#recreate
#id||parent_id||name||URI
0||0||Experimental_Factor_Ontology||NA
1||1596||Osteogenesis imperfecta type 4||http://www.orpha.net/ORDO/Orphanet_216820
2||1826||Mimulus guttatus||http://purl.obolibrary.org/obo/NCBITaxon_4155
3||2165||amyotrophic lateral sclerosis||http://www.ebi.ac.uk/efo/EFO_0000253
4||11025||anal pad specific anlage||http://www.ebi.ac.uk/efo/EFO_0000254
5||13448||amnioserosa anlage in statu nascendi||http://www.ebi.ac.uk/efo/EFO_0000251
6||10652||obsolete_amygdala||http://www.ebi.ac.uk/efo/EFO_0000252
7||10652||obsolete_amnioserosa||http://www.ebi.ac.uk/efo/EFO_0000250
8||2656||anterior endoderm anlage||http://www.ebi.ac.uk/efo/EFO_0000259
9||2656||antennal primordium1||http://www.ebi.ac.uk/efo/EFO_0000257
10||2656||antennal primordium2||http://www.ebi.ac.uk/efo/EFO_0000258
12||1497||angioimmunoblastic T-cell lymphoma||http://www.ebi.ac.uk/efo/EFO_0000255
11||1022||Alexandrium tamarense||http://purl.obolibrary.org/obo/NCBITaxon_2926
14||2656||anlage in statu nascendi||http://www.ebi.ac.uk/efo/EFO_0000256
13||9372||Osteogenesis imperfecta type 5||http://www.orpha.net/ORDO/Orphanet_216828
15||11802||Genetic cardiac rhythm disease||http://www.orpha.net/ORDO/Orphanet_101934
16||583||Autosomal recessive spastic paraplegia type 56||http://www.orpha.net/ORDO/Orphanet_320411
17||2656||adult eye primordium||http://www.ebi.ac.uk/efo/EFO_0000240
18||2656||adult foregut precursor||http://www.ebi.ac.uk/efo/EFO_0000241
19||2656||adult hindgut precursor||http://www.ebi.ac.uk/efo/EFO_0000242
21||15483||Mitochondrial oxidative phosphorylation disorder||http://www.orpha.net/ORDO/Orphanet_223713
20||10652||obsolete_Malpighian tubule||http://www.ebi.ac.uk/efo/EFO_0000243
22||770||GM15590||http://purl.obolibrary.org/obo/CLO_0028103
23||2002||alveolar rhabdomyosarcoma||http://www.ebi.ac.uk/efo/EFO_0000248
24||2165||Alzheimer s disease||http://www.ebi.ac.uk/efo/EFO_0000249
25||2656||adult midgut precursor||http://www.ebi.ac.uk/efo/EFO_0000244
26||2656||adult muscle precursor primordium||http://www.ebi.ac.uk/efo/EFO_0000245
27||2842||age||http://www.ebi.ac.uk/efo/EFO_0000246
28||10652||obsolete_Aicardi syndrome||http://www.ebi.ac.uk/efo/EFO_0000247
29||13470||Autosomal recessive spastic paraplegia type 44||http://www.orpha.net/ORDO/Orphanet_320401
30||10652||obsolete_astrocytic tumor||http://www.ebi.ac.uk/efo/EFO_0000271
31||766||astrocytoma||http://www.ebi.ac.uk/efo/EFO_0000272
32||6244||Limb transversal defect - cardiac anomaly||http://www.orpha.net/ORDO/Orphanet_2492
34||11882||M llerian duct anomalies - limb anomalies||http://www.orpha.net/ORDO/Orphanet_2491
33||1979||asthma||http://www.ebi.ac.uk/efo/EFO_0000270
35||1826||Lilium hybrid division VII||http://purl.obolibrary.org/obo/NCBITaxon_101269
36||8292||atrial fibrillation||http://www.ebi.ac.uk/efo/EFO_0000275
37||10652||obsolete_atrioventricular node||http://www.ebi.ac.uk/efo/EFO_0000276
38||1160||atmosphere||http://www.ebi.ac.uk/efo/EFO_0000273
39||11563||atopic eczema||http://www.ebi.ac.uk/efo/EFO_0000274
40||1761||azoospermia||http://www.ebi.ac.uk/efo/EFO_0000279
41||3229||Cryopyrin-associated periodic syndrome||http://www.orpha.net/ORDO/Orphanet_208650
42||10652||obsolete_cardiac atrium||http://www.ebi.ac.uk/efo/EFO_0000277
44||1403||pancreatitis||http://www.ebi.ac.uk/efo/EFO_0000278
43||7966||Metachondromatosis||http://www.orpha.net/ORDO/Orphanet_2499
45||10567||Syndactyly type 8||http://www.orpha.net/ORDO/Orphanet_2498
47||1022||Emiliania huxleyi||http://purl.obolibrary.org/obo/NCBITaxon_2903
46||7989||Upper limb mesomelic dysplasia||http://www.orpha.net/ORDO/Orphanet_2497
48||583||Spastic paraplegia-optic atrophy-neuropathy syndrome||http://www.orpha.net/ORDO/Orphanet_320406
49||6011||Mesomelia-synostoses syndrome||http://www.orpha.net/ORDO/Orphanet_2496
50||2162||Meningioma||http://www.orpha.net/ORDO/Orphanet_2495
51||5502||Dehalococcoides sp. VS||http://purl.obolibrary.org/obo/NCBITaxon_311424
52||1319||glutamine||http://purl.obolibrary.org/obo/CHEBI_28300
53||1826||Ipomoea batatas||http://purl.obolibrary.org/obo/NCBITaxon_4120
54||5502||Mycobacterium tuberculosis H37Rv||http://purl.obolibrary.org/obo/NCBITaxon_83332
55||5502||Escherichia coli K-12||http://purl.obolibrary.org/obo/NCBITaxon_83333
56||2656||anterior endoderm anlage in statu nascendi||http://www.ebi.ac.uk/efo/EFO_0000260
57||2656||anterior endoderm primordium||http://www.ebi.ac.uk/efo/EFO_0000261
59||5502||Mycobacterium tuberculosis CDC1551||http://purl.obolibrary.org/obo/NCBITaxon_83331
58||7963||Melhem-Fahl syndrome||http://www.orpha.net/ORDO/Orphanet_2482
60||2656||anterior midgut primordium||http://www.ebi.ac.uk/efo/EFO_0000262
61||2656||anterior spiracle specific anlage||http://www.ebi.ac.uk/efo/EFO_0000263
62||8628||antibody||http://www.ebi.ac.uk/efo/EFO_0000264
63||1826||Vitis vinifera||http://purl.obolibrary.org/obo/NCBITaxon_29760
64||10652||obsolete_aorta||http://www.ebi.ac.uk/efo/EFO_0000265
65||2252||Upper limb defect - eye and ear abnormalities||http://www.orpha.net/ORDO/Orphanet_2489
66||1015||aortic stenosis||http://www.ebi.ac.uk/efo/EFO_0000266
67||3392||apical meristem||http://www.ebi.ac.uk/efo/EFO_0000267
68||2656||apoptotic amnioserosa||http://www.ebi.ac.uk/efo/EFO_0000268
69||14816||array design||http://www.ebi.ac.uk/efo/EFO_0000269
70||3560||Melorheostosis||http://www.orpha.net/ORDO/Orphanet_2485
71||1226||Osteodysplasty, Melnick-Needles type||http://www.orpha.net/ORDO/Orphanet_2484
73||11882||Lower limb deficiency - hypospadias||http://www.orpha.net/ORDO/Orphanet_2487
72||1826||Solanum tuberosum||http://purl.obolibrary.org/obo/NCBITaxon_4113
74||5502||Escherichia coli O157:H7||http://purl.obolibrary.org/obo/NCBITaxon_83334
75||10345||Classic pantothenate kinase-associated neurodegeneration||http://www.orpha.net/ORDO/Orphanet_216866
76||10652||obsolete_acute lymphoblastic leukemia||http://www.ebi.ac.uk/efo/EFO_0000219
77||114||acute erythroleukemia||http://www.ebi.ac.uk/efo/EFO_0000218
78||1403||active gastritis||http://www.ebi.ac.uk/efo/EFO_0000217
79||1006||acinar cell carcinoma||http://www.ebi.ac.uk/efo/EFO_0000216
80||2672||abdominal skin||http://www.ebi.ac.uk/efo/EFO_0000214
81||10652||obsolete_abdominal cavity||http://www.ebi.ac.uk/efo/EFO_0000213
82||10652||obsolete_Wilms tumor||http://www.ebi.ac.uk/efo/EFO_0000212
83||1497||unspecified peripheral T-cell lymphoma||http://www.ebi.ac.uk/efo/EFO_0000211
84||10652||obsolete_T lymphocyte||http://www.ebi.ac.uk/efo/EFO_0000210
85||10345||Atypical pantothenate kinase-associated neurodegeneration||http://www.orpha.net/ORDO/Orphanet_216873
86||13701||root meristem||http://purl.obolibrary.org/obo/PO_0006085
87||122||T-cell acute lymphoblastic leukemia||http://www.ebi.ac.uk/efo/EFO_0000209
88||10652||obsolete_K-562 cell||http://purl.obolibrary.org/obo/BTO_0000664
89||12038||primary root apical meristem||http://purl.obolibrary.org/obo/PO_0006081
90||1006||stage I endometrioid carcinoma||http://www.ebi.ac.uk/efo/EFO_0000205
91||10994||baicalin||http://purl.obolibrary.org/obo/CHEBI_2981
92||10652||obsolete_Scott syndrome||http://www.ebi.ac.uk/efo/EFO_0000204
93||10652||obsolete_T-cell lymphoblastic lymphoma||http://www.ebi.ac.uk/efo/EFO_0000207
94||1006||stage II endometrioid carcinoma||http://www.ebi.ac.uk/efo/EFO_0000206
95||10652||obsolete_precursor T lymphoblastic leukemia||http://www.ebi.ac.uk/efo/EFO_0000201
96||7194||plasma cell neoplasm||http://www.ebi.ac.uk/efo/EFO_0000200
97||96||monoclonal gammopathy||http://www.ebi.ac.uk/efo/EFO_0000203
98||10652||obsolete_promyelocytic leukemia||http://www.ebi.ac.uk/efo/EFO_0000202
99||1022||Rhagoletis pomonella||http://purl.obolibrary.org/obo/NCBITaxon_28610
100||5025||Microsporum gallinae||http://purl.obolibrary.org/obo/NCBITaxon_69892
101||5025||Trichophyton soudanense||http://purl.obolibrary.org/obo/NCBITaxon_69891
103||10652||obsolete_adipose tissue brown MMHCC||http://www.ebi.ac.uk/efo/EFO_0000236
102||10994||azithromycin||http://purl.obolibrary.org/obo/CHEBI_2955
104||10652||obsolete_adipose tissue MMHCC||http://www.ebi.ac.uk/efo/EFO_0000235
105||12136||adenosquamous lung carcinoma||http://www.ebi.ac.uk/efo/EFO_0000233
106||5502||Salmonella enterica subsp. enterica serovar Agona||http://purl.obolibrary.org/obo/NCBITaxon_58095
107||2162||adrenal gland pheochromocytoma||http://www.ebi.ac.uk/efo/EFO_0000239
108||10652||obsolete_adrenal cortex||http://www.ebi.ac.uk/efo/EFO_0000237
109||15417||adenoma||http://www.ebi.ac.uk/efo/EFO_0000232
110||1006||adenoid cystic carcinoma||http://www.ebi.ac.uk/efo/EFO_0000231
111||10652||obsolete_adenohypophysis||http://www.ebi.ac.uk/efo/EFO_0000230
112||114||acute myelomonocytic leukemia||http://www.ebi.ac.uk/efo/EFO_0000223
114||1508||acute myeloid leukemia||http://www.ebi.ac.uk/efo/EFO_0000222
113||770||brain cancer cell line||http://purl.obolibrary.org/obo/BTO_0000690
115||8848||acute quadriplegic myopathy||http://www.ebi.ac.uk/efo/EFO_0000225
116||114||acute promyelocytic leukemia||http://www.ebi.ac.uk/efo/EFO_0000224
117||10652||obsolete_adductor mandibulae complex||http://www.ebi.ac.uk/efo/EFO_0000227
118||2656||adaxial cells||http://www.ebi.ac.uk/efo/EFO_0000226
119||10652||obsolete_adenohypophyseal placode||http://www.ebi.ac.uk/efo/EFO_0000229
120||1006||adenocarcinoma||http://www.ebi.ac.uk/efo/EFO_0000228
121||114||acute monocytic leukemia||http://www.ebi.ac.uk/efo/EFO_0000221
122||15411||acute lymphoblastic leukemia||http://www.ebi.ac.uk/efo/EFO_0000220
123||15020||RNA stability design||http://www.ebi.ac.uk/efo/EFO_0001783
124||10652||obsolete_family history design||http://www.ebi.ac.uk/efo/EFO_0001782
125||618||late embryonic stage||http://purl.obolibrary.org/obo/UBERON_0007220
126||10652||obsolete_disease state design||http://www.ebi.ac.uk/efo/EFO_0001781
127||15020||clinical history design||http://www.ebi.ac.uk/efo/EFO_0001780
128||5025||Microsporum distortum||http://purl.obolibrary.org/obo/NCBITaxon_101202
129||2672||breast||http://purl.obolibrary.org/obo/UBERON_0000310
130||12431||Congenital macroglossia||http://www.orpha.net/ORDO/Orphanet_2430
131||1826||Cycas rumphii||http://purl.obolibrary.org/obo/NCBITaxon_58031
133||12372||Hereditary inclusion body myopathy type 4||http://www.orpha.net/ORDO/Orphanet_324381
132||5300||Macrosomia - microphthalmia - cleft palate||http://www.orpha.net/ORDO/Orphanet_2432
134||8247||CD38-positive naive B cell||http://purl.obolibrary.org/obo/CL_0002101
135||7418||Central bilateral macrogyria||http://www.orpha.net/ORDO/Orphanet_2431
136||8247||CD38-negative naive B cell||http://purl.obolibrary.org/obo/CL_0002102
138||15011||translational bias design||http://www.ebi.ac.uk/efo/EFO_0001787
137||10595||IgG-positive double negative memory B cell||http://purl.obolibrary.org/obo/CL_0002103
140||15011||secreted protein identification design||http://www.ebi.ac.uk/efo/EFO_0001786
139||10595||IgG-negative double negative memory B cell||http://purl.obolibrary.org/obo/CL_0002104
141||15011||operon identification design||http://www.ebi.ac.uk/efo/EFO_0001785
142||10494||CD38-positive IgG memory B cell||http://purl.obolibrary.org/obo/CL_0002105
144||15011||genotyping design||http://www.ebi.ac.uk/efo/EFO_0001784
145||142||IgD-positive CD38-positive IgG memory B cell||http://purl.obolibrary.org/obo/CL_0002106
143||5897||Hypo- and hypermelanotic cutaneous macules - retarded growth - intellectual disability||http://www.orpha.net/ORDO/Orphanet_2435
146||4139||Split hand - urinary anomalies - spina bifida||http://www.orpha.net/ORDO/Orphanet_2437
147||10494||CD38-negative IgG memory B cell||http://purl.obolibrary.org/obo/CL_0002108
148||2021||Hand-foot-genital syndrome||http://www.orpha.net/ORDO/Orphanet_2438
149||142||IgD-negative CD38-positive IgG memory B cell||http://purl.obolibrary.org/obo/CL_0002107
150||1171||Patterson-Stevenson-Fontaine syndrome||http://www.orpha.net/ORDO/Orphanet_2439
151||134||B220-positive CD38-positive naive B cell||http://purl.obolibrary.org/obo/CL_0002109
152||5502||Lactobacillus pontis||http://purl.obolibrary.org/obo/NCBITaxon_35787
153||15024||loop design||http://www.ebi.ac.uk/efo/EFO_0001770
154||15026||operator variation design||http://www.ebi.ac.uk/efo/EFO_0001772
155||15026||normalization testing design||http://www.ebi.ac.uk/efo/EFO_0001771
156||3636||late embryo||http://purl.obolibrary.org/obo/UBERON_0000323
157||15026||software variation design||http://www.ebi.ac.uk/efo/EFO_0001778
158||162||B220-positive CD38-negative unswitched memory B cell||http://purl.obolibrary.org/obo/CL_0002112
159||15024||self vs self design||http://www.ebi.ac.uk/efo/EFO_0001777
160||162||B220-low CD38-negative unswitched memory B cell||http://purl.obolibrary.org/obo/CL_0002113
161||134||B220-low CD38-positive naive B cell||http://purl.obolibrary.org/obo/CL_0002110
163||15020||time series design||http://www.ebi.ac.uk/efo/EFO_0001779
162||10487||CD38-negative unswitched memory B cell||http://purl.obolibrary.org/obo/CL_0002111
165||15026||quality control testing design||http://www.ebi.ac.uk/efo/EFO_0001774
164||168||B220-low CD38-positive unswitched memory B cell||http://purl.obolibrary.org/obo/CL_0002116
167||15026||optimization design||http://www.ebi.ac.uk/efo/EFO_0001773
166||10485||IgG-negative class switched memory B cell||http://purl.obolibrary.org/obo/CL_0002117
169||15026||replicate design||http://www.ebi.ac.uk/efo/EFO_0001776
168||10487||CD38-positive unswitched memory B cell||http://purl.obolibrary.org/obo/CL_0002114
172||15026||reference design||http://www.ebi.ac.uk/efo/EFO_0001775
170||168||B220-positive CD38-positive unswitched memory B cell||http://purl.obolibrary.org/obo/CL_0002115
171||5025||Drechslera sp.||http://purl.obolibrary.org/obo/NCBITaxon_67606
174||583||Macrocephaly - spastic paraplegia - dysmorphism||http://www.orpha.net/ORDO/Orphanet_2429
173||5002||Benign recurrent intrahepatic cholestasis||http://www.orpha.net/ORDO/Orphanet_65682
175||166||CD38-positive IgG-negative class switched memory B cell||http://purl.obolibrary.org/obo/CL_0002119
176||2252||Macrocephaly - short stature - paraplegia||http://www.orpha.net/ORDO/Orphanet_2427
177||166||CD38-negative IgG-negative class switched memory B cell||http://purl.obolibrary.org/obo/CL_0002118
178||8190||benzoic acid||http://purl.obolibrary.org/obo/CHEBI_30746
179||2672||colonic mucosa||http://purl.obolibrary.org/obo/UBERON_0000317
181||10994||ethylene glycol||http://purl.obolibrary.org/obo/CHEBI_30742
180||1826||Spartina alterniflora||http://purl.obolibrary.org/obo/NCBITaxon_29706
182||1022||Ustilago maydis||http://purl.obolibrary.org/obo/NCBITaxon_5270
183||7418||Isolated focal cortical dysplasia||http://www.orpha.net/ORDO/Orphanet_65683
184||10994||dibutyl phthalate||http://purl.obolibrary.org/obo/CHEBI_34687
185||770||GM13883||http://purl.obolibrary.org/obo/CLO_0033199
186||12769||Dislocation of the hip - dysmorphism||http://www.orpha.net/ORDO/Orphanet_2412
187||7943||Mixed sclerosing bone dystrophy with extra-skeletal manifestations||http://www.orpha.net/ORDO/Orphanet_324364
189||10994||diazinon||http://purl.obolibrary.org/obo/CHEBI_34682
188||5478||Congenital pulmonary lymphangiectasia||http://www.orpha.net/ORDO/Orphanet_2414
190||1767||Hypergonadotropic hypogonadism - cataract syndrome||http://www.orpha.net/ORDO/Orphanet_2410
191||13496||Ovine herpesvirus 2||http://purl.obolibrary.org/obo/NCBITaxon_10398
192||615||Congenital primary lymphedema||http://www.orpha.net/ORDO/Orphanet_2416
193||194||Constitutional neutropenia||http://www.orpha.net/ORDO/Orphanet_101987
194||201||Primary immunodeficiency due to a defect in innate immunity||http://www.orpha.net/ORDO/Orphanet_101988
195||5292||single-organism metabolic process||http://purl.obolibrary.org/obo/GO_0044710
196||649||single-multicellular organism process||http://purl.obolibrary.org/obo/GO_0044707
198||442||submitted||http://www.ebi.ac.uk/efo/EFO_0001794
197||649||single organism signaling||http://purl.obolibrary.org/obo/GO_0044700
199||442||published||http://www.ebi.ac.uk/efo/EFO_0001796
200||442||in preparation||http://www.ebi.ac.uk/efo/EFO_0001795
201||4135||Primary immunodeficiency||http://www.orpha.net/ORDO/Orphanet_101997
202||9901||Congenital achiasma||http://www.orpha.net/ORDO/Orphanet_324353
203||4571||ethnic group||http://www.ebi.ac.uk/efo/EFO_0001799
204||194||Immunodeficiency due to a complement cascade protein anomaly||http://www.orpha.net/ORDO/Orphanet_101992
205||5700||Lowe-Kohn-Cohen syndrome||http://www.orpha.net/ORDO/Orphanet_2408
206||2252||Lowry-MacLean syndrome||http://www.orpha.net/ORDO/Orphanet_2409
207||5053||LOC syndrome||http://www.orpha.net/ORDO/Orphanet_2407
208||5700||Thickened earlobes - conductive deafness||http://www.orpha.net/ORDO/Orphanet_2405
209||6072||Semilobar holoprosencephaly||http://www.orpha.net/ORDO/Orphanet_220386
210||12769||McKusick-Kaufman syndrome||http://www.orpha.net/ORDO/Orphanet_2473
211||772||capillary endothelial cell||http://purl.obolibrary.org/obo/CL_0002144
212||5048||Genetic chronic primary adrenal insufficiency||http://www.orpha.net/ORDO/Orphanet_101960
213||12769||White forelock with malformations||http://www.orpha.net/ORDO/Orphanet_2475
214||5025||Fusarium solani||http://purl.obolibrary.org/obo/NCBITaxon_169388
215||5300||Medeira-Dennis-Donnai syndrome||http://www.orpha.net/ORDO/Orphanet_2476
217||15549||Megalencephalic leukoencephalopathy with subcortical cysts||http://www.orpha.net/ORDO/Orphanet_2478
216||10652||obsolete_bone MMHCC||http://www.ebi.ac.uk/efo/EFO_0000299
218||4139||Megalocornea-intellectual disability syndrome||http://www.orpha.net/ORDO/Orphanet_2479
219||10652||obsolete_blood||http://www.ebi.ac.uk/efo/EFO_0000296
220||10652||obsolete_blastocyst||http://www.ebi.ac.uk/efo/EFO_0000295
221||2672||bone||http://www.ebi.ac.uk/efo/EFO_0000298
222||1006||bladder carcinoma||http://www.ebi.ac.uk/efo/EFO_0000292
224||5053||Matthew-Wood syndrome||http://www.orpha.net/ORDO/Orphanet_2470
223||10652||obsolete_bladder MMHCC||http://www.ebi.ac.uk/efo/EFO_0000291
226||2252||McDonough syndrome||http://www.orpha.net/ORDO/Orphanet_2471
225||2162||bladder tumor||http://www.ebi.ac.uk/efo/EFO_0000294
227||2672||bladder mucosa||http://www.ebi.ac.uk/efo/EFO_0000293
228||10252||Severe hemophilia B||http://www.orpha.net/ORDO/Orphanet_169793
229||10252||Moderately severe hemophilia B||http://www.orpha.net/ORDO/Orphanet_169796
230||10252||Mild hemophilia B||http://www.orpha.net/ORDO/Orphanet_169799
231||13496||Human herpesvirus 4||http://purl.obolibrary.org/obo/NCBITaxon_10376
232||6770||Marfanoid syndrome, De Silva type||http://www.orpha.net/ORDO/Orphanet_2464
233||13496||Herpesvirus saimiri (strain 11)||http://purl.obolibrary.org/obo/NCBITaxon_10383
235||2252||Shprintzen-Goldberg syndrome||http://www.orpha.net/ORDO/Orphanet_2462
234||9343||echinocyte||http://purl.obolibrary.org/obo/CL_0002155
237||2252||Marfanoid habitus - intellectual disability, autosomal recessive||http://www.orpha.net/ORDO/Orphanet_2463
236||10090||early promyelocyte||http://purl.obolibrary.org/obo/CL_0002154
238||8386||Combined T and B cell immunodeficiency||http://www.orpha.net/ORDO/Orphanet_101972
239||2102||bipolar disorder||http://www.ebi.ac.uk/efo/EFO_0000289
240||7380||MASA syndrome||http://www.orpha.net/ORDO/Orphanet_2466
241||14756||biopsy site||http://www.ebi.ac.uk/efo/EFO_0000288
242||14970||biopsy number||http://www.ebi.ac.uk/efo/EFO_0000287
244||10994||chlorpyrifos||http://purl.obolibrary.org/obo/CHEBI_34631
243||10652||obsolete_biomaterial factor||http://www.ebi.ac.uk/efo/EFO_0000286
245||649||single-organism developmental process||http://purl.obolibrary.org/obo/GO_0044767
246||1824||benign prostatic hyperplasia||http://www.ebi.ac.uk/efo/EFO_0000284
247||13883||behavioral stimulus||http://www.ebi.ac.uk/efo/EFO_0000283
248||12083||Van den Ende-Gupta syndrome||http://www.orpha.net/ORDO/Orphanet_2460
249||2252||Marden-Walker syndrome||http://www.orpha.net/ORDO/Orphanet_2461
250||7925||basal-like carcinoma||http://www.ebi.ac.uk/efo/EFO_0000281
251||10090||late promyelocyte||http://purl.obolibrary.org/obo/CL_0002151
253||2672||presumptive hindbrain||http://purl.obolibrary.org/obo/UBERON_0007277
252||1403||Barrett s esophagus||http://www.ebi.ac.uk/efo/EFO_0000280
254||5965||Hereditary poikiloderma||http://www.orpha.net/ORDO/Orphanet_222628
255||7589||epitheloid cell||http://purl.obolibrary.org/obo/CL_0002150
256||13448||blastocyst||http://purl.obolibrary.org/obo/UBERON_0000358
257||10652||obsolete_bladder||http://www.ebi.ac.uk/efo/EFO_0000290
258||649||single-organism transport||http://purl.obolibrary.org/obo/GO_0044765
259||649||single-organism cellular process||http://purl.obolibrary.org/obo/GO_0044763
260||8386||Immunodeficiency predominantly affecting antibody production||http://www.orpha.net/ORDO/Orphanet_101977
261||8218||CD25-positive, CD27-positive immature gamma-delta T cell||http://purl.obolibrary.org/obo/CL_0002126
262||10064||CD27-negative gamma-delta T cell||http://purl.obolibrary.org/obo/CL_0002125
263||2322||Mandibuloacral dysplasia||http://www.orpha.net/ORDO/Orphanet_2457
264||10471||Tc17 cell||http://purl.obolibrary.org/obo/CL_0002128
265||10465||innate effector T cell||http://purl.obolibrary.org/obo/CL_0002127
266||10721||Rare metabolic liver disease||http://www.orpha.net/ORDO/Orphanet_101940
268||175||B220-positive CD38-positive IgG-negative class switched memory B cell||http://purl.obolibrary.org/obo/CL_0002122
267||10694||Mucocutaneous venous malformations||http://www.orpha.net/ORDO/Orphanet_2451
269||177||CD24-negative CD38-negative IgG-negative class switched memory B cell||http://purl.obolibrary.org/obo/CL_0002121
270||10064||CD27-positive gamma-delta T cell||http://purl.obolibrary.org/obo/CL_0002124
272||175||B220-low CD38-positive IgG-negative class switched memory B cell||http://purl.obolibrary.org/obo/CL_0002123
271||6770||Familial intestinal malrotation - facial anomalies||http://www.orpha.net/ORDO/Orphanet_2454
273||2672||presumptive forebrain midbrain boundary||http://purl.obolibrary.org/obo/UBERON_0007288
274||177||CD24-positive CD38-negative IgG-negative class switched memory B cell||http://purl.obolibrary.org/obo/CL_0002120
275||2672||presumptive shield||http://purl.obolibrary.org/obo/UBERON_0007283
276||2672||presumptive neural plate||http://purl.obolibrary.org/obo/UBERON_0007284
277||2672||presumptive paraxial mesoderm||http://purl.obolibrary.org/obo/UBERON_0007285
278||2672||presumptive floor plate||http://purl.obolibrary.org/obo/UBERON_0007286
279||1171||Acrofacial dysostosis, Kennedy-Teebi type||http://www.orpha.net/ORDO/Orphanet_64542
280||2672||presumptive segmental plate||http://purl.obolibrary.org/obo/UBERON_0007282
281||2672||presumptive midbrain hindbrain boundary||http://purl.obolibrary.org/obo/UBERON_0007281
282||8190||clofibric acid||http://purl.obolibrary.org/obo/CHEBI_34648
283||2672||corpus striatum||http://purl.obolibrary.org/obo/UBERON_0000369
284||9372||Osteogenesis imperfecta type 2||http://www.orpha.net/ORDO/Orphanet_216804
286||1022||Cryptococcus neoformans||http://purl.obolibrary.org/obo/NCBITaxon_5207
285||5267||Rare dyslipidemia||http://www.orpha.net/ORDO/Orphanet_101953
287||3790||X-linked lymphoproliferative disease||http://www.orpha.net/ORDO/Orphanet_2442
288||21||Mitochondrial oxidative phosphorylation disorder due to nuclear DNA anomalies||http://www.orpha.net/ORDO/Orphanet_2443
290||13823||Split hand-split foot malformation||http://www.orpha.net/ORDO/Orphanet_2440
289||10994||LY294002||http://purl.obolibrary.org/obo/CHEBI_65329
291||2672||musculature of body||http://purl.obolibrary.org/obo/UBERON_0000383
292||13689||presumptive pronephric mesoderm||http://purl.obolibrary.org/obo/UBERON_0007297
293||2672||presumptive rhombomere 7||http://purl.obolibrary.org/obo/UBERON_0007294
294||2672||presumptive rhombomere 8||http://purl.obolibrary.org/obo/UBERON_0007295
295||2672||presumptive rhombomere 6||http://purl.obolibrary.org/obo/UBERON_0007293
296||2672||presumptive rhombomere 5||http://purl.obolibrary.org/obo/UBERON_0007292
298||2672||presumptive rhombomere 4||http://purl.obolibrary.org/obo/UBERON_0007291
297||1826||Gossypium arboreum||http://purl.obolibrary.org/obo/NCBITaxon_29729
299||2672||presumptive rhombomere 3||http://purl.obolibrary.org/obo/UBERON_0007290
301||13496||Human herpesvirus 5 strain Towne||http://purl.obolibrary.org/obo/NCBITaxon_10363
300||10994||typhasterol||http://purl.obolibrary.org/obo/CHEBI_27173
302||5502||Bacteroides fragilis YCH46||http://purl.obolibrary.org/obo/NCBITaxon_295405
304||1596||Osteogenesis imperfecta type 3||http://www.orpha.net/ORDO/Orphanet_216812
303||5061||Pituitary deficiency||http://www.orpha.net/ORDO/Orphanet_101957
305||6610||Craniosynostosis - anal anomalies - porokeratosis||http://www.orpha.net/ORDO/Orphanet_85199
306||5317||Ectodermal dysplasia syndrome||http://www.orpha.net/ORDO/Orphanet_79373
307||5954||Syndromic nail anomaly||http://www.orpha.net/ORDO/Orphanet_79370
308||7966||Genochondromatosis type 1||http://www.orpha.net/ORDO/Orphanet_85197
309||7966||Dysspondyloenchondromatosis||http://www.orpha.net/ORDO/Orphanet_85198
310||7939||Familial expansile osteolysis||http://www.orpha.net/ORDO/Orphanet_85195
311||9572||Nodulosis-arthropathy-osteolysis syndrome||http://www.orpha.net/ORDO/Orphanet_85196
312||7942||Idiopathic juvenile osteoporosis||http://www.orpha.net/ORDO/Orphanet_85193
315||13195||Caenorhabditis remanei||http://purl.obolibrary.org/obo/NCBITaxon_31234
313||1022||Melospiza melodia||http://purl.obolibrary.org/obo/NCBITaxon_44397
314||7942||Spondylo-ocular syndrome||http://www.orpha.net/ORDO/Orphanet_85194
316||7942||Singleton-Merten dysplasia||http://www.orpha.net/ORDO/Orphanet_85191
317||7942||Calvarial doughnut lesions - bone fragility||http://www.orpha.net/ORDO/Orphanet_85192
318||10994||thioacetamide||http://purl.obolibrary.org/obo/CHEBI_32497
319||1022||Athelia rolfsii||http://purl.obolibrary.org/obo/NCBITaxon_39291
320||10994||hexachlorobenzene||http://purl.obolibrary.org/obo/CHEBI_5692
321||5951||Alopecia||http://www.orpha.net/ORDO/Orphanet_79364
322||5951||Hypertrichosis||http://www.orpha.net/ORDO/Orphanet_79365
323||5951||Isolated hair shaft abnormality||http://www.orpha.net/ORDO/Orphanet_79366
324||5961||Endosteal sclerosis - cerebellar hypoplasia||http://www.orpha.net/ORDO/Orphanet_85186
325||5965||Other genetic epidermal disease||http://www.orpha.net/ORDO/Orphanet_79360
327||5965||Inherited epidermolysis bullosa||http://www.orpha.net/ORDO/Orphanet_79361
326||7943||Metaphyseal dysplasia, Braun-Tinschert type||http://www.orpha.net/ORDO/Orphanet_85188
328||4740||Diaphyseal medullary stenosis - bone malignancy||http://www.orpha.net/ORDO/Orphanet_85182
329||7943||Craniometadiaphyseal dysplasia, wormian bone type||http://www.orpha.net/ORDO/Orphanet_85184
330||5951||Syndromic hair shaft abnormality||http://www.orpha.net/ORDO/Orphanet_79367
331||5954||Isolated nail anomaly||http://www.orpha.net/ORDO/Orphanet_79369
332||7991||Severe lateral tibial bowing with short stature||http://www.orpha.net/ORDO/Orphanet_324307
333||10187||melanophage||http://purl.obolibrary.org/obo/CL_0002060
334||8696||T-helper 9 cell||http://purl.obolibrary.org/obo/CL_0002061
335||11199||derived mass unit||http://www.ebi.ac.uk/efo/EFO_0001703
336||5838||temperature||http://www.ebi.ac.uk/efo/EFO_0001702
337||10907||Congenital non-bullous ichthyosiform erythroderma||http://www.orpha.net/ORDO/Orphanet_79394
338||8938||Keratoderma hereditarium mutilans with ichthyosis||http://www.orpha.net/ORDO/Orphanet_79395
339||7946||Astley-Kendall dysplasia||http://www.orpha.net/ORDO/Orphanet_85175
340||12736||Generalized epidermolysis bullosa simplex, non-Dowling-Meara type||http://www.orpha.net/ORDO/Orphanet_79399
342||12736||Epidermolysis bullosa simplex, Dowling-Meara type||http://www.orpha.net/ORDO/Orphanet_79396
341||3560||Infantile osteopetrosis with neuroaxonal dysplasia||http://www.orpha.net/ORDO/Orphanet_85179
343||1598||volume||http://www.ebi.ac.uk/efo/EFO_0001715
344||12736||Epidermolysis bullosa simplex with mottled pigmentation||http://www.orpha.net/ORDO/Orphanet_79397
345||5502||Pseudonocardia dioxanivorans||http://purl.obolibrary.org/obo/NCBITaxon_240495
346||7989||Mesomelic dysplasia, Savarirayan type||http://www.orpha.net/ORDO/Orphanet_85170
347||212||IMAGe syndrome||http://www.orpha.net/ORDO/Orphanet_85173
348||5306||Pseudodiastrophic dysplasia||http://www.orpha.net/ORDO/Orphanet_85174
349||2318||Microcephalic osteodysplastic dysplasia, Saul-Wilson type||http://www.orpha.net/ORDO/Orphanet_85172
350||770||GM17128||http://purl.obolibrary.org/obo/CLO_0015128
351||1826||Manihot esculenta||http://purl.obolibrary.org/obo/NCBITaxon_3983
352||770||GM17127||http://purl.obolibrary.org/obo/CLO_0015126
353||10058||Fraction C  precursor B cell||http://purl.obolibrary.org/obo/CL_0002050
354||1826||Ricinus communis||http://purl.obolibrary.org/obo/NCBITaxon_3988
355||10527||CD38-high pre-BCR positive cell||http://purl.obolibrary.org/obo/CL_0002051
356||10058||Fraction D precursor B cell||http://purl.obolibrary.org/obo/CL_0002052
357||10524||CD22-positive, CD38-low small pre-B cell||http://purl.obolibrary.org/obo/CL_0002053
358||10054||Fraction E immature B cell||http://purl.obolibrary.org/obo/CL_0002054
359||10054||CD38-negative immature B cell||http://purl.obolibrary.org/obo/CL_0002055
360||770||GM17124||http://purl.obolibrary.org/obo/CLO_0015121
361||8239||Fraction F mature B cell||http://purl.obolibrary.org/obo/CL_0002056
362||10176||CD14-positive, CD16-negative classical monocyte||http://purl.obolibrary.org/obo/CL_0002057
364||7918||Juvenile Huntington disease||http://www.orpha.net/ORDO/Orphanet_248111
363||10167||Gr1-low non-classical monocyte||http://purl.obolibrary.org/obo/CL_0002058
365||770||GM17126||http://purl.obolibrary.org/obo/CLO_0015124
366||10541||CD8alpha-positive thymic conventional dendritic cell||http://purl.obolibrary.org/obo/CL_0002059
368||1826||Lilium regale||http://purl.obolibrary.org/obo/NCBITaxon_82328
367||770||GM17125||http://purl.obolibrary.org/obo/CLO_0015123
369||7963||Camptodactyly - tall stature - scoliosis - hearing loss||http://www.orpha.net/ORDO/Orphanet_85164
370||325||Severe achondroplasia - developmental delay - acanthosis nigricans||http://www.orpha.net/ORDO/Orphanet_85165
372||15383||Lymphedema||http://www.orpha.net/ORDO/Orphanet_79383
373||10994||sodium nitroprusside||http://purl.obolibrary.org/obo/CHEBI_29321
371||7981||Platyspondylic dysplasia, Torrance type||http://www.orpha.net/ORDO/Orphanet_85166
374||10144||Spondylometaphyseal dysplasia - cone-rod dystrophy||http://www.orpha.net/ORDO/Orphanet_85167
375||15383||Unclassified genetic skin disorder||http://www.orpha.net/ORDO/Orphanet_79385
376||7986||Craniofacial conodysplasia||http://www.orpha.net/ORDO/Orphanet_85168
377||2021||Familial digital arthropathy-brachydactyly||http://www.orpha.net/ORDO/Orphanet_85169
378||15383||Metabolic disease with skin involvement||http://www.orpha.net/ORDO/Orphanet_79387
379||6573||array manufacturer||http://www.ebi.ac.uk/efo/EFO_0001728
380||378||Mucopolysaccharidosis with skin involvement||http://www.orpha.net/ORDO/Orphanet_79388
381||6573||biomaterial provider||http://www.ebi.ac.uk/efo/EFO_0001729
382||15383||Premature aging||http://www.orpha.net/ORDO/Orphanet_79389
383||4706||Facial onset sensory and motor neuronopathy||http://www.orpha.net/ORDO/Orphanet_85162
384||4139||Hypomyelination - congenital cataract||http://www.orpha.net/ORDO/Orphanet_85163
385||1826||Euphorbia esula||http://purl.obolibrary.org/obo/NCBITaxon_3993
386||770||GM17121||http://purl.obolibrary.org/obo/CLO_0015115
387||770||GM17122||http://purl.obolibrary.org/obo/CLO_0015117
388||770||GM17123||http://purl.obolibrary.org/obo/CLO_0015119
389||10463||immature NK T cell stage IV||http://purl.obolibrary.org/obo/CL_0002042
391||11888||Quebec platelet disorder||http://www.orpha.net/ORDO/Orphanet_220436
390||10087||CD34-positive, CD38-negative multipotent progenitor cell||http://purl.obolibrary.org/obo/CL_0002043
392||10463||immature NK T cell stage II||http://purl.obolibrary.org/obo/CL_0002040
393||10463||immature NK T cell stage III||http://purl.obolibrary.org/obo/CL_0002041
394||10112||Early pro-B cell||http://purl.obolibrary.org/obo/CL_0002046
395||13415||Fraction B precursor B cell||http://purl.obolibrary.org/obo/CL_0002047
396||868||Kit-positive, integrin beta7-high basophil mast progenitor cell||http://purl.obolibrary.org/obo/CL_0002044
398||3854||Methanobacteria||http://purl.obolibrary.org/obo/NCBITaxon_183925
397||10112||Fraction A pre-pro B cell||http://purl.obolibrary.org/obo/CL_0002045
399||770||GM17120||http://purl.obolibrary.org/obo/CLO_0015112
401||11506||femtometer||http://www.ebi.ac.uk/efo/EFO_0001721
400||10058||late pro-B cell||http://purl.obolibrary.org/obo/CL_0002048
402||13415||Fraction C precursor B cell||http://purl.obolibrary.org/obo/CL_0002049
403||4406||Bleeding diathesis due to thromboxane synthesis deficiency||http://www.orpha.net/ORDO/Orphanet_220443
404||4736||Micrencephaly - corpus callosum agenesis - abnormal genitalia||http://www.orpha.net/ORDO/Orphanet_2508
405||6573||investigator||http://www.ebi.ac.uk/efo/EFO_0001739
406||6573||institution||http://www.ebi.ac.uk/efo/EFO_0001738
407||6573||hardware manufacturer||http://www.ebi.ac.uk/efo/EFO_0001737
408||8001||Metaphyseal dysplasia - maxillary hypoplasia - brachydacty||http://www.orpha.net/ORDO/Orphanet_2504
409||382||Acroosteolysis-keloid-like lesions-premature aging syndrome||http://www.orpha.net/ORDO/Orphanet_363665
410||375||Multiple benign circumferential skin creases on limbs||http://www.orpha.net/ORDO/Orphanet_2505
411||6573||consortium member||http://www.ebi.ac.uk/efo/EFO_0001731
412||382||Acrogeria||http://www.orpha.net/ORDO/Orphanet_2500
413||6573||consultant||http://www.ebi.ac.uk/efo/EFO_0001732
414||8001||Metaphyseal chondrodysplasia, Spahr type||http://www.orpha.net/ORDO/Orphanet_2501
415||4139||Metaphyseal dysostosis - intellectual disability - conductive deafness||http://www.orpha.net/ORDO/Orphanet_2502
416||6573||biosequence provider||http://www.ebi.ac.uk/efo/EFO_0001730
417||6573||data coder||http://www.ebi.ac.uk/efo/EFO_0001735
418||6573||funder||http://www.ebi.ac.uk/efo/EFO_0001736
419||6573||curator||http://www.ebi.ac.uk/efo/EFO_0001733
421||15365||Congenital vitamin K-dependent coagulation factors deficiency||http://www.orpha.net/ORDO/Orphanet_169826
420||6573||data analyst||http://www.ebi.ac.uk/efo/EFO_0001734
422||8191||cyproheptadine hydrochloride||http://purl.obolibrary.org/obo/CHEBI_59695
423||10994||thyroxine||http://purl.obolibrary.org/obo/CHEBI_30660
424||426||Macrothrombocytopenia with mitral valve insufficiency||http://www.orpha.net/ORDO/Orphanet_220448
425||1022||Plasmodium chabaudi chabaudi||http://purl.obolibrary.org/obo/NCBITaxon_31271
426||4406||Inherited giant platelet disorder||http://www.orpha.net/ORDO/Orphanet_220452
427||15020||innate behavior design||http://www.ebi.ac.uk/efo/EFO_0001749
428||15020||genotype design||http://www.ebi.ac.uk/efo/EFO_0001748
429||2403||Scapuloperoneal amyotrophy||http://www.orpha.net/ORDO/Orphanet_85146
430||2252||Microcephaly - seizures - intellectual disability - heart disease||http://www.orpha.net/ORDO/Orphanet_2519
431||9748||Autosomal recessive chorioretinopathy-microcephaly||http://www.orpha.net/ORDO/Orphanet_2518
432||7419||DNA methylation||http://purl.obolibrary.org/obo/GO_0006306
433||9607||Microcephaly - cardiac defect - lung malsegmentation||http://www.orpha.net/ORDO/Orphanet_2516
434||2252||Microcephaly - cardiomyopathy||http://www.orpha.net/ORDO/Orphanet_2515
435||13306||Autosomal dominant microcephaly||http://www.orpha.net/ORDO/Orphanet_2514
436||6573||software manufacturer||http://www.ebi.ac.uk/efo/EFO_0001740
437||9748||Autosomal recessive primary microcephaly||http://www.orpha.net/ORDO/Orphanet_2512
438||12769||Microcephaly - albinism - digital anomalies||http://www.orpha.net/ORDO/Orphanet_2513
439||6573||submitter||http://www.ebi.ac.uk/efo/EFO_0001741
440||9693||Childhood-onset autosomal recessive myopathy with external ophthalmoplegia||http://www.orpha.net/ORDO/Orphanet_363677
442||15538||publication status||http://www.ebi.ac.uk/efo/EFO_0001742
441||1419||Micro syndrome||http://www.orpha.net/ORDO/Orphanet_2510
443||15020||cell component comparison design||http://www.ebi.ac.uk/efo/EFO_0001743
444||2252||Microbrachycephaly - ptosis - cleft lip||http://www.orpha.net/ORDO/Orphanet_2511
445||15020||cell cycle design||http://www.ebi.ac.uk/efo/EFO_0001744
446||15020||cell type comparison design||http://www.ebi.ac.uk/efo/EFO_0001745
447||15020||development or differentiation design||http://www.ebi.ac.uk/efo/EFO_0001746
448||15020||imprinting design||http://www.ebi.ac.uk/efo/EFO_0001747
449||238||Laron syndrome with immunodeficiency||http://www.orpha.net/ORDO/Orphanet_220465
450||3833||Attenuated familial adenomatous polyposis||http://www.orpha.net/ORDO/Orphanet_220460
451||3049||Familial hyperaldosteronism||http://www.orpha.net/ORDO/Orphanet_235936
452||13470||Autosomal recessive spastic paraplegia type 46||http://www.orpha.net/ORDO/Orphanet_320391
453||2252||Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome||http://www.orpha.net/ORDO/Orphanet_363686
454||13470||Autosomal recessive spastic paraplegia type 45||http://www.orpha.net/ORDO/Orphanet_320396
455||15549||Cystic leukoencephalopathy without megalencephaly||http://www.orpha.net/ORDO/Orphanet_85136
456||2252||2p13.2 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_363680
457||15020||growth condition design||http://www.ebi.ac.uk/efo/EFO_0001759
458||15020||dose response design||http://www.ebi.ac.uk/efo/EFO_0001757
459||15020||genetic modification design||http://www.ebi.ac.uk/efo/EFO_0001758
460||15020||compound treatment design||http://www.ebi.ac.uk/efo/EFO_0001755
461||15020||disease state design||http://www.ebi.ac.uk/efo/EFO_0001756
462||15020||species design||http://www.ebi.ac.uk/efo/EFO_0001753
463||15020||strain or line design||http://www.ebi.ac.uk/efo/EFO_0001754
465||15020||organism status design||http://www.ebi.ac.uk/efo/EFO_0001751
464||9624||Pre-Descemet corneal dystrophy||http://www.orpha.net/ORDO/Orphanet_293462
466||15020||sex design||http://www.ebi.ac.uk/efo/EFO_0001752
467||4139||9p13 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_324313
468||15020||organism part comparison design||http://www.ebi.ac.uk/efo/EFO_0001750
469||8190||uric acid||http://purl.obolibrary.org/obo/CHEBI_27226
470||10994||phosgene||http://purl.obolibrary.org/obo/CHEBI_29365
471||4810||Hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome||http://www.orpha.net/ORDO/Orphanet_363694
473||9965||Bothnia retinal dystrophy||http://www.orpha.net/ORDO/Orphanet_85128
472||10652||obsolete_ex vivo design||http://www.ebi.ac.uk/efo/EFO_0001766
474||15026||hardware variation design||http://www.ebi.ac.uk/efo/EFO_0001767
475||7731||nuocyte||http://purl.obolibrary.org/obo/CL_0002089
476||10652||obsolete_in vitro design||http://www.ebi.ac.uk/efo/EFO_0001768
477||10652||obsolete_in vivo design||http://www.ebi.ac.uk/efo/EFO_0001769
479||15020||stimulus or stress design||http://www.ebi.ac.uk/efo/EFO_0001762
478||770||GM10843||http://purl.obolibrary.org/obo/CLO_0023785
480||15024||all pairs||http://www.ebi.ac.uk/efo/EFO_0001763
481||15024||array platform variation design||http://www.ebi.ac.uk/efo/EFO_0001764
482||770||GM10845||http://purl.obolibrary.org/obo/CLO_0023783
484||15024||dye swap design||http://www.ebi.ac.uk/efo/EFO_0001765
483||10994||dioxygen(2 )||http://purl.obolibrary.org/obo/CHEBI_29371
486||770||GM10842||http://purl.obolibrary.org/obo/CLO_0023784
485||15||Sinoatrial node dysfunction and deafness||http://www.orpha.net/ORDO/Orphanet_324321
487||15020||injury design||http://www.ebi.ac.uk/efo/EFO_0001760
488||15020||pathogenicity design||http://www.ebi.ac.uk/efo/EFO_0001761
489||7731||nongranular leukocyte||http://purl.obolibrary.org/obo/CL_0002087
490||770||GM17775||http://purl.obolibrary.org/obo/CLO_0016638
491||770||GM17776||http://purl.obolibrary.org/obo/CLO_0016636
492||770||GM17779||http://purl.obolibrary.org/obo/CLO_0016635
493||1415||Autosomal recessive limb-girdle muscular dystrophy type 2T||http://www.orpha.net/ORDO/Orphanet_363623
494||770||GM10833||http://purl.obolibrary.org/obo/CLO_0023795
495||770||GM10832||http://purl.obolibrary.org/obo/CLO_0023794
496||1022||Ectocarpus||http://purl.obolibrary.org/obo/NCBITaxon_2879
497||10994||azathioprine||http://purl.obolibrary.org/obo/CHEBI_2948
498||10874||Familial encephalopathy with neuroserpin inclusion bodies||http://www.orpha.net/ORDO/Orphanet_85110
499||6432||Autosomal recessive spastic paraplegia type 55||http://www.orpha.net/ORDO/Orphanet_320375
500||10994||oligomycin A||http://purl.obolibrary.org/obo/CHEBI_28285
501||3019||Palmoplantar keratoderma - XX sex reversal - predisposition to squamous cell carcinoma||http://www.orpha.net/ORDO/Orphanet_85112
502||496||Ectocarpus siliculosus||http://purl.obolibrary.org/obo/NCBITaxon_2880
503||13470||Autosomal recessive spastic paraplegia type 43||http://www.orpha.net/ORDO/Orphanet_320370
504||195||nucleobase-containing small molecule metabolic process||http://purl.obolibrary.org/obo/GO_0055086
505||4139||2q23.1 microduplication syndrome||http://www.orpha.net/ORDO/Orphanet_313947
506||13470||Autosomal recessive spastic paraplegia type 49||http://www.orpha.net/ORDO/Orphanet_320385
507||4430||plant growth regulator||http://purl.obolibrary.org/obo/CHEBI_26155
509||13470||Autosomal recessive spastic paraplegia type 54||http://www.orpha.net/ORDO/Orphanet_320380
508||920||phytohormone||http://purl.obolibrary.org/obo/CHEBI_26158
510||4499||calcium ion homeostasis||http://purl.obolibrary.org/obo/GO_0055074
511||1022||Phaeodactylum tricornutum||http://purl.obolibrary.org/obo/NCBITaxon_2850
512||2672||future spinal cord||http://purl.obolibrary.org/obo/UBERON_0006241
513||382||Mandibular hypoplasia-deafness-progeroid syndrome||http://www.orpha.net/ORDO/Orphanet_363649
514||10253||Moderately severe hemophilia A||http://www.orpha.net/ORDO/Orphanet_169805
515||10253||Severe hemophilia A||http://www.orpha.net/ORDO/Orphanet_169802
516||5502||Vibrio parahaemolyticus RIMD 2210633||http://purl.obolibrary.org/obo/NCBITaxon_223926
517||10253||Mild hemophilia A||http://www.orpha.net/ORDO/Orphanet_169808
518||770||GM14153||http://purl.obolibrary.org/obo/CLO_0034375
519||10994||dimethyl sulfoxide||http://purl.obolibrary.org/obo/CHEBI_28262
520||13471||Autosomal dominant spastic paraplegia type 41||http://www.orpha.net/ORDO/Orphanet_320355
521||2457||Vitamin B12-responsive methylmalonic acidemia type cblA||http://www.orpha.net/ORDO/Orphanet_79310
522||2457||Vitamin B12-responsive methylmalonic acidemia type cblB||http://www.orpha.net/ORDO/Orphanet_79311
523||2448||Vitamin B12-unresponsive methylmalonic acidemia type mut-||http://www.orpha.net/ORDO/Orphanet_79312
524||6650||Isolated oxycephaly||http://www.orpha.net/ORDO/Orphanet_63440
525||2594||L-2-hydroxyglutaric aciduria||http://www.orpha.net/ORDO/Orphanet_79314
526||2594||D-2-hydroxyglutaric aciduria||http://www.orpha.net/ORDO/Orphanet_79315
527||7986||Angel-shaped phalango-epiphyseal dysplasia||http://www.orpha.net/ORDO/Orphanet_63442
528||1851||Phosphoenolpyruvate carboxykinase 1 deficiency||http://www.orpha.net/ORDO/Orphanet_79316
529||1851||Phosphoenolpyruvate carboxykinase 2 deficiency||http://www.orpha.net/ORDO/Orphanet_79317
530||4344||PMM2-CDG||http://www.orpha.net/ORDO/Orphanet_79318
532||4344||MPI-CDG||http://www.orpha.net/ORDO/Orphanet_79319
533||564||Pure or complex X-linked spastic paraplegia||http://www.orpha.net/ORDO/Orphanet_320350
531||7986||Acrocapitofemoral dysplasia||http://www.orpha.net/ORDO/Orphanet_63446
534||770||GM17773||http://purl.obolibrary.org/obo/CLO_0016645
535||770||GM17770||http://purl.obolibrary.org/obo/CLO_0016647
536||770||GM17771||http://purl.obolibrary.org/obo/CLO_0016646
537||770||GM17769||http://purl.obolibrary.org/obo/CLO_0016648
538||2252||20q11.2 microduplication syndrome||http://www.orpha.net/ORDO/Orphanet_363659
540||770||GM17774||http://purl.obolibrary.org/obo/CLO_0016641
539||1125||pathological entity||http://purl.obolibrary.org/obo/MPATH_0
541||770||GM17780||http://purl.obolibrary.org/obo/CLO_0016643
542||770||GM17782||http://purl.obolibrary.org/obo/CLO_0016642
543||9898||X-linked parkinsonism-spasticity syndrome||http://www.orpha.net/ORDO/Orphanet_363654
544||13501||Autosomal dominant spastic paraplegia type 36||http://www.orpha.net/ORDO/Orphanet_320365
546||10994||brassinolide||http://purl.obolibrary.org/obo/CHEBI_28277
545||2672||pigment||http://purl.obolibrary.org/obo/CHEBI_26130
547||4052||Congenital bile acid synthesis defect type 2||http://www.orpha.net/ORDO/Orphanet_79303
548||10397||Progressive familial intrahepatic cholestasis type 2||http://www.orpha.net/ORDO/Orphanet_79304
549||4052||Congenital bile acid synthesis defect type 1||http://www.orpha.net/ORDO/Orphanet_79301
550||4052||Congenital bile acid synthesis defect type 3||http://www.orpha.net/ORDO/Orphanet_79302
551||1022||Trypanosoma brucei gambiense||http://purl.obolibrary.org/obo/NCBITaxon_31285
552||1418||Maternally-inherited spastic paraplegia||http://www.orpha.net/ORDO/Orphanet_320360
553||9675||Patterned dystrophy of the retinal pigment epithelium||http://www.orpha.net/ORDO/Orphanet_63454
554||10397||Progressive familial intrahepatic cholestasis type 3||http://www.orpha.net/ORDO/Orphanet_79305
555||10397||Progressive familial intrahepatic cholestasis type 1||http://www.orpha.net/ORDO/Orphanet_79306
556||770||GM17791||http://purl.obolibrary.org/obo/CLO_0016675
557||770||GM17794||http://purl.obolibrary.org/obo/CLO_0016676
558||770||GM17792||http://purl.obolibrary.org/obo/CLO_0016672
559||770||GM17793||http://purl.obolibrary.org/obo/CLO_0016678
560||4344||GCS1-CDG||http://www.orpha.net/ORDO/Orphanet_79330
562||1826||Nicotiana benthamiana||http://purl.obolibrary.org/obo/NCBITaxon_4100
563||7139||COG7-CDG||http://www.orpha.net/ORDO/Orphanet_79333
561||9918||Rare pervasive developmental disorder||http://www.orpha.net/ORDO/Orphanet_168778
565||5955||B4GALT1-CDG||http://www.orpha.net/ORDO/Orphanet_79332
564||8311||Pure or complex hereditary spastic paraplegia||http://www.orpha.net/ORDO/Orphanet_320335
566||1902||Occipital pachygyria and polymicrogyria||http://www.orpha.net/ORDO/Orphanet_280640
567||1417||X-linked pure spastic paraplegia||http://www.orpha.net/ORDO/Orphanet_320332
568||10994||papaverine||http://purl.obolibrary.org/obo/CHEBI_28241
569||10994||dichloroacetate||http://purl.obolibrary.org/obo/CHEBI_28240
570||1826||Solanum chacoense||http://purl.obolibrary.org/obo/NCBITaxon_4108
571||770||GM17129||http://purl.obolibrary.org/obo/CLO_0015130
572||1826||Petunia x hybrida||http://purl.obolibrary.org/obo/NCBITaxon_4102
573||4344||MGAT2-CDG||http://www.orpha.net/ORDO/Orphanet_79329
574||4344||ALG9-CDG||http://www.orpha.net/ORDO/Orphanet_79328
575||4344||ALG1-CDG||http://www.orpha.net/ORDO/Orphanet_79327
576||4344||ALG2-CDG||http://www.orpha.net/ORDO/Orphanet_79326
577||4344||ALG8-CDG||http://www.orpha.net/ORDO/Orphanet_79325
578||4344||ALG12-CDG||http://www.orpha.net/ORDO/Orphanet_79324
579||7086||MPDU1-CDG||http://www.orpha.net/ORDO/Orphanet_79323
580||7086||DPM1-CDG||http://www.orpha.net/ORDO/Orphanet_79322
581||4344||ALG3-CDG||http://www.orpha.net/ORDO/Orphanet_79321
582||331||Autosomal recessive nail dysplasia||http://www.orpha.net/ORDO/Orphanet_280654
583||564||Pure or complex autosomal recessive spastic paraplegia||http://www.orpha.net/ORDO/Orphanet_320346
584||4344||ALG6-CDG||http://www.orpha.net/ORDO/Orphanet_79320
585||5502||Clostridium botulinum A str. ATCC 3502||http://purl.obolibrary.org/obo/NCBITaxon_413999
586||564||Pure or complex autosomal dominant spastic paraplegia||http://www.orpha.net/ORDO/Orphanet_320342
587||5502||Escherichia coli B str. REL606||http://purl.obolibrary.org/obo/NCBITaxon_413997
588||1171||Acrodysostosis with multiple hormone resistance||http://www.orpha.net/ORDO/Orphanet_280651
589||561||Childhood disintegrative disorder||http://www.orpha.net/ORDO/Orphanet_168782
590||306||Cleft lip/palate - ectodermal dysplasia||http://www.orpha.net/ORDO/Orphanet_320317
591||10994||paclitaxel||http://purl.obolibrary.org/obo/CHEBI_45863
592||5965||Hereditary palmoplantar keratoderma||http://www.orpha.net/ORDO/Orphanet_79357
593||990||Hermansky-Pudlak syndrome type 9||http://www.orpha.net/ORDO/Orphanet_280663
594||15||Heart-hand syndrome, Slovenian type||http://www.orpha.net/ORDO/Orphanet_168796
595||6174||3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form||http://www.orpha.net/ORDO/Orphanet_79351
596||6174||3-phosphoserine phosphatase deficiency||http://www.orpha.net/ORDO/Orphanet_79350
597||5877||PENS syndrome||http://www.orpha.net/ORDO/Orphanet_313936
598||382||LMNA-related cardiocutaneous progeria syndrome||http://www.orpha.net/ORDO/Orphanet_363618
599||770||GM17795||http://purl.obolibrary.org/obo/CLO_0016682
600||770||GM17783||http://purl.obolibrary.org/obo/CLO_0016684
601||770||GM17787||http://purl.obolibrary.org/obo/CLO_0016685
602||770||GM17785||http://purl.obolibrary.org/obo/CLO_0016686
604||2252||Intellectual disability-feeding difficulties-developmental delay-microcephaly syndrome||http://www.orpha.net/ORDO/Orphanet_363611
603||770||GM17790||http://purl.obolibrary.org/obo/CLO_0016687
605||770||GM17789||http://purl.obolibrary.org/obo/CLO_0016688
606||1767||Moyamoya disease - short stature - facial dysmorphism - hypergonadotropic hypogonadism||http://www.orpha.net/ORDO/Orphanet_280679
607||10400||Chondrodysplasia punctata, Toriello type||http://www.orpha.net/ORDO/Orphanet_79347
608||10400||Chondrodysplasia punctata, tibial-metacarpal type||http://www.orpha.net/ORDO/Orphanet_79346
609||10400||Brachytelephalangic chondrodysplasia punctata||http://www.orpha.net/ORDO/Orphanet_79345
610||4191||Congenital muscular dystrophy due to phosphatidylcholine biosynthesis defect||http://www.orpha.net/ORDO/Orphanet_280671
611||10400||Autosomal dominant chondrodysplasia punctata||http://www.orpha.net/ORDO/Orphanet_79344
612||6910||Charcot-Marie-Tooth disease type 1||http://www.orpha.net/ORDO/Orphanet_65753
613||4696||Epilepsy syndrome||http://www.orpha.net/ORDO/Orphanet_166463
614||372||Lipedema||http://www.orpha.net/ORDO/Orphanet_77243
615||372||Primary lymphedema||http://www.orpha.net/ORDO/Orphanet_77240
616||4696||Neurocutaneous syndrome with epilepsy||http://www.orpha.net/ORDO/Orphanet_166466
617||1790||dermatomyositis||http://www.ebi.ac.uk/efo/EFO_0000398
618||1014||developmental stage||http://www.ebi.ac.uk/efo/EFO_0000399
619||6262||Congenitally uncorrected transposition of the great arteries with cardiac malformation||http://www.orpha.net/ORDO/Orphanet_216729
620||10652||obsolete_damage response||http://www.ebi.ac.uk/efo/EFO_0000392
621||4701||Carpenter syndrome||http://www.orpha.net/ORDO/Orphanet_65759
622||9536||Robertsonian translocation||http://www.ebi.ac.uk/efo/EFO_0000393
623||10652||obsolete_cystic fibrosis||http://www.ebi.ac.uk/efo/EFO_0000390
624||14970||damage intensity||http://www.ebi.ac.uk/efo/EFO_0000391
625||2249||dermal neurofibroma||http://www.ebi.ac.uk/efo/EFO_0000397
626||2002||dedifferentiated chondrosarcoma||http://www.ebi.ac.uk/efo/EFO_0000394
627||4335||delivery method||http://www.ebi.ac.uk/efo/EFO_0000395
628||10732||Sudden infant death - dysgenesis of the testes||http://www.orpha.net/ORDO/Orphanet_168593
629||2314||Trichorhinophalangeal syndrome type 1 and 3||http://www.orpha.net/ORDO/Orphanet_77258
630||2856||Gaucher disease type 1||http://www.orpha.net/ORDO/Orphanet_77259
631||2606||Autosomal dominant multiple pterygium syndrome||http://www.orpha.net/ORDO/Orphanet_65743
632||6325||Brain demyelination due to methionine adenosyltransferase deficiency||http://www.orpha.net/ORDO/Orphanet_168598
633||10652||obsolete_cultivar||http://www.ebi.ac.uk/efo/EFO_0000387
635||14970||electrical current||http://www.ebi.ac.uk/efo/EFO_0000388
634||10994||oxidised LDL||http://purl.obolibrary.org/obo/CHEBI_60151
636||4142||Isolated follicle stimulating hormone deficiency||http://www.orpha.net/ORDO/Orphanet_52901
637||2737||cutaneous melanoma||http://www.ebi.ac.uk/efo/EFO_0000389
638||1826||Lactuca sativa||http://purl.obolibrary.org/obo/NCBITaxon_4236
639||10652||obsolete_corpus cardiacum||http://www.ebi.ac.uk/efo/EFO_0000380
640||10652||obsolete_corpus striatum||http://www.ebi.ac.uk/efo/EFO_0000381
642||3043||corpus uteri||http://www.ebi.ac.uk/efo/EFO_0000382
641||5877||Multiple keratoacanthoma, Ferguson-Smith type||http://www.orpha.net/ORDO/Orphanet_65748
643||10652||obsolete_cortex||http://www.ebi.ac.uk/efo/EFO_0000383
644||11620||Crohn s disease||http://www.ebi.ac.uk/efo/EFO_0000384
645||1022||Laccaria bicolor||http://purl.obolibrary.org/obo/NCBITaxon_29883
646||2656||crystal cell specific anlage||http://www.ebi.ac.uk/efo/EFO_0000386
647||9704||Tolosa-Hunt syndrome||http://www.orpha.net/ORDO/Orphanet_64686
648||8191||methyl mercuric(II) chloride||http://purl.obolibrary.org/obo/CHEBI_28216
650||4803||Familial platelet syndrome with predisposition to acute myelogenous leukemia||http://www.orpha.net/ORDO/Orphanet_71290
649||5295||single-organism process||http://purl.obolibrary.org/obo/GO_0044699
652||3883||Hereditary vascular retinopathy||http://www.orpha.net/ORDO/Orphanet_71291
651||10719||Hereditary North American Indian childhood cirrhosis||http://www.orpha.net/ORDO/Orphanet_168583
654||4233||tooth eruption||http://purl.obolibrary.org/obo/GO_0044691
653||1191||Hyperandrogenism due to cortisone reductase deficiency||http://www.orpha.net/ORDO/Orphanet_168588
655||5502||Salmonella enterica subsp. indica||http://purl.obolibrary.org/obo/NCBITaxon_59207
656||1675||coronary artery disease||http://www.ebi.ac.uk/efo/EFO_0000378
657||5502||Salmonella enterica subsp. enterica||http://purl.obolibrary.org/obo/NCBITaxon_59201
658||10652||obsolete_corpus allatum||http://www.ebi.ac.uk/efo/EFO_0000379
659||10652||obsolete_conventional clear cell renal carcinoma||http://www.ebi.ac.uk/efo/EFO_0000376
660||10652||obsolete_cornea structure||http://www.ebi.ac.uk/efo/EFO_0000377
661||10652||obsolete_conjunctiva structure||http://www.ebi.ac.uk/efo/EFO_0000374
662||4401||array control spike calibration||http://www.ebi.ac.uk/efo/EFO_0000375
663||10652||obsolete_congestive cardiomyopathy||http://www.ebi.ac.uk/efo/EFO_0000372
665||10994||danazol||http://purl.obolibrary.org/obo/CHEBI_4315
664||9190||congestive heart failure||http://www.ebi.ac.uk/efo/EFO_0000373
666||4033||chemically induced mutation||http://www.ebi.ac.uk/efo/EFO_0000370
668||10994||dantrolene||http://purl.obolibrary.org/obo/CHEBI_4317
667||10652||obsolete_congenital bilateral absence of the vas deferens||http://www.ebi.ac.uk/efo/EFO_0000371
669||13421||Arthrogryposis - severe scoliosis||http://www.orpha.net/ORDO/Orphanet_65720
670||5300||Native American myopathy||http://www.orpha.net/ORDO/Orphanet_168572
671||13587||Mus musculus x Mus spretus||http://purl.obolibrary.org/obo/NCBITaxon_186842
672||4406||Radio-ulnar synostosis - amegakaryocytic thrombocytopenia||http://www.orpha.net/ORDO/Orphanet_71289
673||10994||rotenone||http://purl.obolibrary.org/obo/CHEBI_28201
674||4139||Hereditary cryohydrocytosis with reduced stomatin||http://www.orpha.net/ORDO/Orphanet_168577
675||2822||compound based treatment||http://www.ebi.ac.uk/efo/EFO_0000369
676||120||colorectal adenocarcinoma||http://www.ebi.ac.uk/efo/EFO_0000365
677||6262||Isolated congenitally uncorrected transposition of the great arteries||http://www.orpha.net/ORDO/Orphanet_216718
678||10652||obsolete_common variable immunodeficiency||http://www.ebi.ac.uk/efo/EFO_0000367
679||9567||minor histocompatibility congenic strain||http://www.ebi.ac.uk/efo/EFO_0000368
680||10652||obsolete_colon||http://www.ebi.ac.uk/efo/EFO_0000361
681||10652||obsolete_colon adenocarcinoma||http://www.ebi.ac.uk/efo/EFO_0000362
682||10652||obsolete_colon carcinoma||http://www.ebi.ac.uk/efo/EFO_0000363
683||676||colon mucinous adenocarcinoma||http://www.ebi.ac.uk/efo/EFO_0000364
684||10652||obsolete_colorectal tumor||http://www.ebi.ac.uk/efo/EFO_0000360
685||12329||Rh deficiency syndrome||http://www.orpha.net/ORDO/Orphanet_71275
686||6322||Encephalopathy due to GLUT1 deficiency||http://www.orpha.net/ORDO/Orphanet_71277
687||14003||Congenital brain dysgenesis due to glutamine synthetase deficiency||http://www.orpha.net/ORDO/Orphanet_71278
688||5700||Split hand - split foot - deafness||http://www.orpha.net/ORDO/Orphanet_71271
689||15570||Ichthyosis hystrix gravior||http://www.orpha.net/ORDO/Orphanet_79504
690||15570||Ichthyosis hystrix of Curth-Macklin||http://www.orpha.net/ORDO/Orphanet_79503
691||1737||Cholesterol-ester transfer protein deficiency||http://www.orpha.net/ORDO/Orphanet_79506
692||5300||Auriculoocular anomalies - cleft lip||http://www.orpha.net/ORDO/Orphanet_71270
694||1022||Cyanidioschyzon merolae||http://purl.obolibrary.org/obo/NCBITaxon_45157
693||5896||DOORS syndrome||http://www.orpha.net/ORDO/Orphanet_79500
695||1564||Punctate palmoplantar keratoderma type 2||http://www.orpha.net/ORDO/Orphanet_79502
697||1564||Punctate palmoplantar keratoderma type 1||http://www.orpha.net/ORDO/Orphanet_79501
696||770||GM17758||http://purl.obolibrary.org/obo/CLO_0016608
698||770||GM17757||http://purl.obolibrary.org/obo/CLO_0016606
699||770||GM17759||http://purl.obolibrary.org/obo/CLO_0016607
700||770||GM17764||http://purl.obolibrary.org/obo/CLO_0016604
702||12378||Hypotonia - failure to thrive - microcephaly||http://www.orpha.net/ORDO/Orphanet_79507
701||770||GM17765||http://purl.obolibrary.org/obo/CLO_0016602
703||10652||obsolete_clinical history age||http://www.ebi.ac.uk/efo/EFO_0000353
704||15538||clinical history||http://www.ebi.ac.uk/efo/EFO_0000352
706||770||GM17762||http://purl.obolibrary.org/obo/CLO_0016600
705||10652||obsolete_clinical factor||http://www.ebi.ac.uk/efo/EFO_0000351
708||2002||clear cell sarcoma of the kidney||http://www.ebi.ac.uk/efo/EFO_0000350
707||770||GM17761||http://purl.obolibrary.org/obo/CLO_0016601
709||10652||obsolete_cochlea structure||http://www.ebi.ac.uk/efo/EFO_0000357
710||2656||clypeo-labral primordium||http://www.ebi.ac.uk/efo/EFO_0000356
711||12498||clinical treatment protocol||http://www.ebi.ac.uk/efo/EFO_0000355
712||10652||obsolete_clinical information||http://www.ebi.ac.uk/efo/EFO_0000354
713||10652||obsolete_cockayne syndrome||http://www.ebi.ac.uk/efo/EFO_0000359
714||6625||Niemann-Pick disease type A||http://www.orpha.net/ORDO/Orphanet_77292
715||4834||Dentinogenesis imperfecta - short stature - hearing loss - intellectual disability||http://www.orpha.net/ORDO/Orphanet_71267
716||2454||Niemann-Pick disease type B||http://www.orpha.net/ORDO/Orphanet_77293
717||4766||Morgagni-Stewart-Morel syndrome||http://www.orpha.net/ORDO/Orphanet_77296
718||14353||Odontoleukodystrophy||http://www.orpha.net/ORDO/Orphanet_77295
719||4122||Anophthalmia/microphthalmia - esophageal atresia||http://www.orpha.net/ORDO/Orphanet_77298
720||13551||Majeed syndrome||http://www.orpha.net/ORDO/Orphanet_77297
721||4139||Microphthalmia - brain atrophy||http://www.orpha.net/ORDO/Orphanet_77299
722||10652||obsolete_chronic myeloid leukemia||http://www.ebi.ac.uk/efo/EFO_0000340
723||1403||chronic pancreatitis||http://www.ebi.ac.uk/efo/EFO_0000342
724||1979||chronic obstructive pulmonary disease||http://www.ebi.ac.uk/efo/EFO_0000341
725||3640||circular visceral mesoderm primordium||http://www.ebi.ac.uk/efo/EFO_0000344
726||10652||obsolete_cingulate cortex||http://www.ebi.ac.uk/efo/EFO_0000343
727||10652||obsolete_classical Hodgkin s lymphoma||http://www.ebi.ac.uk/efo/EFO_0000346
728||2656||circular visceral muscle fibers||http://www.ebi.ac.uk/efo/EFO_0000345
729||120||clear cell adenocarcinoma||http://www.ebi.ac.uk/efo/EFO_0000348
730||11868||classifier prediction||http://www.ebi.ac.uk/efo/EFO_0000347
731||7939||Talo-patello-scaphoid osteolysis||http://www.orpha.net/ORDO/Orphanet_50809
732||1986||clear cell renal carcinoma||http://www.ebi.ac.uk/efo/EFO_0000349
733||4696||Cerebral diseases of vascular origin with epilepsy||http://www.orpha.net/ORDO/Orphanet_166487
734||2856||Gaucher disease type 3||http://www.orpha.net/ORDO/Orphanet_77261
735||7638||Gaucher disease type 2||http://www.orpha.net/ORDO/Orphanet_77260
736||770||colonic cancer cell line||http://purl.obolibrary.org/obo/BTO_0000797
737||2162||chondroblastoma||http://www.ebi.ac.uk/efo/EFO_0000331
738||4728||Zellweger-like syndrome without peroxisomal anomalies||http://www.orpha.net/ORDO/Orphanet_50812
739||114||childhood acute myeloid leukemia||http://www.ebi.ac.uk/efo/EFO_0000330
740||6610||Craniolenticulosutural dysplasia||http://www.orpha.net/ORDO/Orphanet_50814
741||5700||Branchiogenic deafness syndrome||http://www.orpha.net/ORDO/Orphanet_50815
742||4723||Genetic non-syndromic renal or urinary tract malformation||http://www.orpha.net/ORDO/Orphanet_357506
743||5025||Cochliobolus sativus||http://purl.obolibrary.org/obo/NCBITaxon_45130
744||760||Microlissencephaly - micromelia||http://www.orpha.net/ORDO/Orphanet_50810
745||2322||Lipodystrophy - intellectual disability - deafness||http://www.orpha.net/ORDO/Orphanet_50811
746||2063||cognitive decline||http://purl.obolibrary.org/obo/HP_0001268
748||1508||chronic myelogenous leukemia||http://www.ebi.ac.uk/efo/EFO_0000339
747||770||GM17138||http://purl.obolibrary.org/obo/CLO_0015097
749||10652||obsolete_chronic granulomatous disease||http://www.ebi.ac.uk/efo/EFO_0000338
750||1403||chronic gastritis||http://www.ebi.ac.uk/efo/EFO_0000337
751||1766||chromosomal aberration||http://www.ebi.ac.uk/efo/EFO_0000336
752||770||GM17139||http://purl.obolibrary.org/obo/CLO_0015098
753||1986||chromophobe renal cell carcinoma||http://www.ebi.ac.uk/efo/EFO_0000335
754||10652||obsolete_chordoma||http://www.ebi.ac.uk/efo/EFO_0000334
755||2002||chondrosarcoma||http://www.ebi.ac.uk/efo/EFO_0000333
757||2162||chondromyxoid fibroma||http://www.ebi.ac.uk/efo/EFO_0000332
756||5037||Genetic hyperparathyroidism||http://www.orpha.net/ORDO/Orphanet_208596
759||5037||Genetic hypoparathyroidism||http://www.orpha.net/ORDO/Orphanet_208593
758||5502||Rhodopseudomonas palustris CGA009||http://purl.obolibrary.org/obo/NCBITaxon_258594
760||4696||Cerebral malformation with epilepsy||http://www.orpha.net/ORDO/Orphanet_166478
761||10652||obsolete_cerebrospinal fluid||http://www.ebi.ac.uk/efo/EFO_0000329
762||4696||Monogenic disease with epilepsy||http://www.orpha.net/ORDO/Orphanet_166472
763||4696||Idiopathic or cryptogenic familial epilepsy syndrome with identified loci/genes||http://www.orpha.net/ORDO/Orphanet_166475
764||10994||hydroxyzine||http://purl.obolibrary.org/obo/CHEBI_5818
765||5502||Clostridia||http://purl.obolibrary.org/obo/NCBITaxon_186801
766||1002||central nervous system cancer||http://www.ebi.ac.uk/efo/EFO_0000326
767||13883||cellular modification||http://www.ebi.ac.uk/efo/EFO_0000325
768||10652||obsolete_cerebral cortex||http://www.ebi.ac.uk/efo/EFO_0000328
769||10652||obsolete_cerebellum||http://www.ebi.ac.uk/efo/EFO_0000327
770||1125||cell line||http://www.ebi.ac.uk/efo/EFO_0000322
771||10652||obsolete_cell factor||http://www.ebi.ac.uk/efo/EFO_0000321
772||1125||cell type||http://www.ebi.ac.uk/efo/EFO_0000324
773||5838||cell property||http://www.ebi.ac.uk/efo/EFO_0000323
774||2252||Microcephaly - deafness - intellectual disability||http://www.orpha.net/ORDO/Orphanet_2533
775||1826||Vigna unguiculata||http://purl.obolibrary.org/obo/NCBITaxon_3917
776||6899||Microcornea - corectopia - macular hypoplasia||http://www.orpha.net/ORDO/Orphanet_2535
777||1826||Vicia narbonensis||http://purl.obolibrary.org/obo/NCBITaxon_3912
778||2672||ligament||http://purl.obolibrary.org/obo/UBERON_0000211
779||4430||micronutrient||http://purl.obolibrary.org/obo/CHEBI_27027
780||6899||Microcornea - glaucoma - absent frontal sinuses||http://www.orpha.net/ORDO/Orphanet_2536
781||4430||toxin||http://purl.obolibrary.org/obo/CHEBI_27026
782||2450||Pontocerebellar hypoplasia type 2||http://www.orpha.net/ORDO/Orphanet_2524
783||6046||Microcephaly - brain defect - spasticity - hypernatremia||http://www.orpha.net/ORDO/Orphanet_2523
784||2252||Microcephaly - cervical spine fusion anomalies||http://www.orpha.net/ORDO/Orphanet_2522
785||2252||Microcephaly - cleft palate||http://www.orpha.net/ORDO/Orphanet_2521
786||2252||Microcephaly-microcornea syndrome, Seemanova type||http://www.orpha.net/ORDO/Orphanet_2528
787||5478||Microcephaly - lymphedema - chorioretinopathy||http://www.orpha.net/ORDO/Orphanet_2526
788||6899||Microspherophakia - metaphyseal dysplasia||http://www.orpha.net/ORDO/Orphanet_2551
789||2318||Ear-patella-short stature syndrome||http://www.orpha.net/ORDO/Orphanet_2554
790||9622||Mietens syndrome||http://www.orpha.net/ORDO/Orphanet_2557
791||5317||Microphthalmia with linear skin defects syndrome||http://www.orpha.net/ORDO/Orphanet_2556
792||1826||Zingiber officinale||http://purl.obolibrary.org/obo/NCBITaxon_94328
793||5264||cellular protein modification process||http://purl.obolibrary.org/obo/GO_0006464
794||1721||Joubert syndrome with renal defect||http://www.orpha.net/ORDO/Orphanet_220497
795||1022||Crassostrea ariakensis||http://purl.obolibrary.org/obo/NCBITaxon_94323
796||1721||Joubert syndrome with ocular defect||http://www.orpha.net/ORDO/Orphanet_220493
797||1767||Mikati-Najjar-Sahli syndrome||http://www.orpha.net/ORDO/Orphanet_2558
800||1826||Lilium hybrid division I||http://purl.obolibrary.org/obo/NCBITaxon_156532
799||6573||drug role||http://www.ebi.ac.uk/efo/EFO_0001899
798||6897||Isolated anophthalmia - microphthalmia||http://www.orpha.net/ORDO/Orphanet_2542
802||5129||Constitutional deficiency anemia||http://www.orpha.net/ORDO/Orphanet_248296
801||6897||Microphthalmia - cataract||http://www.orpha.net/ORDO/Orphanet_2543
803||10994||3-isobutyl-1-methyl-7H-xanthine||http://purl.obolibrary.org/obo/CHEBI_34795
804||1826||Vigna unguiculata subsp. unguiculata||http://purl.obolibrary.org/obo/NCBITaxon_3920
805||266||Rare hereditary hemochromatosis||http://www.orpha.net/ORDO/Orphanet_220489
806||4775||Oculoauriculovertebral spectrum with radial defects||http://www.orpha.net/ORDO/Orphanet_2549
807||770||myeloid leukemia cell line||http://purl.obolibrary.org/obo/BTO_0000740
808||7675||Aceruloplasminemia||http://www.orpha.net/ORDO/Orphanet_48818
809||7234||X-linked immunoneurologic disorder||http://www.orpha.net/ORDO/Orphanet_2571
810||14507||CD34-positive, CD38-positive megakaryocyte erythroid progenitor cell||http://purl.obolibrary.org/obo/CL_0002005
811||4785||MULIBREY nanism||http://www.orpha.net/ORDO/Orphanet_2576
812||9279||CD34-negative, GlyA-negative proerythroblast||http://purl.obolibrary.org/obo/CL_0002004
814||5501||MURCS association||http://www.orpha.net/ORDO/Orphanet_2578
813||7154||Kit-low, CD34-positive eosinophil progenitor cell||http://purl.obolibrary.org/obo/CL_0002007
815||14507||Kit-positive, CD34-negative megakaryocyte erythroid progenitor cell||http://purl.obolibrary.org/obo/CL_0002006
816||4692||Muscular atrophy - ataxia - retinitis pigmentosa - diabetes mellitus||http://www.orpha.net/ORDO/Orphanet_2579
817||1022||Schizophyllum commune||http://purl.obolibrary.org/obo/NCBITaxon_5334
818||9265||CD34-positive, CD38-positive granulocyte monocyte progenitor||http://purl.obolibrary.org/obo/CL_0002001
819||9622||Spastic ataxia - corneal dystrophy||http://www.orpha.net/ORDO/Orphanet_2572
820||14542||Kit-positive erythroid progenitor cell||http://purl.obolibrary.org/obo/CL_0002000
821||4705||Moyamoya disease||http://www.orpha.net/ORDO/Orphanet_2573
822||14542||CD34-positive, GlyA-negative erythroid progenitor cell||http://purl.obolibrary.org/obo/CL_0002003
823||613||Moynahan syndrome||http://www.orpha.net/ORDO/Orphanet_2574
825||13997||Cystic fibrosis - gastritis - megaloblastic anemia||http://www.orpha.net/ORDO/Orphanet_2575
824||9265||Kit-positive granulocyte monocyte progenitor||http://purl.obolibrary.org/obo/CL_0002002
826||5502||Salmonella enterica subsp. enterica serovar Saintpaul||http://purl.obolibrary.org/obo/NCBITaxon_90105
827||7154||CD34-positive, CD38-positive eosinophil progenitor cell||http://purl.obolibrary.org/obo/CL_0002008
828||871||macrophage dendritic cell progenitor||http://purl.obolibrary.org/obo/CL_0002009
830||831||protein N-linked glycosylation||http://purl.obolibrary.org/obo/GO_0006487
829||6610||Goodman syndrome||http://www.orpha.net/ORDO/Orphanet_65798
831||793||protein glycosylation||http://purl.obolibrary.org/obo/GO_0006486
832||872||pre-conventional dendritic cell||http://purl.obolibrary.org/obo/CL_0002010
833||1306||M bius syndrome - axonal neuropathy - hypogonadotropic hypogonadism||http://www.orpha.net/ORDO/Orphanet_2560
834||3854||Methanococcus maripaludis||http://purl.obolibrary.org/obo/NCBITaxon_39152
835||9276||CD71-negative, GlyA-positive orthochromatic erythroblast||http://purl.obolibrary.org/obo/CL_0002018
836||9276||Kit-negative, Ly-76 high orthochromatophilic erythroblasts||http://purl.obolibrary.org/obo/CL_0002017
838||10994||imidacloprid||http://purl.obolibrary.org/obo/CHEBI_5870
839||2021||Mononen-Karnes-Senac syndrome||http://www.orpha.net/ORDO/Orphanet_2565
837||9274||CD71-low, GlyA-positive polychromatic erythroblast||http://purl.obolibrary.org/obo/CL_0002016
840||9274||Kit-negative, Ly-76 high polychromatophilic erythroblast||http://purl.obolibrary.org/obo/CL_0002015
841||4701||MOMO syndrome||http://www.orpha.net/ORDO/Orphanet_2563
842||9286||Kit-negative, Ly-76 high basophilic erythroblast||http://purl.obolibrary.org/obo/CL_0002014
845||6244||Tetramelic monodactyly||http://www.orpha.net/ORDO/Orphanet_2564
844||9286||GlyA-positive basophillic erythroblast||http://purl.obolibrary.org/obo/CL_0002013
843||10839||Persistent combined dystonia||http://www.orpha.net/ORDO/Orphanet_391711
846||306||Ackerman syndrome||http://www.orpha.net/ORDO/Orphanet_2561
847||9279||Kit-low proerythroblast||http://purl.obolibrary.org/obo/CL_0002012
848||828||Kit-positive macrophage dendritic cell progenitor||http://purl.obolibrary.org/obo/CL_0002011
849||13496||Iridovirus||http://purl.obolibrary.org/obo/NCBITaxon_10487
850||13352||Ly-76 high reticulocyte||http://purl.obolibrary.org/obo/CL_0002019
851||7860||Hereditary myoclonus - progressive distal muscular atrophy||http://www.orpha.net/ORDO/Orphanet_2590
852||5025||Hypocrea virens||http://purl.obolibrary.org/obo/NCBITaxon_29875
853||5877||Infantile myofibromatosis||http://www.orpha.net/ORDO/Orphanet_2591
854||9343||GlyA-positive erythrocyte||http://purl.obolibrary.org/obo/CL_0002021
855||13352||GlyA-positive reticulocytes||http://purl.obolibrary.org/obo/CL_0002020
856||8791||Tubular aggregate myopathy||http://www.orpha.net/ORDO/Orphanet_2593
857||9277||CD34-positive, CD41-positive, CD42-positive megakaryocyte progenitor cell||http://purl.obolibrary.org/obo/CL_0002023
858||9856||Spinocerebellar ataxia type 29||http://www.orpha.net/ORDO/Orphanet_208513
859||9343||Ly-76 high positive erythrocyte||http://purl.obolibrary.org/obo/CL_0002022
861||5055||Myopathy and diabetes mellitus||http://www.orpha.net/ORDO/Orphanet_2596
860||9277||CD34-positive, CD41-positive, CD42-negative megakaryocyte progenitor cell||http://purl.obolibrary.org/obo/CL_0002025
863||5700||Mitochondrial myopathy - lactic acidosis - deafness||http://www.orpha.net/ORDO/Orphanet_2597
862||9277||Kit-positive megakaryocyte progenitor cell||http://purl.obolibrary.org/obo/CL_0002024
865||6432||Mitochondrial myopathy and sideroblastic anemia||http://www.orpha.net/ORDO/Orphanet_2598
864||9266||CD9-positive, CD41-positive megakaryocyte cell||http://purl.obolibrary.org/obo/CL_0002027
866||9266||CD34-negative, CD41-positive, CD42-positive megakaryocyte cell||http://purl.obolibrary.org/obo/CL_0002026
867||10093||Fc-epsilon RIalpha-low mast cell progenitor||http://purl.obolibrary.org/obo/CL_0002029
868||10085||basophil mast progenitor cell||http://purl.obolibrary.org/obo/CL_0002028
869||5502||Mycobacterium smegmatis str. MC2 155||http://purl.obolibrary.org/obo/NCBITaxon_246196
870||2490||Autosomal dominant cerebellar ataxia type 2||http://www.orpha.net/ORDO/Orphanet_208508
871||772||hematopoietic oligopotent progenitor cell||http://purl.obolibrary.org/obo/CL_0002032
872||772||hematopoietic lineage restricted progenitor cell||http://purl.obolibrary.org/obo/CL_0002031
873||7151||Fc-epsilon RIalpha-high basophil progenitor cell||http://purl.obolibrary.org/obo/CL_0002030
874||4139||Shoulder and girdle defects - familial intellectual disability||http://www.orpha.net/ORDO/Orphanet_2580
875||4695||Ataxia - pancytopenia||http://www.orpha.net/ORDO/Orphanet_2585
876||10087||Slamf1-positive multipotent progenitor cell||http://purl.obolibrary.org/obo/CL_0002036
877||10087||Slamf1-negative multipotent progenitor cell||http://purl.obolibrary.org/obo/CL_0002035
878||14091||long term hematopoietic stem cell||http://purl.obolibrary.org/obo/CL_0002034
879||1022||Moniezia benedeni||http://purl.obolibrary.org/obo/NCBITaxon_218196
880||14091||short term hematopoietic stem cell||http://purl.obolibrary.org/obo/CL_0002033
881||1022||Coprinopsis cinerea||http://purl.obolibrary.org/obo/NCBITaxon_5346
882||4692||Myoclonus - cerebellar ataxia - deafness||http://www.orpha.net/ORDO/Orphanet_2589
883||10463||immature NK T cell stage I||http://purl.obolibrary.org/obo/CL_0002039
884||5191||Myeloperoxidase deficiency||http://www.orpha.net/ORDO/Orphanet_2587
885||8696||T follicular helper cell||http://purl.obolibrary.org/obo/CL_0002038
886||2252||Myhre syndrome||http://www.orpha.net/ORDO/Orphanet_2588
887||8208||CD2-positive, CD5-positive, CD44-positive alpha-beta intraepithelial T cell||http://purl.obolibrary.org/obo/CL_0002037
888||1022||Lentinula edodes||http://purl.obolibrary.org/obo/NCBITaxon_5353
889||5502||Ruegeria pomeroyi DSS-3||http://purl.obolibrary.org/obo/NCBITaxon_246200
890||9623||Epithelial recurrent erosion dystrophy||http://www.orpha.net/ORDO/Orphanet_293381
891||799||DNA synthesis inhibitor||http://purl.obolibrary.org/obo/CHEBI_59517
892||10994||imatinib||http://purl.obolibrary.org/obo/CHEBI_45783
893||5502||Streptococcus pyogenes MGAS6180||http://purl.obolibrary.org/obo/NCBITaxon_319701
894||1826||Medicago truncatula||http://purl.obolibrary.org/obo/NCBITaxon_3880
895||1826||Medicago sativa||http://purl.obolibrary.org/obo/NCBITaxon_3879
896||9623||Grayson-Wilbrandt corneal dystrophy||http://www.orpha.net/ORDO/Orphanet_293375
897||5896||Autosomal dominant deafness-onychodystrophy syndrome||http://www.orpha.net/ORDO/Orphanet_79499
898||1257||X-linked congenital generalized hypertrichosis||http://www.orpha.net/ORDO/Orphanet_79495
899||5877||Brooke-Spiegler syndrome||http://www.orpha.net/ORDO/Orphanet_79493
900||323||Pili gemini||http://www.orpha.net/ORDO/Orphanet_79492
901||770||GM17768||http://purl.obolibrary.org/obo/CLO_0016597
902||1022||Phanerochaete chrysosporium||http://purl.obolibrary.org/obo/NCBITaxon_5306
903||5502||Magnetospirillum magneticum AMB-1||http://purl.obolibrary.org/obo/NCBITaxon_342108
904||5502||Brucella melitensis bv. 1 str. 16M||http://purl.obolibrary.org/obo/NCBITaxon_224914
905||770||GM17767||http://purl.obolibrary.org/obo/CLO_0016593
906||770||GM17766||http://purl.obolibrary.org/obo/CLO_0016594
907||5025||Arthroderma racemosum||http://purl.obolibrary.org/obo/NCBITaxon_231010
909||2252||Muscular hypertrophy - hepatomegaly - polyhydramnios||http://www.orpha.net/ORDO/Orphanet_324416
908||1826||Pisum sativum||http://purl.obolibrary.org/obo/NCBITaxon_3888
910||1826||Phaseolus coccineus||http://purl.obolibrary.org/obo/NCBITaxon_3886
911||1826||Phaseolus vulgaris||http://purl.obolibrary.org/obo/NCBITaxon_3885
912||5502||Bradyrhizobium japonicum USDA 110||http://purl.obolibrary.org/obo/NCBITaxon_224911
913||15||X-linked intellectual disability - cardiomegaly - congestive heart failure||http://www.orpha.net/ORDO/Orphanet_324410
914||7858||Paroxysmal dystonia||http://www.orpha.net/ORDO/Orphanet_200037
915||3834||Phakomatosis cesiomarmorata||http://www.orpha.net/ORDO/Orphanet_79484
916||3834||Phakomatosis spilorosea||http://www.orpha.net/ORDO/Orphanet_79485
917||3834||Phakomatosis cesioflammea||http://www.orpha.net/ORDO/Orphanet_79483
918||6306||Methylmalonic acidemia without homocystinuria||http://www.orpha.net/ORDO/Orphanet_293355
919||1022||Microcebus murinus||http://purl.obolibrary.org/obo/NCBITaxon_30608
920||4430||hormone role||http://www.ebi.ac.uk/efo/EFO_0001824
921||5668||pathological||http://purl.obolibrary.org/obo/PATO_0001869
922||5502||Ralstonia solanacearum UW551||http://purl.obolibrary.org/obo/NCBITaxon_342110
923||1826||Trifolium repens||http://purl.obolibrary.org/obo/NCBITaxon_3899
924||4344||ALG13-CDG||http://www.orpha.net/ORDO/Orphanet_324422
925||15174||Familial visceral myopathy||http://www.orpha.net/ORDO/Orphanet_2604
926||8910||Isolated NADH-CoQ reductase deficiency||http://www.orpha.net/ORDO/Orphanet_2609
927||2252||N syndrome||http://www.orpha.net/ORDO/Orphanet_2608
928||10994||afimoxifene||http://purl.obolibrary.org/obo/CHEBI_44616
929||4139||Developmental and speech delay due to SOX5 deficiency||http://www.orpha.net/ORDO/Orphanet_313892
930||4785||Short stature-optic atrophy-Pelger-Hu t anomaly syndrome||http://www.orpha.net/ORDO/Orphanet_391677
931||4139||Myopathy - growth delay - intellectual disability - hypospadias||http://www.orpha.net/ORDO/Orphanet_2601
932||4785||3M syndrome||http://www.orpha.net/ORDO/Orphanet_2616
933||3121||Nakajo-Nishimura syndrome||http://www.orpha.net/ORDO/Orphanet_2615
934||307||Nail-patella syndrome||http://www.orpha.net/ORDO/Orphanet_2614
935||3753||Nail-patella-like renal disease||http://www.orpha.net/ORDO/Orphanet_2613
936||10143||Brachydactylous dwarfism, Mseleni type||http://www.orpha.net/ORDO/Orphanet_2619
938||15167||Congenital enteropathy due to enteropeptidase deficiency||http://www.orpha.net/ORDO/Orphanet_168601
937||2252||Bird headed-dwarfism, Montreal type||http://www.orpha.net/ORDO/Orphanet_2617
939||8191||potassium chloride||http://purl.obolibrary.org/obo/CHEBI_32588
940||10994||4-hydroxy-2-nonenal||http://purl.obolibrary.org/obo/CHEBI_32585
941||1735||Homozygous familial hypercholesterolemia||http://www.orpha.net/ORDO/Orphanet_391665
942||5965||Seborrhea-like dermatitis with psoriasiform elements||http://www.orpha.net/ORDO/Orphanet_168606
943||5877||Linear nevus sebaceus syndrome||http://www.orpha.net/ORDO/Orphanet_2612
944||5261||Mitochondrial non-syndromic sensorineural deafness with susceptibility to aminoglycoside exposure||http://www.orpha.net/ORDO/Orphanet_168609
946||12715||Autosomal recessive axonal neuropathy with neuromyotonia||http://www.orpha.net/ORDO/Orphanet_324442
945||10734||12p12.1 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_313884
947||15549||Leukoencephalopathy with mild cerebellar ataxia and white matter edema||http://www.orpha.net/ORDO/Orphanet_363540
948||1415||Autosomal recessive limb-girdle muscular dystrophy due to desmin deficiency||http://www.orpha.net/ORDO/Orphanet_363543
949||1022||Apis mellifera mellifera||http://purl.obolibrary.org/obo/NCBITaxon_44477
950||7248||Low birth weight - dwarfism - dysgammaglobulinemia||http://www.orpha.net/ORDO/Orphanet_2621
951||7986||Geleophysic dysplasia||http://www.orpha.net/ORDO/Orphanet_2623
952||1826||Glycine soja||http://purl.obolibrary.org/obo/NCBITaxon_3848
953||1826||Glycine max||http://purl.obolibrary.org/obo/NCBITaxon_3847
954||6244||Fibular aplasia - complex brachydactyly||http://www.orpha.net/ORDO/Orphanet_2639
955||10611||Mild Canavan disease||http://www.orpha.net/ORDO/Orphanet_314918
956||2318||Microcephalic osteodysplastic primordial dwarfism type II||http://www.orpha.net/ORDO/Orphanet_2637
957||2318||Microcephalic osteodysplastic primordial dwarfism types I and III||http://www.orpha.net/ORDO/Orphanet_2636
958||3540||Metatropic dysplasia||http://www.orpha.net/ORDO/Orphanet_2635
959||5025||Fusarium sp.||http://purl.obolibrary.org/obo/NCBITaxon_29916
960||1022||Callipepla californica||http://purl.obolibrary.org/obo/NCBITaxon_67771
961||5502||Actinobacillus pleuropneumoniae serovar 3||http://purl.obolibrary.org/obo/NCBITaxon_434270
962||7989||Mesomelic dwarfism, Nievergelt type||http://www.orpha.net/ORDO/Orphanet_2633
963||12973||Feingold syndrome type 1||http://www.orpha.net/ORDO/Orphanet_391641
964||7989||Mesomelic dwarfism, Reinhardt-Pfeiffer type||http://www.orpha.net/ORDO/Orphanet_2634
965||5300||Mesomelic dwarfism - cleft palate - camptodactyly||http://www.orpha.net/ORDO/Orphanet_2631
966||7989||Langer mesomelic dysplasia||http://www.orpha.net/ORDO/Orphanet_2632
967||12973||Feingold syndrome type 2||http://www.orpha.net/ORDO/Orphanet_391646
968||10611||Severe Canavan disease||http://www.orpha.net/ORDO/Orphanet_314911
969||770||GM17130||http://purl.obolibrary.org/obo/CLO_0015085
970||1006||breast carcinoma||http://www.ebi.ac.uk/efo/EFO_0000305
972||4139||Intellectual disability-strabismus syndrome||http://www.orpha.net/ORDO/Orphanet_363528
971||970||breast tumor luminal||http://www.ebi.ac.uk/efo/EFO_0000306
973||770||GM17131||http://purl.obolibrary.org/obo/CLO_0015087
974||7991||FGFR2-related bent bone dysplasia||http://www.orpha.net/ORDO/Orphanet_313855
976||120||breast adenocarcinoma||http://www.ebi.ac.uk/efo/EFO_0000304
975||770||GM17136||http://purl.obolibrary.org/obo/CLO_0015088
978||4139||Hypohidrosis-enamel hypoplasia-palmoplantar keratoderma-intellectual disability syndrome||http://www.orpha.net/ORDO/Orphanet_363523
977||10652||obsolete_bone marrow MMHCC||http://www.ebi.ac.uk/efo/EFO_0000301
979||10652||obsolete_brain||http://www.ebi.ac.uk/efo/EFO_0000302
980||1680||prothoracic leg disc||http://purl.obolibrary.org/obo/FBbt_00001781
981||4706||Infantile cerebellar-retinal degeneration||http://www.orpha.net/ORDO/Orphanet_313850
982||2430||Oculocutaneous albinism type 3||http://www.orpha.net/ORDO/Orphanet_79433
983||9833||Oculocutaneous albinism type 1B||http://www.orpha.net/ORDO/Orphanet_79434
984||2430||Oculocutaneous albinism type 4||http://www.orpha.net/ORDO/Orphanet_79435
985||3731||arthralgia||http://purl.obolibrary.org/obo/HP_0002829
986||770||GM17137||http://purl.obolibrary.org/obo/CLO_0015090
988||770||GM17134||http://purl.obolibrary.org/obo/CLO_0015093
987||5877||Generalized basaloid follicular hamartoma syndrome||http://www.orpha.net/ORDO/Orphanet_168632
990||1831||Hermansky-Pudlak syndrome||http://www.orpha.net/ORDO/Orphanet_79430
989||1497||Burkitts lymphoma||http://www.ebi.ac.uk/efo/EFO_0000309
991||12136||bronchoalveolar adenocarcinoma||http://www.ebi.ac.uk/efo/EFO_0000308
992||9833||Oculocutaneous albinism type 1A||http://www.orpha.net/ORDO/Orphanet_79431
993||2672||bronchial epithelium||http://www.ebi.ac.uk/efo/EFO_0000307
995||2430||Oculocutaneous albinism type 2||http://www.orpha.net/ORDO/Orphanet_79432
994||770||GM17135||http://purl.obolibrary.org/obo/CLO_0015094
996||3114||X-linked non progressive cerebellar ataxia||http://www.orpha.net/ORDO/Orphanet_314978
997||3640||cardiac mesoderm primordium||http://www.ebi.ac.uk/efo/EFO_0000315
998||4803||Familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome||http://www.orpha.net/ORDO/Orphanet_313846
999||10652||obsolete_cardiac ventricle||http://www.ebi.ac.uk/efo/EFO_0000317
1000||770||GM17835||http://purl.obolibrary.org/obo/CLO_0016520
1001||10652||obsolete_calpainopathy||http://www.ebi.ac.uk/efo/EFO_0000310
1002||2162||cancer||http://www.ebi.ac.uk/efo/EFO_0000311
1005||14756||cancer site||http://www.ebi.ac.uk/efo/EFO_0000312
1004||770||GM17831||http://purl.obolibrary.org/obo/CLO_0016522
1003||266||Mitochondrial DNA depletion syndrome, hepatocerebrorenal form||http://www.orpha.net/ORDO/Orphanet_363534
1007||770||GM17828||http://purl.obolibrary.org/obo/CLO_0016521
1006||1002||carcinoma||http://www.ebi.ac.uk/efo/EFO_0000313
1008||770||GM17840||http://purl.obolibrary.org/obo/CLO_0016524
1009||770||GM17839||http://purl.obolibrary.org/obo/CLO_0016523
1010||770||GM17838||http://purl.obolibrary.org/obo/CLO_0016526
1011||770||GM17837||http://purl.obolibrary.org/obo/CLO_0016525
1012||770||GM17827||http://purl.obolibrary.org/obo/CLO_0016528
1013||770||GM17841||http://purl.obolibrary.org/obo/CLO_0016527
1014||7111||process||http://www.ifomis.org/bfo/1.1/span#ProcessualEntity
1015||1391||cardiovascular disease||http://www.ebi.ac.uk/efo/EFO_0000319
1016||1015||cardiomyopathy||http://www.ebi.ac.uk/efo/EFO_0000318
1017||770||GM17133||http://purl.obolibrary.org/obo/CLO_0015082
1018||770||GM17132||http://purl.obolibrary.org/obo/CLO_0015081
1019||13678||imaginal disc||http://purl.obolibrary.org/obo/FBbt_00001761
1020||770||GM17818||http://purl.obolibrary.org/obo/CLO_0016511
1021||770||GM17817||http://purl.obolibrary.org/obo/CLO_0016510
1023||1732||Hereditary persistence of alpha-fetoprotein||http://www.orpha.net/ORDO/Orphanet_168615
1022||5005||Eukaryota||http://purl.obolibrary.org/obo/NCBITaxon_2759
1024||5126||Rare hemorrhagic disorder due to a constitutional platelet anomaly||http://www.orpha.net/ORDO/Orphanet_71202
1025||13695||eye-antennal disc||http://purl.obolibrary.org/obo/FBbt_00001766
1026||770||GM17833||http://purl.obolibrary.org/obo/CLO_0016519
1027||770||GM17826||http://purl.obolibrary.org/obo/CLO_0016518
1028||770||GM17825||http://purl.obolibrary.org/obo/CLO_0016517
1029||770||GM17824||http://purl.obolibrary.org/obo/CLO_0016516
1030||770||GM17823||http://purl.obolibrary.org/obo/CLO_0016515
1031||9372||Osteogenesis imperfecta type 1||http://www.orpha.net/ORDO/Orphanet_216796
1032||10275||Transient bullous dermolysis of the newborn||http://www.orpha.net/ORDO/Orphanet_79411
1034||323||Woolly hair nevus||http://www.orpha.net/ORDO/Orphanet_79414
1033||6299||Oscheius tipulae||http://purl.obolibrary.org/obo/NCBITaxon_141969
1036||4705||Coats plus syndrome||http://www.orpha.net/ORDO/Orphanet_313838
1035||6903||Renal-hepatic-pancreatic dysplasia||http://www.orpha.net/ORDO/Orphanet_294415
1037||10994||phosphate||http://purl.obolibrary.org/obo/CHEBI_26020
1038||1732||Congenital deficiency in alpha-fetoprotein||http://www.orpha.net/ORDO/Orphanet_168612
1039||10275||Pretibial dystrophic epidermolysis bullosa||http://www.orpha.net/ORDO/Orphanet_79410
1040||8190||aristolochic acid||http://purl.obolibrary.org/obo/CHEBI_2825
1041||770||GM17812||http://purl.obolibrary.org/obo/CLO_0016500
1042||10994||3,3 ,4,4 -tetrachlorobiphenyl||http://purl.obolibrary.org/obo/CHEBI_1367
1043||5499||Autosomal thrombocytopenia with normal platelets||http://www.orpha.net/ORDO/Orphanet_168629
1045||13689||posterior lateral line||http://purl.obolibrary.org/obo/UBERON_0006334
1044||9558||Retinal cavernous hemangioma||http://www.orpha.net/ORDO/Orphanet_71213
1046||770||GM17815||http://purl.obolibrary.org/obo/CLO_0016506
1047||770||GM17806||http://purl.obolibrary.org/obo/CLO_0016505
1048||770||GM17814||http://purl.obolibrary.org/obo/CLO_0016508
1049||770||GM17813||http://purl.obolibrary.org/obo/CLO_0016507
1050||770||GM17810||http://purl.obolibrary.org/obo/CLO_0016502
1051||770||GM17809||http://purl.obolibrary.org/obo/CLO_0016501
1053||770||GM17808||http://purl.obolibrary.org/obo/CLO_0016504
1052||10275||Recessive dystrophic epidermolysis bullosa inversa||http://www.orpha.net/ORDO/Orphanet_79409
1054||770||GM17807||http://purl.obolibrary.org/obo/CLO_0016503
1055||5578||Severe generalized recessive dystrophic epidermolysis bullosa||http://www.orpha.net/ORDO/Orphanet_79408
1056||10278||Late-onset junctional epidermolysis bullosa||http://www.orpha.net/ORDO/Orphanet_79406
1057||5578||Junctional epidermolysis bullosa, Herlitz type||http://www.orpha.net/ORDO/Orphanet_79404
1058||10278||Junctional epidermolysis bullosa inversa||http://www.orpha.net/ORDO/Orphanet_79405
1060||770||GM17816||http://purl.obolibrary.org/obo/CLO_0016509
1059||5585||Generalized junctional epidermolysis bullosa, non-Herlitz type||http://www.orpha.net/ORDO/Orphanet_79402
1061||10278||Junctional epidermolysis bullosa - pyloric atresia||http://www.orpha.net/ORDO/Orphanet_79403
1062||12736||Localized epidermolysis bullosa simplex||http://www.orpha.net/ORDO/Orphanet_79400
1063||12736||Epidermolysis bullosa simplex, Ogna type||http://www.orpha.net/ORDO/Orphanet_79401
1064||4999||Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency||http://www.orpha.net/ORDO/Orphanet_71212
1065||6610||Familial scaphocephaly syndrome, McGillivray type||http://www.orpha.net/ORDO/Orphanet_168624
1066||7972||Dysplasia of head of femur, Meyer type||http://www.orpha.net/ORDO/Orphanet_168621
1067||1022||Solea senegalensis||http://purl.obolibrary.org/obo/NCBITaxon_28829
1068||10994||theophylline||http://purl.obolibrary.org/obo/CHEBI_28177
1069||1022||Sarcophaga crassipalpis||http://purl.obolibrary.org/obo/NCBITaxon_59312
1070||2322||Atypical Werner syndrome||http://www.orpha.net/ORDO/Orphanet_79474
1071||4509||Porphyria variegata||http://www.orpha.net/ORDO/Orphanet_79473
1072||7671||Griscelli disease type 1||http://www.orpha.net/ORDO/Orphanet_79476
1073||7671||Griscelli disease type 3||http://www.orpha.net/ORDO/Orphanet_79478
1074||5882||Griscelli disease type 2||http://www.orpha.net/ORDO/Orphanet_79477
1075||770||GM17745||http://purl.obolibrary.org/obo/CLO_0016567
1076||770||GM17744||http://purl.obolibrary.org/obo/CLO_0016568
1077||1022||Pyropia yezoensis||http://purl.obolibrary.org/obo/NCBITaxon_2788
1079||770||GM17753||http://purl.obolibrary.org/obo/CLO_0016560
1078||9718||Optic nerve edema-splenomegaly syndrome||http://www.orpha.net/ORDO/Orphanet_313800
1080||770||GM17752||http://purl.obolibrary.org/obo/CLO_0016561
1081||770||GM17749||http://purl.obolibrary.org/obo/CLO_0016564
1082||770||GM17747||http://purl.obolibrary.org/obo/CLO_0016565
1083||770||GM17746||http://purl.obolibrary.org/obo/CLO_0016566
1084||15549||Hereditary diffuse leukoencephalopathy with axonal spheroids and pigmented glia||http://www.orpha.net/ORDO/Orphanet_313808
1085||5025||Trichophyton longifusum||http://purl.obolibrary.org/obo/NCBITaxon_446639
1086||4179||concentration of||http://purl.obolibrary.org/obo/PATO_0000033
1087||8190||pirinixic acid||http://purl.obolibrary.org/obo/CHEBI_32509
1088||10994||2,3,7,8-tetrachlorodibenzodioxine||http://purl.obolibrary.org/obo/CHEBI_28119
1089||770||GM17754||http://purl.obolibrary.org/obo/CLO_0016558
1091||14325||lymphadenitis||http://purl.obolibrary.org/obo/HP_0002840
1090||770||GM17756||http://purl.obolibrary.org/obo/CLO_0016554
1092||770||GM17755||http://purl.obolibrary.org/obo/CLO_0016555
1093||192||Milroy disease||http://www.orpha.net/ORDO/Orphanet_79452
1094||6596||docosahexaenoic acid||http://purl.obolibrary.org/obo/CHEBI_28125
1095||4139||Severe intellectual disability and progressive spastic paraplegia||http://www.orpha.net/ORDO/Orphanet_280763
1096||1826||Carthamus tinctorius||http://purl.obolibrary.org/obo/NCBITaxon_4222
1097||192||Non hereditary congenital primary lymphedema||http://www.orpha.net/ORDO/Orphanet_79450
1098||10551||Follicular atrophoderma-basal cell carcinoma||http://www.orpha.net/ORDO/Orphanet_79459
1099||5317||Oley syndrome||http://www.orpha.net/ORDO/Orphanet_79458
1100||5959||Cataract-congenital heart disease-neural tube defect syndrome||http://www.orpha.net/ORDO/Orphanet_314993
1101||5502||Lactobacillus rossiae||http://purl.obolibrary.org/obo/NCBITaxon_231049
1104||1826||Helianthus annuus||http://purl.obolibrary.org/obo/NCBITaxon_4232
1102||9383||Pseudohypoparathyroidism type 1A||http://www.orpha.net/ORDO/Orphanet_79443
1103||10994||ponasterone A||http://purl.obolibrary.org/obo/CHEBI_28135
1105||5300||Auricular abnormalities - cleft lip with or without cleft palate - ocular abnormalities||http://www.orpha.net/ORDO/Orphanet_77300
1106||12769||Oculo-oto-facial dysplasia||http://www.orpha.net/ORDO/Orphanet_77302
1107||6022||Monosomy 9q22.3||http://www.orpha.net/ORDO/Orphanet_77301
1109||2606||X-linked lethal multiple pterygium syndrome||http://www.orpha.net/ORDO/Orphanet_79447
1108||4705||Not NOTCH3-related small vessel disease of the brain||http://www.orpha.net/ORDO/Orphanet_77304
1110||5502||Salmonella enterica subsp. enterica serovar Dublin||http://purl.obolibrary.org/obo/NCBITaxon_98360
1111||9383||Pseudopseudohypoparathyroidism||http://www.orpha.net/ORDO/Orphanet_79445
1112||9383||Pseudohypoparathyroidism type 1C||http://www.orpha.net/ORDO/Orphanet_79444
1113||13448||embryonic ganglion mother cell||http://www.ebi.ac.uk/efo/EFO_0000459
1114||13448||embryonic frontal ganglion||http://www.ebi.ac.uk/efo/EFO_0000458
1115||13448||embryonic foregut sensory structure||http://www.ebi.ac.uk/efo/EFO_0000457
1116||13448||embryonic foregut||http://www.ebi.ac.uk/efo/EFO_0000456
1117||13448||embryonic esophagus||http://www.ebi.ac.uk/efo/EFO_0000455
1118||13448||embryonic esophageal ganglion||http://www.ebi.ac.uk/efo/EFO_0000454
1119||13448||embryonic epipharynx||http://www.ebi.ac.uk/efo/EFO_0000453
1120||13448||embryonic dorsal epidermis||http://www.ebi.ac.uk/efo/EFO_0000452
1121||13448||embryonic dorsal apodeme||http://www.ebi.ac.uk/efo/EFO_0000451
1122||13448||embryonic cuprophilic cell||http://www.ebi.ac.uk/efo/EFO_0000450
1123||1124||Male infertility with spermatogenesis disorder||http://www.orpha.net/ORDO/Orphanet_399775
1124||1140||Male infertility due to sperm disorder||http://www.orpha.net/ORDO/Orphanet_399771
1126||13448||embryonic central nervous system||http://www.ebi.ac.uk/efo/EFO_0000447
1125||7111||material entity||http://www.ifomis.org/bfo/1.1/snap#MaterialEntity
1127||13448||embryonic central brain surface glia||http://www.ebi.ac.uk/efo/EFO_0000446
1128||13448||embryonic corpus cardiacum||http://www.ebi.ac.uk/efo/EFO_0000449
1129||13448||embryonic corpus allatum||http://www.ebi.ac.uk/efo/EFO_0000448
1130||13448||embryonic central brain mushroom body||http://www.ebi.ac.uk/efo/EFO_0000443
1131||13448||embryonic central brain glia||http://www.ebi.ac.uk/efo/EFO_0000442
1132||13448||embryonic central brain pars intercerebralis||http://www.ebi.ac.uk/efo/EFO_0000445
1133||13448||embryonic central brain neuron||http://www.ebi.ac.uk/efo/EFO_0000444
1134||5502||Synechocystis sp. PCC 6803||http://purl.obolibrary.org/obo/NCBITaxon_1148
1135||13448||embryonic central brain||http://www.ebi.ac.uk/efo/EFO_0000441
1136||13448||embryonic brain||http://www.ebi.ac.uk/efo/EFO_0000440
1137||1826||Citrus sinensis||http://purl.obolibrary.org/obo/NCBITaxon_2711
1138||10080||Late infantile neuronal ceroid lipofuscinosis||http://www.orpha.net/ORDO/Orphanet_168491
1139||3352||Arabidopsis suecica||http://purl.obolibrary.org/obo/NCBITaxon_45249
1140||5520||Male infertility due to gonadal dysgenesis or sperm disorder||http://www.orpha.net/ORDO/Orphanet_399764
1141||5025||Tuber melanosporum||http://purl.obolibrary.org/obo/NCBITaxon_39416
1142||120||esophageal adenocarcinoma||http://www.ebi.ac.uk/efo/EFO_0000478
1143||1826||Citrus limon||http://purl.obolibrary.org/obo/NCBITaxon_2708
1144||10652||obsolete_epithelial cell of lung||http://www.ebi.ac.uk/efo/EFO_0000476
1145||1393||Insulin-resistance syndrome type A||http://www.orpha.net/ORDO/Orphanet_2297
1146||15422||essential thrombocythemia||http://www.ebi.ac.uk/efo/EFO_0000479
1147||1393||Insulin-resistance syndrome type B||http://www.orpha.net/ORDO/Orphanet_2298
1148||2822||environmental stress||http://www.ebi.ac.uk/efo/EFO_0000470
1149||10898||Ehlers-Danlos syndrome type 11||http://www.orpha.net/ORDO/Orphanet_2295
1150||2165||epilepsy||http://www.ebi.ac.uk/efo/EFO_0000474
1151||1153||epigenetic status||http://www.ebi.ac.uk/efo/EFO_0000473
1152||7991||Congenital bowing of long bones||http://www.orpha.net/ORDO/Orphanet_2292
1153||15538||epigenetic factor||http://www.ebi.ac.uk/efo/EFO_0000472
1154||3866||Microvillus inclusion disease||http://www.orpha.net/ORDO/Orphanet_2290
1155||5502||Synechococcus elongatus PCC 7942||http://purl.obolibrary.org/obo/NCBITaxon_1140
1156||13496||Human adenovirus 7||http://purl.obolibrary.org/obo/NCBITaxon_10519
1157||1015||endocarditis||http://www.ebi.ac.uk/efo/EFO_0000465
1158||1979||emphysema||http://www.ebi.ac.uk/efo/EFO_0000464
1159||1006||endometrioid carcinoma||http://www.ebi.ac.uk/efo/EFO_0000466
1161||2090||Solitary median maxillary central incisor syndrome||http://www.orpha.net/ORDO/Orphanet_2286
1160||1125||environmental factor||http://www.ebi.ac.uk/efo/EFO_0000469
1163||1619||Fused mandibular incisors||http://www.orpha.net/ORDO/Orphanet_2287
1162||10652||obsolete_environment||http://www.ebi.ac.uk/efo/EFO_0000468
1164||4706||Neuronal intranuclear inclusion disease||http://www.orpha.net/ORDO/Orphanet_2289
1166||2252||Dysmorphism - short stature - deafness - disorder of sex development||http://www.orpha.net/ORDO/Orphanet_2282
1165||1022||Acropora millepora||http://purl.obolibrary.org/obo/NCBITaxon_45264
1167||4695||Primary basilar impression||http://www.orpha.net/ORDO/Orphanet_2285
1168||13448||embryonic gastric caecum||http://www.ebi.ac.uk/efo/EFO_0000460
1169||10652||obsolete_Emery-Dreifuss muscular dystrophy||http://www.ebi.ac.uk/efo/EFO_0000463
1170||2021||Intellectual disability-brachydactyly-Pierre Robin syndrome||http://www.orpha.net/ORDO/Orphanet_364577
1172||1123||Male infertility with spermatogenesis disorder due to single gene mutation||http://www.orpha.net/ORDO/Orphanet_399786
1171||1174||Acrofacial dysostosis||http://www.orpha.net/ORDO/Orphanet_364574
1173||13496||Human adenovirus 41||http://purl.obolibrary.org/obo/NCBITaxon_10524
1174||6249||Dysostosis with limb and face anomalies as a major feature||http://www.orpha.net/ORDO/Orphanet_364571
1175||1761||fetal growth restriction||http://www.ebi.ac.uk/efo/EFO_0000495
1176||704||family history||http://www.ebi.ac.uk/efo/EFO_0000493
1177||11868||feature extraction||http://www.ebi.ac.uk/efo/EFO_0000494
1178||4692||Ichthyosis - hepatosplenomegaly - cerebellar degeneration||http://www.orpha.net/ORDO/Orphanet_2274
1179||10652||obsolete_facioscapulohumeral muscular dystrophy||http://www.ebi.ac.uk/efo/EFO_0000491
1180||321||Ichthyosis follicularis - alopecia - photophobia||http://www.orpha.net/ORDO/Orphanet_2273
1181||10652||obsolete_familial combined hyperlipidemia||http://www.ebi.ac.uk/efo/EFO_0000492
1182||5317||Ichthyosis - oral and digital anomalies||http://www.orpha.net/ORDO/Orphanet_2272
1184||14867||Congenital ichthyosis - microcephalus - tetraplegia||http://www.orpha.net/ORDO/Orphanet_2271
1183||4335||extraction protocol||http://www.ebi.ac.uk/efo/EFO_0000490
1185||7319||Ichthyosis - intellectual disability - dwarfism - renal impairment||http://www.orpha.net/ORDO/Orphanet_2278
1186||4734||Primary bone dysplasia||http://www.orpha.net/ORDO/Orphanet_364526
1187||109||follicular thyroid adenoma||http://www.ebi.ac.uk/efo/EFO_0000499
1188||2162||fibromatosis||http://www.ebi.ac.uk/efo/EFO_0000497
1189||13496||Guanarito virus||http://purl.obolibrary.org/obo/NCBITaxon_45219
1190||5838||morphology||http://purl.obolibrary.org/obo/PATO_0000051
1191||5048||Adrenogenital syndrome||http://www.orpha.net/ORDO/Orphanet_181412
1192||10994||glucitol||http://purl.obolibrary.org/obo/CHEBI_30911
1193||13496||Amapari virus||http://purl.obolibrary.org/obo/NCBITaxon_45218
1194||2846||event free survival time||http://www.ebi.ac.uk/efo/EFO_0000482
1195||12507||exercise||http://www.ebi.ac.uk/efo/EFO_0000483
1196||10652||obsolete_experiment type||http://www.ebi.ac.uk/efo/EFO_0000484
1197||10652||obsolete_experimental design||http://www.ebi.ac.uk/efo/EFO_0000485
1198||2252||Hypospadias - intellectual disability, Goldblatt type||http://www.orpha.net/ORDO/Orphanet_2261
1199||14970||event death||http://www.ebi.ac.uk/efo/EFO_0000480
1200||10652||obsolete_event distant metastases||http://www.ebi.ac.uk/efo/EFO_0000481
1201||14891||Ichthyosis-cheek-eyebrow syndrome||http://www.orpha.net/ORDO/Orphanet_2267
1202||4139||Hypotrichosis-intellectual disability, Lopes type||http://www.orpha.net/ORDO/Orphanet_2266
1203||306||Ichthyosis - alopecia - eclabion - ectropion - intellectual disability||http://www.orpha.net/ORDO/Orphanet_2269
1205||13883||exposure||http://www.ebi.ac.uk/efo/EFO_0000487
1204||4255||ICF syndrome||http://www.orpha.net/ORDO/Orphanet_2268
1206||13992||external control ratio||http://www.ebi.ac.uk/efo/EFO_0000488
1208||11622||extra-adrenal sympathetic paraganglioma||http://www.ebi.ac.uk/efo/EFO_0000489
1207||5502||Rhizobium etli CFN 42||http://purl.obolibrary.org/obo/NCBITaxon_347834
1209||10143||Spondyloepimetaphyseal dysplasia, Genevi ve type||http://www.orpha.net/ORDO/Orphanet_168454
1210||10862||Benign partial infantile seizures||http://www.orpha.net/ORDO/Orphanet_166311
1211||759||Syndrome with hypoparathyroidism||http://www.orpha.net/ORDO/Orphanet_181402
1213||10143||Spondyloepimetaphyseal dysplasia - abnormal dentition||http://www.orpha.net/ORDO/Orphanet_168451
1212||10994||methoprene||http://purl.obolibrary.org/obo/CHEBI_34839
1214||11882||Radial hypoplasia - triphalangeal thumbs - hypospadias - maxillary diastema||http://www.orpha.net/ORDO/Orphanet_2252
1215||6246||Thumb deformity - alopecia - pigmentation anomaly||http://www.orpha.net/ORDO/Orphanet_2251
1216||1306||Hyposmia - nasal and ocular hypoplasia - hypogonadotropic hypogonadism||http://www.orpha.net/ORDO/Orphanet_2250
1217||1022||Amblyomma americanum||http://purl.obolibrary.org/obo/NCBITaxon_6943
1219||1022||Rhipicephalus microplus||http://purl.obolibrary.org/obo/NCBITaxon_6941
1218||5053||Familial primary pulmonary hypoplasia||http://www.orpha.net/ORDO/Orphanet_2257
1220||7319||Fibulo-ulnar hypoplasia - renal anomalies||http://www.orpha.net/ORDO/Orphanet_2256
1221||5055||Pancreatic hypoplasia - diabetes - congenital heart disease||http://www.orpha.net/ORDO/Orphanet_2255
1222||2450||Pontocerebellar hypoplasia type 1||http://www.orpha.net/ORDO/Orphanet_2254
1224||1022||Ixodes scapularis||http://purl.obolibrary.org/obo/NCBITaxon_6945
1223||9681||Foveal hypoplasia - presenile cataract||http://www.orpha.net/ORDO/Orphanet_2253
1225||10080||Congenital neuronal ceroid lipofuscinosis||http://www.orpha.net/ORDO/Orphanet_168486
1226||1186||Frontootopalatodigital syndrome||http://www.orpha.net/ORDO/Orphanet_364541
1227||7482||purine nucleotide metabolic process||http://purl.obolibrary.org/obo/GO_0006163
1228||1227||purine nucleotide biosynthetic process||http://purl.obolibrary.org/obo/GO_0006164
1229||7319||Megacystis-microcolon-intestinal hypoperistalsis syndrome||http://www.orpha.net/ORDO/Orphanet_2241
1230||6244||Ulna hypoplasia - intellectual disability||http://www.orpha.net/ORDO/Orphanet_2249
1231||1234||deviation(from_normal)||http://purl.obolibrary.org/obo/PATO_0000069
1232||1186||Primary bone dysplasia with micromelia||http://www.orpha.net/ORDO/Orphanet_364536
1233||1022||Neolamprologus brichardi||http://purl.obolibrary.org/obo/NCBITaxon_32507
1235||1186||Primary bone dysplasia with progressive ossification of skin, skeletal muscle, fascia, tendons and ligaments||http://www.orpha.net/ORDO/Orphanet_364531
1234||5838||qualitative||http://purl.obolibrary.org/obo/PATO_0000068
1236||13496||Human papillomavirus||http://purl.obolibrary.org/obo/NCBITaxon_10566
1237||4139||Primary non-essential cutis verticis gyrata||http://www.orpha.net/ORDO/Orphanet_357225
1238||1249||Familial isolated hypoparathyroidism due to agenesis of parathyroid gland||http://www.orpha.net/ORDO/Orphanet_2239
1239||5025||Candida parapsilosis||http://purl.obolibrary.org/obo/NCBITaxon_5480
1240||1729||overgrowth||http://purl.obolibrary.org/obo/HP_0001548
1242||1767||Primary hypergonadotropic hypogonadism - partial alopecia||http://www.orpha.net/ORDO/Orphanet_2232
1241||5025||Candida glabrata||http://purl.obolibrary.org/obo/NCBITaxon_5478
1243||1767||Hypogonadism - mitral valve prolapse - intellectual disability||http://www.orpha.net/ORDO/Orphanet_2233
1244||1767||Male hypergonadotropic hypogonadism - intellectual disability - skeletal anomalies||http://www.orpha.net/ORDO/Orphanet_2234
1246||1595||ascites||http://purl.obolibrary.org/obo/HP_0001541
1245||1306||Hypogonadotropic hypogonadism - retinitis pigmentosa||http://www.orpha.net/ORDO/Orphanet_2235
1247||5126||Rare thrombotic disorder due to a constitutional coagulation factors defect||http://www.orpha.net/ORDO/Orphanet_248361
1248||1211||Hypoparathyroidism - deafness - renal disease||http://www.orpha.net/ORDO/Orphanet_2237
1249||759||Familial isolated hypoparathyroidism||http://www.orpha.net/ORDO/Orphanet_2238
1250||1306||Hypogonadotropic hypogonadism - frontoparietal alopecia||http://www.orpha.net/ORDO/Orphanet_2230
1251||1022||Anopheles gambiae S||http://purl.obolibrary.org/obo/NCBITaxon_377270
1252||5937||Severe combined immunodeficiency due to CARD11 deficiency||http://www.orpha.net/ORDO/Orphanet_357237
1253||1767||Dilated cardiomyopathy - hypergonadotropic hypogonadism||http://www.orpha.net/ORDO/Orphanet_2229
1254||306||Hypodontia - dysplasia of nails||http://www.orpha.net/ORDO/Orphanet_2228
1255||5025||Candida albicans||http://purl.obolibrary.org/obo/NCBITaxon_5476
1256||10994||neocarzinostatin chromophore||http://purl.obolibrary.org/obo/CHEBI_29655
1257||306||Hypertrichosis lanuginosa congenita||http://www.orpha.net/ORDO/Orphanet_2222
1258||306||Hypertrichosis cubiti - short stature||http://www.orpha.net/ORDO/Orphanet_2220
1259||14068||Hypertryptophanemia||http://www.orpha.net/ORDO/Orphanet_2224
1260||8611||Tetrahydrobiopterin-responsive hyperphenylalaninemia/phenylketonuria||http://www.orpha.net/ORDO/Orphanet_293284
1262||10994||N-nitrosodiethylamine||http://purl.obolibrary.org/obo/CHEBI_34873
1261||5502||Eubacterium rectale||http://purl.obolibrary.org/obo/NCBITaxon_39491
1263||5502||Burkholderia pseudomallei||http://purl.obolibrary.org/obo/NCBITaxon_28450
1264||5502||Streptococcus pneumoniae TIGR4||http://purl.obolibrary.org/obo/NCBITaxon_170187
1265||322||Cervical hypertrichosis - peripheral neuropathy||http://www.orpha.net/ORDO/Orphanet_2218
1266||1434||Benign partial epilepsy with secondarily generalized seizures in infancy||http://www.orpha.net/ORDO/Orphanet_166302
1267||2252||Hypertelorism-microtia-facial clefting syndrome||http://www.orpha.net/ORDO/Orphanet_2213
1268||1210||Benign infantile seizures associated to mild gastroenteritis||http://www.orpha.net/ORDO/Orphanet_166305
1269||12083||Malignant hyperthermia - arthrogryposis - torticollis||http://www.orpha.net/ORDO/Orphanet_2215
1270||1210||Benign infantile focal epilepsy with midline spikes and wave during sleep||http://www.orpha.net/ORDO/Orphanet_166308
1271||11882||Hypertelorism - hypospadias - polysyndactyly syndrome||http://www.orpha.net/ORDO/Orphanet_2211
1272||5025||Zymoseptoria tritici||http://purl.obolibrary.org/obo/NCBITaxon_1047171
1273||1669||melanoma cell line||http://purl.obolibrary.org/obo/BTO_0000849
1274||2307||nucleobase-containing compound metabolic process||http://purl.obolibrary.org/obo/GO_0006139
1275||1833||Maternal hyperphenylalaninemia||http://www.orpha.net/ORDO/Orphanet_2209
1276||756||Familial primary hyperparathyroidism||http://www.orpha.net/ORDO/Orphanet_2207
1277||7963||Ankylosing vertebral hyperostosis with tylosis||http://www.orpha.net/ORDO/Orphanet_2206
1278||7943||Dysplastic cortical hyperostosis||http://www.orpha.net/ORDO/Orphanet_2204
1280||2063||abnormality of the integument||http://purl.obolibrary.org/obo/HP_0001574
1279||5700||Palmoplantar keratoderma-deafness syndrome||http://www.orpha.net/ORDO/Orphanet_2202
1281||13972||Hyperlysinemia||http://www.orpha.net/ORDO/Orphanet_2203
1282||12316||Focal palmoplantar and gingival keratoderma||http://www.orpha.net/ORDO/Orphanet_2200
1283||5004||Palmoplantar keratoderma-spastic paralysis syndrome||http://www.orpha.net/ORDO/Orphanet_2201
1284||10994||nocodazole||http://purl.obolibrary.org/obo/CHEBI_34892
1285||5502||Cyanobacteria||http://purl.obolibrary.org/obo/NCBITaxon_1117
1286||7391||Mus musculus musculus||http://purl.obolibrary.org/obo/NCBITaxon_39442
1287||8191||tetrachloromethane||http://purl.obolibrary.org/obo/CHEBI_27385
1288||5502||Xanthomonas oryzae pv. oryzae KACC10331||http://purl.obolibrary.org/obo/NCBITaxon_291331
1289||1022||Teleopsis quinqueguttata||http://purl.obolibrary.org/obo/NCBITaxon_139650
1290||1022||Teleopsis whitei||http://purl.obolibrary.org/obo/NCBITaxon_139651
1291||5502||Citrobacter rodentium||http://purl.obolibrary.org/obo/NCBITaxon_67825
1292||1022||Teleopsis dalmanni||http://purl.obolibrary.org/obo/NCBITaxon_139649
1293||10994||4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone||http://purl.obolibrary.org/obo/CHEBI_32692
1294||11347||Hyperinsulinism due to HNF1A deficiency||http://www.orpha.net/ORDO/Orphanet_324575
1295||8190||folic acid||http://purl.obolibrary.org/obo/CHEBI_27470
1296||10994||genistein||http://purl.obolibrary.org/obo/CHEBI_28088
1297||7050||Autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain||http://www.orpha.net/ORDO/Orphanet_324585
1299||4228||Rare intellectual disability without developmental anomaly||http://www.orpha.net/ORDO/Orphanet_101685
1298||8791||Benign Samaritan congenital myopathy||http://www.orpha.net/ORDO/Orphanet_324581
1301||10994||piperonylbutoxide||http://purl.obolibrary.org/obo/CHEBI_32687
1300||7858||Familial dyskinesia and facial myokymia||http://www.orpha.net/ORDO/Orphanet_324588
1302||4732||Rare genetic dystonia||http://www.orpha.net/ORDO/Orphanet_391799
1303||4454||chromium||http://purl.obolibrary.org/obo/CHEBI_28073
1304||6420||Early-onset spastic ataxia-neuropathy syndrome||http://www.orpha.net/ORDO/Orphanet_313772
1305||1826||Cucumis melo subsp. melo||http://purl.obolibrary.org/obo/NCBITaxon_412675
1306||4513||Rare disorder with hypogonadotropic hypogonadism||http://www.orpha.net/ORDO/Orphanet_181387
1307||1568||Hypogonadotropic hypogonadism associated with other endocrinopathies||http://www.orpha.net/ORDO/Orphanet_181390
1308||5004||Hypopigmentation-punctate palmoplantar keratoderma syndrome||http://www.orpha.net/ORDO/Orphanet_324561
1309||5061||Growth hormone insensitivity syndrome||http://www.orpha.net/ORDO/Orphanet_181393
1310||12343||Hemolytic anemia due to glyceraldehyde-3-phosphate dehydrogenase deficiency||http://www.orpha.net/ORDO/Orphanet_248305
1311||9894||Pontocerebellar hypoplasia type 8||http://www.orpha.net/ORDO/Orphanet_324569
1312||10994||rifampicin||http://purl.obolibrary.org/obo/CHEBI_28077
1313||5039||Rare hyperthyroidism||http://www.orpha.net/ORDO/Orphanet_181399
1314||5039||Rare hypothyroidism||http://www.orpha.net/ORDO/Orphanet_181396
1315||6432||Combined oxidative phosphorylation defect type 11||http://www.orpha.net/ORDO/Orphanet_324535
1316||4775||Orofaciodigital syndrome||http://www.orpha.net/ORDO/Orphanet_140997
1317||2252||Jawad syndrome||http://www.orpha.net/ORDO/Orphanet_313795
1318||10140||Oculoauriculofrontonasal syndrome||http://www.orpha.net/ORDO/Orphanet_398156
1319||8190||amino acid||http://purl.obolibrary.org/obo/CHEBI_33709
1320||10994||methyltestosterone||http://purl.obolibrary.org/obo/CHEBI_27436
1321||2252||20p13 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_313781
1322||2252||Aphonia - deafness - retinal dystrophy - bifid halluces - intellectual disability||http://www.orpha.net/ORDO/Orphanet_324540
1323||10994||glyburide||http://purl.obolibrary.org/obo/CHEBI_5441
1324||1022||Ptomaphagus||http://purl.obolibrary.org/obo/NCBITaxon_351534
1325||306||Focal facial dermal dysplasia||http://www.orpha.net/ORDO/Orphanet_398166
1326||2063||abnormal phenotype of the cardiovascular system||http://purl.obolibrary.org/obo/HP_0001626
1327||8303||Non-syndromic genetic deafness||http://www.orpha.net/ORDO/Orphanet_87884
1328||7377||RHYNS syndrome||http://www.orpha.net/ORDO/Orphanet_140976
1329||770||GM17797||http://purl.obolibrary.org/obo/CLO_0016494
1330||770||GM17796||http://purl.obolibrary.org/obo/CLO_0016493
1331||770||GM17803||http://purl.obolibrary.org/obo/CLO_0016496
1332||770||GM17802||http://purl.obolibrary.org/obo/CLO_0016495
1333||770||GM17805||http://purl.obolibrary.org/obo/CLO_0016498
1334||770||GM17804||http://purl.obolibrary.org/obo/CLO_0016497
1335||770||GM17811||http://purl.obolibrary.org/obo/CLO_0016499
1336||1326||prolonged QT interval||http://purl.obolibrary.org/obo/HP_0001657
1337||1325||Focal facial dermal dysplasia type II||http://www.orpha.net/ORDO/Orphanet_398173
1338||2252||Sialidosis type 2||http://www.orpha.net/ORDO/Orphanet_87876
1339||4705||Primary central nervous system vasculitis||http://www.orpha.net/ORDO/Orphanet_140989
1340||4266||Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation||http://www.orpha.net/ORDO/Orphanet_324525
1341||770||GM17798||http://purl.obolibrary.org/obo/CLO_0016489
1342||11889||Isolated delta-storage pool disease||http://www.orpha.net/ORDO/Orphanet_248340
1343||1022||Cryptococcus||http://purl.obolibrary.org/obo/NCBITaxon_5415
1344||770||GM17800||http://purl.obolibrary.org/obo/CLO_0016491
1345||770||GM17801||http://purl.obolibrary.org/obo/CLO_0016492
1346||1325||Focal facial dermal dysplasia type IV||http://www.orpha.net/ORDO/Orphanet_398189
1347||770||GM17799||http://purl.obolibrary.org/obo/CLO_0016490
1348||8190||10-trans,12-cis-octadecadienoic acid||http://purl.obolibrary.org/obo/CHEBI_44526
1349||4661||vancomycin||http://purl.obolibrary.org/obo/CHEBI_28001
1350||426||Autosomal dominant macrothrombocytopenia||http://www.orpha.net/ORDO/Orphanet_140957
1351||10994||camphorsulfonic acid||http://purl.obolibrary.org/obo/CHEBI_55379
1352||5838||mass||http://purl.obolibrary.org/obo/PATO_0000125
1353||10633||Syndactyly - telecanthus - anogenital and renal malformations||http://www.orpha.net/ORDO/Orphanet_140952
1354||10994||kinetin||http://purl.obolibrary.org/obo/CHEBI_27407
1355||2063||abnormality of the immune system||http://purl.obolibrary.org/obo/HP_0002715
1356||10144||Spondylometaphyseal dysplasia, Golden type||http://www.orpha.net/ORDO/Orphanet_168544
1357||1355||recurrent infection||http://purl.obolibrary.org/obo/HP_0002719
1358||7319||Saldino-Mainzer syndrome||http://www.orpha.net/ORDO/Orphanet_140969
1359||5502||Bacillus cereus ATCC 14579||http://purl.obolibrary.org/obo/NCBITaxon_226900
1360||10144||Axial spondylometaphyseal dysplasia||http://www.orpha.net/ORDO/Orphanet_168549
1361||5300||Bilateral microtia - deafness - cleft palate||http://www.orpha.net/ORDO/Orphanet_140963
1362||5502||Calyptogena kilmeri gill symbiont||http://purl.obolibrary.org/obo/NCBITaxon_72600
1364||12317||Palmoplantar keratoderma, Nagashima type||http://www.orpha.net/ORDO/Orphanet_140966
1363||5502||Calyptogena pacifica gill symbiont||http://purl.obolibrary.org/obo/NCBITaxon_72603
1365||10994||desferrioxamine B||http://purl.obolibrary.org/obo/CHEBI_4356
1366||12539||X-linked severe congenital neutropenia||http://www.orpha.net/ORDO/Orphanet_86788
1367||2700||gonorrhea||http://purl.obolibrary.org/obo/DOID_7551
1368||10144||Spondylometaphyseal dysplasia - bowed forearms - facial dysmorphism||http://www.orpha.net/ORDO/Orphanet_168552
1369||10144||Spondylometaphyseal dysplasia, A4 type||http://www.orpha.net/ORDO/Orphanet_168555
1370||212||46,XY disorder of sex development - adrenal insufficiency due to CYP11A1 deficiency||http://www.orpha.net/ORDO/Orphanet_168558
1371||770||GM17850||http://purl.obolibrary.org/obo/CLO_0016450
1372||770||GM17847||http://purl.obolibrary.org/obo/CLO_0016455
1374||770||GM17846||http://purl.obolibrary.org/obo/CLO_0016456
1373||306||Lelis syndrome||http://www.orpha.net/ORDO/Orphanet_140936
1375||770||GM17845||http://purl.obolibrary.org/obo/CLO_0016453
1376||770||GM17844||http://purl.obolibrary.org/obo/CLO_0016454
1377||7955||Patella aplasia/hypoplasia||http://www.orpha.net/ORDO/Orphanet_86789
1379||770||GM17842||http://purl.obolibrary.org/obo/CLO_0016457
1378||5918||Linear atrophoderma of Moulin||http://www.orpha.net/ORDO/Orphanet_140933
1380||770||GM17843||http://purl.obolibrary.org/obo/CLO_0016458
1381||3019||46,XY gonadal dysgenesis - motor and sensory neuropathy||http://www.orpha.net/ORDO/Orphanet_168563
1382||5912||H syndrome||http://www.orpha.net/ORDO/Orphanet_168569
1383||6432||Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3||http://www.orpha.net/ORDO/Orphanet_168566
1384||5868||CLOVE syndrome||http://www.orpha.net/ORDO/Orphanet_140944
1385||770||GM17852||http://purl.obolibrary.org/obo/CLO_0016449
1386||1309||Short stature due to primary acid-labile subunit deficiency||http://www.orpha.net/ORDO/Orphanet_140941
1387||5502||Lactobacillus rhamnosus GG||http://purl.obolibrary.org/obo/NCBITaxon_568703
1388||1194||disease free survival||http://www.ebi.ac.uk/efo/EFO_0000409
1389||4834||Suarez-Stickler syndrome||http://www.orpha.net/ORDO/Orphanet_166277
1390||5519||Rare male infertility due to testicular endocrine disorder||http://www.orpha.net/ORDO/Orphanet_399685
1391||9803||disease||http://www.ebi.ac.uk/efo/EFO_0000408
1392||1016||dilated cardiomyopathy||http://www.ebi.ac.uk/efo/EFO_0000407
1393||5055||Rare insulin-resistance syndrome||http://www.orpha.net/ORDO/Orphanet_181368
1394||1319||phenylalanine||http://purl.obolibrary.org/obo/CHEBI_28044
1395||13496||Paramecium bursaria Chlorella virus 1||http://purl.obolibrary.org/obo/NCBITaxon_10506
1396||4834||Goldblatt syndrome||http://www.orpha.net/ORDO/Orphanet_166272
1398||1485||diabetes mellitus||http://www.ebi.ac.uk/efo/EFO_0000400
1397||5055||Thiamine-responsive megaloblastic anemia syndrome||http://www.orpha.net/ORDO/Orphanet_49827
1400||11443||Autosomal monosomy||http://www.orpha.net/ORDO/Orphanet_102020
1399||1485||diabetic nephropathy||http://www.ebi.ac.uk/efo/EFO_0000401
1401||1790||diffuse scleroderma||http://www.ebi.ac.uk/efo/EFO_0000404
1403||1391||digestive system disease||http://www.ebi.ac.uk/efo/EFO_0000405
1402||5700||Stapes ankylosis with broad thumbs and toes||http://www.orpha.net/ORDO/Orphanet_140917
1404||120||diffuse gastric adenocarcinoma||http://www.ebi.ac.uk/efo/EFO_0000402
1405||1497||diffuse large B-cell lymphoma||http://www.ebi.ac.uk/efo/EFO_0000403
1406||2656||dorsal histoblast nest abdominal||http://www.ebi.ac.uk/efo/EFO_0000418
1408||2656||dorsal epidermis primordium||http://www.ebi.ac.uk/efo/EFO_0000417
1409||5877||Porokeratotic eccrine ostial and dermal duct nevus||http://www.orpha.net/ORDO/Orphanet_166286
1407||10272||Childhood absence epilepsy||http://www.orpha.net/ORDO/Orphanet_64280
1410||2656||dorsal imaginal precursor||http://www.ebi.ac.uk/efo/EFO_0000419
1411||10898||X-linked Ehlers-Danlos syndrome||http://www.orpha.net/ORDO/Orphanet_75497
1412||4014||Ehlers-Danlos syndrome, progeroid type||http://www.orpha.net/ORDO/Orphanet_75496
1413||15||Familial sick sinus syndrome||http://www.orpha.net/ORDO/Orphanet_166282
1414||10174||Autosomal dominant limb-girdle muscular dystrophy||http://www.orpha.net/ORDO/Orphanet_102014
1416||1415||Autosomal recessive limb-girdle muscular dystrophy type 2J||http://www.orpha.net/ORDO/Orphanet_140922
1415||10174||Autosomal recessive limb-girdle muscular dystrophy||http://www.orpha.net/ORDO/Orphanet_102015
1417||8311||Pure hereditary spastic paraplegia||http://www.orpha.net/ORDO/Orphanet_102012
1418||8311||Complex hereditary spastic paraplegia||http://www.orpha.net/ORDO/Orphanet_102013
1419||2683||Other syndrome with lissencephaly as a major feature||http://www.orpha.net/ORDO/Orphanet_102010
1420||763||Benign familial neonatal-infantile seizures||http://www.orpha.net/ORDO/Orphanet_140927
1421||2683||Lissencephaly type 3||http://www.orpha.net/ORDO/Orphanet_102011
1422||9803||disease staging||http://www.ebi.ac.uk/efo/EFO_0000410
1423||10652||obsolete_disease state||http://www.ebi.ac.uk/efo/EFO_0000411
1424||13175||distant metastasis free survival||http://www.ebi.ac.uk/efo/EFO_0000412
1425||2656||dorsal apodeme specific anlage||http://www.ebi.ac.uk/efo/EFO_0000413
1426||10652||obsolete_ectoderm||http://www.ebi.ac.uk/efo/EFO_0000414
1427||2656||dorsal ectoderm anlage in statu nascendi||http://www.ebi.ac.uk/efo/EFO_0000415
1429||10994||(-)-demecolcine||http://purl.obolibrary.org/obo/CHEBI_4393
1428||2656||dorsal ectoderm primordium||http://www.ebi.ac.uk/efo/EFO_0000416
1430||1434||Benign partial epilepsy of infancy with complex partial seizures||http://www.orpha.net/ORDO/Orphanet_166299
1431||10652||obsolete_Duchenne muscular dystrophy||http://www.ebi.ac.uk/efo/EFO_0000429
1432||14970||dose||http://www.ebi.ac.uk/efo/EFO_0000428
1433||2683||Classic lissencephaly||http://www.orpha.net/ORDO/Orphanet_102009
1435||772||retinal cell||http://purl.obolibrary.org/obo/CL_0009004
1434||1210||Benign non-familial infantile seizures||http://www.orpha.net/ORDO/Orphanet_166295
1436||2656||dorsal trunk specific anlage||http://www.ebi.ac.uk/efo/EFO_0000426
1437||2656||dorsomedial neurosecretory cell||http://www.ebi.ac.uk/efo/EFO_0000427
1438||2656||dorsal ridge||http://www.ebi.ac.uk/efo/EFO_0000424
1439||2656||dorsal pharyngeal muscle primordium||http://www.ebi.ac.uk/efo/EFO_0000422
1440||2656||dorsal prothoracic pharyngeal muscle||http://www.ebi.ac.uk/efo/EFO_0000423
1441||10652||obsolete_dorsal mesothoracic disc||http://www.ebi.ac.uk/efo/EFO_0000420
1442||2656||dorsal metathoracic disc||http://www.ebi.ac.uk/efo/EFO_0000421
1443||13496||Kyasanur forest disease virus||http://purl.obolibrary.org/obo/NCBITaxon_33743
1444||13448||embryonic antennal sense organ||http://www.ebi.ac.uk/efo/EFO_0000439
1445||120||ductal adenocarcinoma||http://www.ebi.ac.uk/efo/EFO_0000430
1446||2656||ectoderm anlage in statu nascendi||http://www.ebi.ac.uk/efo/EFO_0000435
1447||3653||plant embryo||http://www.ebi.ac.uk/efo/EFO_0000436
1448||2021||Brachydactyly type B2||http://www.orpha.net/ORDO/Orphanet_140908
1449||2002||embryonal rhabdomyosarcoma||http://www.ebi.ac.uk/efo/EFO_0000437
1450||13448||embryonic anal pad||http://www.ebi.ac.uk/efo/EFO_0000438
1451||1737||Hyperlipidemia due to hepatic triglyceride lipase deficiency||http://www.orpha.net/ORDO/Orphanet_140905
1452||10652||obsolete_ductal breast carcinoma||http://www.ebi.ac.uk/efo/EFO_0000431
1453||970||ductal carcinoma in situ||http://www.ebi.ac.uk/efo/EFO_0000432
1454||2842||duration||http://www.ebi.ac.uk/efo/EFO_0000433
1455||10994||2-nitrofluorene||http://purl.obolibrary.org/obo/CHEBI_1224
1456||4571||ecotype||http://www.ebi.ac.uk/efo/EFO_0000434
1457||12461||Congenital analbuminemia||http://www.orpha.net/ORDO/Orphanet_86816
1458||10652||obsolete_mitochondrial disorder||http://www.ebi.ac.uk/efo/EFO_0000591
1459||9597||Aplasia of lacrimal and salivary glands||http://www.orpha.net/ORDO/Orphanet_86815
1461||2672||visual cortex||http://purl.obolibrary.org/obo/UBERON_0000411
1460||2252||Alport syndrome - intellectual disability - midface hypoplasia - elliptocytosis||http://www.orpha.net/ORDO/Orphanet_86818
1462||12346||Hemolytic anemia due to adenylate kinase deficiency||http://www.orpha.net/ORDO/Orphanet_86817
1464||15441||monophasic synovial sarcoma||http://www.ebi.ac.uk/efo/EFO_0000595
1463||1415||Autosomal recessive limb-girdle muscular dystrophy type 2K||http://www.orpha.net/ORDO/Orphanet_86812
1465||7852||Benign adult familial myoclonic epilepsy||http://www.orpha.net/ORDO/Orphanet_86814
1466||9965||Helicoid peripapillary chorioretinal degeneration||http://www.orpha.net/ORDO/Orphanet_86813
1467||10652||obsolete_mixed lobular and ductal breast carcinoma||http://www.ebi.ac.uk/efo/EFO_0000592
1468||1471||129/Sv||http://www.ebi.ac.uk/efo/EFO_0000599
1469||1391||intussusception||http://purl.obolibrary.org/obo/HP_0002576
1470||1471||129S6||http://www.ebi.ac.uk/efo/EFO_0000598
1471||13587||129 mouse strain||http://www.ebi.ac.uk/efo/EFO_0000597
1473||9753||rectal bleeding||http://purl.obolibrary.org/obo/HP_0002573
1472||10652||obsolete_motoneuron||http://www.ebi.ac.uk/efo/EFO_0000596
1474||321||Atrichia with papular lesions||http://www.orpha.net/ORDO/Orphanet_86819
1475||1826||Panax ginseng||http://purl.obolibrary.org/obo/NCBITaxon_4054
1476||4857||Dentinogenesis imperfecta type 3||http://www.orpha.net/ORDO/Orphanet_166265
1477||13470||Autosomal recessive spastic paraplegia type 59||http://www.orpha.net/ORDO/Orphanet_401795
1478||4857||Dentinogenesis imperfecta type 2||http://www.orpha.net/ORDO/Orphanet_166260
1479||970||medullary breast carcinoma||http://www.ebi.ac.uk/efo/EFO_0000580
1480||2683||Lissencephaly with cerebellar hypoplasia||http://www.orpha.net/ORDO/Orphanet_86823
1481||5343||meningitis infection||http://www.ebi.ac.uk/efo/EFO_0000584
1482||1421||Lissencephaly type 3 - metacarpal bone dysplasia||http://www.orpha.net/ORDO/Orphanet_86822
1483||14537||mesenchymal stem cell||http://www.ebi.ac.uk/efo/EFO_0000586
1484||1002||mesothelioma||http://www.ebi.ac.uk/efo/EFO_0000588
1485||1391||metabolic disease||http://www.ebi.ac.uk/efo/EFO_0000589
1486||13496||Watermelon mosaic virus||http://purl.obolibrary.org/obo/NCBITaxon_146500
1487||3659||Familial avascular necrosis of femoral head||http://www.orpha.net/ORDO/Orphanet_86820
1488||1421||Lissencephaly type 3 - familial fetal akinesia sequence||http://www.orpha.net/ORDO/Orphanet_86821
1489||10994||diclofenac sodium||http://purl.obolibrary.org/obo/CHEBI_4509
1490||1491||external encapsulating structure part||http://purl.obolibrary.org/obo/GO_0044462
1491||3744||cell part||http://purl.obolibrary.org/obo/GO_0044464
1492||772||lymphoblast||http://www.ebi.ac.uk/efo/EFO_0000572
1493||12136||lung adenocarcinoma||http://www.ebi.ac.uk/efo/EFO_0000571
1494||10652||obsolete_lobular breast carcinoma||http://www.ebi.ac.uk/efo/EFO_0000570
1495||1813||media||http://www.ebi.ac.uk/efo/EFO_0000579
1496||10652||obsolete_material type||http://www.ebi.ac.uk/efo/EFO_0000577
1497||1682||lymphoma||http://www.ebi.ac.uk/efo/EFO_0000574
1498||1826||Capsicum annuum||http://purl.obolibrary.org/obo/NCBITaxon_4072
1499||10994||pentachloronitrobenzene||http://purl.obolibrary.org/obo/CHEBI_34908
1500||1491||neuron projection||http://purl.obolibrary.org/obo/GO_0043005
1501||10994||paraquat||http://purl.obolibrary.org/obo/CHEBI_34905
1502||13883||labelling||http://www.ebi.ac.uk/efo/EFO_0000562
1503||13883||knock in expression||http://www.ebi.ac.uk/efo/EFO_0000561
1504||1160||light||http://www.ebi.ac.uk/efo/EFO_0000568
1505||2002||liposarcoma||http://www.ebi.ac.uk/efo/EFO_0000569
1506||2002||leiomyosarcoma||http://www.ebi.ac.uk/efo/EFO_0000564
1507||1006||large cell neuroendocrine carcinoma||http://www.ebi.ac.uk/efo/EFO_0000563
1508||1682||leukemia||http://www.ebi.ac.uk/efo/EFO_0000565
1509||13496||Human herpesvirus 6B||http://purl.obolibrary.org/obo/NCBITaxon_32604
1510||13496||Myoviridae||http://purl.obolibrary.org/obo/NCBITaxon_10662
1511||10994||permethrin||http://purl.obolibrary.org/obo/CHEBI_34911
1512||9898||Early-onset parkinsonism - intellectual disability||http://www.orpha.net/ORDO/Orphanet_2379
1514||13770||Laurin-Sandrow syndrome||http://www.orpha.net/ORDO/Orphanet_2378
1513||1619||Hereditary dentin defect||http://www.orpha.net/ORDO/Orphanet_167759
1515||1306||Laurence-Moon syndrome||http://www.orpha.net/ORDO/Orphanet_2377
1516||11899||Laryngeal abductor paralysis - intellectual disability||http://www.orpha.net/ORDO/Orphanet_2375
1518||12098||Congenital laryngeal web||http://www.orpha.net/ORDO/Orphanet_2374
1517||1826||Linum usitatissimum||http://purl.obolibrary.org/obo/NCBITaxon_4006
1520||12098||Congenital laryngomalacia||http://www.orpha.net/ORDO/Orphanet_2373
1519||1022||Nematostella vectensis||http://purl.obolibrary.org/obo/NCBITaxon_45351
1521||5306||Lethal Larsen-like syndrome||http://www.orpha.net/ORDO/Orphanet_2371
1522||7949||Larsen-like osseous dysplasia - short stature||http://www.orpha.net/ORDO/Orphanet_2370
1523||1560||plastid part||http://purl.obolibrary.org/obo/GO_0044435
1524||1523||chloroplast part||http://purl.obolibrary.org/obo/GO_0044434
1525||1560||cytoplasmic vesicle part||http://purl.obolibrary.org/obo/GO_0044433
1526||1561||cytoskeletal part||http://purl.obolibrary.org/obo/GO_0044430
1527||5502||Rhodobacter sphaeroides||http://purl.obolibrary.org/obo/NCBITaxon_1063
1528||12014||Female infertility due to gonadal dysgenesis||http://www.orpha.net/ORDO/Orphanet_399877
1529||6572||Glycogen storage disease due to lactate dehydrogenase deficiency||http://www.orpha.net/ORDO/Orphanet_2364
1530||4834||Lacrimoauriculodentodigital syndrome||http://www.orpha.net/ORDO/Orphanet_2363
1531||1560||mitochondrial part||http://purl.obolibrary.org/obo/GO_0044429
1532||3744||membrane part||http://purl.obolibrary.org/obo/GO_0044425
1533||1561||nuclear part||http://purl.obolibrary.org/obo/GO_0044428
1536||3744||organelle part||http://purl.obolibrary.org/obo/GO_0044422
1534||2672||Perirhinal cortex||http://purl.obolibrary.org/obo/UBERON_0006083
1535||5502||Salmonella enterica subsp. enterica serovar Typhimurium||http://purl.obolibrary.org/obo/NCBITaxon_90371
1537||3744||extracellular region part||http://purl.obolibrary.org/obo/GO_0044421
1538||5502||Salmonella enterica subsp. enterica serovar Typhi||http://purl.obolibrary.org/obo/NCBITaxon_90370
1539||1491||intracellular part||http://purl.obolibrary.org/obo/GO_0044424
1540||5502||Bordetella holmesii||http://purl.obolibrary.org/obo/NCBITaxon_35814
1541||5502||Proteus mirabilis HI4320||http://purl.obolibrary.org/obo/NCBITaxon_529507
1542||1022||Polistes metricus||http://purl.obolibrary.org/obo/NCBITaxon_91422
1543||6899||Nasopalpebral lipoma - coloboma - telecanthus||http://www.orpha.net/ORDO/Orphanet_2399
1544||5868||Familial symmetric lipomatosis||http://www.orpha.net/ORDO/Orphanet_2398
1545||5868||Encephalocraniocutaneous lipomatosis||http://www.orpha.net/ORDO/Orphanet_2396
1546||8896||Lichstenstein syndrome||http://www.orpha.net/ORDO/Orphanet_2390
1547||8736||Pyruvate dehydrogenase E3 deficiency||http://www.orpha.net/ORDO/Orphanet_2394
1548||5005||synthetic construct||http://purl.obolibrary.org/obo/NCBITaxon_32630
1549||5502||Rhodospirillum rubrum||http://purl.obolibrary.org/obo/NCBITaxon_1085
1550||3744||synapse part||http://purl.obolibrary.org/obo/GO_0044456
1551||4890||Leukoencephalopathy-palmoplantar keratoderma syndrome||http://www.orpha.net/ORDO/Orphanet_2386
1552||5838||viability||http://purl.obolibrary.org/obo/PATO_0000169
1553||325||Choreoacanthocytosis||http://www.orpha.net/ORDO/Orphanet_2388
1554||331||Leukonychia totalis||http://www.orpha.net/ORDO/Orphanet_2387
1555||1568||Rare disorder with female infertility due to a congenital hypogonadotropic hypogonadism||http://www.orpha.net/ORDO/Orphanet_399846
1556||5524||Monosomy 22q13||http://www.orpha.net/ORDO/Orphanet_48652
1557||7981||Legg-Calv -Perthes disease||http://www.orpha.net/ORDO/Orphanet_2380
1558||10860||Lennox-Gastaut syndrome||http://www.orpha.net/ORDO/Orphanet_2382
1559||5502||Rhodopseudomonas palustris||http://purl.obolibrary.org/obo/NCBITaxon_1076
1560||1539||cytoplasmic part||http://purl.obolibrary.org/obo/GO_0044444
1561||6096||intracellular organelle part||http://purl.obolibrary.org/obo/GO_0044446
1562||5838||rate||http://purl.obolibrary.org/obo/PATO_0000161
1563||325||Keratosis follicularis - dwarfism - cerebral atrophy||http://www.orpha.net/ORDO/Orphanet_2339
1564||13988||Isolated punctate palmoplantar keratoderma||http://www.orpha.net/ORDO/Orphanet_2338
1565||770||AG13066||http://purl.obolibrary.org/obo/CLO_0022132
1566||7662||Autosomal dominant keratitis||http://www.orpha.net/ORDO/Orphanet_2334
1567||12401||Non-epidermolytic palmoplantar keratoderma||http://www.orpha.net/ORDO/Orphanet_2337
1568||12030||Rare female infertility due to a congenital hypogonadotropic hypogonadism||http://www.orpha.net/ORDO/Orphanet_399839
1569||2252||KBG syndrome||http://www.orpha.net/ORDO/Orphanet_2332
1570||1211||Kenny-Caffey syndrome||http://www.orpha.net/ORDO/Orphanet_2333
1571||6244||Karsch-Neugebauer syndrome||http://www.orpha.net/ORDO/Orphanet_2329
1572||13496||Lactococcus phage c2||http://purl.obolibrary.org/obo/NCBITaxon_31537
1573||2252||Kapur-Toriello syndrome||http://www.orpha.net/ORDO/Orphanet_2328
1574||10277||Epidermolysis bullosa simplex with anodontia/hypodontia||http://www.orpha.net/ORDO/Orphanet_2325
1575||1306||Kallmann syndrome - heart disease||http://www.orpha.net/ORDO/Orphanet_2326
1576||1211||Sanjad-Sakati syndrome||http://www.orpha.net/ORDO/Orphanet_2323
1577||4139||Kaler-Garrity-Stern syndrome||http://www.orpha.net/ORDO/Orphanet_2324
1578||2252||Kabuki syndrome||http://www.orpha.net/ORDO/Orphanet_2322
1579||4713||Malignant migrating partial seizures of infancy||http://www.orpha.net/ORDO/Orphanet_293181
1580||10994||sodium valproate||http://purl.obolibrary.org/obo/CHEBI_9925
1581||10994||sulmazole||http://purl.obolibrary.org/obo/CHEBI_34988
1582||382||Xeroderma pigmentosum-Cockayne syndrome complex||http://www.orpha.net/ORDO/Orphanet_220295
1583||2672||testis||http://purl.obolibrary.org/obo/UBERON_0000473
1584||3020||female reproductive system||http://purl.obolibrary.org/obo/UBERON_0000474
1585||5295||interspecies interaction between organisms||http://purl.obolibrary.org/obo/GO_0044419
1586||11882||Schilbach-Rott syndrome||http://www.orpha.net/ORDO/Orphanet_2353
1588||5025||Alternaria alternata||http://purl.obolibrary.org/obo/NCBITaxon_5599
1587||6920||heterogeneous||http://purl.obolibrary.org/obo/HP_0001425
1589||7955||Familial clubfoot due to PITX1 point mutation||http://www.orpha.net/ORDO/Orphanet_293150
1590||770||ND06449||http://purl.obolibrary.org/obo/CLO_0018566
1591||1124||Male infertility due to sperm motility disorder||http://www.orpha.net/ORDO/Orphanet_399813
1592||5987||Arachnoid cyst||http://www.orpha.net/ORDO/Orphanet_2356
1593||9869||Infantile-onset ascending hereditary spastic paralysis||http://www.orpha.net/ORDO/Orphanet_293168
1594||7074||Muscular pseudohypertrophy - hypothyroidism||http://www.orpha.net/ORDO/Orphanet_2349
1595||2063||abnormality of the abdomen||http://purl.obolibrary.org/obo/HP_0001438
1596||15289||Rare disease with dentinogenesis imperfecta||http://www.orpha.net/ORDO/Orphanet_167762
1597||5025||Penicillium islandicum||http://purl.obolibrary.org/obo/NCBITaxon_28573
1599||1585||symbiosis, encompassing mutualism through parasitism||http://purl.obolibrary.org/obo/GO_0044403
1598||1190||size||http://www.ebi.ac.uk/efo/EFO_0001695
1600||5025||Penicillium funiculosum||http://purl.obolibrary.org/obo/NCBITaxon_28572
1601||7068||Keratosis follicularis spinulosa decalvans||http://www.orpha.net/ORDO/Orphanet_2340
1603||1172||Male infertility with teratozoospermia due to single gene mutation||http://www.orpha.net/ORDO/Orphanet_399808
1602||6650||Isolated cloverleaf skull syndrome||http://www.orpha.net/ORDO/Orphanet_2343
1604||770||AG13150||http://purl.obolibrary.org/obo/CLO_0022101
1605||4312||Haim-Munk syndrome||http://www.orpha.net/ORDO/Orphanet_2342
1606||1172||Male infertility with azoospermia or oligozoospermia due to single gene mutation||http://www.orpha.net/ORDO/Orphanet_399805
1610||13151||Skin fragility-woolly hair-palmoplantar keratoderma syndrome||http://www.orpha.net/ORDO/Orphanet_293165
1608||1598||area||http://www.ebi.ac.uk/efo/EFO_0001696
1607||770||AG13145||http://purl.obolibrary.org/obo/CLO_0022107
1609||8026||Lethal Kniest-like dysplasia||http://www.orpha.net/ORDO/Orphanet_2347
1611||2322||Familial partial lipodystrophy, Dunnigan type||http://www.orpha.net/ORDO/Orphanet_2348
1612||7963||Isolated Klippel-Feil syndrome||http://www.orpha.net/ORDO/Orphanet_2345
1613||1687||Angioosteohypertrophic syndrome||http://www.orpha.net/ORDO/Orphanet_2346
1614||238||Cryptosporidiosis - chronic cholangitis - liver disease||http://www.orpha.net/ORDO/Orphanet_357329
1615||2672||septum of telencephalon||http://purl.obolibrary.org/obo/UBERON_0000446
1616||1826||Nicotiana tabacum||http://purl.obolibrary.org/obo/NCBITaxon_4097
1617||10994||verapamil||http://purl.obolibrary.org/obo/CHEBI_9948
1618||2672||decidua basalis||http://purl.obolibrary.org/obo/UBERON_0000453
1619||15289||Rare odontal or periodontal disorder||http://www.orpha.net/ORDO/Orphanet_164001
1620||2672||prefrontal cortex||http://purl.obolibrary.org/obo/UBERON_0000451
1621||1826||Solanum lycopersicum||http://purl.obolibrary.org/obo/NCBITaxon_4081
1622||1826||Solanum pimpinellifolium||http://purl.obolibrary.org/obo/NCBITaxon_4084
1624||13770||Syndactyly - camptodactyly and clinodactyly of fifth fingers - bifid toes||http://www.orpha.net/ORDO/Orphanet_357332
1623||11172||coleorhiza emergence stage||http://purl.obolibrary.org/obo/PO_0025475
1625||2714||simian immunodeficiency virus infection||http://www.ebi.ac.uk/efo/EFO_0001675
1626||4430||placebo||http://www.ebi.ac.uk/efo/EFO_0001674
1627||2672||anatomical system||http://purl.obolibrary.org/obo/UBERON_0000467
1628||5025||Aspergillus versicolor||http://purl.obolibrary.org/obo/NCBITaxon_46472
1629||10652||obsolete_mediastinal lymph node||http://www.ebi.ac.uk/efo/EFO_0001670
1630||306||Johnson neuroectodermal syndrome||http://www.orpha.net/ORDO/Orphanet_2316
1631||1721||Joubert syndrome with oculorenal defect||http://www.orpha.net/ORDO/Orphanet_2318
1632||5300||Juberg-Hayward syndrome||http://www.orpha.net/ORDO/Orphanet_2319
1633||2714||influenza infection||http://www.ebi.ac.uk/efo/EFO_0001669
1635||4276||Autosomal recessive spondylocostal dysostosis||http://www.orpha.net/ORDO/Orphanet_2311
1634||2714||human papilloma virus infection||http://www.ebi.ac.uk/efo/EFO_0001668
1636||770||CEM/C1||http://www.ebi.ac.uk/efo/EFO_0001667
1637||6244||Absence deformity of leg - cataract||http://www.orpha.net/ORDO/Orphanet_2310
1638||1015||aortic aneurysm||http://www.ebi.ac.uk/efo/EFO_0001666
1639||10721||Transient familial neonatal hyperbilirubinemia||http://www.orpha.net/ORDO/Orphanet_2312
1642||2672||foreskin||http://www.ebi.ac.uk/efo/EFO_0001664
1640||306||Johanson-Blizzard syndrome||http://www.orpha.net/ORDO/Orphanet_2315
1641||1326||Abnormality of the vasculature||http://purl.obolibrary.org/obo/HP_0002597
1644||1006||prostate carcinoma||http://www.ebi.ac.uk/efo/EFO_0001663
1643||5882||Autosomal dominant hyper-IgE syndrome||http://www.orpha.net/ORDO/Orphanet_2314
1645||1679||ventral||http://www.ebi.ac.uk/efo/EFO_0001662
1646||1679||proximal||http://www.ebi.ac.uk/efo/EFO_0001661
1647||1679||medial||http://www.ebi.ac.uk/efo/EFO_0001660
1648||6244||IVIC syndrome||http://www.orpha.net/ORDO/Orphanet_2307
1649||5983||Jacobsen syndrome||http://www.orpha.net/ORDO/Orphanet_2308
1650||13306||Isotretinoin-like syndrome||http://www.orpha.net/ORDO/Orphanet_2306
1651||307||Pachyonychia congenita||http://www.orpha.net/ORDO/Orphanet_2309
1653||1679||lateral||http://www.ebi.ac.uk/efo/EFO_0001657
1652||6771||Multiple intestinal atresia||http://www.orpha.net/ORDO/Orphanet_2300
1654||1679||dorsal||http://www.ebi.ac.uk/efo/EFO_0001656
1655||1679||right||http://www.ebi.ac.uk/efo/EFO_0001659
1656||1679||left||http://www.ebi.ac.uk/efo/EFO_0001658
1657||1679||apical||http://www.ebi.ac.uk/efo/EFO_0001653
1658||10652||obsolete_primordium||http://www.ebi.ac.uk/efo/EFO_0001652
1659||1679||distal||http://www.ebi.ac.uk/efo/EFO_0001655
1661||1679||basal||http://www.ebi.ac.uk/efo/EFO_0001654
1660||6770||Congenital short bowel syndrome||http://www.orpha.net/ORDO/Orphanet_2301
1662||10994||haloperidol||http://purl.obolibrary.org/obo/CHEBI_5613
1663||1678||precursor||http://www.ebi.ac.uk/efo/EFO_0001651
1664||1678||placode||http://www.ebi.ac.uk/efo/EFO_0001650
1665||10994||halothane||http://purl.obolibrary.org/obo/CHEBI_5615
1666||1687||Angioosteohypotrophic syndrome||http://www.orpha.net/ORDO/Orphanet_75508
1667||770||ND02852||http://purl.obolibrary.org/obo/CLO_0015209
1668||15||Progressive sensorineural hearing loss - hypertrophic cardiomyopathy||http://www.orpha.net/ORDO/Orphanet_228012
1669||770||cancer cell line||http://www.ebi.ac.uk/efo/EFO_0001639
1670||10898||Ehlers-Danlos syndrome, fibronectinemic type||http://www.orpha.net/ORDO/Orphanet_75501
1671||2672||inferior colliculus||http://purl.obolibrary.org/obo/UBERON_0001946
1672||2672||superior colliculus||http://purl.obolibrary.org/obo/UBERON_0001945
1673||770||B cell derived cell line||http://www.ebi.ac.uk/efo/EFO_0001640
1674||14364||lateral mesenchyme derived from mesoderm||http://purl.obolibrary.org/obo/UBERON_0007683
1675||1015||coronary heart disease||http://www.ebi.ac.uk/efo/EFO_0001645
1676||5838||anatomical modifier||http://www.ebi.ac.uk/efo/EFO_0001646
1677||6766||Severe combined immunodeficiency due to CORO1A deficiency||http://www.orpha.net/ORDO/Orphanet_228003
1678||1676||tissue modifier||http://www.ebi.ac.uk/efo/EFO_0001647
1680||1678||anlage||http://purl.obolibrary.org/obo/UBERON_0007688
1679||1676||geometric modifier||http://www.ebi.ac.uk/efo/EFO_0001648
1681||770||epithelial cell derived cell line||http://www.ebi.ac.uk/efo/EFO_0001641
1682||1002||lymphoid neoplasm||http://www.ebi.ac.uk/efo/EFO_0001642
1684||770||kidney derived cell line||http://www.ebi.ac.uk/efo/EFO_0001643
1683||4994||Idiopathic CD4 lymphocytopenia||http://www.orpha.net/ORDO/Orphanet_228000
1685||3502||stria vascularis||http://www.ebi.ac.uk/efo/EFO_0001644
1686||10652||obsolete_anlage||http://www.ebi.ac.uk/efo/EFO_0001649
1687||4734||Congenital vascular bone syndrome||http://www.orpha.net/ORDO/Orphanet_235832
1688||5025||Fusarium oxysporum||http://purl.obolibrary.org/obo/NCBITaxon_5507
1689||5025||Cochliobolus lunatus||http://purl.obolibrary.org/obo/NCBITaxon_5503
1690||2672||preoptic area||http://purl.obolibrary.org/obo/UBERON_0001928
1691||2672||supraoptic nucleus||http://purl.obolibrary.org/obo/UBERON_0001929
1692||2672||lateral geniculate body||http://purl.obolibrary.org/obo/UBERON_0001926
1693||2672||medial geniculate body||http://purl.obolibrary.org/obo/UBERON_0001927
1694||5126||Rare thrombotic disorder due to a constitutional platelet anomaly||http://www.orpha.net/ORDO/Orphanet_248401
1695||5025||Gibberella zeae||http://purl.obolibrary.org/obo/NCBITaxon_5518
1696||5025||Fusarium sporotrichioides||http://purl.obolibrary.org/obo/NCBITaxon_5514
1697||5502||Salmonella enterica subsp. enterica serovar Java||http://purl.obolibrary.org/obo/NCBITaxon_224729
1698||4454||Zinc||http://purl.obolibrary.org/obo/CHEBI_27363
1699||7817||Familial hypodysfibrinogenemia||http://www.orpha.net/ORDO/Orphanet_248408
1700||11433||mammary gland||http://purl.obolibrary.org/obo/UBERON_0001911
1701||5502||Paenibacillus||http://purl.obolibrary.org/obo/NCBITaxon_44249
1702||1022||Sylvia communis||http://purl.obolibrary.org/obo/NCBITaxon_216193
1703||8365||Familial clubfoot due to 5q31 microdeletion||http://www.orpha.net/ORDO/Orphanet_293144
1704||5025||Metarhizium||http://purl.obolibrary.org/obo/NCBITaxon_5529
1705||5502||Actinobacillus pleuropneumoniae serovar 5||http://purl.obolibrary.org/obo/NCBITaxon_44294
1706||7852||Familial cortical myoclonus||http://www.orpha.net/ORDO/Orphanet_319189
1707||306||Chondroectodermal dysplasia with night blindness||http://www.orpha.net/ORDO/Orphanet_319195
1708||14513||superior cervical ganglion||http://purl.obolibrary.org/obo/UBERON_0001989
1710||2672||placenta||http://purl.obolibrary.org/obo/UBERON_0001987
1709||5984||Diencephalic-mesencephalic junction dysplasia||http://www.orpha.net/ORDO/Orphanet_319192
1711||2672||endothelium||http://purl.obolibrary.org/obo/UBERON_0001986
1712||5025||Metarhizium anisopliae||http://purl.obolibrary.org/obo/NCBITaxon_5530
1713||770||ND01737||http://purl.obolibrary.org/obo/CLO_0016362
1714||2672||capillary||http://purl.obolibrary.org/obo/UBERON_0001982
1715||13470||Autosomal recessive spastic paraplegia type 53||http://www.orpha.net/ORDO/Orphanet_319199
1716||2672||blood vessel||http://purl.obolibrary.org/obo/UBERON_0001981
1717||10994||Vitamin D||http://purl.obolibrary.org/obo/CHEBI_27300
1718||5025||Hypocrea lixii||http://purl.obolibrary.org/obo/NCBITaxon_5544
1719||1729||growth delay||http://purl.obolibrary.org/obo/HP_0001510
1721||11831||Joubert syndrome and related disorders||http://www.orpha.net/ORDO/Orphanet_140874
1722||2658||bile||http://purl.obolibrary.org/obo/UBERON_0001970
1720||1022||Leishmania chagasi||http://purl.obolibrary.org/obo/NCBITaxon_44271
1723||5502||Dehalococcoides||http://purl.obolibrary.org/obo/NCBITaxon_61434
1724||2252||Distal 17p13.1 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_319171
1725||2672||blood plasma||http://purl.obolibrary.org/obo/UBERON_0001969
1726||5025||Trichophyton rubrum||http://purl.obolibrary.org/obo/NCBITaxon_5551
1727||5502||Streptococcus pyogenes MGAS5005||http://purl.obolibrary.org/obo/NCBITaxon_293653
1728||2252||Wiedemann-Steiner syndrome||http://www.orpha.net/ORDO/Orphanet_319182
1729||2063||growth abnormality||http://purl.obolibrary.org/obo/HP_0001507
1730||10652||obsolete_genetic factor||http://www.ebi.ac.uk/efo/EFO_0000509
1731||5838||generation||http://www.ebi.ac.uk/efo/EFO_0000507
1733||1735||Major hypertriglyceridemia||http://www.orpha.net/ORDO/Orphanet_181425
1732||1391||genetic disorder||http://www.ebi.ac.uk/efo/EFO_0000508
1735||285||Rare hyperlipidemia||http://www.orpha.net/ORDO/Orphanet_181422
1734||10652||obsolete_gastrointestinal stromal tumor||http://www.ebi.ac.uk/efo/EFO_0000505
1736||1766||gene knock out||http://www.ebi.ac.uk/efo/EFO_0000506
1737||1735||Hyperalphalipoproteinemia||http://www.orpha.net/ORDO/Orphanet_181428
1738||10994||tacrine||http://purl.obolibrary.org/obo/CHEBI_45980
1740||1641||Venous abnormality||http://purl.obolibrary.org/obo/HP_0002624
1739||120||gastric intestinal type adenocarcinoma||http://www.ebi.ac.uk/efo/EFO_0000504
1741||120||gastric adenocarcinoma||http://www.ebi.ac.uk/efo/EFO_0000503
1742||2162||ganglioneuroblastoma||http://www.ebi.ac.uk/efo/EFO_0000502
1743||2477||X-linked dyserythropoetic anemia with abnormal platelets and neutropenia||http://www.orpha.net/ORDO/Orphanet_363727
1744||1006||follicular thyroid carcinoma||http://www.ebi.ac.uk/efo/EFO_0000501
1745||2439||Alexander disease type II||http://www.orpha.net/ORDO/Orphanet_363722
1746||2162||ganglioneuroma||http://www.ebi.ac.uk/efo/EFO_0000500
1748||1740||Varicose veins||http://purl.obolibrary.org/obo/HP_0002619
1747||10143||Spondyloepimetaphyseal dysplasia - hypotrichosis||http://www.orpha.net/ORDO/Orphanet_168443
1749||285||Rare hypolipidemia||http://www.orpha.net/ORDO/Orphanet_181431
1750||12161||glaucoma||http://www.ebi.ac.uk/efo/EFO_0000516
1751||10143||Spondyloepimetaphyseal dysplasia, Bieganski type||http://www.orpha.net/ORDO/Orphanet_168448
1752||10652||obsolete_glial cell (sensu Vertebrata)||http://www.ebi.ac.uk/efo/EFO_0000518
1753||31||glioblastoma multiforme||http://www.ebi.ac.uk/efo/EFO_0000519
1754||285||Rare syndromic dyslipidemia||http://www.orpha.net/ORDO/Orphanet_181437
1755||8444||Congenital myopathy with internal nuclei and atypical cores||http://www.orpha.net/ORDO/Orphanet_319160
1756||10994||nimesulide||http://purl.obolibrary.org/obo/CHEBI_44445
1757||8903||Classic multiminicore myopathy||http://www.orpha.net/ORDO/Orphanet_324604
1759||1826||Cleome gynandra||http://purl.obolibrary.org/obo/NCBITaxon_190802
1758||5300||X-linked cleft palate and ankyloglossia||http://www.orpha.net/ORDO/Orphanet_324601
1760||14970||genotype||http://www.ebi.ac.uk/efo/EFO_0000513
1761||1391||reproductive system disease||http://www.ebi.ac.uk/efo/EFO_0000512
1762||10652||obsolete_brain tumor glioblastoma||http://www.ebi.ac.uk/efo/EFO_0000515
1763||2162||germ cell tumor||http://www.ebi.ac.uk/efo/EFO_0000514
1764||5502||Lactobacillus paralimentarius||http://purl.obolibrary.org/obo/NCBITaxon_83526
1765||5838||genetic trait||http://www.ebi.ac.uk/efo/EFO_0000511
1766||13883||genetic modification||http://www.ebi.ac.uk/efo/EFO_0000510
1767||1390||Rare disorder with hypergonadotropic hypogonadism||http://www.orpha.net/ORDO/Orphanet_181441
1768||8697||X-linked sideroblastic anemia||http://www.orpha.net/ORDO/Orphanet_75563
1769||2997||Autosomal dominant Charcot-Marie-Tooth disease type 2 due to KIF5A mutation||http://www.orpha.net/ORDO/Orphanet_324611
1770||9305||Neurofibromatosis type 1 due to NF1mutation or intragenic deletion||http://www.orpha.net/ORDO/Orphanet_363700
1772||2252||Craniofaciofrontodigital syndrome||http://www.orpha.net/ORDO/Orphanet_363705
1771||770||ND06229||http://purl.obolibrary.org/obo/CLO_0029036
1773||2672||olfactory epithelium||http://purl.obolibrary.org/obo/UBERON_0001997
1774||539||ulcer||http://purl.obolibrary.org/obo/MPATH_579
1775||10994||trifluoperazine||http://purl.obolibrary.org/obo/CHEBI_45951
1776||10994||hydroxyurea||http://purl.obolibrary.org/obo/CHEBI_44423
1777||9856||Spinocerebellar ataxia type 37||http://www.orpha.net/ORDO/Orphanet_363710
1778||2439||Alexander disease type I||http://www.orpha.net/ORDO/Orphanet_363717
1779||9899||Proximal myopathy with extrapyramidal signs||http://www.orpha.net/ORDO/Orphanet_401768
1780||15519||Pancytopenia-developmental delay syndrome||http://www.orpha.net/ORDO/Orphanet_401764
1781||15417||insulinoma||http://www.ebi.ac.uk/efo/EFO_0000549
1782||10652||obsolete_inner cell mass||http://www.ebi.ac.uk/efo/EFO_0000547
1783||1125||instrument||http://www.ebi.ac.uk/efo/EFO_0000548
1784||1761||infertility||http://www.ebi.ac.uk/efo/EFO_0000545
1785||9803||injury||http://www.ebi.ac.uk/efo/EFO_0000546
1786||10652||obsolete_individual genetic characteristic||http://www.ebi.ac.uk/efo/EFO_0000543
1787||9451||infection||http://www.ebi.ac.uk/efo/EFO_0000544
1788||10994||immunoprecipitate||http://www.ebi.ac.uk/efo/EFO_0000541
1789||4981||individual||http://www.ebi.ac.uk/efo/EFO_0000542
1790||1391||immune system disease||http://www.ebi.ac.uk/efo/EFO_0000540
1791||5877||Gardner syndrome||http://www.orpha.net/ORDO/Orphanet_79665
1792||1022||Spermophilus tridecemlineatus||http://purl.obolibrary.org/obo/NCBITaxon_43179
1793||5502||Ruegeria pomeroyi||http://purl.obolibrary.org/obo/NCBITaxon_89184
1794||1015||ischemia||http://www.ebi.ac.uk/efo/EFO_0000556
1795||617||juvenile dermatomyositis||http://www.ebi.ac.uk/efo/EFO_0000557
1796||2002||Kaposi s sarcoma||http://www.ebi.ac.uk/efo/EFO_0000558
1797||2860||keratinizing squamous cell carcinoma||http://www.ebi.ac.uk/efo/EFO_0000559
1798||7925||invasive ductal and lobular carcinoma||http://www.ebi.ac.uk/efo/EFO_0000552
1799||970||invasive lobular carcinoma||http://www.ebi.ac.uk/efo/EFO_0000553
1800||13883||irradiate||http://www.ebi.ac.uk/efo/EFO_0000554
1801||1403||irritable bowel syndrome||http://www.ebi.ac.uk/efo/EFO_0000555
1802||1015||intracranial hemorrhage NOS||http://www.ebi.ac.uk/efo/EFO_0000551
1803||13480||Autosomal recessive spastic paraplegia type 62||http://www.orpha.net/ORDO/Orphanet_401785
1804||13496||BK polyomavirus||http://purl.obolibrary.org/obo/NCBITaxon_10629
1805||10652||obsolete_hereditary spastic paraplegia||http://www.ebi.ac.uk/efo/EFO_0000529
1806||8611||Mild hyperphenylalaninemia||http://www.orpha.net/ORDO/Orphanet_79651
1807||1022||Cafeteria roenbergensis||http://purl.obolibrary.org/obo/NCBITaxon_33653
1809||13470||Autosomal recessive spastic paraplegia type 61||http://www.orpha.net/ORDO/Orphanet_401780
1808||2252||Colobomatous microphthalmia-obesity-hypogenitalism-intellectual disability syndrome||http://www.orpha.net/ORDO/Orphanet_363741
1810||10652||obsolete_glioma||http://www.ebi.ac.uk/efo/EFO_0000520
1811||10652||obsolete_hematological neoplasm||http://www.ebi.ac.uk/efo/EFO_0000525
1812||10652||obsolete_hemopoietic progenitor cell||http://www.ebi.ac.uk/efo/EFO_0000526
1813||4430||growth condition||http://www.ebi.ac.uk/efo/EFO_0000523
1814||1391||head disease||http://www.ebi.ac.uk/efo/EFO_0000524
1815||11348||Autosomal recessive hyperinsulinism due to Kir6.2 deficiency||http://www.orpha.net/ORDO/Orphanet_79644
1816||4139||Optic atrophy-intellectual disability syndrome||http://www.orpha.net/ORDO/Orphanet_401777
1817||11348||Autosomal recessive hyperinsulinism due to SUR1 deficiency||http://www.orpha.net/ORDO/Orphanet_79643
1818||1016||hypertrophic cardiomyopathy||http://www.ebi.ac.uk/efo/EFO_0000538
1819||3043||hippocampus||http://www.ebi.ac.uk/efo/EFO_0000530
1820||4430||host||http://www.ebi.ac.uk/efo/EFO_0000532
1821||10652||obsolete_Huntington s disease||http://www.ebi.ac.uk/efo/EFO_0000533
1822||1160||hydrostatic pressure||http://www.ebi.ac.uk/efo/EFO_0000534
1823||10652||obsolete_hyperglycemia||http://www.ebi.ac.uk/efo/EFO_0000535
1824||1391||hyperplasia||http://www.ebi.ac.uk/efo/EFO_0000536
1825||1015||hypertension||http://www.ebi.ac.uk/efo/EFO_0000537
1826||1022||Viridiplantae||http://purl.obolibrary.org/obo/NCBITaxon_33090
1828||2515||Isolated aniridia||http://www.orpha.net/ORDO/Orphanet_250923
1827||9816||Ocular albinism||http://www.orpha.net/ORDO/Orphanet_284804
1829||5502||Escherichia coli O157:H7 str. Sakai||http://purl.obolibrary.org/obo/NCBITaxon_386585
1830||5502||Enterococcus faecalis||http://purl.obolibrary.org/obo/NCBITaxon_1351
1831||5911||Syndromic oculocutaneous albinism||http://www.orpha.net/ORDO/Orphanet_284811
1832||5502||Lactococcus lactis||http://purl.obolibrary.org/obo/NCBITaxon_1358
1834||5502||Lactococcus lactis subsp. cremoris||http://purl.obolibrary.org/obo/NCBITaxon_1359
1833||6267||Disorder of phenylalanine metabolism||http://www.orpha.net/ORDO/Orphanet_284814
1835||5502||Enterococcus faecium||http://purl.obolibrary.org/obo/NCBITaxon_1352
1836||5502||Enterococcus hirae||http://purl.obolibrary.org/obo/NCBITaxon_1354
1837||1022||Entamoeba invadens||http://purl.obolibrary.org/obo/NCBITaxon_33085
1838||8846||Autosomal dominant optic atrophy and peripheral neuropathy||http://www.orpha.net/ORDO/Orphanet_250932
1839||6267||Disorder of tyrosine metabolism||http://www.orpha.net/ORDO/Orphanet_284818
1840||5502||Lactococcus lactis subsp. lactis||http://purl.obolibrary.org/obo/NCBITaxon_1360
1841||10994||benzo(a)pyrene||http://purl.obolibrary.org/obo/CHEBI_29865
1842||10994||arsenite(3-)||http://purl.obolibrary.org/obo/CHEBI_29866
1843||1852||Qualitative or quantitative defects of FKRP||http://www.orpha.net/ORDO/Orphanet_207119
1844||10994||(R)-lactic acid||http://purl.obolibrary.org/obo/CHEBI_42111
1845||3514||TARP syndrome||http://www.orpha.net/ORDO/Orphanet_2886
1846||5911||Piebaldism||http://www.orpha.net/ORDO/Orphanet_2884
1848||2395||Qualitative or quantitative defects of myotubularin||http://www.orpha.net/ORDO/Orphanet_207110
1847||5911||Piebald trait - neurologic defects||http://www.orpha.net/ORDO/Orphanet_2885
1849||1826||Syntrichia ruralis||http://purl.obolibrary.org/obo/NCBITaxon_38588
1850||1754||Sitosterolemia||http://www.orpha.net/ORDO/Orphanet_2882
1851||6321||Phosphoenolpyruvate carboxykinase deficiency||http://www.orpha.net/ORDO/Orphanet_2880
1852||7577||Qualitative or quantitative defects of protein involved in O-glycosylation of alpha-dystroglycan||http://www.orpha.net/ORDO/Orphanet_207113
1853||2672||subthalamic nucleus||http://purl.obolibrary.org/obo/UBERON_0001906
1854||323||Pili torti||http://www.orpha.net/ORDO/Orphanet_2889
1855||1022||Scyliorhinus canicula||http://purl.obolibrary.org/obo/NCBITaxon_7830
1856||5300||Pierre Robin syndrome - faciodigital anomaly||http://www.orpha.net/ORDO/Orphanet_2888
1857||2672||epithelium of small intestine||http://purl.obolibrary.org/obo/UBERON_0001902
1859||11433||pineal body||http://purl.obolibrary.org/obo/UBERON_0001905
1858||10813||Progressive supranuclear palsy - progressive non fluent aphasia||http://www.orpha.net/ORDO/Orphanet_240112
1861||770||ND00397||http://purl.obolibrary.org/obo/CLO_0027048
1860||10813||Progressive supranuclear palsy - corticobasal syndrome||http://www.orpha.net/ORDO/Orphanet_240103
1862||306||Pili torti - onychodysplasia||http://www.orpha.net/ORDO/Orphanet_2890
1864||5502||Streptococcus equi||http://purl.obolibrary.org/obo/NCBITaxon_1336
1863||5502||Polaromonas sp. JS666||http://purl.obolibrary.org/obo/NCBITaxon_296591
1865||4139||Pitt-Hopkins syndrome||http://www.orpha.net/ORDO/Orphanet_2896
1866||1852||Qualitative or quantitative defects of fukutin||http://www.orpha.net/ORDO/Orphanet_207122
1867||5985||Pityriasis rubra pilaris||http://www.orpha.net/ORDO/Orphanet_2897
1868||2252||X-linked intellectual disability - plagiocephaly||http://www.orpha.net/ORDO/Orphanet_2898
1869||330||Pili torti - developmental delay - neurological abnormalities||http://www.orpha.net/ORDO/Orphanet_2891
1870||306||Pilodental dysplasia - refractive errors||http://www.orpha.net/ORDO/Orphanet_2892
1871||5300||Pilotto syndrome||http://www.orpha.net/ORDO/Orphanet_2894
1872||4834||Brachyolmia-amelogenesis imperfecta syndrome||http://www.orpha.net/ORDO/Orphanet_2899
1873||1316||Orofaciodigital syndrome type 12||http://www.orpha.net/ORDO/Orphanet_141327
1874||5502||Streptococcus mutans||http://purl.obolibrary.org/obo/NCBITaxon_1309
1875||5502||Streptococcus thermophilus||http://purl.obolibrary.org/obo/NCBITaxon_1308
1876||5502||Streptococcus suis||http://purl.obolibrary.org/obo/NCBITaxon_1307
1877||5502||Streptococcus sanguinis||http://purl.obolibrary.org/obo/NCBITaxon_1305
1878||5502||Streptococcus oralis||http://purl.obolibrary.org/obo/NCBITaxon_1303
1879||5502||Streptococcus gordonii||http://purl.obolibrary.org/obo/NCBITaxon_1302
1880||6610||Acrocephalopolydactyly||http://www.orpha.net/ORDO/Orphanet_221054
1881||2395||Qualitative or quantitative defects of calpain||http://www.orpha.net/ORDO/Orphanet_207104
1882||2395||Qualitative or quantitative defects of perlecan||http://www.orpha.net/ORDO/Orphanet_207101
1883||5502||Streptococcus pneumoniae||http://purl.obolibrary.org/obo/NCBITaxon_1313
1884||5502||Streptococcus pyogenes||http://purl.obolibrary.org/obo/NCBITaxon_1314
1885||2395||Qualitative or quantitative defects of TRIM32||http://www.orpha.net/ORDO/Orphanet_207107
1886||5502||Streptococcus agalactiae||http://purl.obolibrary.org/obo/NCBITaxon_1311
1887||2252||Biemond syndrome type 2||http://www.orpha.net/ORDO/Orphanet_141333
1888||9558||Hereditary cerebral cavernous malformation||http://www.orpha.net/ORDO/Orphanet_221061
1889||1316||Orofaciodigital syndrome type 13||http://www.orpha.net/ORDO/Orphanet_141330
1890||8190||alendronic acid||http://purl.obolibrary.org/obo/CHEBI_2567
1892||1022||Spea bombifrons||http://purl.obolibrary.org/obo/NCBITaxon_233779
1891||1022||Leishmania tarentolae||http://purl.obolibrary.org/obo/NCBITaxon_5689
1893||1022||Trypanosoma cruzi||http://purl.obolibrary.org/obo/NCBITaxon_5693
1894||1022||Trypanosoma brucei||http://purl.obolibrary.org/obo/NCBITaxon_5691
1895||10994||propylparaben||http://purl.obolibrary.org/obo/CHEBI_32063
1896||1022||Trypanosoma vivax||http://purl.obolibrary.org/obo/NCBITaxon_5699
1897||10994||aldicarb||http://purl.obolibrary.org/obo/CHEBI_2555
1898||770||Lu135||http://www.ebi.ac.uk/efo/EFO_0002828
1899||770||MIN6||http://www.ebi.ac.uk/efo/EFO_0002829
1900||770||KS-IMM||http://www.ebi.ac.uk/efo/EFO_0002826
1901||770||LC-1F||http://www.ebi.ac.uk/efo/EFO_0002827
1902||760||Non-syndromic cerebral malformation due to abnormal neuronal migration||http://www.orpha.net/ORDO/Orphanet_163209
1904||2194||Rothmund-Thomson syndrome type 2||http://www.orpha.net/ORDO/Orphanet_221016
1903||7419||RNA interference||http://purl.obolibrary.org/obo/GO_0016246
1905||306||Dermatopathia pigmentosa reticularis||http://www.orpha.net/ORDO/Orphanet_86920
1906||13543||Drosophila santomea||http://purl.obolibrary.org/obo/NCBITaxon_129105
1907||12317||Hereditary palmoplantar keratoderma, Gamborg-Nielsen type||http://www.orpha.net/ORDO/Orphanet_86923
1908||770||CTLL-2||http://www.ebi.ac.uk/efo/EFO_0002821
1909||770||CM7-1||http://www.ebi.ac.uk/efo/EFO_0002820
1910||10652||obsolete_Jurkat||http://www.ebi.ac.uk/efo/EFO_0002825
1911||770||HCT116||http://www.ebi.ac.uk/efo/EFO_0002824
1912||10652||obsolete_H69||http://www.ebi.ac.uk/efo/EFO_0002823
1913||770||D10.G4.1||http://www.ebi.ac.uk/efo/EFO_0002822
1914||770||MS428||http://www.ebi.ac.uk/efo/EFO_0002837
1915||770||MS589||http://www.ebi.ac.uk/efo/EFO_0002838
1916||770||MSTO-211H||http://www.ebi.ac.uk/efo/EFO_0002839
1917||1920||interaction with host via secreted substance involved in symbiotic interaction||http://purl.obolibrary.org/obo/GO_0052048
1918||2395||Qualitative or quantitative defects of glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase -||http://www.orpha.net/ORDO/Orphanet_209203
1920||1585||interaction with other organism via secreted substance involved in symbiotic interaction||http://purl.obolibrary.org/obo/GO_0052047
1919||10862||Myoclonic epilepsy in non-progressive encephalopathies||http://www.orpha.net/ORDO/Orphanet_86913
1921||5478||Lymphedema - atrial septal defects - facial changes||http://www.orpha.net/ORDO/Orphanet_86915
1922||5478||Lymphedema - cerebral arteriovenous anomaly||http://www.orpha.net/ORDO/Orphanet_86914
1923||5478||Lymphedema - cleft palate||http://www.orpha.net/ORDO/Orphanet_86917
1925||12318||Keratosis palmaris et plantaris - clinodactyly||http://www.orpha.net/ORDO/Orphanet_86919
1924||770||MKN1||http://www.ebi.ac.uk/efo/EFO_0002830
1926||12318||Diffuse palmoplantar keratoderma-acrocyanosis syndrome||http://www.orpha.net/ORDO/Orphanet_86918
1927||770||MKN45||http://www.ebi.ac.uk/efo/EFO_0002832
1928||770||MKN28||http://www.ebi.ac.uk/efo/EFO_0002831
1929||770||MKN74||http://www.ebi.ac.uk/efo/EFO_0002834
1930||770||MS-1||http://www.ebi.ac.uk/efo/EFO_0002836
1931||5295||reproductive process||http://purl.obolibrary.org/obo/GO_0000003
1932||770||MRC5||http://www.ebi.ac.uk/efo/EFO_0002835
1933||10994||paraquat dichloride||http://purl.obolibrary.org/obo/CHEBI_28786
1934||770||QG56||http://www.ebi.ac.uk/efo/EFO_0002848
1935||770||R11||http://www.ebi.ac.uk/efo/EFO_0002849
1936||254||Hereditary sclerosing poikiloderma, Weary type||http://www.orpha.net/ORDO/Orphanet_221039
1937||760||Hypothalamic hamartomas with gelastic seizures||http://www.orpha.net/ORDO/Orphanet_86906
1938||5502||Streptococcus mutans UA159||http://purl.obolibrary.org/obo/NCBITaxon_210007
1939||770||PC-9||http://www.ebi.ac.uk/efo/EFO_0002847
1940||770||PC-7||http://www.ebi.ac.uk/efo/EFO_0002846
1941||770||PC-6||http://www.ebi.ac.uk/efo/EFO_0002845
1942||770||PC-14||http://www.ebi.ac.uk/efo/EFO_0002844
1943||6432||Combined oxidative phosphorylation defect type 8||http://www.orpha.net/ORDO/Orphanet_319504
1944||770||PC-10||http://www.ebi.ac.uk/efo/EFO_0002843
1946||770||PC-1||http://www.ebi.ac.uk/efo/EFO_0002842
1945||10862||Myoclonic epilepsy of infancy||http://www.orpha.net/ORDO/Orphanet_86909
1947||10994||ethylenediaminetetraacetic acid||http://purl.obolibrary.org/obo/CHEBI_42191
1949||770||NCI-N87||http://www.ebi.ac.uk/efo/EFO_0002841
1948||6432||Combined oxidative phosphorylation defect type 9||http://www.orpha.net/ORDO/Orphanet_319509
1950||770||N231||http://www.ebi.ac.uk/efo/EFO_0002840
1951||5300||Stickler syndrome type 3||http://www.orpha.net/ORDO/Orphanet_166100
1952||10994||coumarin||http://purl.obolibrary.org/obo/CHEBI_28794
1954||770||SK-N-AS||http://www.ebi.ac.uk/efo/EFO_0002859
1953||8846||FASTKD2-related infantile mitochondrial encephalomyopathy||http://www.orpha.net/ORDO/Orphanet_166105
1955||10994||serotonin||http://purl.obolibrary.org/obo/CHEBI_28790
1956||254||Poikiloderma with neutropenia||http://www.orpha.net/ORDO/Orphanet_221046
1957||254||Hereditary sclerosing poikiloderma with tendon and pulmonary involvement||http://www.orpha.net/ORDO/Orphanet_221043
1958||10994||disopyramide||http://purl.obolibrary.org/obo/CHEBI_4657
1959||770||RERF-LC-AI||http://www.ebi.ac.uk/efo/EFO_0002850
1960||10994||disulfiram||http://purl.obolibrary.org/obo/CHEBI_4659
1961||6432||Combined oxidative phosphorylation defect type 13||http://www.orpha.net/ORDO/Orphanet_319514
1963||4139||Intellectual disability, Birk-Barel type||http://www.orpha.net/ORDO/Orphanet_166108
1962||770||SCH||http://www.ebi.ac.uk/efo/EFO_0002856
1964||770||SBC-5||http://www.ebi.ac.uk/efo/EFO_0002855
1965||770||SK-ES-1||http://www.ebi.ac.uk/efo/EFO_0002858
1966||770||SHEP-SF||http://www.ebi.ac.uk/efo/EFO_0002857
1967||10994||agarose||http://purl.obolibrary.org/obo/CHEBI_2511
1968||770||RERF-LC-MS||http://www.ebi.ac.uk/efo/EFO_0002852
1970||770||RERF-LC-KJ||http://www.ebi.ac.uk/efo/EFO_0002851
1969||6432||Combined oxidative phosphorylation defect type 14||http://www.orpha.net/ORDO/Orphanet_319519
1971||770||SBC-3||http://www.ebi.ac.uk/efo/EFO_0002854
1972||770||RM 82||http://www.ebi.ac.uk/efo/EFO_0002853
1973||5502||Bacillus anthracis||http://purl.obolibrary.org/obo/NCBITaxon_1392
1974||5502||Bacillus amyloliquefaciens||http://purl.obolibrary.org/obo/NCBITaxon_1390
1975||5967||Bazex syndrome||http://www.orpha.net/ORDO/Orphanet_166113
1976||14756||sampling site||http://www.ebi.ac.uk/efo/EFO_0000688
1977||2842||sampling time||http://www.ebi.ac.uk/efo/EFO_0000689
1978||1022||Carcinus maenas||http://purl.obolibrary.org/obo/NCBITaxon_6759
1979||1391||respiratory system disease||http://www.ebi.ac.uk/efo/EFO_0000684
1980||5103||rheumatoid arthritis||http://www.ebi.ac.uk/efo/EFO_0000685
1981||14970||risk status||http://www.ebi.ac.uk/efo/EFO_0000686
1984||3560||Isolated osteopoikilosis||http://www.orpha.net/ORDO/Orphanet_166119
1982||10652||obsolete_sample factor||http://www.ebi.ac.uk/efo/EFO_0000687
1983||10994||aflatoxin B1||http://purl.obolibrary.org/obo/CHEBI_2504
1985||6432||Combined oxidative phosphorylation defect type 15||http://www.orpha.net/ORDO/Orphanet_319524
1986||2229||renal cell carcinoma||http://www.ebi.ac.uk/efo/EFO_0000681
1987||10652||obsolete_renal clear cell carcinoma||http://www.ebi.ac.uk/efo/EFO_0000682
1988||6573||replicate||http://www.ebi.ac.uk/efo/EFO_0000683
1989||5502||Candidatus Pelagibacter ubique HTCC1062||http://purl.obolibrary.org/obo/NCBITaxon_335992
1990||1826||Senecio cambrensis||http://purl.obolibrary.org/obo/NCBITaxon_285720
1991||760||Polymicrogyria with optic nerve hypoplasia||http://www.orpha.net/ORDO/Orphanet_250972
1992||8193||mesalamine||http://purl.obolibrary.org/obo/CHEBI_6775
1993||5103||Sjogren syndrome||http://www.ebi.ac.uk/efo/EFO_0000699
1994||10652||obsolete_sickle cell disease||http://www.ebi.ac.uk/efo/EFO_0000697
1995||1006||signet ring cell carcinoma||http://www.ebi.ac.uk/efo/EFO_0000698
1996||2252||AICA-ribosiduria||http://www.orpha.net/ORDO/Orphanet_250977
1997||5838||sex||http://www.ebi.ac.uk/efo/EFO_0000695
1998||8586||Autosomal recessive mendelian susceptibility to mycobacterial diseases due to a partial deficiency||http://www.orpha.net/ORDO/Orphanet_319539
1999||13883||shear stressing||http://www.ebi.ac.uk/efo/EFO_0000696
2000||15475||schwannoma||http://www.ebi.ac.uk/efo/EFO_0000693
2001||2714||severe acute respiratory syndrome||http://www.ebi.ac.uk/efo/EFO_0000694
2002||1002||sarcoma||http://www.ebi.ac.uk/efo/EFO_0000691
2003||8586||Autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency||http://www.orpha.net/ORDO/Orphanet_319535
2004||2102||schizophrenia||http://www.ebi.ac.uk/efo/EFO_0000692
2005||10652||obsolete_sarcoidosis||http://www.ebi.ac.uk/efo/EFO_0000690
2006||5502||Bacillus cereus||http://purl.obolibrary.org/obo/NCBITaxon_1396
2007||1783||hybridization station||http://purl.obolibrary.org/obo/OBI_0400111
2008||10994||doxorubicin||http://purl.obolibrary.org/obo/CHEBI_28748
2009||1783||liquid handler||http://purl.obolibrary.org/obo/OBI_0400112
2010||1783||oligonucleotide synthesizer||http://purl.obolibrary.org/obo/OBI_0400113
2011||1783||sonicator||http://purl.obolibrary.org/obo/OBI_0400114
2013||1783||hybridization chamber||http://purl.obolibrary.org/obo/OBI_0400110
2012||259||cell division||http://purl.obolibrary.org/obo/GO_0051301
2014||770||4483||http://www.ebi.ac.uk/efo/EFO_0002809
2015||770||4475||http://www.ebi.ac.uk/efo/EFO_0002808
2017||1783||spectrophotometer||http://purl.obolibrary.org/obo/OBI_0400115
2016||770||4470||http://www.ebi.ac.uk/efo/EFO_0002807
2018||1783||thermal cycler||http://purl.obolibrary.org/obo/OBI_0400116
2019||7169||retroperitoneum||http://www.ebi.ac.uk/efo/EFO_0002806
2020||1783||vacuum dryer||http://purl.obolibrary.org/obo/OBI_0400117
2021||6246||Syndrome with brachydactyly||http://www.orpha.net/ORDO/Orphanet_69028
2022||10652||obsolete_pelvis||http://www.ebi.ac.uk/efo/EFO_0002805
2023||1783||vortexer||http://purl.obolibrary.org/obo/OBI_0400118
2024||770||TH-2||http://www.ebi.ac.uk/efo/EFO_0002804
2025||770||SK-N-SH_RA||http://www.ebi.ac.uk/efo/EFO_0002802
2027||770||TH-1||http://www.ebi.ac.uk/efo/EFO_0002803
2026||5849||1q21.1 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_250989
2028||770||SAEC||http://www.ebi.ac.uk/efo/EFO_0002800
2029||770||SKMC||http://www.ebi.ac.uk/efo/EFO_0002801
2030||6180||Autosomal recessive Stickler syndrome||http://www.orpha.net/ORDO/Orphanet_250984
2031||5502||Lactococcus garvieae||http://purl.obolibrary.org/obo/NCBITaxon_1363
2032||8586||Autosomal dominant mendelian susceptibility to mycobacterial diseases due to a partial deficiency||http://www.orpha.net/ORDO/Orphanet_319543
2033||2003||Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR2 deficiency||http://www.orpha.net/ORDO/Orphanet_319547
2034||11488||DNA sequencer||http://purl.obolibrary.org/obo/OBI_0400103
2035||1022||Thalassiosira pseudonana CCMP1335||http://purl.obolibrary.org/obo/NCBITaxon_296543
2036||770||Calu3||http://www.ebi.ac.uk/efo/EFO_0002819
2037||1783||heating block||http://purl.obolibrary.org/obo/OBI_0400108
2038||1783||homogenizer||http://purl.obolibrary.org/obo/OBI_0400109
2039||1783||centrifuge||http://purl.obolibrary.org/obo/OBI_0400106
2040||770||C3H10T1/2||http://www.ebi.ac.uk/efo/EFO_0002816
2041||1783||computer||http://purl.obolibrary.org/obo/OBI_0400107
2042||770||BJAB||http://www.ebi.ac.uk/efo/EFO_0002815
2044||1783||array scanner||http://purl.obolibrary.org/obo/OBI_0400104
2043||770||CADO ES1||http://www.ebi.ac.uk/efo/EFO_0002818
2047||1783||arrayer||http://purl.obolibrary.org/obo/OBI_0400105
2045||770||Caco-2/TC7||http://www.ebi.ac.uk/efo/EFO_0002817
2046||5502||Exiguobacterium sibiricum 255-15||http://purl.obolibrary.org/obo/NCBITaxon_262543
2048||770||3T3-F442A||http://www.ebi.ac.uk/efo/EFO_0002811
2049||770||AB2.2||http://www.ebi.ac.uk/efo/EFO_0002812
2051||770||ABC-1||http://www.ebi.ac.uk/efo/EFO_0002813
2050||5849||1q41q42 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_250999
2052||770||AZ-521||http://www.ebi.ac.uk/efo/EFO_0002814
2053||10246||1q21.1 microduplication syndrome||http://www.orpha.net/ORDO/Orphanet_250994
2054||770||1205-Lu||http://www.ebi.ac.uk/efo/EFO_0002810
2055||2003||Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency||http://www.orpha.net/ORDO/Orphanet_319552
2056||2194||Rothmund-Thomson syndrome type 1||http://www.orpha.net/ORDO/Orphanet_221008
2057||2003||Mendelian susceptibility to mycobacterial diseases due to complete IL12B deficiency||http://www.orpha.net/ORDO/Orphanet_319558
2058||5657||Hereditary cerebral hemorrhage with amyloidosis, Piedmont type||http://www.orpha.net/ORDO/Orphanet_324703
2059||1391||whooping cough||http://www.ebi.ac.uk/efo/EFO_0000650
2060||5502||Helicobacter pylori 26695||http://purl.obolibrary.org/obo/NCBITaxon_85962
2061||10652||obsolete_phenotypic factor||http://www.ebi.ac.uk/efo/EFO_0000652
2062||1022||Vulpes vulpes||http://purl.obolibrary.org/obo/NCBITaxon_9627
2064||5502||Helicobacter pylori J99||http://purl.obolibrary.org/obo/NCBITaxon_85963
2063||5838||phenotype||http://www.ebi.ac.uk/efo/EFO_0000651
2065||1826||Saccharum officinarum||http://purl.obolibrary.org/obo/NCBITaxon_4547
2066||970||phyllodes tumor||http://www.ebi.ac.uk/efo/EFO_0000653
2068||2249||plexiform neurofibroma||http://www.ebi.ac.uk/efo/EFO_0000658
2067||1826||Cenchrus americanus||http://purl.obolibrary.org/obo/NCBITaxon_4543
2069||10652||obsolete_platform||http://www.ebi.ac.uk/efo/EFO_0000657
2070||5838||ploidy||http://www.ebi.ac.uk/efo/EFO_0000659
2071||8526||Pelizaeus-Merzbacher disease, connatal form||http://www.orpha.net/ORDO/Orphanet_280210
2072||3854||Methanobrevibacter ruminantium||http://purl.obolibrary.org/obo/NCBITaxon_83816
2073||5657||Hereditary cerebral hemorrhage with amyloidosis, Iowa type||http://www.orpha.net/ORDO/Orphanet_324708
2074||2713||Inherited cancer-predisposing syndrome due to biallelic BRCA2 mutations||http://www.orpha.net/ORDO/Orphanet_319462
2075||8526||Pelizaeus-Merzbacher disease, classic form||http://www.orpha.net/ORDO/Orphanet_280219
2077||1826||Oryza nivara||http://purl.obolibrary.org/obo/NCBITaxon_4536
2076||4430||pathogen||http://www.ebi.ac.uk/efo/EFO_0000643
2079||1006||papillary thyroid carcinoma||http://www.ebi.ac.uk/efo/EFO_0000641
2078||5025||Aspergillus carbonarius||http://purl.obolibrary.org/obo/NCBITaxon_40993
2080||1986||papillary renal cell carcinoma||http://www.ebi.ac.uk/efo/EFO_0000640
2081||6573||experiment performer||http://www.ebi.ac.uk/efo/EFO_0000647
2082||10652||obsolete_percent oxygen concentration||http://www.ebi.ac.uk/efo/EFO_0000646
2083||10652||obsolete_percent oxygen||http://www.ebi.ac.uk/efo/EFO_0000645
2084||13883||pathogen test||http://www.ebi.ac.uk/efo/EFO_0000644
2085||8001||Metaphyseal chondrodysplasia - retinitis pigmentosa||http://www.orpha.net/ORDO/Orphanet_166035
2086||13036||period of infection||http://www.ebi.ac.uk/efo/EFO_0000648
2087||1814||periodontitis||http://www.ebi.ac.uk/efo/EFO_0000649
2088||10141||Multiple epiphyseal dysplasia, with miniepiphyses||http://www.orpha.net/ORDO/Orphanet_166032
2089||1022||Ursus americanus||http://purl.obolibrary.org/obo/NCBITaxon_9643
2090||6072||Microform holoprosencephaly||http://www.orpha.net/ORDO/Orphanet_280200
2091||13496||Podoviridae||http://purl.obolibrary.org/obo/NCBITaxon_10744
2092||8001||Metaphyseal chondrodysplasia, Kaitila type||http://www.orpha.net/ORDO/Orphanet_166038
2093||5155||Familial isolated restrictive cardiomyopathy||http://www.orpha.net/ORDO/Orphanet_75249
2095||1826||Oryza rufipogon||http://purl.obolibrary.org/obo/NCBITaxon_4529
2094||4571||prognostic subgroup||http://www.ebi.ac.uk/efo/EFO_0000672
2097||1826||Oryza longistaminata||http://purl.obolibrary.org/obo/NCBITaxon_4528
2096||10652||obsolete_progeria syndrome||http://www.ebi.ac.uk/efo/EFO_0000671
2098||306||Pure hair and nail ectodermal dysplasia||http://www.orpha.net/ORDO/Orphanet_69084
2099||306||Ectodermal dysplasia with natal teeth, Turnpenny type||http://www.orpha.net/ORDO/Orphanet_69083
2100||306||Odonto-tricho-ungual-digito-palmar syndrome||http://www.orpha.net/ORDO/Orphanet_69082
2101||2162||pterygium||http://www.ebi.ac.uk/efo/EFO_0000678
2103||13496||SARS coronavirus||http://purl.obolibrary.org/obo/NCBITaxon_227859
2104||1826||Lolium perenne||http://purl.obolibrary.org/obo/NCBITaxon_4522
2102||1391||mental or behavioural disorder||http://www.ebi.ac.uk/efo/EFO_0000677
2105||1022||Acanthopleura||http://purl.obolibrary.org/obo/NCBITaxon_61362
2106||1022||Homo sapiens||http://purl.obolibrary.org/obo/NCBITaxon_9606
2107||10652||obsolete_rat strain||http://www.ebi.ac.uk/efo/EFO_0000679
2109||1022||Paxillus filamentosus||http://purl.obolibrary.org/obo/NCBITaxon_85986
2108||10652||obsolete_protocol||http://www.ebi.ac.uk/efo/EFO_0000674
2110||120||prostate adenocarcinoma||http://www.ebi.ac.uk/efo/EFO_0000673
2111||2211||Pongo pygmaeus pygmaeus||http://purl.obolibrary.org/obo/NCBITaxon_9602
2112||1790||psoriasis||http://www.ebi.ac.uk/efo/EFO_0000676
2113||1022||Pongo sp.||http://purl.obolibrary.org/obo/NCBITaxon_9603
2114||10652||obsolete_protocol factor||http://www.ebi.ac.uk/efo/EFO_0000675
2115||1022||Canis lupus||http://purl.obolibrary.org/obo/NCBITaxon_9612
2116||8526||Null syndrome||http://www.orpha.net/ORDO/Orphanet_280234
2117||1826||Oryza sativa||http://purl.obolibrary.org/obo/NCBITaxon_4530
2118||9894||Pontocerebellar hypoplasia type 5||http://www.orpha.net/ORDO/Orphanet_166068
2119||6322||Renal glucosuria||http://www.orpha.net/ORDO/Orphanet_69076
2120||9894||Pontocerebellar hypoplasia type 4||http://www.orpha.net/ORDO/Orphanet_166063
2121||12433||Acute myeloid leukemia with CEBPA somatic mutations||http://www.orpha.net/ORDO/Orphanet_319480
2123||10652||obsolete_polymorphonuclear leukocyte||http://www.ebi.ac.uk/efo/EFO_0000661
2122||10994||adrenaline||http://purl.obolibrary.org/obo/CHEBI_33568
2124||15416||polycystic ovary syndrome||http://www.ebi.ac.uk/efo/EFO_0000660
2126||12433||Inherited acute myeloid leukemia||http://www.orpha.net/ORDO/Orphanet_319465
2125||10994||methoxychlor||http://purl.obolibrary.org/obo/CHEBI_6842
2127||10652||obsolete_pretreatment||http://www.ebi.ac.uk/efo/EFO_0000669
2128||1015||preeclampsia||http://www.ebi.ac.uk/efo/EFO_0000668
2129||1015||portal hypertension||http://www.ebi.ac.uk/efo/EFO_0000666
2130||10652||obsolete_porphyria||http://www.ebi.ac.uk/efo/EFO_0000665
2131||1826||Hordeum vulgare||http://purl.obolibrary.org/obo/NCBITaxon_4513
2132||1022||Canis lupus familiaris||http://purl.obolibrary.org/obo/NCBITaxon_9615
2133||1125||pool||http://www.ebi.ac.uk/efo/EFO_0000663
2134||2162||polyp||http://www.ebi.ac.uk/efo/EFO_0000662
2135||266||Hepatoencephalopathy due to combined oxidative phosphorylation deficiency type 1||http://www.orpha.net/ORDO/Orphanet_137681
2136||8526||Pelizaeus-Merzbacher disease, transitional form||http://www.orpha.net/ORDO/Orphanet_280224
2137||8526||Pelizaeus-Merzbacher disease in female carriers||http://www.orpha.net/ORDO/Orphanet_280229
2138||1783||water bath||http://purl.obolibrary.org/obo/OBI_0400155
2139||770||YCC16||http://www.ebi.ac.uk/efo/EFO_0002879
2140||770||YCC10||http://www.ebi.ac.uk/efo/EFO_0002877
2141||770||YCC11||http://www.ebi.ac.uk/efo/EFO_0002878
2142||770||WM793-P2N1||http://www.ebi.ac.uk/efo/EFO_0002875
2144||770||YCC1||http://www.ebi.ac.uk/efo/EFO_0002876
2143||1015||myocardial infarction||http://www.ebi.ac.uk/efo/EFO_0000612
2145||1505||myxoid liposarcoma||http://www.ebi.ac.uk/efo/EFO_0000613
2146||770||WM793||http://www.ebi.ac.uk/efo/EFO_0002873
2148||2165||narcolepsy||http://www.ebi.ac.uk/efo/EFO_0000614
2147||770||WM793-P1N1||http://www.ebi.ac.uk/efo/EFO_0002874
2149||770||WB-F344||http://www.ebi.ac.uk/efo/EFO_0002871
2151||2672||nucleus accumbens||http://purl.obolibrary.org/obo/UBERON_0001882
2150||770||WE-68||http://www.ebi.ac.uk/efo/EFO_0002872
2154||2672||bed nucleus of stria terminalis||http://purl.obolibrary.org/obo/UBERON_0001880
2152||2658||ascitic fluid||http://purl.obolibrary.org/obo/UBERON_0007795
2153||770||VH-64||http://www.ebi.ac.uk/efo/EFO_0002870
2155||14201||choroid plexus||http://purl.obolibrary.org/obo/UBERON_0001886
2156||6609||Von Willebrand disease type 2||http://www.orpha.net/ORDO/Orphanet_166081
2158||13689||terminal nerve||http://purl.obolibrary.org/obo/UBERON_0002924
2157||10808||amygdala||http://purl.obolibrary.org/obo/UBERON_0001876
2159||10813||Progressive supranuclear palsy - parkinsonism||http://www.orpha.net/ORDO/Orphanet_240085
2160||2156||Von Willebrand disease type 2A||http://www.orpha.net/ORDO/Orphanet_166084
2161||1316||Orofaciodigital syndrome type 5||http://www.orpha.net/ORDO/Orphanet_2919
2163||2156||Von Willebrand disease type 2B||http://www.orpha.net/ORDO/Orphanet_166087
2162||1391||neoplasm||http://www.ebi.ac.uk/efo/EFO_0000616
2165||1391||nervous system disease||http://www.ebi.ac.uk/efo/EFO_0000618
2164||4834||Postaxial polydactyly - dental and vertebral anomalies||http://www.orpha.net/ORDO/Orphanet_2916
2166||13770||Polydactyly-myopia syndrome||http://www.orpha.net/ORDO/Orphanet_2917
2167||10652||obsolete_nerve cell||http://www.ebi.ac.uk/efo/EFO_0000617
2168||2021||Poland syndrome||http://www.orpha.net/ORDO/Orphanet_2911
2169||7956||Polydactyly||http://www.orpha.net/ORDO/Orphanet_2913
2170||770||TE85||http://www.ebi.ac.uk/efo/EFO_0002866
2171||770||TMK1||http://www.ebi.ac.uk/efo/EFO_0002867
2172||770||TT3E||http://www.ebi.ac.uk/efo/EFO_0002868
2173||770||U2OS||http://www.ebi.ac.uk/efo/EFO_0002869
2175||13587||BALB/c||http://www.ebi.ac.uk/efo/EFO_0000602
2174||770||STA-ET-1||http://www.ebi.ac.uk/efo/EFO_0002862
2176||13587||BALB/cByJ||http://www.ebi.ac.uk/efo/EFO_0000603
2177||770||STA-ET-2.1||http://www.ebi.ac.uk/efo/EFO_0002863
2179||1826||Zea mays||http://purl.obolibrary.org/obo/NCBITaxon_4577
2180||1471||129X1/SvJ||http://www.ebi.ac.uk/efo/EFO_0000600
2178||770||T24||http://www.ebi.ac.uk/efo/EFO_0002864
2182||1471||129xC57BL/6||http://www.ebi.ac.uk/efo/EFO_0000601
2181||770||TC71||http://www.ebi.ac.uk/efo/EFO_0002865
2183||2672||forebrain||http://purl.obolibrary.org/obo/UBERON_0001890
2184||2672||midbrain||http://purl.obolibrary.org/obo/UBERON_0001891
2187||13448||rhombomere||http://purl.obolibrary.org/obo/UBERON_0001892
2188||10994||methapyrilene||http://purl.obolibrary.org/obo/CHEBI_6820
2185||2201||Familial papillary or follicular thyroid carcinoma||http://www.orpha.net/ORDO/Orphanet_319487
2186||770||SK-N-MC||http://www.ebi.ac.uk/efo/EFO_0002860
2189||2672||telencephalon||http://purl.obolibrary.org/obo/UBERON_0001893
2190||770||SQ-5||http://www.ebi.ac.uk/efo/EFO_0002861
2191||2672||diencephalon||http://purl.obolibrary.org/obo/UBERON_0001894
2192||2672||medulla oblongata||http://purl.obolibrary.org/obo/UBERON_0001896
2193||2672||thalamus||http://purl.obolibrary.org/obo/UBERON_0001897
2194||254||Rothmund-Thomson syndrome||http://www.orpha.net/ORDO/Orphanet_2909
2195||7086||SRD5A3-CDG||http://www.orpha.net/ORDO/Orphanet_324737
2196||6244||Limb-mammary syndrome||http://www.orpha.net/ORDO/Orphanet_69085
2198||306||Anhidrotic ectodermal dysplasia - immunodeficiency - osteopetrosis - lymphedema||http://www.orpha.net/ORDO/Orphanet_69088
2197||8756||Hereditary acrokeratotic poikiloderma, Weary type||http://www.orpha.net/ORDO/Orphanet_2907
2202||306||Naegeli-Franceschetti-Jadassohn syndrome||http://www.orpha.net/ORDO/Orphanet_69087
2200||327||Kindler syndrome||http://www.orpha.net/ORDO/Orphanet_2908
2201||5971||Familial nonmedullary thyroid carcinoma||http://www.orpha.net/ORDO/Orphanet_319494
2199||6432||Pontocerebellar hypoplasia type 6||http://www.orpha.net/ORDO/Orphanet_166073
2203||5502||Streptococcus pneumoniae R6||http://purl.obolibrary.org/obo/NCBITaxon_171101
2205||6609||Von Willebrand disease type 1||http://www.orpha.net/ORDO/Orphanet_166078
2204||10652||obsolete_mouse strain||http://www.ebi.ac.uk/efo/EFO_0000607
2206||5180||C57BL/6J||http://www.ebi.ac.uk/efo/EFO_0000606
2208||10652||obsolete_C57BL/6||http://www.ebi.ac.uk/efo/EFO_0000605
2207||10732||Familial spontaneous pneumothorax||http://www.orpha.net/ORDO/Orphanet_2903
2209||5180||C57BL/10||http://www.ebi.ac.uk/efo/EFO_0000604
2210||5502||Cronobacter muytjensii||http://purl.obolibrary.org/obo/NCBITaxon_413501
2211||1022||Pongo pygmaeus||http://purl.obolibrary.org/obo/NCBITaxon_9600
2212||5502||Cronobacter turicensis||http://purl.obolibrary.org/obo/NCBITaxon_413502
2214||1022||Pongo abelii||http://purl.obolibrary.org/obo/NCBITaxon_9601
2215||7953||Leri pleonosteosis||http://www.orpha.net/ORDO/Orphanet_2900
2213||10813||Progressive supranuclear palsy - pure akinesia with gait freezing||http://www.orpha.net/ORDO/Orphanet_240094
2217||14970||operator variation||http://www.ebi.ac.uk/efo/EFO_0000633
2216||11067||gram per kilogram||http://www.ebi.ac.uk/efo/EFO_0002897
2219||1826||Triticum durum||http://purl.obolibrary.org/obo/NCBITaxon_4567
2218||335||gram per meter squared||http://www.ebi.ac.uk/efo/EFO_0002898
2220||770||MKN7||http://www.ebi.ac.uk/efo/EFO_0002895
2221||1125||organism part||http://www.ebi.ac.uk/efo/EFO_0000635
2223||11476||microRNA profiling by high throughput sequencing||http://www.ebi.ac.uk/efo/EFO_0002896
2224||1826||Triticum aestivum||http://purl.obolibrary.org/obo/NCBITaxon_4565
2222||10652||obsolete_organism status||http://www.ebi.ac.uk/efo/EFO_0000636
2225||31||oligoastrocytoma||http://www.ebi.ac.uk/efo/EFO_0000630
2227||11067||microgram per kilogram||http://www.ebi.ac.uk/efo/EFO_0002899
2226||10652||obsolete_oligoastroglioma||http://www.ebi.ac.uk/efo/EFO_0000631
2228||766||oligodendroglioma||http://www.ebi.ac.uk/efo/EFO_0000632
2229||1006||renal carcinoma||http://www.ebi.ac.uk/efo/EFO_0002890
2230||1763||choriocarcinoma||http://www.ebi.ac.uk/efo/EFO_0002893
2231||2737||amelanotic skin melanoma||http://www.ebi.ac.uk/efo/EFO_0002894
2233||770||prostate derived cell line||http://www.ebi.ac.uk/efo/EFO_0002891
2232||5657||Hereditary cerebral hemorrhage with amyloidosis, Arctic type||http://www.orpha.net/ORDO/Orphanet_324723
2234||1006||thyroid carcinoma||http://www.ebi.ac.uk/efo/EFO_0002892
2235||4464||Cholesteryl ester storage disease||http://www.orpha.net/ORDO/Orphanet_75234
2237||1826||Spinacia oleracea||http://purl.obolibrary.org/obo/NCBITaxon_3562
2236||4464||Wolman disease||http://www.orpha.net/ORDO/Orphanet_75233
2238||2672||epithalamus||http://purl.obolibrary.org/obo/UBERON_0001899
2239||2672||hypothalamus||http://purl.obolibrary.org/obo/UBERON_0001898
2240||2846||overall survival||http://www.ebi.ac.uk/efo/EFO_0000638
2241||2002||osteosarcoma||http://www.ebi.ac.uk/efo/EFO_0000637
2242||9169||central nervous system development||http://purl.obolibrary.org/obo/GO_0007417
2243||120||papillary cystadenocarcinoma||http://www.ebi.ac.uk/efo/EFO_0000639
2244||770||mammary gland cell line||http://www.ebi.ac.uk/efo/EFO_0002884
2246||15417||nevus||http://www.ebi.ac.uk/efo/EFO_0000625
2245||770||breast cancer cell line||http://www.ebi.ac.uk/efo/EFO_0002885
2249||15475||neurofibroma||http://www.ebi.ac.uk/efo/EFO_0000622
2248||1826||Setaria italica||http://purl.obolibrary.org/obo/NCBITaxon_4555
2247||770||stem cell derived cell line||http://www.ebi.ac.uk/efo/EFO_0002886
2250||770||mouse cell line||http://www.ebi.ac.uk/efo/EFO_0002887
2251||770||Homo sapiens cell line||http://www.ebi.ac.uk/efo/EFO_0002888
2252||4715||Multiple congenital anomalies/dysmorphic syndrome-intellectual disability||http://www.orpha.net/ORDO/Orphanet_102283
2254||2162||neuroblastoma||http://www.ebi.ac.uk/efo/EFO_0000621
2253||1826||Sorghum bicolor||http://purl.obolibrary.org/obo/NCBITaxon_4558
2255||770||YCC3||http://www.ebi.ac.uk/efo/EFO_0002880
2256||10994||metformin||http://purl.obolibrary.org/obo/CHEBI_6801
2257||4259||response to glucocorticoid stimulus||http://purl.obolibrary.org/obo/GO_0051384
2258||770||YCC6||http://www.ebi.ac.uk/efo/EFO_0002881
2259||770||YCC7||http://www.ebi.ac.uk/efo/EFO_0002882
2261||770||haemopoietic system cell line||http://www.ebi.ac.uk/efo/EFO_0002883
2260||5657||Hereditary cerebral hemorrhage with amyloidosis, Italian type||http://www.orpha.net/ORDO/Orphanet_324713
2262||6609||Von Willebrand disease type 3||http://www.orpha.net/ORDO/Orphanet_166096
2263||5657||Hereditary cerebral hemorrhage with amyloidosis, Flemish type||http://www.orpha.net/ORDO/Orphanet_324718
2265||245||brain development||http://purl.obolibrary.org/obo/GO_0007420
2264||8193||methamphetamine||http://purl.obolibrary.org/obo/CHEBI_6809
2266||2156||Von Willebrand disease type 2N||http://www.orpha.net/ORDO/Orphanet_166093
2267||2156||Von Willebrand disease type 2M||http://www.orpha.net/ORDO/Orphanet_166090
2268||15020||observational design||http://www.ebi.ac.uk/efo/EFO_0000629
2269||14970||number of injections||http://www.ebi.ac.uk/efo/EFO_0000627
2270||10652||obsolete_nucleic acid extracted||http://www.ebi.ac.uk/efo/EFO_0000626
2271||7782||Alpha-B crystallin-related late-onset distal myopathy||http://www.orpha.net/ORDO/Orphanet_399058
2272||382||Prog ria - short stature - pigmented nevi||http://www.orpha.net/ORDO/Orphanet_2959
2273||11899||X-linked intellectual disability - dysmorphism - cerebral atrophy||http://www.orpha.net/ORDO/Orphanet_2958
2274||2319||Patent ductus arteriosus - bicuspid aortic valve - hand anomalies||http://www.orpha.net/ORDO/Orphanet_228190
2275||11882||Guttmacher syndrome||http://www.orpha.net/ORDO/Orphanet_2957
2276||2021||Prata-Liberal-Goncalves syndrome||http://www.orpha.net/ORDO/Orphanet_2956
2277||1826||Lepidium sativum||http://purl.obolibrary.org/obo/NCBITaxon_33125
2278||3019||Lung fibrosis - immunodeficiency - 46,XX gonadal dysgenesis||http://www.orpha.net/ORDO/Orphanet_137631
2279||8024||Overgrowth - macrocephaly - facial dysmorphism||http://www.orpha.net/ORDO/Orphanet_137634
2280||14353||Leukoencephalopathy - ataxia - hypodontia - hypomyelination||http://www.orpha.net/ORDO/Orphanet_137639
2281||12083||Adducted thumbs - arthrogryposis, Christian type||http://www.orpha.net/ORDO/Orphanet_2952
2282||4014||Ehlers-Danlos syndrome, musculocontractural type||http://www.orpha.net/ORDO/Orphanet_2953
2283||13770||Triphalangeal thumb - polysyndactyly syndrome||http://www.orpha.net/ORDO/Orphanet_2950
2284||2397||Pelizaeus-Merzbacher-like disease due to AIMP1 mutation||http://www.orpha.net/ORDO/Orphanet_280293
2285||238||Absent thumb - short stature - immunodeficiency||http://www.orpha.net/ORDO/Orphanet_2951
2287||13770||Triphalangeal thumbs - brachyectrodactyly||http://www.orpha.net/ORDO/Orphanet_2947
2286||1022||Leishmania infantum||http://purl.obolibrary.org/obo/NCBITaxon_5671
2288||504||nucleoside phosphate metabolic process||http://purl.obolibrary.org/obo/GO_0006753
2289||6978||ATP biosynthetic process||http://purl.obolibrary.org/obo/GO_0006754
2290||2397||Pelizaeus-Merzbacher-like disease due to HSPD1 mutation||http://www.orpha.net/ORDO/Orphanet_280288
2291||15||Brachydactyly - long thumb||http://www.orpha.net/ORDO/Orphanet_2946
2293||3866||Intractable diarrhea - choanal atresia - eye anomalies||http://www.orpha.net/ORDO/Orphanet_137622
2292||2672||internal ear||http://purl.obolibrary.org/obo/UBERON_0001846
2294||2672||cochlea||http://purl.obolibrary.org/obo/UBERON_0001844
2295||4261||Glycogen storage disease due to muscle and heart glycogen synthase deficiency||http://www.orpha.net/ORDO/Orphanet_137625
2296||9918||Familial advanced sleep-phase syndrome||http://www.orpha.net/ORDO/Orphanet_164736
2297||9607||Cardiac anomalies - heterotaxy||http://www.orpha.net/ORDO/Orphanet_137628
2298||1826||Casuarina glauca||http://purl.obolibrary.org/obo/NCBITaxon_3522
2300||2395||Qualitative or quantitative defects of integrin alpha-7||http://www.orpha.net/ORDO/Orphanet_207098
2299||2063||abnormality of blood and blood-forming tissues||http://purl.obolibrary.org/obo/HP_0001871
2301||2397||Pelizaeus-Merzbacher-like disease due to GJC2 mutation||http://www.orpha.net/ORDO/Orphanet_280282
2302||760||Porencephaly||http://www.orpha.net/ORDO/Orphanet_2940
2303||1022||Leishmania major||http://purl.obolibrary.org/obo/NCBITaxon_5664
2304||1022||Leishmania mexicana||http://purl.obolibrary.org/obo/NCBITaxon_5665
2306||13770||Crossed polysyndactyly||http://www.orpha.net/ORDO/Orphanet_2935
2305||4810||Dominant hypophosphatemia with nephrolithiasis or osteoporosis||http://www.orpha.net/ORDO/Orphanet_244305
2308||12769||Polysyndactyly - cardiac malformation||http://www.orpha.net/ORDO/Orphanet_2934
2307||6085||cellular aromatic compound metabolic process||http://purl.obolibrary.org/obo/GO_0006725
2309||2395||Qualitative or quantitative defects of merosin||http://www.orpha.net/ORDO/Orphanet_207094
2310||1022||Karenia brevis||http://purl.obolibrary.org/obo/NCBITaxon_156230
2311||1022||Leishmania donovani||http://purl.obolibrary.org/obo/NCBITaxon_5661
2313||2395||Qualitative or quantitative defects of collagen 6||http://www.orpha.net/ORDO/Orphanet_207090
2312||1022||Leishmania braziliensis||http://purl.obolibrary.org/obo/NCBITaxon_5660
2314||306||Trichorhinophalangeal syndrome||http://www.orpha.net/ORDO/Orphanet_324764
2315||1826||Alnus glutinosa||http://purl.obolibrary.org/obo/NCBITaxon_3517
2316||9898||Autosomal dominant striatal neurodegeneration||http://www.orpha.net/ORDO/Orphanet_228169
2317||306||Cronkhite-Canada syndrome||http://www.orpha.net/ORDO/Orphanet_2930
2318||2252||Microcephalic primordial dwarfism||http://www.orpha.net/ORDO/Orphanet_324761
2319||6246||Heart-hand syndrome||http://www.orpha.net/ORDO/Orphanet_228184
2320||2252||Preaxial polydactyly - colobomata - intellectual disability||http://www.orpha.net/ORDO/Orphanet_2921
2321||10719||Isolated polycystic liver disease||http://www.orpha.net/ORDO/Orphanet_2924
2323||2395||Qualitative or quantitative defects of dystrophin||http://www.orpha.net/ORDO/Orphanet_207085
2322||4717||Genetic progeroid syndrome||http://www.orpha.net/ORDO/Orphanet_363245
2324||6912||Polyneuropathy - hand defect||http://www.orpha.net/ORDO/Orphanet_2926
2325||4139||Polymicrogyria - turricephaly - hypogenitalism||http://www.orpha.net/ORDO/Orphanet_2925
2326||4139||Polyneuropathy - intellectual disability - acromicria - premature menopause||http://www.orpha.net/ORDO/Orphanet_2928
2327||3833||Juvenile polyposis syndrome||http://www.orpha.net/ORDO/Orphanet_2929
2328||2672||cerebral hemisphere||http://purl.obolibrary.org/obo/UBERON_0001869
2329||1022||Agrotis ipsilon||http://purl.obolibrary.org/obo/NCBITaxon_56364
2330||2672||globus pallidus||http://purl.obolibrary.org/obo/UBERON_0001875
2331||2672||caudate nucleus||http://purl.obolibrary.org/obo/UBERON_0001873
2332||2672||parietal lobe||http://purl.obolibrary.org/obo/UBERON_0001872
2334||2672||temporal lobe||http://purl.obolibrary.org/obo/UBERON_0001871
2333||5877||Segmental outgrowth - lipomatosis - arteriovenous malformation - epidermal nevus||http://www.orpha.net/ORDO/Orphanet_137608
2335||2672||frontal cortex||http://purl.obolibrary.org/obo/UBERON_0001870
2336||1022||Cryptococcus neoformans var. grubii||http://purl.obolibrary.org/obo/NCBITaxon_178876
2337||5912||Legius syndrome||http://www.orpha.net/ORDO/Orphanet_137605
2338||8191||potassium bromide||http://purl.obolibrary.org/obo/CHEBI_32030
2339||4344||RFT1-CDG||http://www.orpha.net/ORDO/Orphanet_244310
2340||1826||Betula pendula||http://purl.obolibrary.org/obo/NCBITaxon_3505
2341||2997||Autosomal dominant Charcot-Marie-Tooth disease type 2M||http://www.orpha.net/ORDO/Orphanet_228179
2345||10994||benzodiazepine||http://purl.obolibrary.org/obo/CHEBI_22720
2343||2997||Autosomal dominant Charcot-Marie-Tooth disease type 2N||http://www.orpha.net/ORDO/Orphanet_228174
2344||2395||Qualitative or quantitative defects of caveolin-3||http://www.orpha.net/ORDO/Orphanet_207078
2342||8298||iron deficiency anemia||http://purl.obolibrary.org/obo/HP_0001891
2346||2252||Oliver syndrome||http://www.orpha.net/ORDO/Orphanet_2920
2347||15||Histiocytoid cardiomyopathy||http://www.orpha.net/ORDO/Orphanet_137675
2348||7981||Czech dysplasia, metatarsal type||http://www.orpha.net/ORDO/Orphanet_137678
2349||12360||Distal anoctaminopathy||http://www.orpha.net/ORDO/Orphanet_399096
2350||2392||Qualitative or quantitative defects of delta-sarcoglycan||http://www.orpha.net/ORDO/Orphanet_207070
2351||14540||weight loss||http://purl.obolibrary.org/obo/HP_0001824
2352||2355||organic cyclic compound biosynthetic process||http://purl.obolibrary.org/obo/GO_1901362
2355||14860||organic cyclic compound metabolic process||http://purl.obolibrary.org/obo/GO_1901360
2354||2395||Qualitative or quantitative defects of dysferlin||http://www.orpha.net/ORDO/Orphanet_207073
2353||9934||Ptosis - strabismus - ectopic pupils||http://www.orpha.net/ORDO/Orphanet_2999
2357||1826||Bromus secalinus||http://purl.obolibrary.org/obo/NCBITaxon_4502
2358||1022||Mustela putorius furo||http://purl.obolibrary.org/obo/NCBITaxon_9669
2356||9934||Ptosis - vocal cord paralysis||http://www.orpha.net/ORDO/Orphanet_2997
2359||2392||Qualitative or quantitative defects of gamma-sarcoglycan||http://www.orpha.net/ORDO/Orphanet_207067
2360||1419||Baraitser-Winter syndrome||http://www.orpha.net/ORDO/Orphanet_2995
2361||12769||Short stature - craniofacial anomalies - genital hypoplasia||http://www.orpha.net/ORDO/Orphanet_2994
2362||2606||Autosomal recessive multiple pterygium syndrome||http://www.orpha.net/ORDO/Orphanet_2990
2363||12358||KLHL9-related childhood-onset distal myopathy||http://www.orpha.net/ORDO/Orphanet_399081
2365||12358||Finnish upper limb-onset distal myopathy||http://www.orpha.net/ORDO/Orphanet_399086
2364||2366||phosphate-containing compound metabolic process||http://purl.obolibrary.org/obo/GO_0006796
2366||6085||phosphorus metabolic process||http://purl.obolibrary.org/obo/GO_0006793
2367||10694||Capillary malformation - arteriovenous malformation||http://www.orpha.net/ORDO/Orphanet_137667
2369||10994||benzenetriols||http://purl.obolibrary.org/obo/CHEBI_22707
2368||1022||Felis catus||http://purl.obolibrary.org/obo/NCBITaxon_9685
2370||2392||Qualitative or quantitative defects of alpha-sarcoglycan||http://www.orpha.net/ORDO/Orphanet_207060
2371||1022||Dermacentor andersoni||http://purl.obolibrary.org/obo/NCBITaxon_34620
2372||5918||Antecubital pterygium syndrome||http://www.orpha.net/ORDO/Orphanet_2987
2373||2252||Pterygium colli - intellectual disability - digital anomalies||http://www.orpha.net/ORDO/Orphanet_2988
2375||2392||Qualitative or quantitative defects of beta-sarcoglycan||http://www.orpha.net/ORDO/Orphanet_207063
2374||9631||Pterygium of the conjunctiva, familial form||http://www.orpha.net/ORDO/Orphanet_2989
2376||5502||Lactobacillus kimchii||http://purl.obolibrary.org/obo/NCBITaxon_103818
2377||3019||Disorder of sex development - intellectual disability||http://www.orpha.net/ORDO/Orphanet_2983
2378||2252||Pseudoprogeria syndrome||http://www.orpha.net/ORDO/Orphanet_2985
2379||6899||Acro-oto-ocular syndrome||http://www.orpha.net/ORDO/Orphanet_2980
2380||11842||Distal hereditary motor neuropathy||http://www.orpha.net/ORDO/Orphanet_53739
2381||2713||Familial papillary renal cell carcinoma||http://www.orpha.net/ORDO/Orphanet_47044
2382||2395||Qualitative or quantitative defects of protein SERCA1||http://www.orpha.net/ORDO/Orphanet_209199
2384||10994||caerulein||http://purl.obolibrary.org/obo/CHEBI_59219
2383||41||Familial cold urticaria||http://www.orpha.net/ORDO/Orphanet_47045
2385||2395||Qualitative or quantitative defects of plectin||http://www.orpha.net/ORDO/Orphanet_209196
2386||11433||lacrimal gland||http://purl.obolibrary.org/obo/UBERON_0001817
2387||2252||Microcephaly - intellectual disability - phalangeal and neurological anomalies||http://www.orpha.net/ORDO/Orphanet_137658
2388||2672||conjunctiva||http://purl.obolibrary.org/obo/UBERON_0001811
2389||2252||Microcephaly - digital anomalies - intellectual disability||http://www.orpha.net/ORDO/Orphanet_137653
2390||2395||Qualitative or quantitative defects of selenoprotein N1||http://www.orpha.net/ORDO/Orphanet_209193
2391||15174||Chronic intestinal pseudoobstruction||http://www.orpha.net/ORDO/Orphanet_2978
2392||2395||Qualitative or quantitative defects of sarcoglycan||http://www.orpha.net/ORDO/Orphanet_207052
2393||5048||Pseudoleprechaunism syndrome, Patterson type||http://www.orpha.net/ORDO/Orphanet_2976
2394||6276||Peroxisomal acyl-CoA oxidase deficiency||http://www.orpha.net/ORDO/Orphanet_2971
2397||15549||Pelizaeus-Merzbacher-like disease||http://www.orpha.net/ORDO/Orphanet_280270
2396||742||Prune belly syndrome||http://www.orpha.net/ORDO/Orphanet_2970
2395||5893||Qualitative or quantitative protein defects in neuromuscular diseases||http://www.orpha.net/ORDO/Orphanet_207049
2398||3019||46,XX disorder of sex development - skeletal anomalies||http://www.orpha.net/ORDO/Orphanet_2975
2399||5681||46,XX disorder of sex development - anorectal anomalies||http://www.orpha.net/ORDO/Orphanet_2973
2400||4834||Non-eruption of teeth - maxillary hypoplasia - genu valgum||http://www.orpha.net/ORDO/Orphanet_2972
2401||2395||Qualitative or quantitative defects of emerin||http://www.orpha.net/ORDO/Orphanet_209188
2402||2672||gingiva||http://purl.obolibrary.org/obo/UBERON_0001828
2403||2395||Qualitative or quantitative defects of beta-myosin heavy chain (MYH7)||http://www.orpha.net/ORDO/Orphanet_209185
2404||2395||Qualitative or quantitative defects of nebulin||http://www.orpha.net/ORDO/Orphanet_209182
2405||1400||Ring chromosome||http://www.orpha.net/ORDO/Orphanet_363203
2406||15||Idiopathic ventricular fibrillation, not Brugada type||http://www.orpha.net/ORDO/Orphanet_228140
2407||204||Properdin deficiency||http://www.orpha.net/ORDO/Orphanet_2966
2408||6294||Protein R deficiency||http://www.orpha.net/ORDO/Orphanet_2967
2409||5191||Leukocyte adhesion deficiency||http://www.orpha.net/ORDO/Orphanet_2968
2410||5877||Proteus-like syndrome||http://www.orpha.net/ORDO/Orphanet_2969
2411||9986||Wyburn-Mason syndrome||http://www.orpha.net/ORDO/Orphanet_53719
2412||1022||Callorhinchus milii||http://purl.obolibrary.org/obo/NCBITaxon_7868
2413||382||De Barsy syndrome||http://www.orpha.net/ORDO/Orphanet_2962
2415||1732||Rare genetic eye disease||http://www.orpha.net/ORDO/Orphanet_101435
2414||5037||Tumoral calcinosis||http://www.orpha.net/ORDO/Orphanet_53715
2416||12769||Autosomal dominant prognathism||http://www.orpha.net/ORDO/Orphanet_2964
2417||382||Progeroid syndrome, Petty type||http://www.orpha.net/ORDO/Orphanet_2963
2418||11433||parotid gland||http://purl.obolibrary.org/obo/UBERON_0001831
2419||4907||Medium chain acyl-CoA dehydrogenase deficiency||http://www.orpha.net/ORDO/Orphanet_42
2420||212||X-linked adrenoleukodystrophy||http://www.orpha.net/ORDO/Orphanet_43
2421||212||Neonatal adrenoleukodystrophy||http://www.orpha.net/ORDO/Orphanet_44
2422||6266||Adenosine monophosphate deaminase deficiency||http://www.orpha.net/ORDO/Orphanet_45
2423||4728||Adenylosuccinate lyase deficiency||http://www.orpha.net/ORDO/Orphanet_46
2424||4238||X-linked agammaglobulinemia||http://www.orpha.net/ORDO/Orphanet_47
2425||5538||Congenital bilateral absence of vas deferens||http://www.orpha.net/ORDO/Orphanet_48
2426||7990||Acromesomelic dysplasia, Maroteaux type||http://www.orpha.net/ORDO/Orphanet_40
2427||5912||Dyschromatosis symmetrica hereditaria||http://www.orpha.net/ORDO/Orphanet_41
2428||3643||skin tags||http://purl.obolibrary.org/obo/HP_0010609
2429||1826||Festuca brevipila||http://purl.obolibrary.org/obo/NCBITaxon_98746
2430||5911||Oculocutaneous albinism||http://www.orpha.net/ORDO/Orphanet_55
2431||378||Alkaptonuria||http://www.orpha.net/ORDO/Orphanet_56
2432||1022||Danio rerio||http://purl.obolibrary.org/obo/NCBITaxon_7955
2434||3560||Albers-Sch nberg osteopetrosis||http://www.orpha.net/ORDO/Orphanet_53
2433||5502||Prochlorococcus marinus||http://purl.obolibrary.org/obo/NCBITaxon_1219
2435||1827||X-linked recessive ocular albinism||http://www.orpha.net/ORDO/Orphanet_54
2436||533||Allan-Herndon-Dudley syndrome||http://www.orpha.net/ORDO/Orphanet_59
2437||6572||Glycogen storage disease due to aldolase A deficiency||http://www.orpha.net/ORDO/Orphanet_57
2438||1022||Carassius auratus||http://purl.obolibrary.org/obo/NCBITaxon_7957
2439||4706||Alexander disease||http://www.orpha.net/ORDO/Orphanet_58
2440||4139||Aicardi-Gouti res syndrome||http://www.orpha.net/ORDO/Orphanet_51
2441||5967||Alagille syndrome||http://www.orpha.net/ORDO/Orphanet_52
2442||760||Aicardi syndrome||http://www.orpha.net/ORDO/Orphanet_50
2443||1022||Cyprinus carpio||http://purl.obolibrary.org/obo/NCBITaxon_7962
2444||10352||Fumaric aciduria||http://www.orpha.net/ORDO/Orphanet_24
2445||6371||Glutaryl-CoA dehydrogenase deficiency||http://www.orpha.net/ORDO/Orphanet_25
2446||6294||Methylmalonic acidemia with homocystinuria||http://www.orpha.net/ORDO/Orphanet_26
2447||11842||Rare hereditary disease with peripheral neuropathy||http://www.orpha.net/ORDO/Orphanet_207015
2448||918||Vitamin B12-unresponsive methylmalonic acidemia||http://www.orpha.net/ORDO/Orphanet_27
2450||13125||Spinal muscular atrophy associated with central nervous system anomaly||http://www.orpha.net/ORDO/Orphanet_207012
2449||1022||Hypophthalmichthys||http://purl.obolibrary.org/obo/NCBITaxon_7963
2451||6272||3-hydroxy-3-methylglutaric aciduria||http://www.orpha.net/ORDO/Orphanet_20
2452||6328||4-hydroxybutyric aciduria||http://www.orpha.net/ORDO/Orphanet_22
2453||6302||Argininosuccinic aciduria||http://www.orpha.net/ORDO/Orphanet_23
2454||2447||Rare hereditary metabolic disease with peripheral neuropathy||http://www.orpha.net/ORDO/Orphanet_207018
2455||770||GM15324||http://purl.obolibrary.org/obo/CLO_0027182
2456||5237||Mevalonic aciduria||http://www.orpha.net/ORDO/Orphanet_29
2457||918||Vitamin B12-responsive methylmalonic acidemia||http://www.orpha.net/ORDO/Orphanet_28
2459||2447||Rare hereditary neurologic disease with peripheral neuropathy||http://www.orpha.net/ORDO/Orphanet_207025
2458||378||Acrodermatitis enteropathica||http://www.orpha.net/ORDO/Orphanet_37
2460||5935||Acrokeratoelastoidosis of Costa||http://www.orpha.net/ORDO/Orphanet_38
2461||6306||Propionic acidemia||http://www.orpha.net/ORDO/Orphanet_35
2462||2459||Cerebellar ataxia with peripheral neuropathy||http://www.orpha.net/ORDO/Orphanet_207028
2463||2252||Acrocallosal syndrome||http://www.orpha.net/ORDO/Orphanet_36
2465||2447||Rare hereditary systemic disease with peripheral neuropathy||http://www.orpha.net/ORDO/Orphanet_207021
2464||6306||Isovaleric acidemia||http://www.orpha.net/ORDO/Orphanet_33
2466||10352||Oxoglutaricaciduria||http://www.orpha.net/ORDO/Orphanet_31
2467||6288||Glutathione synthetase deficiency||http://www.orpha.net/ORDO/Orphanet_32
2468||8193||acrylamide||http://purl.obolibrary.org/obo/CHEBI_28619
2469||6264||Hereditary orotic aciduria||http://www.orpha.net/ORDO/Orphanet_30
2470||10994||1,4-dichlorobenzene||http://purl.obolibrary.org/obo/CHEBI_28618
2471||2459||Rare disease with corpus callosum agenesis associated with peripheral neuropathy||http://www.orpha.net/ORDO/Orphanet_207031
2473||770||CCD-18Co cell||http://purl.obolibrary.org/obo/BTO_0004059
2472||770||AG11696||http://purl.obolibrary.org/obo/CLO_0022362
2474||6573||dye role||http://purl.obolibrary.org/obo/CHEBI_37960
2475||6610||Antley-Bixler syndrome||http://www.orpha.net/ORDO/Orphanet_83
2476||4572||Hereditary thrombophilia due to congenital antithrombin deficiency||http://www.orpha.net/ORDO/Orphanet_82
2477||13551||Congenital dyserythropoietic anemia||http://www.orpha.net/ORDO/Orphanet_85
2478||5912||Fanconi anemia||http://www.orpha.net/ORDO/Orphanet_84
2479||5767||Apert syndrome||http://www.orpha.net/ORDO/Orphanet_87
2481||618||plant structure development stage||http://purl.obolibrary.org/obo/PO_0009012
2480||4629||Familial abdominal aortic aneurysm||http://www.orpha.net/ORDO/Orphanet_86
2482||2288||nucleoside phosphate biosynthetic process||http://purl.obolibrary.org/obo/GO_1901293
2483||770||AG11726||http://purl.obolibrary.org/obo/CLO_0022371
2484||4931||Aromatase deficiency||http://www.orpha.net/ORDO/Orphanet_91
2485||6302||Argininemia||http://www.orpha.net/ORDO/Orphanet_90
2486||2454||Ataxia with vitamin E deficiency||http://www.orpha.net/ORDO/Orphanet_96
2487||2462||Friedreich ataxia||http://www.orpha.net/ORDO/Orphanet_95
2488||6595||Aspartylglucosaminuria||http://www.orpha.net/ORDO/Orphanet_93
2489||3655||vascular leaf||http://purl.obolibrary.org/obo/PO_0009025
2490||4692||Autosomal dominant cerebellar ataxia||http://www.orpha.net/ORDO/Orphanet_99
2492||799||histamine antagonist||http://purl.obolibrary.org/obo/CHEBI_37956
2491||10735||Autosomal recessive spastic ataxia of Charlevoix-Saguenay||http://www.orpha.net/ORDO/Orphanet_98
2493||7944||Familial paroxysmal ataxia||http://www.orpha.net/ORDO/Orphanet_97
2494||10994||curcumin||http://purl.obolibrary.org/obo/CHEBI_3962
2495||1826||Polytrichum juniperinum||http://purl.obolibrary.org/obo/NCBITaxon_129213
2496||4267||Alpha-mannosidosis||http://www.orpha.net/ORDO/Orphanet_61
2497||266||Alpha-1-antitrypsin deficiency||http://www.orpha.net/ORDO/Orphanet_60
2498||5700||Alport syndrome||http://www.orpha.net/ORDO/Orphanet_63
2499||1415||Autosomal recessive limb-girdle muscular dystrophy type 2D||http://www.orpha.net/ORDO/Orphanet_62
2500||9626||Leber congenital amaurosis||http://www.orpha.net/ORDO/Orphanet_65
2501||4701||Alstr m syndrome||http://www.orpha.net/ORDO/Orphanet_64
2502||5502||Burkholderia cenocepacia||http://purl.obolibrary.org/obo/NCBITaxon_95486
2503||1326||phenotypic abnormality of the aorta||http://purl.obolibrary.org/obo/HP_0001679
2504||1826||Aquilegia formosa||http://purl.obolibrary.org/obo/NCBITaxon_223430
2505||1687||Gorham-Stout disease||http://www.orpha.net/ORDO/Orphanet_73
2506||4139||Angelman syndrome||http://www.orpha.net/ORDO/Orphanet_72
2507||3856||Chylomicron retention disease||http://www.orpha.net/ORDO/Orphanet_71
2508||10994||sulpiride||http://purl.obolibrary.org/obo/CHEBI_32168
2509||9869||Proximal spinal muscular atrophy||http://www.orpha.net/ORDO/Orphanet_70
2510||10994||acyclovir||http://purl.obolibrary.org/obo/CHEBI_2453
2511||1022||Anguilla anguilla||http://purl.obolibrary.org/obo/NCBITaxon_7936
2512||799||phenothiazine antipsychotic drug||http://purl.obolibrary.org/obo/CHEBI_37930
2514||15365||Congenital alpha2 antiplasmin deficiency||http://www.orpha.net/ORDO/Orphanet_79
2513||10994||methyltrienolone||http://purl.obolibrary.org/obo/CHEBI_379896
2515||9654||Aniridia||http://www.orpha.net/ORDO/Orphanet_77
2516||1226||Frank-Ter Haar syndrome||http://www.orpha.net/ORDO/Orphanet_137834
2517||5961||X-linked intellectual disability - cerebellar hypoplasia||http://www.orpha.net/ORDO/Orphanet_137831
2518||10994||leukotriene D4||http://purl.obolibrary.org/obo/CHEBI_28666
2519||4139||Pitt-Hopkins-like syndrome||http://www.orpha.net/ORDO/Orphanet_221150
2520||8315||Classical progressive supranuclear palsy||http://www.orpha.net/ORDO/Orphanet_240071
2521||10652||obsolete_endocrine system||http://www.ebi.ac.uk/efo/EFO_0002969
2523||14537||embryonic stem cell derived neuronal stem cell||http://www.ebi.ac.uk/efo/EFO_0002968
2522||10994||enalapril||http://purl.obolibrary.org/obo/CHEBI_4784
2524||773||pluripotent||http://www.ebi.ac.uk/efo/EFO_0002967
2525||772||pancreatic cell||http://www.ebi.ac.uk/efo/EFO_0002966
2526||770||AG14446||http://purl.obolibrary.org/obo/CLO_0022320
2527||772||nervous system cell||http://www.ebi.ac.uk/efo/EFO_0002963
2528||772||animal reproductive system cell||http://www.ebi.ac.uk/efo/EFO_0002962
2529||770||NTera2 derived dopaminergic neuronal like cells||http://www.ebi.ac.uk/efo/EFO_0002961
2530||770||BG03||http://www.ebi.ac.uk/efo/EFO_0002960
2531||1022||Euphausia superba||http://purl.obolibrary.org/obo/NCBITaxon_6819
2532||1826||Populus fremontii x Populus angustifolia||http://purl.obolibrary.org/obo/NCBITaxon_352374
2533||5025||Candida tenuis||http://purl.obolibrary.org/obo/NCBITaxon_45596
2534||10266||2q31.1 microduplication syndrome||http://www.orpha.net/ORDO/Orphanet_294026
2535||2545||ILSXISS19/TejJ||http://www.ebi.ac.uk/efo/EFO_0002977
2536||2545||ILSXISS16/TejJ||http://www.ebi.ac.uk/efo/EFO_0002976
2537||2545||ILSXISS23/TejJ||http://www.ebi.ac.uk/efo/EFO_0002979
2538||2545||ILSXISS22/TejJ||http://www.ebi.ac.uk/efo/EFO_0002978
2539||325||Neonatal inflammatory skin and bowel disease||http://www.orpha.net/ORDO/Orphanet_294023
2540||2545||ILSXISS7/TejJ||http://www.ebi.ac.uk/efo/EFO_0002973
2541||2545||ILSXISS3/TejJ||http://www.ebi.ac.uk/efo/EFO_0002972
2542||2545||ILSXISS14/TejJ||http://www.ebi.ac.uk/efo/EFO_0002975
2543||2545||ILSXISS13/TejJ||http://www.ebi.ac.uk/efo/EFO_0002974
2544||5502||Deinococcus radiodurans||http://purl.obolibrary.org/obo/NCBITaxon_1299
2545||13587||ILSXISS#/Tej||http://www.ebi.ac.uk/efo/EFO_0002971
2546||1391||muscular disease||http://www.ebi.ac.uk/efo/EFO_0002970
2547||5502||Deinococcus||http://purl.obolibrary.org/obo/NCBITaxon_1298
2548||4609||dehydroepiandrosterone||http://purl.obolibrary.org/obo/CHEBI_28689
2549||6046||Microcephaly-capillary malformation syndrome||http://www.orpha.net/ORDO/Orphanet_294016
2550||10994||cytarabine||http://purl.obolibrary.org/obo/CHEBI_28680
2551||5838||parous||http://www.ebi.ac.uk/efo/EFO_0002947
2552||618||postnatal||http://www.ebi.ac.uk/efo/EFO_0002948
2553||12296||transcription profiling by MPSS||http://www.ebi.ac.uk/efo/EFO_0002942
2554||12296||transcription profiling by SAGE||http://www.ebi.ac.uk/efo/EFO_0002941
2555||770||zebrafish cell line||http://www.ebi.ac.uk/efo/EFO_0002940
2556||10652||obsolete_alpha-1-antitrypsin deficiency||http://www.ebi.ac.uk/efo/EFO_0002946
2557||1016||familial cardiomyopathy||http://www.ebi.ac.uk/efo/EFO_0002945
2558||1183||nucleic acid extraction protocol||http://www.ebi.ac.uk/efo/EFO_0002944
2559||12296||transcription profiling by RT-PCR||http://www.ebi.ac.uk/efo/EFO_0002943
2560||238||Combined immunodeficiency with facio-oculo-skeletal anomalies||http://www.orpha.net/ORDO/Orphanet_221139
2561||5502||Buchnera aphidicola (Schizaphis graminum)||http://purl.obolibrary.org/obo/NCBITaxon_98794
2562||10138||Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies||http://www.orpha.net/ORDO/Orphanet_221145
2564||772||experimental cell||http://www.ebi.ac.uk/efo/EFO_0002958
2563||4454||copper||http://purl.obolibrary.org/obo/CHEBI_28694
2565||770||NTera2||http://www.ebi.ac.uk/efo/EFO_0002959
2566||5838||virgin||http://www.ebi.ac.uk/efo/EFO_0002951
2567||1931||pregnancy||http://www.ebi.ac.uk/efo/EFO_0002950
2568||5025||Penicillium viridicatum||http://purl.obolibrary.org/obo/NCBITaxon_60134
2569||772||reproductive system cell||http://www.ebi.ac.uk/efo/EFO_0002955
2570||773||differentiated||http://www.ebi.ac.uk/efo/EFO_0002954
2571||770||2102Ep||http://www.ebi.ac.uk/efo/EFO_0002957
2572||772||musculo-skeletal system cell||http://www.ebi.ac.uk/efo/EFO_0002956
2573||770||ES-E14 cell||http://purl.obolibrary.org/obo/BTO_0005136
2574||7981||Multiple epiphyseal dysplasia, Beighton type||http://www.orpha.net/ORDO/Orphanet_166011
2575||12633||microgram per kilogram per day||http://www.ebi.ac.uk/efo/EFO_0002929
2576||12633||International Unit per milliliter||http://www.ebi.ac.uk/efo/EFO_0002928
2577||11507||International Unit||http://www.ebi.ac.uk/efo/EFO_0002927
2578||770||ENCODE cell line||http://www.ebi.ac.uk/efo/EFO_0002926
2579||10141||Multiple epiphyseal dysplasia, Lowry type||http://www.orpha.net/ORDO/Orphanet_166016
2580||13883||ENCODE functional genome mapping||http://www.ebi.ac.uk/efo/EFO_0002925
2581||2603||Aneurysm - osteoarthritis syndrome||http://www.orpha.net/ORDO/Orphanet_284984
2582||10994||6alpha-methylprednisolone||http://purl.obolibrary.org/obo/CHEBI_6888
2583||5502||Leuconostoc mesenteroides||http://purl.obolibrary.org/obo/NCBITaxon_1245
2584||5502||Oenococcus oeni||http://purl.obolibrary.org/obo/NCBITaxon_1247
2585||2252||Congenital cataracts - facial dysmorphism - neuropathy||http://www.orpha.net/ORDO/Orphanet_48431
2586||10652||obsolete_retinoblastoma||http://www.ebi.ac.uk/efo/EFO_0002923
2587||13883||HapMap haplotype mapping||http://www.ebi.ac.uk/efo/EFO_0002924
2588||1006||vulvar carcinoma||http://www.ebi.ac.uk/efo/EFO_0002921
2589||770||normal cell line||http://www.ebi.ac.uk/efo/EFO_0002922
2590||2002||vulva sarcoma||http://www.ebi.ac.uk/efo/EFO_0002920
2591||6420||Fatal infantile lactic acidosis with methylmalonic aciduria||http://www.orpha.net/ORDO/Orphanet_17
2593||6277||Distal renal tubular acidosis||http://www.orpha.net/ORDO/Orphanet_18
2592||10141||Multiple epiphyseal dysplasia, Al-Gazali type||http://www.orpha.net/ORDO/Orphanet_166024
2594||6371||2-hydroxyglutaric aciduria||http://www.orpha.net/ORDO/Orphanet_19
2595||770||lymphoma or leukaemia cell line||http://www.ebi.ac.uk/efo/EFO_0002937
2596||770||rat cell line||http://www.ebi.ac.uk/efo/EFO_0002936
2597||766||medulloblastoma||http://www.ebi.ac.uk/efo/EFO_0002939
2598||1006||hypopharyngeal carcinoma||http://www.ebi.ac.uk/efo/EFO_0002938
2599||2252||Pseudoaminopterin syndrome||http://www.orpha.net/ORDO/Orphanet_221120
2600||5259||secretory granule membrane||http://purl.obolibrary.org/obo/GO_0030667
2601||5959||Fowler syndrome||http://www.orpha.net/ORDO/Orphanet_221126
2602||5502||Ruminococcus||http://purl.obolibrary.org/obo/NCBITaxon_1263
2603||6054||Marfan and Marfan-related disorder||http://www.orpha.net/ORDO/Orphanet_284993
2604||5502||Pediococcus pentosaceus||http://purl.obolibrary.org/obo/NCBITaxon_1255
2605||5502||Pediococcus acidilactici||http://purl.obolibrary.org/obo/NCBITaxon_1254
2606||13025||Multiple pterygium syndrome||http://www.orpha.net/ORDO/Orphanet_294060
2607||2725||coated vesicle membrane||http://purl.obolibrary.org/obo/GO_0030662
2608||4472||48,XXYY syndrome||http://www.orpha.net/ORDO/Orphanet_10
2609||770||HapMap cell line||http://www.ebi.ac.uk/efo/EFO_0002933
2610||770||lung cancer cell line||http://www.ebi.ac.uk/efo/EFO_0002934
2611||770||Drosophila melanogaster cell line||http://www.ebi.ac.uk/efo/EFO_0002935
2613||4898||Pentasomy X||http://www.orpha.net/ORDO/Orphanet_11
2612||10141||Multiple epiphyseal dysplasia, with severe proximal femoral dysplasia||http://www.orpha.net/ORDO/Orphanet_166029
2614||2454||Abetalipoproteinemia||http://www.orpha.net/ORDO/Orphanet_14
2615||7749||6-pyruvoyl-tetrahydropterin synthase deficiency||http://www.orpha.net/ORDO/Orphanet_13
2617||12633||milligram per kilogram per day||http://www.ebi.ac.uk/efo/EFO_0002930
2616||9682||Blue cone monochromatism||http://www.orpha.net/ORDO/Orphanet_16
2618||12633||unit per kilogram||http://www.ebi.ac.uk/efo/EFO_0002931
2619||1232||Achondroplasia||http://www.orpha.net/ORDO/Orphanet_15
2620||2221||whole organism||http://www.ebi.ac.uk/efo/EFO_0002906
2621||12632||weight percent||http://www.ebi.ac.uk/efo/EFO_0002904
2622||8190||lipoteichoic Acid||http://purl.obolibrary.org/obo/CHEBI_28640
2623||4263||microscopy assay||http://www.ebi.ac.uk/efo/EFO_0002909
2624||4263||motility assay||http://www.ebi.ac.uk/efo/EFO_0002908
2625||4263||population growth assay||http://www.ebi.ac.uk/efo/EFO_0002907
2626||10994||2,4-dinitrophenol||http://purl.obolibrary.org/obo/CHEBI_42017
2627||5502||Micrococcus luteus||http://purl.obolibrary.org/obo/NCBITaxon_1270
2628||1826||Festuca rubra subsp. fallax||http://purl.obolibrary.org/obo/NCBITaxon_98754
2629||1826||Festuca rubra subsp. littoralis||http://purl.obolibrary.org/obo/NCBITaxon_98755
2630||5502||Streptomyces coelicolor A3(2)||http://purl.obolibrary.org/obo/NCBITaxon_100226
2631||5502||Ruminococcus flavefaciens||http://purl.obolibrary.org/obo/NCBITaxon_1265
2632||8783||Marfan syndrome type 1||http://www.orpha.net/ORDO/Orphanet_284963
2633||11065||micromole per liter||http://www.ebi.ac.uk/efo/EFO_0002901
2634||11056||milligram per kilogram||http://www.ebi.ac.uk/efo/EFO_0002902
2635||11065||micromole per kilogram||http://www.ebi.ac.uk/efo/EFO_0002900
2636||10652||obsolete_rectal carcinoma||http://www.ebi.ac.uk/efo/EFO_0002915
2637||2002||uterine sarcoma||http://www.ebi.ac.uk/efo/EFO_0002914
2638||11205||ovarian serous adenocarcinoma||http://www.ebi.ac.uk/efo/EFO_0002917
2640||1006||esophageal carcinoma||http://www.ebi.ac.uk/efo/EFO_0002916
2639||7949||Reunion Island s Larsen syndrome||http://www.orpha.net/ORDO/Orphanet_294049
2641||1006||uterine carcinoma||http://www.ebi.ac.uk/efo/EFO_0002919
2643||2002||rhabdomyosarcoma||http://www.ebi.ac.uk/efo/EFO_0002918
2642||10141||Multiple epiphyseal dysplasia due to collagen 9 anomaly||http://www.orpha.net/ORDO/Orphanet_166002
2644||5502||Staphylococcus epidermidis||http://purl.obolibrary.org/obo/NCBITaxon_1282
2645||5502||Staphylococcus haemolyticus||http://purl.obolibrary.org/obo/NCBITaxon_1283
2646||5502||Staphylococcus aureus||http://purl.obolibrary.org/obo/NCBITaxon_1280
2647||5502||Staphylococcus carnosus||http://purl.obolibrary.org/obo/NCBITaxon_1281
2648||4454||phosphorus||http://purl.obolibrary.org/obo/CHEBI_28659
2649||2603||Neonatal Marfan syndrome||http://www.orpha.net/ORDO/Orphanet_284979
2650||8783||Marfan syndrome type 2||http://www.orpha.net/ORDO/Orphanet_284973
2651||13883||characterization of functional areas of human genome||http://www.ebi.ac.uk/efo/EFO_0002912
2652||1497||Cutaneous T-cell lymphoma||http://www.ebi.ac.uk/efo/EFO_0002913
2653||10652||obsolete_appendage||http://www.ebi.ac.uk/efo/EFO_0000799
2654||1627||hematopoietic system||http://www.ebi.ac.uk/efo/EFO_0000798
2655||1826||Musa acuminata||http://purl.obolibrary.org/obo/NCBITaxon_4641
2656||2672||animal developmental tissue||http://www.ebi.ac.uk/efo/EFO_0000795
2657||10652||obsolete_gland||http://www.ebi.ac.uk/efo/EFO_0000797
2658||2672||animal fluid||http://www.ebi.ac.uk/efo/EFO_0000796
2659||10652||obsolete_cardiovascular system||http://www.ebi.ac.uk/efo/EFO_0000791
2660||10652||obsolete_adipose tissue||http://www.ebi.ac.uk/efo/EFO_0000790
2661||10652||obsolete_digestive system component||http://www.ebi.ac.uk/efo/EFO_0000793
2662||2672||craniofacial tissue||http://www.ebi.ac.uk/efo/EFO_0000792
2663||1826||Cannabis sativa||http://purl.obolibrary.org/obo/NCBITaxon_3483
2664||13496||SARS coronavirus Tor2||http://purl.obolibrary.org/obo/NCBITaxon_227984
2665||10898||Ehlers-Danlos syndrome, periodontitis type||http://www.orpha.net/ORDO/Orphanet_75392
2666||13496||Tomato yellow leaf curl virus||http://purl.obolibrary.org/obo/NCBITaxon_10832
2667||1393||Familial partial lipodystrophy associated with PLIN1 mutations||http://www.orpha.net/ORDO/Orphanet_280356
2668||194||Immunodeficiency with natural-killer cell deficiency and adrenal insufficiency||http://www.orpha.net/ORDO/Orphanet_75391
2670||2674||plant component||http://www.ebi.ac.uk/efo/EFO_0000789
2669||1022||Tursiops truncatus||http://purl.obolibrary.org/obo/NCBITaxon_9739
2671||2674||fungal component||http://www.ebi.ac.uk/efo/EFO_0000788
2673||3229||NLRP12-associated hereditary periodic fever syndrome||http://www.orpha.net/ORDO/Orphanet_247868
2672||2674||animal component||http://www.ebi.ac.uk/efo/EFO_0000787
2674||2221||anatomy basic component||http://www.ebi.ac.uk/efo/EFO_0000786
2675||2252||X-linked creatine transporter deficiency||http://www.orpha.net/ORDO/Orphanet_52503
2676||1790||myositis||http://www.ebi.ac.uk/efo/EFO_0000783
2677||2714||Hibiscus chlorotic ringspot virus infection||http://www.ebi.ac.uk/efo/EFO_0000782
2678||2700||Pectobacterium carotovorum infection||http://www.ebi.ac.uk/efo/EFO_0000781
2679||2700||Enterococcus faecalis infection||http://www.ebi.ac.uk/efo/EFO_0000780
2680||1826||Eschscholzia californica||http://purl.obolibrary.org/obo/NCBITaxon_3467
2681||5918||Genetic dermis elastic tissue disorder||http://www.orpha.net/ORDO/Orphanet_228215
2682||1826||Papaver somniferum||http://purl.obolibrary.org/obo/NCBITaxon_3469
2683||760||Lissencephaly||http://www.orpha.net/ORDO/Orphanet_48471
2684||2252||Brain malformation - congenital heart disease - postaxial polydactyly||http://www.orpha.net/ORDO/Orphanet_75389
2685||196||excretion||http://purl.obolibrary.org/obo/GO_0007588
2686||9681||Cystoid macular dystrophy||http://www.orpha.net/ORDO/Orphanet_75381
2687||9965||Oguchi disease||http://www.orpha.net/ORDO/Orphanet_75382
2688||12360||Nebulin-related early-onset distal myopathy||http://www.orpha.net/ORDO/Orphanet_399103
2689||1150||temporal lobe epilepsy||http://www.ebi.ac.uk/efo/EFO_0000773
2690||2700||pneumococcal infection||http://www.ebi.ac.uk/efo/EFO_0000772
2691||2700||Whipple s disease||http://www.ebi.ac.uk/efo/EFO_0000775
2692||10652||obsolete_tuberculosis||http://www.ebi.ac.uk/efo/EFO_0000774
2694||2700||human granulocytic anaplasmosis||http://www.ebi.ac.uk/efo/EFO_0000777
2693||9675||Occult macular dystrophy||http://www.orpha.net/ORDO/Orphanet_247834
2695||2700||Aeromonas hydrophila infection||http://www.ebi.ac.uk/efo/EFO_0000776
2697||2714||Drosophila C virus infection||http://www.ebi.ac.uk/efo/EFO_0000779
2696||1022||Delphinapterus leucas||http://purl.obolibrary.org/obo/NCBITaxon_9749
2698||2700||anthrax infection||http://www.ebi.ac.uk/efo/EFO_0000778
2699||8793||Autosomal recessive myogenic arthrogryposis multiplex congenita||http://www.orpha.net/ORDO/Orphanet_319332
2700||5343||bacterial disease||http://www.ebi.ac.uk/efo/EFO_0000771
2701||1484||malignant pleural mesothelioma||http://www.ebi.ac.uk/efo/EFO_0000770
2702||6854||Familial drusen||http://www.orpha.net/ORDO/Orphanet_75376
2703||9680||Central areolar choroidal dystrophy||http://www.orpha.net/ORDO/Orphanet_75377
2704||9690||Bradyopsia||http://www.orpha.net/ORDO/Orphanet_75374
2705||196||blood coagulation||http://purl.obolibrary.org/obo/GO_0007596
2706||2319||Carney complex-trismus-pseudocamptodactyly syndrome||http://www.orpha.net/ORDO/Orphanet_319340
2707||9965||Oligocone trichromacy||http://www.orpha.net/ORDO/Orphanet_75378
2708||9965||Progressive bifocal chorioretinal atrophy||http://www.orpha.net/ORDO/Orphanet_75373
2709||1415||Autosomal recessive limb-girdle muscular dystrophy type 2P||http://www.orpha.net/ORDO/Orphanet_280333
2710||10994||monocrotaline||http://purl.obolibrary.org/obo/CHEBI_6980
2712||2714||HIV infection||http://www.ebi.ac.uk/efo/EFO_0000764
2711||5657||Hereditary cerebral hemorrhage with amyloidosis, Dutch type||http://www.orpha.net/ORDO/Orphanet_100006
2713||4803||Inherited renal cancer-predisposing syndrome||http://www.orpha.net/ORDO/Orphanet_319328
2714||5343||viral disease||http://www.ebi.ac.uk/efo/EFO_0000763
2715||109||hepatocellular adenoma||http://www.ebi.ac.uk/efo/EFO_0000762
2716||1022||Trypanosoma brucei brucei||http://purl.obolibrary.org/obo/NCBITaxon_5702
2717||1979||idiopathic pulmonary fibrosis||http://www.ebi.ac.uk/efo/EFO_0000768
2718||1016||idiopathic cardiomyopathy||http://www.ebi.ac.uk/efo/EFO_0000767
2719||10652||obsolete_hereditary leiomyomatosis and renal cell cancer||http://www.ebi.ac.uk/efo/EFO_0000766
2720||2712||AIDS||http://www.ebi.ac.uk/efo/EFO_0000765
2721||15475||malignant peripheral nerve sheath tumor||http://www.ebi.ac.uk/efo/EFO_0000760
2722||1826||Humulus lupulus||http://purl.obolibrary.org/obo/NCBITaxon_3486
2723||1022||Anopheles funestus||http://purl.obolibrary.org/obo/NCBITaxon_62324
2724||2725||transport vesicle membrane||http://purl.obolibrary.org/obo/GO_0030658
2725||1525||cytoplasmic vesicle membrane||http://purl.obolibrary.org/obo/GO_0030659
2726||10734||Distal monosomy 12p||http://www.orpha.net/ORDO/Orphanet_280325
2727||2714||Epstein-Barr virus infection||http://www.ebi.ac.uk/efo/EFO_0000769
2728||5657||Hereditary cerebral hemorrhage with amyloidosis, Icelandic type||http://www.orpha.net/ORDO/Orphanet_100008
2729||10994||alpha-methyl-L-tyrosine||http://purl.obolibrary.org/obo/CHEBI_6912
2730||2395||Qualitative or quantitative defects of myotilin||http://www.orpha.net/ORDO/Orphanet_209224
2731||2672||optic disc||http://purl.obolibrary.org/obo/UBERON_0001783
2732||1826||Persea americana||http://purl.obolibrary.org/obo/NCBITaxon_3435
2733||10652||obsolete_re-sequencing||http://www.ebi.ac.uk/efo/EFO_0000754
2734||1480||Lissencephaly with cerebellar hypoplasia type A||http://www.orpha.net/ORDO/Orphanet_100011
2735||10652||obsolete_colorectal carcinoma||http://www.ebi.ac.uk/efo/EFO_0000755
2736||1480||Lissencephaly with cerebellar hypoplasia type B||http://www.orpha.net/ORDO/Orphanet_100012
2737||1006||melanoma||http://www.ebi.ac.uk/efo/EFO_0000756
2738||1480||Lissencephaly with cerebellar hypoplasia type C||http://www.orpha.net/ORDO/Orphanet_100013
2739||10652||obsolete_muscular dystrophy||http://www.ebi.ac.uk/efo/EFO_0000757
2742||13883||genotyping||http://www.ebi.ac.uk/efo/EFO_0000750
2741||1480||Lissencephaly with cerebellar hypoplasia type D||http://www.orpha.net/ORDO/Orphanet_100014
2740||5292||nitrogen compound metabolic process||http://purl.obolibrary.org/obo/GO_0006807
2743||13883||methylation profiling||http://www.ebi.ac.uk/efo/EFO_0000751
2744||1480||Lissencephaly with cerebellar hypoplasia type E||http://www.orpha.net/ORDO/Orphanet_100015
2745||13299||metabolomic profiling||http://www.ebi.ac.uk/efo/EFO_0000752
2746||1480||Lissencephaly with cerebellar hypoplasia type F||http://www.orpha.net/ORDO/Orphanet_100016
2747||13883||microRNA profiling by array||http://www.ebi.ac.uk/efo/EFO_0000753
2749||1826||Lilium longiflorum||http://purl.obolibrary.org/obo/NCBITaxon_4690
2748||10994||quinidine||http://purl.obolibrary.org/obo/CHEBI_28593
2750||15417||lipoma||http://www.ebi.ac.uk/efo/EFO_0000759
2751||10652||obsolete_limb-girdle muscular dystrophy||http://www.ebi.ac.uk/efo/EFO_0000758
2752||4477||Pseudo-von Willebrand disease||http://www.orpha.net/ORDO/Orphanet_52530
2753||10994||mexiletine||http://purl.obolibrary.org/obo/CHEBI_6916
2754||10994||miconazole||http://purl.obolibrary.org/obo/CHEBI_6923
2755||5502||Streptococcus dysgalactiae subsp. dysgalactiae||http://purl.obolibrary.org/obo/NCBITaxon_99822
2756||13883||proteomic profiling||http://www.ebi.ac.uk/efo/EFO_0000746
2757||5502||Salmonella enterica subsp. enterica serovar Kentucky||http://purl.obolibrary.org/obo/NCBITaxon_192955
2758||1826||Allium cepa||http://purl.obolibrary.org/obo/NCBITaxon_4679
2759||10994||felodipine||http://purl.obolibrary.org/obo/CHEBI_585948
2760||13883||comparative genomic hybridization by array||http://www.ebi.ac.uk/efo/EFO_0000749
2761||13883||ChIP-Chip||http://www.ebi.ac.uk/efo/EFO_0000748
2762||13299||antigen profiling||http://www.ebi.ac.uk/efo/EFO_0000747
2763||3683||transport||http://purl.obolibrary.org/obo/GO_0006810
2764||2545||ILSXISS79/TejJ||http://www.ebi.ac.uk/efo/EFO_0002992
2765||2545||ILSXISS80/TejJ||http://www.ebi.ac.uk/efo/EFO_0002993
2766||2545||ILSXISS62/TejJ||http://www.ebi.ac.uk/efo/EFO_0002990
2769||2545||ILSXISS66/TejJ||http://www.ebi.ac.uk/efo/EFO_0002991
2768||5502||Haemophilus influenzae R2866||http://purl.obolibrary.org/obo/NCBITaxon_262728
2767||6893||Hypoplastic amelogenesis imperfecta||http://www.orpha.net/ORDO/Orphanet_100031
2770||8047||RNA||http://purl.obolibrary.org/obo/CHEBI_33697
2771||2770||messenger RNA||http://purl.obolibrary.org/obo/CHEBI_33699
2772||1022||Zalophus californianus||http://purl.obolibrary.org/obo/NCBITaxon_9704
2774||2545||ILSXISS92/TejJ||http://www.ebi.ac.uk/efo/EFO_0002998
2773||2002||undifferentiated sarcoma||http://www.ebi.ac.uk/efo/EFO_0000730
2776||2545||ILSXISS94/TejJ||http://www.ebi.ac.uk/efo/EFO_0002999
2775||2162||uterine fibroid||http://www.ebi.ac.uk/efo/EFO_0000731
2777||4430||auxin||http://purl.obolibrary.org/obo/CHEBI_22676
2780||2545||ILSXISS89/TejJ||http://www.ebi.ac.uk/efo/EFO_0002996
2778||6573||vehicle role||http://www.ebi.ac.uk/efo/EFO_0000732
2779||6893||Hypocalcified amelogenesis imperfecta||http://www.orpha.net/ORDO/Orphanet_100032
2782||2545||ILSXISS90/TejJ||http://www.ebi.ac.uk/efo/EFO_0002997
2781||6893||Hypomaturation amelogenesis imperfecta||http://www.orpha.net/ORDO/Orphanet_100033
2783||10652||obsolete_virus strain||http://www.ebi.ac.uk/efo/EFO_0000733
2785||12143||vitamin B12 deficiency||http://www.ebi.ac.uk/efo/EFO_0000734
2786||2545||ILSXISS84/TejJ||http://www.ebi.ac.uk/efo/EFO_0002994
2784||6893||Hypomaturation-hypoplastic amelogenesis imperfecta with taurodontism||http://www.orpha.net/ORDO/Orphanet_100034
2787||13883||washing||http://www.ebi.ac.uk/efo/EFO_0000735
2788||2545||ILSXISS86/TejJ||http://www.ebi.ac.uk/efo/EFO_0002995
2789||2002||well-differentiated sarcoma||http://www.ebi.ac.uk/efo/EFO_0000737
2790||1505||well-differentiated liposarcoma||http://www.ebi.ac.uk/efo/EFO_0000736
2791||12329||Hereditary cryohydrocytosis with normal stomatin||http://www.orpha.net/ORDO/Orphanet_398088
2792||10652||obsolete_white blood cell||http://www.ebi.ac.uk/efo/EFO_0000738
2793||15170||Congenital chloride diarrhea||http://www.orpha.net/ORDO/Orphanet_53689
2794||2672||vagus nerve||http://purl.obolibrary.org/obo/UBERON_0001759
2795||9680||North Carolina macular dystrophy||http://www.orpha.net/ORDO/Orphanet_75327
2796||2545||ILSXISS24/TejJ||http://www.ebi.ac.uk/efo/EFO_0002980
2797||2545||ILSXISS25/TejJ||http://www.ebi.ac.uk/efo/EFO_0002981
2800||2672||corneal epithelium||http://purl.obolibrary.org/obo/UBERON_0001772
2799||2545||ILSXISS26/TejJ||http://www.ebi.ac.uk/efo/EFO_0002982
2798||5502||Streptomyces tanashiensis||http://purl.obolibrary.org/obo/NCBITaxon_67367
2801||2545||ILSXISS51/TejJ||http://www.ebi.ac.uk/efo/EFO_0002987
2802||9826||Primary interstitial lung disease specific to childhood due to pulmonary surfactant protein anomalies||http://www.orpha.net/ORDO/Orphanet_100049
2803||15538||test result||http://www.ebi.ac.uk/efo/EFO_0000720
2804||2545||ILSXISS52/TejJ||http://www.ebi.ac.uk/efo/EFO_0002988
2805||11122||Esophageal duplication cyst||http://www.orpha.net/ORDO/Orphanet_100047
2806||2545||ILSXISS56/TejJ||http://www.ebi.ac.uk/efo/EFO_0002989
2807||11122||Tubular duplication of the esophagus||http://www.orpha.net/ORDO/Orphanet_100048
2809||2545||ILSXISS41/TejJ||http://www.ebi.ac.uk/efo/EFO_0002983
2810||7050||Autosomal dominant intermediate Charcot-Marie-Tooth disease type C||http://www.orpha.net/ORDO/Orphanet_100045
2808||10652||obsolete_time to development of distant metastases||http://www.ebi.ac.uk/efo/EFO_0000723
2813||2842||timepoint||http://www.ebi.ac.uk/efo/EFO_0000724
2811||2545||ILSXISS48/TejJ||http://www.ebi.ac.uk/efo/EFO_0002984
2812||7050||Autosomal dominant intermediate Charcot-Marie-Tooth disease type D||http://www.orpha.net/ORDO/Orphanet_100046
2815||2842||time||http://www.ebi.ac.uk/efo/EFO_0000721
2816||2545||ILSXISS49/TejJ||http://www.ebi.ac.uk/efo/EFO_0002985
2814||7050||Autosomal dominant intermediate Charcot-Marie-Tooth disease type A||http://www.orpha.net/ORDO/Orphanet_100043
2818||2545||ILSXISS50/TejJ||http://www.ebi.ac.uk/efo/EFO_0002986
2819||7050||Autosomal dominant intermediate Charcot-Marie-Tooth disease type B||http://www.orpha.net/ORDO/Orphanet_100044
2817||10652||obsolete_time before disease progression||http://www.ebi.ac.uk/efo/EFO_0000722
2820||10652||obsolete_tumor||http://www.ebi.ac.uk/efo/EFO_0000728
2822||13883||treatment||http://www.ebi.ac.uk/efo/EFO_0000727
2821||4987||GRACILE syndrome||http://www.orpha.net/ORDO/Orphanet_53693
2825||14963||Lethal arthrogryposis - anterior horn cell disease||http://www.orpha.net/ORDO/Orphanet_53696
2823||13883||transfection||http://www.ebi.ac.uk/efo/EFO_0000726
2824||2832||Prader-Willi-like syndrome due to point mutation||http://www.orpha.net/ORDO/Orphanet_398079
2826||2403||Hyaline body myopathy||http://www.orpha.net/ORDO/Orphanet_53698
2827||5295||aging||http://purl.obolibrary.org/obo/GO_0007568
2828||7942||Gnathodiaphyseal dysplasia||http://www.orpha.net/ORDO/Orphanet_53697
2829||11620||ulcerative colitis||http://www.ebi.ac.uk/efo/EFO_0000729
2830||2672||iris||http://purl.obolibrary.org/obo/UBERON_0001769
2832||1306||Prader-Willi-like syndrome||http://www.orpha.net/ORDO/Orphanet_398073
2831||5414||Congenital lactase deficiency||http://www.orpha.net/ORDO/Orphanet_53690
2833||5502||Streptococcus infantis||http://purl.obolibrary.org/obo/NCBITaxon_68892
2834||4705||Retinal arterial tortuosity||http://www.orpha.net/ORDO/Orphanet_75326
2836||4931||Osteosclerosis - ichthyosis - premature ovarian failure||http://www.orpha.net/ORDO/Orphanet_75325
2835||9628||Congenital cornea plana||http://www.orpha.net/ORDO/Orphanet_53691
2837||2672||larynx||http://purl.obolibrary.org/obo/UBERON_0001737
2838||2672||uvula||http://purl.obolibrary.org/obo/UBERON_0001734
2839||11433||submandibular gland||http://purl.obolibrary.org/obo/UBERON_0001736
2840||14165||adipose tissue of abdominal region||http://purl.obolibrary.org/obo/UBERON_0007808
2841||14970||exposure temperature||http://www.ebi.ac.uk/efo/EFO_0000718
2842||14970||temporal measurement||http://www.ebi.ac.uk/efo/EFO_0000719
2843||10652||obsolete_syndrome||http://www.ebi.ac.uk/efo/EFO_0000716
2844||1790||systemic scleroderma||http://www.ebi.ac.uk/efo/EFO_0000717
2846||13036||survival time||http://www.ebi.ac.uk/efo/EFO_0000714
2845||8565||Prader-Willi syndrome due to point mutation||http://www.orpha.net/ORDO/Orphanet_398069
2847||9803||survival probability||http://www.ebi.ac.uk/efo/EFO_0000715
2848||1015||subarachnoid hemorrhage||http://www.ebi.ac.uk/efo/EFO_0000713
2849||1015||stroke||http://www.ebi.ac.uk/efo/EFO_0000712
2850||10652||obsolete_strain factor||http://www.ebi.ac.uk/efo/EFO_0000711
2852||11305||Hereditary angioedema type 3||http://www.orpha.net/ORDO/Orphanet_100054
2851||10652||obsolete_strain||http://www.ebi.ac.uk/efo/EFO_0000710
2853||11305||Hereditary angioedema type 2||http://www.orpha.net/ORDO/Orphanet_100051
2854||11305||Hereditary angioedema type 1||http://www.orpha.net/ORDO/Orphanet_100050
2855||10994||sodium hydroxide||http://purl.obolibrary.org/obo/CHEBI_32145
2856||3659||Rare hereditary disease with avascular necrosis||http://www.orpha.net/ORDO/Orphanet_399185
2857||10994||sodium metaarsenite||http://purl.obolibrary.org/obo/CHEBI_29678
2859||2672||lymphoid tissue||http://purl.obolibrary.org/obo/UBERON_0001744
2858||1022||Aureococcus anophagefferens||http://purl.obolibrary.org/obo/NCBITaxon_44056
2860||1006||squamous cell carcinoma||http://www.ebi.ac.uk/efo/EFO_0000707
2861||12136||squamous cell lung carcinoma||http://www.ebi.ac.uk/efo/EFO_0000708
2862||2002||spindle cell tumor||http://www.ebi.ac.uk/efo/EFO_0000705
2863||1790||spondyloarthropathy||http://www.ebi.ac.uk/efo/EFO_0000706
2864||772||integumental cell||http://www.ebi.ac.uk/efo/EFO_0000700
2865||12136||small cell lung carcinoma||http://www.ebi.ac.uk/efo/EFO_0000702
2866||1391||skin disease||http://www.ebi.ac.uk/efo/EFO_0000701
2867||5502||Salmonella enterica subsp. enterica serovar Muenster||http://purl.obolibrary.org/obo/NCBITaxon_82689
2868||10036||Semantic dementia||http://www.orpha.net/ORDO/Orphanet_100069
2869||12275||pedicel||http://purl.obolibrary.org/obo/PO_0009052
2870||5502||Thermotoga maritima||http://purl.obolibrary.org/obo/NCBITaxon_2336
2871||5502||Thermotoga neapolitana||http://purl.obolibrary.org/obo/NCBITaxon_2337
2872||2672||eyelid||http://purl.obolibrary.org/obo/UBERON_0001711
2873||5502||Xylella fastidiosa||http://purl.obolibrary.org/obo/NCBITaxon_2371
2874||14513||cranial ganglion||http://purl.obolibrary.org/obo/UBERON_0001714
2875||9800||Neurological conditions associated with aminoacylase 1 deficiency||http://www.orpha.net/ORDO/Orphanet_137754
2876||2672||oculomotor nuclear complex||http://purl.obolibrary.org/obo/UBERON_0001715
2877||13496||Melon necrotic spot virus||http://purl.obolibrary.org/obo/NCBITaxon_11987
2878||4850||Nasal obstruction||http://purl.obolibrary.org/obo/HP_0001742
2879||8191||sapropterin dihydrochloride||http://purl.obolibrary.org/obo/CHEBI_32120
2880||10994||2,2 -bipyridine||http://purl.obolibrary.org/obo/CHEBI_30351
2881||1826||Liriodendron tulipifera||http://purl.obolibrary.org/obo/NCBITaxon_3415
2882||11457||Mosaic trisomy 3||http://www.orpha.net/ORDO/Orphanet_100071
2884||259||cell cycle process||http://purl.obolibrary.org/obo/GO_0022402
2883||7902||Progressive non-fluent aphasia||http://www.orpha.net/ORDO/Orphanet_100070
2885||5502||Calyptogena magnifica symbiont||http://purl.obolibrary.org/obo/NCBITaxon_2361
2886||2672||tongue||http://purl.obolibrary.org/obo/UBERON_0001723
2887||2672||oropharynx||http://purl.obolibrary.org/obo/UBERON_0001729
2888||10994||tunicamycin||http://purl.obolibrary.org/obo/CHEBI_29699
2889||1022||Physarum polycephalum||http://purl.obolibrary.org/obo/NCBITaxon_5791
2890||10994||thiostrepton||http://purl.obolibrary.org/obo/CHEBI_29693
2891||10994||Cy3 dye||http://purl.obolibrary.org/obo/CHEBI_37987
2892||10994||Cy5 dye||http://purl.obolibrary.org/obo/CHEBI_37989
2893||1022||Dictyostelium purpureum||http://purl.obolibrary.org/obo/NCBITaxon_5786
2894||10994||metoprolol||http://purl.obolibrary.org/obo/CHEBI_6904
2895||12769||Lethal congenital contracture syndrome type 2||http://www.orpha.net/ORDO/Orphanet_137776
2896||1826||Festuca arundinacea||http://purl.obolibrary.org/obo/NCBITaxon_4606
2897||5146||Multiple polyglandular tumor||http://www.orpha.net/ORDO/Orphanet_100094
2898||1022||Ictalurus punctatus||http://purl.obolibrary.org/obo/NCBITaxon_7998
2899||6285||Dimethylglycine dehydrogenase deficiency||http://www.orpha.net/ORDO/Orphanet_243343
2900||2672||nail||http://purl.obolibrary.org/obo/UBERON_0001705
2901||2874||geniculate ganglion||http://purl.obolibrary.org/obo/UBERON_0001700
2902||1022||Trichomonas vaginalis||http://purl.obolibrary.org/obo/NCBITaxon_5722
2903||4139||Recessive intellectual disability - motor dysfunction - multiple joint contractures||http://www.orpha.net/ORDO/Orphanet_280384
2904||1022||Naegleria gruberi||http://purl.obolibrary.org/obo/NCBITaxon_5762
2905||8566||Erythropoietic uroporphyria associated with myeloid malignancy||http://www.orpha.net/ORDO/Orphanet_280379
2906||1022||Equus caballus||http://purl.obolibrary.org/obo/NCBITaxon_9796
2907||5502||Bartonella grahamii||http://purl.obolibrary.org/obo/NCBITaxon_33045
2908||5502||Caldicellulosiruptor saccharolyticus||http://purl.obolibrary.org/obo/NCBITaxon_44001
2909||1022||Entamoeba histolytica||http://purl.obolibrary.org/obo/NCBITaxon_5759
2910||14454||response to clopidogrel||http://purl.obolibrary.org/obo/GO_1903493
2912||12769||Lethal congenital contracture syndrome type 3||http://www.orpha.net/ORDO/Orphanet_137783
2911||4259||response to simvastatin||http://purl.obolibrary.org/obo/GO_1903491
2913||6248||response to aspirin||http://purl.obolibrary.org/obo/GO_1903492
2914||1393||Autosomal codominant severe lipodystrophic laminopathy||http://www.orpha.net/ORDO/Orphanet_280365
2915||10994||antimony(0)||http://purl.obolibrary.org/obo/CHEBI_30304
2916||1022||Strongyloides ratti||http://purl.obolibrary.org/obo/NCBITaxon_34506
2917||5025||Fusarium equiseti||http://purl.obolibrary.org/obo/NCBITaxon_61235
2918||1022||Tetraodon nigroviridis||http://purl.obolibrary.org/obo/NCBITaxon_99883
2919||1022||Giardia intestinalis||http://purl.obolibrary.org/obo/NCBITaxon_5741
2920||2681||Familial anetoderma||http://www.orpha.net/ORDO/Orphanet_228277
2921||9691||Spinocerebellar ataxia with axonal neuropathy type 2||http://www.orpha.net/ORDO/Orphanet_64753
2922||6900||Hereditary sensory and autonomic neuropathy type 5||http://www.orpha.net/ORDO/Orphanet_64752
2923||5877||Becker nevus syndrome||http://www.orpha.net/ORDO/Orphanet_64755
2924||5877||Nevus comedonicus syndrome||http://www.orpha.net/ORDO/Orphanet_64754
2925||10994||epigallocatechin gallate||http://purl.obolibrary.org/obo/CHEBI_4806
2926||6917||Hereditary motor and sensory neuropathy type 5||http://www.orpha.net/ORDO/Orphanet_64751
2927||1022||Epinephelus coioides||http://purl.obolibrary.org/obo/NCBITaxon_94232
2928||5700||High myopia-sensorineural deafness syndrome||http://www.orpha.net/ORDO/Orphanet_363396
2929||7963||Autosomal dominant spondylocostal dysostosis||http://www.orpha.net/ORDO/Orphanet_1797
2930||7943||Dysostosis, Stanescu type||http://www.orpha.net/ORDO/Orphanet_1798
2931||7986||Peripheral dysostosis||http://www.orpha.net/ORDO/Orphanet_1795
2932||5300||Oculomaxillofacial dysostosis||http://www.orpha.net/ORDO/Orphanet_1794
2933||4775||Frontofacionasal dysplasia||http://www.orpha.net/ORDO/Orphanet_1791
2934||4766||Hypomandibular faciocranial dysostosis||http://www.orpha.net/ORDO/Orphanet_1790
2935||5502||Caldicellulosiruptor bescii||http://purl.obolibrary.org/obo/NCBITaxon_31899
2936||508||plant growth hormone||http://purl.obolibrary.org/obo/CHEBI_37848
2938||193||Cyclic neutropenia||http://www.orpha.net/ORDO/Orphanet_2686
2937||920||growth hormone||http://purl.obolibrary.org/obo/CHEBI_37845
2939||5502||Clostridium beijerinckii||http://purl.obolibrary.org/obo/NCBITaxon_1520
2940||14963||Hypomyelination neuropathy - arthrogryposis||http://www.orpha.net/ORDO/Orphanet_2680
2941||5700||Knuckle pads-leukonychia-sensorineural deafness-palmoplantar hyperkeratosis syndrome||http://www.orpha.net/ORDO/Orphanet_2698
2942||7319||Arthrogryposis - renal dysfunction - cholestasis||http://www.orpha.net/ORDO/Orphanet_2697
2943||12769||Median nodule of the upper lip||http://www.orpha.net/ORDO/Orphanet_2699
2944||5700||Neutropenia - monocytopenia - deafness||http://www.orpha.net/ORDO/Orphanet_2690
2945||5502||Clostridium kluyveri||http://purl.obolibrary.org/obo/NCBITaxon_1534
2946||5700||Nephrosis - deafness - urinary tract - digital malformations||http://www.orpha.net/ORDO/Orphanet_2669
2947||5700||Nephropathy-deafness-hyperparathyroidism syndrome||http://www.orpha.net/ORDO/Orphanet_2668
2948||5502||Lactobacillus plantarum||http://purl.obolibrary.org/obo/NCBITaxon_1590
2950||12747||response to temozolomide||http://purl.obolibrary.org/obo/GO_1990054
2949||5502||Lactobacillus pentosus||http://purl.obolibrary.org/obo/NCBITaxon_1589
2951||5502||Lactobacillus helveticus||http://purl.obolibrary.org/obo/NCBITaxon_1587
2952||5502||Lactobacillus hilgardii||http://purl.obolibrary.org/obo/NCBITaxon_1588
2953||6432||Hypotonia with lactic acidemia and hyperammonemia||http://www.orpha.net/ORDO/Orphanet_137908
2954||5502||Lactobacillus delbrueckii subsp. bulgaricus||http://purl.obolibrary.org/obo/NCBITaxon_1585
2955||9718||Isolated optic nerve hypoplasia||http://www.orpha.net/ORDO/Orphanet_137902
2956||5502||Weissella confusa||http://purl.obolibrary.org/obo/NCBITaxon_1583
2957||9718||Syndromic optic nerve hypoplasia||http://www.orpha.net/ORDO/Orphanet_137905
2958||5502||Lactobacillus delbrueckii||http://purl.obolibrary.org/obo/NCBITaxon_1584
2959||12769||Keipert syndrome||http://www.orpha.net/ORDO/Orphanet_2662
2961||5502||Bartonella henselae||http://purl.obolibrary.org/obo/NCBITaxon_38323
2960||6899||Nathalie syndrome||http://www.orpha.net/ORDO/Orphanet_2663
2962||1491||postsynaptic density||http://purl.obolibrary.org/obo/GO_0014069
2963||7377||Adult familial nephronophthisis - spastic quadriparesia||http://www.orpha.net/ORDO/Orphanet_2666
2964||11842||Infantile axonal neuropathy||http://www.orpha.net/ORDO/Orphanet_2679
2965||1826||Pyrus communis||http://purl.obolibrary.org/obo/NCBITaxon_23211
2966||5085||Autism - facial port-wine stain||http://www.orpha.net/ORDO/Orphanet_137911
2967||4259||response to opiate||http://purl.obolibrary.org/obo/GO_0014072
2968||5502||Lactobacillus reuteri||http://purl.obolibrary.org/obo/NCBITaxon_1598
2969||5502||Lactobacillus sakei||http://purl.obolibrary.org/obo/NCBITaxon_1599
2970||6573||amphiprotic solvent role||http://purl.obolibrary.org/obo/CHEBI_4836
2971||5502||Lactobacillus gasseri||http://purl.obolibrary.org/obo/NCBITaxon_1596
2972||3753||Pierson syndrome||http://www.orpha.net/ORDO/Orphanet_2670
2973||5502||Lactobacillus paracasei||http://purl.obolibrary.org/obo/NCBITaxon_1597
2974||1421||Neu-Laxova syndrome||http://www.orpha.net/ORDO/Orphanet_2671
2975||2252||Neurofaciodigitorenal syndrome||http://www.orpha.net/ORDO/Orphanet_2673
2976||12322||Cyprus facial-neuromusculoskeletal syndrome||http://www.orpha.net/ORDO/Orphanet_2674
2977||2252||Neuroectodermal-endocrine syndrome||http://www.orpha.net/ORDO/Orphanet_2676
2978||1826||Arachis hypogaea||http://purl.obolibrary.org/obo/NCBITaxon_3818
2979||5912||Neurofibromatosis type 6||http://www.orpha.net/ORDO/Orphanet_2678
2980||2252||Short stature - intellectual disability - eye anomalies - cleft lip/palate||http://www.orpha.net/ORDO/Orphanet_2649
2981||5502||Desulfovibrio halophilus||http://purl.obolibrary.org/obo/NCBITaxon_45629
2982||3540||Parastremmatic dwarfism||http://www.orpha.net/ORDO/Orphanet_2646
2983||10652||obsolete_normal||http://purl.obolibrary.org/obo/EFO_0000761
2984||9656||Iridocorneal endothelial syndrome||http://www.orpha.net/ORDO/Orphanet_64734
2985||5502||Clostridium baratii||http://purl.obolibrary.org/obo/NCBITaxon_1561
2986||4194||Ovarian hyperstimulation syndrome||http://www.orpha.net/ORDO/Orphanet_64739
2987||7966||Osteoglophonic dwarfism||http://www.orpha.net/ORDO/Orphanet_2645
2988||5502||Psychrobacter arcticus 273-4||http://purl.obolibrary.org/obo/NCBITaxon_259536
2989||2318||Microcephalic primordial dwarfism, Toriello type||http://www.orpha.net/ORDO/Orphanet_2643
2990||10144||Micromelic dwarfism, Fryns type||http://www.orpha.net/ORDO/Orphanet_2641
2991||2252||Lenz-Majewski hyperostotic dwarfism||http://www.orpha.net/ORDO/Orphanet_2658
2992||5502||Lactobacillus brevis||http://purl.obolibrary.org/obo/NCBITaxon_1580
2993||5502||Lactobacillus casei||http://purl.obolibrary.org/obo/NCBITaxon_1582
2994||5502||Lactobacillus buchneri||http://purl.obolibrary.org/obo/NCBITaxon_1581
2995||6912||Dejerine-Sottas syndrome||http://www.orpha.net/ORDO/Orphanet_64748
2996||5700||X-linked Charcot-Marie-Tooth disease||http://www.orpha.net/ORDO/Orphanet_64747
2997||6917||Autosomal dominant Charcot-Marie-Tooth disease type 2||http://www.orpha.net/ORDO/Orphanet_64746
2998||5502||Lactobacillus||http://purl.obolibrary.org/obo/NCBITaxon_1578
3000||5502||Lactobacillus acidophilus||http://purl.obolibrary.org/obo/NCBITaxon_1579
2999||6921||Charcot-Marie-Tooth disease type 4||http://www.orpha.net/ORDO/Orphanet_64749
3001||5700||Osteochondrodysplatic nanism - deafness - retinitis pigmentosa||http://www.orpha.net/ORDO/Orphanet_2653
3002||1232||Thanatophoric dysplasia||http://www.orpha.net/ORDO/Orphanet_2655
3003||2252||Dwarfism - intellectual disability - eye abnormality||http://www.orpha.net/ORDO/Orphanet_2650
3004||3015||sensory perception of smell||http://purl.obolibrary.org/obo/GO_0007608
3005||7947||Blomstrand lethal chondrodysplasia||http://www.orpha.net/ORDO/Orphanet_50945
3006||10994||insulin||http://purl.obolibrary.org/obo/CHEBI_5931
3007||10994||ethionamide||http://purl.obolibrary.org/obo/CHEBI_4885
3008||306||Sch pf-Schulz-Passarge syndrome||http://www.orpha.net/ORDO/Orphanet_50944
3009||325||Keratolytic winter erythema||http://www.orpha.net/ORDO/Orphanet_50943
3010||13304||Keratosis palmoplantaris striata||http://www.orpha.net/ORDO/Orphanet_50942
3011||11433||seminal vesicle||http://purl.obolibrary.org/obo/UBERON_0000998
3012||2672||ejaculatory duct||http://purl.obolibrary.org/obo/UBERON_0000999
3013||2672||vagina||http://purl.obolibrary.org/obo/UBERON_0000996
3014||5295||cellular component organization||http://purl.obolibrary.org/obo/GO_0016043
3015||5295||sensory perception||http://purl.obolibrary.org/obo/GO_0007600
3016||450||APC-related attenuated familial adenomatous polyposis||http://www.orpha.net/ORDO/Orphanet_247806
3017||1022||Biomphalaria glabrata||http://purl.obolibrary.org/obo/NCBITaxon_6526
3018||770||ND01173||http://purl.obolibrary.org/obo/CLO_0028397
3019||3042||Syndrome with disorder of sex development of gynecological interest||http://www.orpha.net/ORDO/Orphanet_325638
3020||1627||reproductive system||http://purl.obolibrary.org/obo/UBERON_0000990
3022||2672||oviduct||http://purl.obolibrary.org/obo/UBERON_0000993
3021||10994||ethambutol||http://purl.obolibrary.org/obo/CHEBI_4877
3023||3042||46,XY disorder of sex development of gynecological interest||http://www.orpha.net/ORDO/Orphanet_325632
3024||2672||uterus||http://purl.obolibrary.org/obo/UBERON_0000995
3025||2672||spermathecum||http://purl.obolibrary.org/obo/UBERON_0000994
3026||10994||dexibuprofen||http://purl.obolibrary.org/obo/CHEBI_43415
3028||14759||haltere||http://purl.obolibrary.org/obo/UBERON_0000987
3027||10994||1,2-dibromoethane||http://purl.obolibrary.org/obo/CHEBI_28534
3029||2672||pons||http://purl.obolibrary.org/obo/UBERON_0000988
3030||2672||penis||http://purl.obolibrary.org/obo/UBERON_0000989
3031||306||Ectodermal dysplasia - syndactyly syndrome||http://www.orpha.net/ORDO/Orphanet_247820
3032||4005||mitotic cell cycle||http://purl.obolibrary.org/obo/GO_0000278
3033||7426||Bilateral parasagittal parieto-occipital polymicrogyria||http://www.orpha.net/ORDO/Orphanet_208441
3034||7426||Bilateral generalized polymicrogyria||http://www.orpha.net/ORDO/Orphanet_208447
3035||7426||Bilateral frontal polymicrogyria||http://www.orpha.net/ORDO/Orphanet_208444
3036||5502||Lactobacillus helveticus DPC 4571||http://purl.obolibrary.org/obo/NCBITaxon_405566
3037||306||Ectodermal dysplasia - cutaneous syndactyly syndrome||http://www.orpha.net/ORDO/Orphanet_247827
3038||1022||Aplysia californica||http://purl.obolibrary.org/obo/NCBITaxon_6500
3039||5025||Epidermophyton floccosum||http://purl.obolibrary.org/obo/NCBITaxon_34391
3040||1022||Moniezia expansa||http://purl.obolibrary.org/obo/NCBITaxon_28841
3041||11830||Autosomal recessive ataxia due to PEX10 deficiency||http://www.orpha.net/ORDO/Orphanet_247815
3042||4194||Genetic disorder of sex development of gynecological interest||http://www.orpha.net/ORDO/Orphanet_325665
3044||4173||piperazine||http://purl.obolibrary.org/obo/CHEBI_28568
3043||2672||brain||http://purl.obolibrary.org/obo/UBERON_0000955
3045||2672||cerebral cortex||http://purl.obolibrary.org/obo/UBERON_0000956
3046||10994||methotrexate||http://purl.obolibrary.org/obo/CHEBI_44185
3048||1627||endocrine system||http://purl.obolibrary.org/obo/UBERON_0000949
3047||1022||Sterkiella histriomuscorum||http://purl.obolibrary.org/obo/NCBITaxon_94289
3049||5048||Genetic hyperaldosteronism||http://www.orpha.net/ORDO/Orphanet_371861
3050||2672||stomach||http://purl.obolibrary.org/obo/UBERON_0000945
3051||2672||heart||http://purl.obolibrary.org/obo/UBERON_0000948
3052||1716||aorta||http://purl.obolibrary.org/obo/UBERON_0000947
3053||10994||adrenocorticotropic hormone||http://purl.obolibrary.org/obo/CHEBI_3892
3054||10926||femur||http://purl.obolibrary.org/obo/UBERON_0000981
3055||13448||chordo neural hinge||http://purl.obolibrary.org/obo/UBERON_0007097
3056||10994||aphidicolin||http://purl.obolibrary.org/obo/CHEBI_2766
3057||6035||cytoplasmic membrane-bounded vesicle||http://purl.obolibrary.org/obo/GO_0016023
3058||3744||membrane||http://purl.obolibrary.org/obo/GO_0016020
3059||10926||tibia||http://purl.obolibrary.org/obo/UBERON_0000979
3060||2672||pleura||http://purl.obolibrary.org/obo/UBERON_0000977
3061||10926||humerus||http://purl.obolibrary.org/obo/UBERON_0000976
3062||2672||neck||http://purl.obolibrary.org/obo/UBERON_0000974
3063||2672||eye||http://purl.obolibrary.org/obo/UBERON_0000970
3064||14759||antenna||http://purl.obolibrary.org/obo/UBERON_0000972
3065||11914||response to etoposide||http://purl.obolibrary.org/obo/GO_190252
3066||12338||microtubule cytoskeleton organization||http://purl.obolibrary.org/obo/GO_0000226
3067||6046||Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly||http://www.orpha.net/ORDO/Orphanet_402364
3068||5295||behavior||http://purl.obolibrary.org/obo/GO_0007610
3069||2672||cornea||http://purl.obolibrary.org/obo/UBERON_0000964
3070||2672||retina||http://purl.obolibrary.org/obo/UBERON_0000966
3071||3063||lens of camera-type eye||http://purl.obolibrary.org/obo/UBERON_0000965
3072||1716||artery||http://purl.obolibrary.org/obo/UBERON_0001637
3074||1716||vein||http://purl.obolibrary.org/obo/UBERON_0001638
3073||5502||Salmonella enterica||http://purl.obolibrary.org/obo/NCBITaxon_28901
3075||3084||basal plate||http://www.ebi.ac.uk/efo/EFO_0001904
3077||770||cervical cancer cell line||http://purl.obolibrary.org/obo/BTO_0001967
3076||10652||obsolete_prostate||http://www.ebi.ac.uk/efo/EFO_0000858
3079||10652||obsolete_blood plasma||http://www.ebi.ac.uk/efo/EFO_0001905
3078||10652||obsolete_pituitary||http://www.ebi.ac.uk/efo/EFO_0000857
3081||3904||articular cartilage||http://www.ebi.ac.uk/efo/EFO_0001902
3080||7966||Inclusion body myopathy with Paget disease of bone and frontotemporal dementia||http://www.orpha.net/ORDO/Orphanet_52430
3084||2656||nervous system developmental tissue||http://www.ebi.ac.uk/efo/EFO_0001903
3083||2063||Abnormality of the endocrine system||http://purl.obolibrary.org/obo/HP_0000818
3082||10652||obsolete_salivary gland||http://www.ebi.ac.uk/efo/EFO_0000859
3085||1679||caudal||http://www.ebi.ac.uk/efo/EFO_0001908
3086||3134||caudal fin||http://www.ebi.ac.uk/efo/EFO_0001909
3087||10652||obsolete_capillary||http://www.ebi.ac.uk/efo/EFO_0001906
3088||3715||dorsal skin||http://www.ebi.ac.uk/efo/EFO_0001907
3089||10652||obsolete_caecum||http://www.ebi.ac.uk/efo/EFO_0000850
3090||1022||Sus scrofa||http://purl.obolibrary.org/obo/NCBITaxon_9823
3092||10652||obsolete_duodenum||http://www.ebi.ac.uk/efo/EFO_0000851
3091||10719||Growth retardation-mild developmental delay-chronic hepatitis syndrome||http://www.orpha.net/ORDO/Orphanet_391366
3093||10652||obsolete_adrenal medulla||http://www.ebi.ac.uk/efo/EFO_0000852
3094||1678||aerial part||http://www.ebi.ac.uk/efo/EFO_0001901
3095||10382||Carnitine palmitoyl transferase II deficiency, myopathic form||http://www.orpha.net/ORDO/Orphanet_228302
3096||10652||obsolete_gall bladder||http://www.ebi.ac.uk/efo/EFO_0000853
3098||3854||Methanosarcina barkeri||http://purl.obolibrary.org/obo/NCBITaxon_2208
3097||10652||obsolete_mammary gland||http://www.ebi.ac.uk/efo/EFO_0000854
3100||3854||Methanosarcina mazei||http://purl.obolibrary.org/obo/NCBITaxon_2209
3099||10652||obsolete_pancreas||http://www.ebi.ac.uk/efo/EFO_0000855
3101||10652||obsolete_islet of Langerhans||http://www.ebi.ac.uk/efo/EFO_0000856
3102||10382||Carnitine palmitoyl transferase II deficiency, severe infantile form||http://www.orpha.net/ORDO/Orphanet_228305
3103||10382||Carnitine palmitoyl transferase II deficiency, neonatal form||http://www.orpha.net/ORDO/Orphanet_228308
3104||2672||trigeminal nerve||http://purl.obolibrary.org/obo/UBERON_0001645
3105||3753||Familial steroid-resistant nephrotic syndrome with sensorineural deafness||http://www.orpha.net/ORDO/Orphanet_280406
3107||2672||appendix||http://www.ebi.ac.uk/efo/EFO_0000849
3106||4717||Familial omphalocele syndrome with facial dysmorphism||http://www.orpha.net/ORDO/Orphanet_280403
3108||10652||obsolete_rectum||http://www.ebi.ac.uk/efo/EFO_0000848
3109||10652||obsolete_anal region||http://www.ebi.ac.uk/efo/EFO_0000847
3110||10652||obsolete_sigmoid colon||http://www.ebi.ac.uk/efo/EFO_0000846
3111||4139||Intellectual disability-severe speech delay-mild dysmorphism syndrome||http://www.orpha.net/ORDO/Orphanet_391372
3112||10652||obsolete_large intestine||http://www.ebi.ac.uk/efo/EFO_0000840
3113||10652||obsolete_small intestine||http://www.ebi.ac.uk/efo/EFO_0000841
3114||4692||X-linked cerebellar ataxia||http://www.orpha.net/ORDO/Orphanet_247765
3115||3131||Congenital microcephaly-severe encephalopathy-progressive cerebral atrophy syndrome||http://www.orpha.net/ORDO/Orphanet_391376
3116||10994||sapphyrin||http://purl.obolibrary.org/obo/CHEBI_36779
3117||10652||obsolete_transverse colon||http://www.ebi.ac.uk/efo/EFO_0000844
3118||10652||obsolete_descending colon||http://www.ebi.ac.uk/efo/EFO_0000845
3120||3019||Atypical Mayer-Rokitansky-K ster-Hauser syndrome||http://www.orpha.net/ORDO/Orphanet_247768
3119||10652||obsolete_ascending colon||http://www.ebi.ac.uk/efo/EFO_0000843
3121||6054||Proteasome disability syndrome||http://www.orpha.net/ORDO/Orphanet_324977
3122||3083||Abnormality of the thyroid gland||http://purl.obolibrary.org/obo/HP_0000820
3124||1826||Oryza sativa Indica Group||http://purl.obolibrary.org/obo/NCBITaxon_39946
3123||10652||obsolete_hindlimb muscle||http://www.ebi.ac.uk/efo/EFO_0001928
3126||11842||Familial episodic pain syndrome||http://www.orpha.net/ORDO/Orphanet_391384
3127||3432||hip||http://www.ebi.ac.uk/efo/EFO_0001929
3125||1826||Oryza sativa Japonica Group||http://purl.obolibrary.org/obo/NCBITaxon_39947
3128||2670||gynoecium||http://www.ebi.ac.uk/efo/EFO_0001926
3130||3432||head capsule||http://www.ebi.ac.uk/efo/EFO_0001927
3129||10652||obsolete_stylopod||http://www.ebi.ac.uk/efo/EFO_0000879
3132||12224||flower bud||http://www.ebi.ac.uk/efo/EFO_0001924
3131||5795||Disorder of asparagine metabolism||http://www.orpha.net/ORDO/Orphanet_391381
3133||2672||gum||http://www.ebi.ac.uk/efo/EFO_0001925
3134||14759||fin||http://www.ebi.ac.uk/efo/EFO_0000875
3135||10652||obsolete_floor of mouth||http://www.ebi.ac.uk/efo/EFO_0001923
3136||2672||female accessory gland||http://www.ebi.ac.uk/efo/EFO_0001922
3137||10652||obsolete_vertebrate limb||http://www.ebi.ac.uk/efo/EFO_0000876
3139||14017||autopod||http://www.ebi.ac.uk/efo/EFO_0000877
3138||10652||obsolete_extraocular muscle||http://www.ebi.ac.uk/efo/EFO_0001921
3140||10652||obsolete_entorhinal cortex||http://www.ebi.ac.uk/efo/EFO_0001920
3141||10652||obsolete_zeugopod||http://www.ebi.ac.uk/efo/EFO_0000878
3142||10652||obsolete_lymph||http://www.ebi.ac.uk/efo/EFO_0000871
3144||5501||Classic Mayer-Rokitansky-K ster-Hauser syndrome||http://www.orpha.net/ORDO/Orphanet_247775
3143||10652||obsolete_lymph node||http://www.ebi.ac.uk/efo/EFO_0000872
3145||10652||obsolete_lymph vessel||http://www.ebi.ac.uk/efo/EFO_0000873
3147||3126||Familial episodic pain syndrome with predominantly upper body involvement||http://www.orpha.net/ORDO/Orphanet_391389
3148||4717||Genetic disorder of sex development||http://www.orpha.net/ORDO/Orphanet_325690
3146||10652||obsolete_antenna||http://www.ebi.ac.uk/efo/EFO_0000874
3149||2654||lymphatic system||http://www.ebi.ac.uk/efo/EFO_0000870
3150||3148||Genetic 46,XX disorder of sex development||http://www.orpha.net/ORDO/Orphanet_325697
3151||1826||Lotus filicaulis||http://purl.obolibrary.org/obo/NCBITaxon_264956
3153||10994||ajmaline||http://purl.obolibrary.org/obo/CHEBI_28462
3152||10652||obsolete_corneal epithelium||http://www.ebi.ac.uk/efo/EFO_0001917
3154||10652||obsolete_decidua basalis||http://www.ebi.ac.uk/efo/EFO_0001918
3155||10652||obsolete_dorsal raphe nucleus||http://www.ebi.ac.uk/efo/EFO_0001919
3156||3126||Familial episodic pain syndrome with predominantly lower limb involvement||http://www.orpha.net/ORDO/Orphanet_391392
3157||10652||obsolete_cervix epithelium||http://www.ebi.ac.uk/efo/EFO_0001913
3158||10652||obsolete_brain ventricle||http://www.ebi.ac.uk/efo/EFO_0001914
3160||10652||obsolete_spleen||http://www.ebi.ac.uk/efo/EFO_0000869
3159||10652||obsolete_choroid plexus||http://www.ebi.ac.uk/efo/EFO_0001915
3162||2672||conjunctival epithelium||http://www.ebi.ac.uk/efo/EFO_0001916
3161||10652||obsolete_bone marrow||http://www.ebi.ac.uk/efo/EFO_0000868
3163||3084||brain structure developmental tissue||http://www.ebi.ac.uk/efo/EFO_0001910
3164||3043||meninges||http://www.ebi.ac.uk/efo/EFO_0000867
3166||10652||obsolete_neurohemal organ||http://www.ebi.ac.uk/efo/EFO_0000864
3165||10652||obsolete_caudate putamen||http://www.ebi.ac.uk/efo/EFO_0001912
3168||5700||Branchio-otic syndrome||http://www.orpha.net/ORDO/Orphanet_52429
3169||10652||obsolete_caudal ganglionic eminence||http://www.ebi.ac.uk/efo/EFO_0001911
3167||10652||obsolete_pineal gland||http://www.ebi.ac.uk/efo/EFO_0000865
3172||10994||campestanol||http://purl.obolibrary.org/obo/CHEBI_36799
3170||6854||Retinitis punctata albescens||http://www.orpha.net/ORDO/Orphanet_52427
3171||10652||obsolete_hatching gland||http://www.ebi.ac.uk/efo/EFO_0000863
3174||6888||Hereditary sensory and autonomic neuropathy type 7||http://www.orpha.net/ORDO/Orphanet_391397
3173||10652||obsolete_thymus||http://www.ebi.ac.uk/efo/EFO_0000860
3175||10652||obsolete_thyroid||http://www.ebi.ac.uk/efo/EFO_0000861
3176||2874||trigeminal ganglion||http://purl.obolibrary.org/obo/UBERON_0001675
3177||3074||central retinal vein||http://purl.obolibrary.org/obo/UBERON_0001673
3178||8024||CLAPO syndrome||http://www.orpha.net/ORDO/Orphanet_168984
3179||772||kidney cell||http://purl.obolibrary.org/obo/CL_1000497
3181||2252||Epiphyseal dysplasia - hearing loss - dysmorphism||http://www.orpha.net/ORDO/Orphanet_1825
3180||1138||CLN2 disease||http://www.orpha.net/ORDO/Orphanet_228349
3182||7453||mandible||http://purl.obolibrary.org/obo/UBERON_0001684
3183||1226||Frontometaphyseal dysplasia||http://www.orpha.net/ORDO/Orphanet_1826
3184||1171||Acromelic frontonasal dysplasia||http://www.orpha.net/ORDO/Orphanet_1827
3185||14513||invertebrate ganglion||http://www.ebi.ac.uk/efo/EFO_0000890
3186||7966||Dysplasia epiphysealis hemimelica||http://www.orpha.net/ORDO/Orphanet_1822
3187||5502||Bacillus cereus G9842||http://purl.obolibrary.org/obo/NCBITaxon_405531
3188||7972||Lowry-Wood syndrome||http://www.orpha.net/ORDO/Orphanet_1824
3189||10652||obsolete_peripheral nervous system||http://www.ebi.ac.uk/efo/EFO_0000891
3191||1022||Plasmodium falciparum||http://purl.obolibrary.org/obo/NCBITaxon_5833
3190||10652||obsolete_parasympathetic nervous system||http://www.ebi.ac.uk/efo/EFO_0000894
3193||15365||East Texas bleeding disorder||http://www.orpha.net/ORDO/Orphanet_391320
3192||10652||obsolete_sympathetic nervous system||http://www.ebi.ac.uk/efo/EFO_0000893
3194||10652||obsolete_ventral nerve cord||http://www.ebi.ac.uk/efo/EFO_0000896
3195||6825||CLN4A disease||http://www.orpha.net/ORDO/Orphanet_228340
3196||10652||obsolete_enteric nervous system||http://www.ebi.ac.uk/efo/EFO_0000895
3197||10652||obsolete_somatic nervous system||http://www.ebi.ac.uk/efo/EFO_0000898
3198||14172||pharyngeal nervous system||http://www.ebi.ac.uk/efo/EFO_0000897
3199||6831||CLN3 disease||http://www.orpha.net/ORDO/Orphanet_228346
3201||6825||CLN4B disease||http://www.orpha.net/ORDO/Orphanet_228343
3200||7943||X-linked calvarial hyperostosis||http://www.orpha.net/ORDO/Orphanet_391327
3202||10652||obsolete_ganglion||http://www.ebi.ac.uk/efo/EFO_0000899
3203||1022||Crassostrea virginica||http://purl.obolibrary.org/obo/NCBITaxon_6565
3204||7942||X-linked osteoporosis with fractures||http://www.orpha.net/ORDO/Orphanet_391330
3205||1138||CLN5 disease||http://www.orpha.net/ORDO/Orphanet_228360
3206||10994||anastrozole||http://purl.obolibrary.org/obo/CHEBI_2704
3207||306||Ectodermal dysplasia, Berlin type||http://www.orpha.net/ORDO/Orphanet_1816
3208||1826||Fagus sylvatica||http://purl.obolibrary.org/obo/NCBITaxon_28930
3209||306||Ectodermal dysplasia - intellectual disability - central nervous system malformation||http://www.orpha.net/ORDO/Orphanet_1812
3210||10652||obsolete_digit||http://www.ebi.ac.uk/efo/EFO_0000881
3211||8356||Autosomal dominant hypohidrotic ectodermal dysplasia||http://www.orpha.net/ORDO/Orphanet_1810
3212||307||Odontomicronychial dysplasia||http://www.orpha.net/ORDO/Orphanet_1811
3213||10652||obsolete_wing||http://www.ebi.ac.uk/efo/EFO_0000885
3214||14759||invertebrate limb||http://www.ebi.ac.uk/efo/EFO_0000884
3215||10652||obsolete_hindlimb||http://www.ebi.ac.uk/efo/EFO_0000883
3216||10652||obsolete_forelimb||http://www.ebi.ac.uk/efo/EFO_0000882
3218||3389||smooth muscle||http://www.ebi.ac.uk/efo/EFO_0000889
3217||1138||CLN8 disease||http://www.orpha.net/ORDO/Orphanet_228354
3219||1022||Plasmodium berghei||http://purl.obolibrary.org/obo/NCBITaxon_5821
3220||2672||external ear||http://purl.obolibrary.org/obo/UBERON_0001691
3222||306||Ectodermal dysplasia, trichoodontoonychial type||http://www.orpha.net/ORDO/Orphanet_1818
3221||10652||obsolete_liver||http://www.ebi.ac.uk/efo/EFO_0000887
3224||6831||CLN9 disease||http://www.orpha.net/ORDO/Orphanet_228357
3223||10652||obsolete_haltere||http://www.ebi.ac.uk/efo/EFO_0000886
3225||1022||Mytilus trossulus||http://purl.obolibrary.org/obo/NCBITaxon_6551
3226||15549||Hypomyelination with brain stem and spinal cord involvement and leg spasticity||http://www.orpha.net/ORDO/Orphanet_363412
3227||1826||Populus maximowiczii x Populus nigra||http://purl.obolibrary.org/obo/NCBITaxon_343990
3228||770||JURKAT E-6.1 cell||http://purl.obolibrary.org/obo/BTO_0001948
3229||6054||Hereditary periodic fever syndrome||http://www.orpha.net/ORDO/Orphanet_324924
3230||1138||CLN1 disease||http://www.orpha.net/ORDO/Orphanet_228329
3231||7991||Kyphomelic dysplasia||http://www.orpha.net/ORDO/Orphanet_1801
3232||7943||Ghosal hematodiaphyseal dysplasia||http://www.orpha.net/ORDO/Orphanet_1802
3233||7973||Thoracomelic dysplasia||http://www.orpha.net/ORDO/Orphanet_1803
3234||6897||Dyssegmental dysplasia - glaucoma||http://www.orpha.net/ORDO/Orphanet_1804
3235||306||Ectodermal dysplasia - blindness||http://www.orpha.net/ORDO/Orphanet_1806
3237||1022||Mytilus californianus||http://purl.obolibrary.org/obo/NCBITaxon_6549
3236||1325||Focal facial dermal dysplasia type III||http://www.orpha.net/ORDO/Orphanet_1807
3238||306||Hidrotic ectodermal dysplasia, Christianson-Fourie type||http://www.orpha.net/ORDO/Orphanet_1808
3239||306||Hidrotic ectodermal dysplasia, Halal type||http://www.orpha.net/ORDO/Orphanet_1809
3240||2021||Temtamy preaxial brachydactyly syndrome||http://www.orpha.net/ORDO/Orphanet_363417
3241||8846||Growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome||http://www.orpha.net/ORDO/Orphanet_391348
3242||1022||Toxoplasma gondii||http://purl.obolibrary.org/obo/NCBITaxon_5811
3243||4706||Fatal post-viral neurodegenerative disorder||http://www.orpha.net/ORDO/Orphanet_391343
3244||288||SURF1-related Charcot-Marie-Tooth disease type 4||http://www.orpha.net/ORDO/Orphanet_391351
3245||1022||Cervus nippon||http://purl.obolibrary.org/obo/NCBITaxon_9863
3246||4706||Severe neurodegenerative syndrome with lipodystrophy||http://www.orpha.net/ORDO/Orphanet_363400
3247||5502||Caulobacter crescentus NA1000||http://purl.obolibrary.org/obo/NCBITaxon_565050
3248||1022||Cervus elaphus||http://purl.obolibrary.org/obo/NCBITaxon_9860
3249||6038||extracellular membrane-bounded organelle||http://purl.obolibrary.org/obo/GO_0065010
3250||1138||CLN10 disease||http://www.orpha.net/ORDO/Orphanet_228337
3251||5502||Lactobacillus paraplantarum||http://purl.obolibrary.org/obo/NCBITaxon_60520
3252||8791||Fetal akinesia-cerebral and retinal hemorrhage syndrome||http://www.orpha.net/ORDO/Orphanet_363409
3255||2670||leaf component||http://www.ebi.ac.uk/efo/EFO_0001983
3254||1316||Orofaciodigital syndrome type 8||http://www.orpha.net/ORDO/Orphanet_2755
3253||6097||5q14.3 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_228384
3256||1316||Joubert syndrome with orofaciodigital defect||http://www.orpha.net/ORDO/Orphanet_2754
3257||10652||obsolete_presomitic mesoderm||http://www.ebi.ac.uk/efo/EFO_0001982
3259||2672||pulmonary alveolus||http://www.ebi.ac.uk/efo/EFO_0001985
3258||1316||Orofaciodigital syndrome type 4||http://www.orpha.net/ORDO/Orphanet_2753
3261||3655||rosette leaf||http://www.ebi.ac.uk/efo/EFO_0001984
3260||1316||Orofaciodigital syndrome type 3||http://www.orpha.net/ORDO/Orphanet_2752
3262||1316||Orofaciodigital syndrome type 2||http://www.orpha.net/ORDO/Orphanet_2751
3263||10652||obsolete_cerebral peduncle||http://www.ebi.ac.uk/efo/EFO_0001987
3267||14207||lung structure||http://www.ebi.ac.uk/efo/EFO_0001986
3265||306||Orofaciodigital syndrome type 1||http://www.orpha.net/ORDO/Orphanet_2750
3264||1022||Theileria parva||http://purl.obolibrary.org/obo/NCBITaxon_5875
3266||10143||Spondylo-megaepiphyseal-metaphyseal dysplasia||http://www.orpha.net/ORDO/Orphanet_228387
3268||10652||obsolete_lateral geniculate nucleus||http://www.ebi.ac.uk/efo/EFO_0001988
3271||325||Bullous dystrophy, macular type||http://www.orpha.net/ORDO/Orphanet_1867
3269||799||alpha-adrenergic antagonist||http://purl.obolibrary.org/obo/CHEBI_37890
3270||5502||Lactobacillus frumenti||http://purl.obolibrary.org/obo/NCBITaxon_104955
3273||12553||Focal, segmental or multifocal dystonia||http://www.orpha.net/ORDO/Orphanet_1866
3272||3854||Sulfolobus solfataricus||http://purl.obolibrary.org/obo/NCBITaxon_2287
3274||10652||obsolete_mesoderm||http://www.ebi.ac.uk/efo/EFO_0001981
3275||7969||Dyssegmental dysplasia, Silverman-Handmaker type||http://www.orpha.net/ORDO/Orphanet_1865
3276||10652||obsolete_pleura||http://www.ebi.ac.uk/efo/EFO_0001980
3277||6087||Congenital valvular dysplasia||http://www.orpha.net/ORDO/Orphanet_1864
3278||3002||Thanatophoric dysplasia type 1||http://www.orpha.net/ORDO/Orphanet_1860
3280||3296||Autosomal recessive congenital cerebellar ataxia due to GRID2 deficiency||http://www.orpha.net/ORDO/Orphanet_363432
3279||321||Frontonasal dysplasia with alopecia and genital anomaly||http://www.orpha.net/ORDO/Orphanet_228390
3281||7963||Imperforate oropharynx - costo vetebral anomalies||http://www.orpha.net/ORDO/Orphanet_2759
3282||1316||Orofaciodigital syndrome type 10||http://www.orpha.net/ORDO/Orphanet_2756
3283||10652||obsolete_optic disc||http://www.ebi.ac.uk/efo/EFO_0001974
3284||6899||Ophthalmomandibulomelic dysplasia||http://www.orpha.net/ORDO/Orphanet_2741
3286||9597||Ptosis - upper ocular movement limitation - absence of lacrimal punctum||http://www.orpha.net/ORDO/Orphanet_228396
3285||10652||obsolete_olfactory system||http://www.ebi.ac.uk/efo/EFO_0001973
3288||15121||Hypotonia-cerebral atrophy-hyperglycinemia syndrome||http://www.orpha.net/ORDO/Orphanet_363424
3289||5959||Horizontal gaze palsy with progressive scoliosis||http://www.orpha.net/ORDO/Orphanet_2744
3287||10652||obsolete_olfactory epithelium||http://www.ebi.ac.uk/efo/EFO_0001972
3290||3043||nucleus of terminal stria||http://www.ebi.ac.uk/efo/EFO_0001971
3291||2252||Ophthalmoplegia - intellectual disability - lingua scrotalis||http://www.orpha.net/ORDO/Orphanet_2743
3292||10652||obsolete_perirhinal cortex||http://www.ebi.ac.uk/efo/EFO_0001978
3293||10652||obsolete_palatine tonsil||http://www.ebi.ac.uk/efo/EFO_0001977
3294||10291||8q12 microduplication syndrome||http://www.orpha.net/ORDO/Orphanet_228399
3295||10652||obsolete_oropharynx||http://www.ebi.ac.uk/efo/EFO_0001976
3296||6305||Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome||http://www.orpha.net/ORDO/Orphanet_363429
3297||10652||obsolete_oral cavity||http://www.ebi.ac.uk/efo/EFO_0001975
3298||1826||Matthiola incana||http://purl.obolibrary.org/obo/NCBITaxon_3724
3299||2021||Skeletal dysplasia - epilepsy - short stature||http://www.orpha.net/ORDO/Orphanet_1858
3300||5486||Spondyloenchondrodysplasia||http://www.orpha.net/ORDO/Orphanet_1855
3301||10652||obsolete_myometrium||http://www.ebi.ac.uk/efo/EFO_0001970
3302||7981||Spondyloperipheral dysplasia - short ulna||http://www.orpha.net/ORDO/Orphanet_1856
3303||7319||Renal dysplasia - megalocystis - sirenomelia||http://www.orpha.net/ORDO/Orphanet_1850
3304||10994||lysobisphosphatidic acid||http://purl.obolibrary.org/obo/CHEBI_60815
3305||742||Multicystic dysplastic kidney||http://www.orpha.net/ORDO/Orphanet_1851
3306||9965||X-linked retinal dysplasia||http://www.orpha.net/ORDO/Orphanet_1852
3307||3854||Sulfolobus acidocaldarius||http://purl.obolibrary.org/obo/NCBITaxon_2285
3308||1174||Oromandibular-limb hypogenesis syndrome||http://www.orpha.net/ORDO/Orphanet_2749
3309||10652||obsolete_plantaris muscle||http://www.ebi.ac.uk/efo/EFO_0001979
3310||2252||Opitz G/BBB syndrome||http://www.orpha.net/ORDO/Orphanet_2745
3311||7984||Opsismodysplasia||http://www.orpha.net/ORDO/Orphanet_2746
3312||5502||Lactobacillus delbrueckii subsp. bulgaricus ATCC BAA-365||http://purl.obolibrary.org/obo/NCBITaxon_321956
3313||1138||CLN7 disease||http://www.orpha.net/ORDO/Orphanet_228366
3315||1826||Capsella bursa-pastoris||http://purl.obolibrary.org/obo/NCBITaxon_3719
3314||7989||Omodysplasia||http://www.orpha.net/ORDO/Orphanet_2733
3316||5700||Olivopontocerebellar atrophy - deafness||http://www.orpha.net/ORDO/Orphanet_2732
3317||306||Taurodontia - absent teeth - sparse hair||http://www.orpha.net/ORDO/Orphanet_2731
3319||1022||Plasmodium vivax||http://purl.obolibrary.org/obo/NCBITaxon_5855
3318||1138||CLN6 disease||http://www.orpha.net/ORDO/Orphanet_228363
3320||6244||Postaxial tetramelic oligodactyly||http://www.orpha.net/ORDO/Orphanet_2730
3321||7966||Bone dysplasia, Azouz type||http://www.orpha.net/ORDO/Orphanet_1844
3322||1826||Brassica rapa||http://purl.obolibrary.org/obo/NCBITaxon_3711
3323||7319||Infundibulopelvic stenosis - multicystic kidney||http://www.orpha.net/ORDO/Orphanet_1849
3324||742||Bilateral renal agenesis||http://www.orpha.net/ORDO/Orphanet_1848
3326||2252||Severe intellectual disability-short stature-behavioral troubles-facial dysmorphism syndrome||http://www.orpha.net/ORDO/Orphanet_391307
3325||1826||Brassica oleracea||http://purl.obolibrary.org/obo/NCBITaxon_3712
3327||3854||Thermoproteus tenax||http://purl.obolibrary.org/obo/NCBITaxon_2271
3328||4728||Leukoencephalopathy with brain stem and spinal cord involvement - high lactate||http://www.orpha.net/ORDO/Orphanet_137898
3329||8026||Bone dysplasia, lethal Holmgren type||http://www.orpha.net/ORDO/Orphanet_1842
3330||5508||Iniencephaly||http://www.orpha.net/ORDO/Orphanet_63259
3332||3341||Autosomal dominant childhood-onset proximal spinal muscular atrophy with contractures||http://www.orpha.net/ORDO/Orphanet_363454
3331||2252||Lethal omphalocele-cleft palate syndrome||http://www.orpha.net/ORDO/Orphanet_2736
3333||1603||Male infertility due to large-headed multiflagellar polyploid spermatozoa||http://www.orpha.net/ORDO/Orphanet_137893
3334||1022||Plasmodium yoelii||http://purl.obolibrary.org/obo/NCBITaxon_5861
3335||762||Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression||http://www.orpha.net/ORDO/Orphanet_391316
3336||12715||Severe early-onset axonal neuropathy due to NEFL deficiency||http://www.orpha.net/ORDO/Orphanet_228374
3339||1826||Brassica napus||http://purl.obolibrary.org/obo/NCBITaxon_3708
3337||306||Odonto-onycho dysplasia - alopecia||http://www.orpha.net/ORDO/Orphanet_2722
3338||4994||Susceptibility to viral and mycobacterial infections||http://www.orpha.net/ORDO/Orphanet_391311
3342||1826||Brassica juncea||http://purl.obolibrary.org/obo/NCBITaxon_3707
3340||306||Odonto-onycho-dermal dysplasia||http://www.orpha.net/ORDO/Orphanet_2721
3341||8035||Autosomal dominant childhood-onset proximal spinal muscular atrophy||http://www.orpha.net/ORDO/Orphanet_363447
3343||10652||obsolete_seedling||http://www.ebi.ac.uk/efo/EFO_0001992
3345||7947||Lethal osteosclerotic bone dysplasia||http://www.orpha.net/ORDO/Orphanet_1832
3344||10652||obsolete_superior frontal gyrus||http://www.ebi.ac.uk/efo/EFO_0001991
3346||10652||obsolete_orbitofrontal cortex||http://www.ebi.ac.uk/efo/EFO_0001990
3347||7319||Axial mesodermal dysplasia spectrum||http://www.orpha.net/ORDO/Orphanet_1834
3349||3352||Arabidopsis thaliana||http://purl.obolibrary.org/obo/NCBITaxon_3702
3350||5025||Ogataea angusta||http://purl.obolibrary.org/obo/NCBITaxon_870730
3348||8001||Ulna metaphyseal dysplasia syndrome||http://www.orpha.net/ORDO/Orphanet_1837
3352||1826||Arabidopsis||http://purl.obolibrary.org/obo/NCBITaxon_3701
3351||7989||Mesomelic dysplasia, Kantaputra type||http://www.orpha.net/ORDO/Orphanet_1836
3353||5882||Hereditary mucoepithelial dysplasia||http://www.orpha.net/ORDO/Orphanet_1839
3354||4775||Auriculocondylar syndrome||http://www.orpha.net/ORDO/Orphanet_137888
3355||3854||Pyrococcus furiosus||http://purl.obolibrary.org/obo/NCBITaxon_2261
3356||3753||Schimke immuno-osseous dysplasia||http://www.orpha.net/ORDO/Orphanet_1830
3357||306||Odontotrichomelic syndrome||http://www.orpha.net/ORDO/Orphanet_2723
3358||2252||Developmental delay-microcephaly-facial dysmorphism syndrome, Hutterite type||http://www.orpha.net/ORDO/Orphanet_363444
3359||4834||Odontomatosis - aortae esophagus stenosis||http://www.orpha.net/ORDO/Orphanet_2724
3360||15044||Blepharophimosis-intellectual disability syndrome, Ohdo type||http://www.orpha.net/ORDO/Orphanet_2728
3361||2252||Okamoto syndrome||http://www.orpha.net/ORDO/Orphanet_2729
3362||1022||Plasmodium knowlesi||http://purl.obolibrary.org/obo/NCBITaxon_5850
3363||266||FTH1-related iron overload||http://www.orpha.net/ORDO/Orphanet_247790
3364||3854||Haloferax volcanii||http://purl.obolibrary.org/obo/NCBITaxon_2246
3365||5502||Staphylococcus aureus subsp. aureus RN4220||http://purl.obolibrary.org/obo/NCBITaxon_561307
3366||5414||Juvenile cataract - microcornea - renal glucosuria||http://www.orpha.net/ORDO/Orphanet_247794
3367||306||Oculodentodigital dysplasia||http://www.orpha.net/ORDO/Orphanet_2710
3368||10652||obsolete_umbilical vein||http://www.ebi.ac.uk/efo/EFO_0001940
3370||2654||blood component||http://www.ebi.ac.uk/efo/EFO_0001941
3369||450||MUTYH-related attenuated familial adenomatous polyposis||http://www.orpha.net/ORDO/Orphanet_247798
3372||14165||brown fat||http://www.ebi.ac.uk/efo/EFO_0000812
3371||10652||obsolete_umbilical cord blood||http://www.ebi.ac.uk/efo/EFO_0001942
3374||14165||fat body sensu amphibia||http://www.ebi.ac.uk/efo/EFO_0000811
3373||3432||thigh||http://www.ebi.ac.uk/efo/EFO_0001943
3376||14165||fat body sensu invertebrata||http://www.ebi.ac.uk/efo/EFO_0000810
3377||5502||Listeria monocytogenes||http://purl.obolibrary.org/obo/NCBITaxon_1639
3375||10652||obsolete_superior temporal gyrus||http://www.ebi.ac.uk/efo/EFO_0001944
3378||10652||obsolete_superior cervical ganglion||http://www.ebi.ac.uk/efo/EFO_0001945
3380||2670||shoot apex||http://www.ebi.ac.uk/efo/EFO_0001947
3379||1831||Oculocerebral hypopigmentation syndrome, Cross type||http://www.orpha.net/ORDO/Orphanet_2719
3381||10652||obsolete_heart||http://www.ebi.ac.uk/efo/EFO_0000815
3382||13496||Lymphocytic choriomeningitis virus||http://purl.obolibrary.org/obo/NCBITaxon_11623
3383||306||Oculotrichodysplasia||http://www.orpha.net/ORDO/Orphanet_2718
3384||10652||obsolete_soleus muscle||http://www.ebi.ac.uk/efo/EFO_0001946
3385||10652||obsolete_vein||http://www.ebi.ac.uk/efo/EFO_0000816
3388||14165||white fat||http://www.ebi.ac.uk/efo/EFO_0000813
3386||13496||Lassa virus Josiah||http://purl.obolibrary.org/obo/NCBITaxon_11622
3387||13306||Oculotrichoanal syndrome||http://www.orpha.net/ORDO/Orphanet_2717
3390||12358||Distal myopathy with posterior leg and anterior hand involvement||http://www.orpha.net/ORDO/Orphanet_63273
3389||291||muscle||http://www.ebi.ac.uk/efo/EFO_0001949
3392||2670||shoot component||http://www.ebi.ac.uk/efo/EFO_0001948
3391||7319||Oculo-skeletal-renal syndrome||http://www.orpha.net/ORDO/Orphanet_2716
3393||10652||obsolete_artery||http://www.ebi.ac.uk/efo/EFO_0000814
3394||13496||Lassa virus||http://purl.obolibrary.org/obo/NCBITaxon_11620
3395||10652||obsolete_myocardium||http://www.ebi.ac.uk/efo/EFO_0000819
3396||2252||Oculo-palato-cerebral syndrome||http://www.orpha.net/ORDO/Orphanet_2714
3398||306||Oculoosteocutaneous syndrome||http://www.orpha.net/ORDO/Orphanet_2713
3397||10652||obsolete_blood vessel||http://www.ebi.ac.uk/efo/EFO_0000817
3401||3072||carotid artery||http://www.ebi.ac.uk/efo/EFO_0000818
3400||2252||Oculofaciocardiodental syndrome||http://www.orpha.net/ORDO/Orphanet_2712
3399||1393||Laminopathy type Decaudain-Vigouroux||http://www.orpha.net/ORDO/Orphanet_137871
3402||13496||Mopeia virus||http://purl.obolibrary.org/obo/NCBITaxon_11629
3403||13496||Machupo virus||http://purl.obolibrary.org/obo/NCBITaxon_11628
3404||1826||Pyrus pyrifolia||http://purl.obolibrary.org/obo/NCBITaxon_3767
3405||10898||Ehlers-Danlos syndrome, arthrochalasic type||http://www.orpha.net/ORDO/Orphanet_1899
3406||10994||calcium ionophore||http://purl.obolibrary.org/obo/CHEBI_22986
3407||5502||Lactobacillus salivarius||http://purl.obolibrary.org/obo/NCBITaxon_1624
3408||13448||hypoblast||http://www.ebi.ac.uk/efo/EFO_0001930
3409||5502||Lactobacillus sanfranciscensis||http://purl.obolibrary.org/obo/NCBITaxon_1625
3410||4454||calcium||http://purl.obolibrary.org/obo/CHEBI_22984
3411||13448||wing disc||http://www.ebi.ac.uk/efo/EFO_0001933
3412||10652||obsolete_vomeronasal organ||http://www.ebi.ac.uk/efo/EFO_0001934
3413||3653||hypocotyl||http://www.ebi.ac.uk/efo/EFO_0001931
3414||10652||obsolete_muscular system||http://www.ebi.ac.uk/efo/EFO_0000801
3415||10652||obsolete_hypopharynx||http://www.ebi.ac.uk/efo/EFO_0001932
3416||10652||obsolete_liver and biliary system||http://www.ebi.ac.uk/efo/EFO_0000800
3418||10652||obsolete_nervous system||http://www.ebi.ac.uk/efo/EFO_0000802
3417||10652||obsolete_quadricep muscle||http://www.ebi.ac.uk/efo/EFO_0001938
3419||3883||HERNS syndrome||http://www.orpha.net/ORDO/Orphanet_63261
3420||1627||renal system||http://www.ebi.ac.uk/efo/EFO_0000803
3421||10652||obsolete_vastus lateralis||http://www.ebi.ac.uk/efo/EFO_0001937
3422||5508||Craniorachischisis||http://www.orpha.net/ORDO/Orphanet_63260
3423||10652||obsolete_ventral striatum||http://www.ebi.ac.uk/efo/EFO_0001936
3424||10652||obsolete_respiratory system structure||http://www.ebi.ac.uk/efo/EFO_0000804
3425||2252||Oculocerebrofacial syndrome, Kaufman type||http://www.orpha.net/ORDO/Orphanet_2707
3427||10652||obsolete_ventral tegmental area||http://www.ebi.ac.uk/efo/EFO_0001935
3426||10652||obsolete_sensory system||http://www.ebi.ac.uk/efo/EFO_0000805
3428||10652||obsolete_skeletal system||http://www.ebi.ac.uk/efo/EFO_0000806
3430||321||Noonan syndrome-like disorder with loose anagen hair||http://www.orpha.net/ORDO/Orphanet_2701
3429||10652||obsolete_integumental system||http://www.ebi.ac.uk/efo/EFO_0000807
3431||13496||Tacaribe virus||http://purl.obolibrary.org/obo/NCBITaxon_11631
3432||2672||animal body part||http://www.ebi.ac.uk/efo/EFO_0000808
3433||7319||Ochoa syndrome||http://www.orpha.net/ORDO/Orphanet_2704
3435||1627||animal reproductive system||http://www.ebi.ac.uk/efo/EFO_0000809
3434||10652||obsolete_urine||http://www.ebi.ac.uk/efo/EFO_0001939
3436||15464||extra-ocular muscle||http://purl.obolibrary.org/obo/UBERON_0001601
3437||306||EEM syndrome||http://www.orpha.net/ORDO/Orphanet_1897
3439||3854||Halobacterium salinarum||http://purl.obolibrary.org/obo/NCBITaxon_2242
3438||6244||EEC syndrome||http://www.orpha.net/ORDO/Orphanet_1896
3441||4139||Intellectual disability - spasticity - ectrodactyly||http://www.orpha.net/ORDO/Orphanet_1891
3440||9869||Madras motor neuron disease||http://www.orpha.net/ORDO/Orphanet_137867
3442||4834||Oculodental syndrome, Rutherfurd type||http://www.orpha.net/ORDO/Orphanet_2709
3443||13770||Ectrodactyly - polydactyly||http://www.orpha.net/ORDO/Orphanet_1892
3444||1826||Malus x domestica||http://purl.obolibrary.org/obo/NCBITaxon_3750
3445||5502||Lactobacillus farciminis||http://purl.obolibrary.org/obo/NCBITaxon_1612
3446||3072||coronary artery||http://purl.obolibrary.org/obo/UBERON_0001621
3448||2672||male accessory gland||http://www.ebi.ac.uk/efo/EFO_0001964
3447||10652||obsolete_intestine||http://www.ebi.ac.uk/efo/EFO_0000834
3449||10652||obsolete_tongue||http://www.ebi.ac.uk/efo/EFO_0000833
3450||10652||obsolete_mandible||http://www.ebi.ac.uk/efo/EFO_0001965
3451||10652||obsolete_retina structure||http://www.ebi.ac.uk/efo/EFO_0000832
3452||10652||obsolete_ligament||http://www.ebi.ac.uk/efo/EFO_0001966
3454||3459||carbohydrate derivative biosynthetic process||http://purl.obolibrary.org/obo/GO_1901137
3455||778||medial collateral ligament||http://www.ebi.ac.uk/efo/EFO_0001967
3453||10652||obsolete_cranium||http://www.ebi.ac.uk/efo/EFO_0000831
3456||14107||taste system||http://www.ebi.ac.uk/efo/EFO_0000830
3457||2670||lateral root||http://www.ebi.ac.uk/efo/EFO_0001960
3459||14860||carbohydrate derivative metabolic process||http://purl.obolibrary.org/obo/GO_1901135
3458||11835||lateral ventricle||http://www.ebi.ac.uk/efo/EFO_0001961
3461||5502||Lactobacillus fermentum||http://purl.obolibrary.org/obo/NCBITaxon_1613
3460||10652||obsolete_brain stem||http://www.ebi.ac.uk/efo/EFO_0001962
3463||5502||Lactobacillus fructivorans||http://purl.obolibrary.org/obo/NCBITaxon_1614
3462||10652||obsolete_locus coeruleus||http://www.ebi.ac.uk/efo/EFO_0001963
3464||4454||cadmium||http://purl.obolibrary.org/obo/CHEBI_22977
3465||10994||cadmium compounds||http://purl.obolibrary.org/obo/CHEBI_22978
3466||2672||tooth||http://www.ebi.ac.uk/efo/EFO_0000839
3467||10652||obsolete_stomach||http://www.ebi.ac.uk/efo/EFO_0000837
3468||10652||obsolete_medulla of thymus||http://www.ebi.ac.uk/efo/EFO_0001969
3469||10652||obsolete_larynx||http://www.ebi.ac.uk/efo/EFO_0000838
3470||10652||obsolete_medial geniculate nucleus||http://www.ebi.ac.uk/efo/EFO_0001968
3471||10652||obsolete_esophagus||http://www.ebi.ac.uk/efo/EFO_0000835
3472||14135||pharynx structure||http://www.ebi.ac.uk/efo/EFO_0000836
3473||306||Hypohidrotic ectodermal dysplasia - hypothyroidism - ciliary dyskinesia||http://www.orpha.net/ORDO/Orphanet_1882
3474||13496||Puumala virus||http://purl.obolibrary.org/obo/NCBITaxon_11604
3475||2603||Isolated ectopia lentis||http://www.orpha.net/ORDO/Orphanet_1885
3476||13496||Seoul virus||http://purl.obolibrary.org/obo/NCBITaxon_11608
3477||1826||Prunus persica||http://purl.obolibrary.org/obo/NCBITaxon_3760
3478||9687||Ectopia lentis - chorioretinal dystrophy - myopia||http://www.orpha.net/ORDO/Orphanet_1884
3479||306||Ectodermal dysplasia - sensorineural deafness||http://www.orpha.net/ORDO/Orphanet_1883
3480||9934||Oculogastrointestinal muscular dystrophy||http://www.orpha.net/ORDO/Orphanet_1876
3481||12322||Muscular dystrophy - white matter spongiosis||http://www.orpha.net/ORDO/Orphanet_1877
3482||1415||Autosomal recessive limb-girdle muscular dystrophy type 2H||http://www.orpha.net/ORDO/Orphanet_1878
3483||3560||Melorheostosis with osteopoikilosis||http://www.orpha.net/ORDO/Orphanet_1879
3484||3121||JMP syndrome||http://www.orpha.net/ORDO/Orphanet_324999
3485||14877||heart component||http://www.ebi.ac.uk/efo/EFO_0001955
3486||10652||obsolete_endocardium||http://www.ebi.ac.uk/efo/EFO_0000821
3488||10652||obsolete_pericardium||http://www.ebi.ac.uk/efo/EFO_0000820
3487||10652||obsolete_interventricular septum||http://www.ebi.ac.uk/efo/EFO_0001956
3490||1826||Fragaria x ananassa||http://purl.obolibrary.org/obo/NCBITaxon_3747
3491||799||adrenergic antagonist||http://purl.obolibrary.org/obo/CHEBI_37887
3489||10652||obsolete_external carotid artery||http://www.ebi.ac.uk/efo/EFO_0001953
3492||3072||division of carotid artery||http://www.ebi.ac.uk/efo/EFO_0001954
3493||3043||inferior parietal lobule||http://www.ebi.ac.uk/efo/EFO_0001951
3495||1022||Paramecium tetraurelia||http://purl.obolibrary.org/obo/NCBITaxon_5888
3494||5502||Lactobacillus alimentarius||http://purl.obolibrary.org/obo/NCBITaxon_1602
3496||10652||obsolete_internal carotid artery||http://www.ebi.ac.uk/efo/EFO_0001952
3497||5502||Lactobacillus amylovorus||http://purl.obolibrary.org/obo/NCBITaxon_1604
3498||10652||obsolete_midgut||http://www.ebi.ac.uk/efo/EFO_0001950
3499||14107||nose structure||http://www.ebi.ac.uk/efo/EFO_0000828
3500||10652||obsolete_mouth structure||http://www.ebi.ac.uk/efo/EFO_0000825
3502||14107||ear||http://www.ebi.ac.uk/efo/EFO_0000826
3501||13496||Tomato spotted wilt virus||http://purl.obolibrary.org/obo/NCBITaxon_11613
3503||2672||joint component||http://www.ebi.ac.uk/efo/EFO_0001958
3505||10652||obsolete_knee joint||http://www.ebi.ac.uk/efo/EFO_0001957
3504||10652||obsolete_eye structure||http://www.ebi.ac.uk/efo/EFO_0000827
3506||9675||Progressive cone dystrophy||http://www.orpha.net/ORDO/Orphanet_1871
3507||5502||Streptococcus thermophilus CNRZ1066||http://purl.obolibrary.org/obo/NCBITaxon_299768
3508||13496||Junin virus||http://purl.obolibrary.org/obo/NCBITaxon_11619
3509||4834||Jalili syndrome||http://www.orpha.net/ORDO/Orphanet_1873
3510||9681||Cone rod dystrophy||http://www.orpha.net/ORDO/Orphanet_1872
3511||8793||Congenital muscular dystrophy - infantile cataract - hypogonadism||http://www.orpha.net/ORDO/Orphanet_1875
3512||10994||17alpha-ethynylestradiol||http://purl.obolibrary.org/obo/CHEBI_4903
3513||10994||amphotericin B||http://purl.obolibrary.org/obo/CHEBI_2682
3514||12083||Genetic syndromic Pierre Robin syndrome||http://www.orpha.net/ORDO/Orphanet_363294
3515||10994||benzo(a)pyrene diolepoxide 1||http://purl.obolibrary.org/obo/CHEBI_30614
3516||2672||mucosa of tongue||http://purl.obolibrary.org/obo/UBERON_0005020
3517||5502||Sphingomonas sp. NM05||http://purl.obolibrary.org/obo/NCBITaxon_352164
3518||10994||citalopram||http://purl.obolibrary.org/obo/CHEBI_3723
3519||10994||amoxicillin||http://purl.obolibrary.org/obo/CHEBI_2676
3520||5502||Bacillus subtilis||http://purl.obolibrary.org/obo/NCBITaxon_1423
3521||10994||clofibrate||http://purl.obolibrary.org/obo/CHEBI_3750
3522||5502||Rhodococcus jostii RHA1||http://purl.obolibrary.org/obo/NCBITaxon_101510
3523||11617||protein kinase C inhibitor||http://purl.obolibrary.org/obo/CHEBI_37700
3525||5502||Bacillus thuringiensis||http://purl.obolibrary.org/obo/NCBITaxon_1428
3524||8191||clomipramine hydrochloride||http://purl.obolibrary.org/obo/CHEBI_3755
3526||10994||eugenol||http://purl.obolibrary.org/obo/CHEBI_4917
3527||770||GM15245||http://purl.obolibrary.org/obo/CLO_0027391
3528||10994||methyleugenol||http://purl.obolibrary.org/obo/CHEBI_4918
3529||10994||etoposide||http://purl.obolibrary.org/obo/CHEBI_4911
3530||10994||clindamycin||http://purl.obolibrary.org/obo/CHEBI_3745
3531||3854||Methanococcus||http://purl.obolibrary.org/obo/NCBITaxon_2184
3532||7962||Familial osteodysplasia, Anderson type||http://www.orpha.net/ORDO/Orphanet_2769
3533||7991||Blount disease||http://www.orpha.net/ORDO/Orphanet_2768
3534||7966||Carpotarsal osteochondromatosis||http://www.orpha.net/ORDO/Orphanet_2767
3535||7948||Osteocraniostenosis||http://www.orpha.net/ORDO/Orphanet_2763
3536||3573||Aggrecan-related bone disorder||http://www.orpha.net/ORDO/Orphanet_364817
3537||1235||Progressive osseous heteroplasia||http://www.orpha.net/ORDO/Orphanet_2762
3538||4740||OSLAM syndrome||http://www.orpha.net/ORDO/Orphanet_2760
3539||13689||neural keel||http://purl.obolibrary.org/obo/UBERON_0007135
3540||3573||TRPV4-related bone disorder||http://www.orpha.net/ORDO/Orphanet_364820
3541||5912||Osteopathia striata - pigmentary dermopathy - white forelock||http://www.orpha.net/ORDO/Orphanet_2779
3542||7319||Multicentric carpo-tarsal osteolysis with or without nephropathy||http://www.orpha.net/ORDO/Orphanet_2774
3543||7939||Autosomal recessive distal osteolysis syndrome||http://www.orpha.net/ORDO/Orphanet_2776
3544||3560||Osteomesopyknosis||http://www.orpha.net/ORDO/Orphanet_2777
3545||12144||pharyngeal pouch 5||http://purl.obolibrary.org/obo/UBERON_0007126
3546||7939||Nasu-Hakola disease||http://www.orpha.net/ORDO/Orphanet_2770
3548||12144||pharyngeal pouch 6||http://purl.obolibrary.org/obo/UBERON_0007127
3547||1596||Bruck syndrome||http://www.orpha.net/ORDO/Orphanet_2771
3549||7942||Congenital osteogenesis imperfecta - microcephaly - cataracts||http://www.orpha.net/ORDO/Orphanet_2772
3550||7942||Osteogenesis imperfecta - retinopathy - seizures - intellectual disability||http://www.orpha.net/ORDO/Orphanet_2773
3551||12144||pharyngeal pouch 1||http://purl.obolibrary.org/obo/UBERON_0007122
3552||12144||pharyngeal pouch 2||http://purl.obolibrary.org/obo/UBERON_0007123
3553||12144||pharyngeal pouch 3||http://purl.obolibrary.org/obo/UBERON_0007124
3554||12144||pharyngeal pouch 4||http://purl.obolibrary.org/obo/UBERON_0007125
3555||10994||bleomycin||http://purl.obolibrary.org/obo/CHEBI_22907
3557||10994||diarsenic trioxide||http://purl.obolibrary.org/obo/CHEBI_30621
3556||3148||Genetic 46,XY disorder of sex development||http://www.orpha.net/ORDO/Orphanet_325706
3558||7943||Lateral meningocele syndrome||http://www.orpha.net/ORDO/Orphanet_2789
3559||3560||Autosomal dominant osteopetrosis type 1||http://www.orpha.net/ORDO/Orphanet_2783
3560||7943||Osteopetrosis||http://www.orpha.net/ORDO/Orphanet_2781
3561||7942||Osteoporosis - macrocephaly - blindness - joint hyperlaxity||http://www.orpha.net/ORDO/Orphanet_2787
3562||4139||Osteoporosis - pseudoglioma||http://www.orpha.net/ORDO/Orphanet_2788
3563||3560||Osteopetrosis with renal tubular acidosis||http://www.orpha.net/ORDO/Orphanet_2785
3564||7942||Osteoporosis - oculocutaneous hypopigmentation syndrome||http://www.orpha.net/ORDO/Orphanet_2786
3565||2658||venom||http://purl.obolibrary.org/obo/UBERON_0007113
3566||3560||Osteopathia striata - cranial sclerosis||http://www.orpha.net/ORDO/Orphanet_2780
3567||6064||phytogenic insecticide||http://purl.obolibrary.org/obo/CHEBI_22917
3568||4775||Otofaciocervical syndrome||http://www.orpha.net/ORDO/Orphanet_2792
3569||1022||Amphiura filiformis||http://purl.obolibrary.org/obo/NCBITaxon_82378
3570||5918||Pachydermoperiostosis||http://www.orpha.net/ORDO/Orphanet_2796
3571||1826||Selaginella moellendorffii||http://purl.obolibrary.org/obo/NCBITaxon_88036
3572||760||Pachygyria - intellectual disability - epilepsy||http://www.orpha.net/ORDO/Orphanet_2798
3573||4734||Rare bone disease related to a common gene or pathway defect||http://www.orpha.net/ORDO/Orphanet_364803
3574||10994||exemestane||http://purl.obolibrary.org/obo/CHEBI_4953
3575||3556||Genetic 46,XY disorder of sex development of endocrine origin||http://www.orpha.net/ORDO/Orphanet_325713
3576||7943||Autosomal dominant osteosclerosis, Worth type||http://www.orpha.net/ORDO/Orphanet_2790
3577||4834||Otodental syndrome||http://www.orpha.net/ORDO/Orphanet_2791
3578||196||callus formation||http://purl.obolibrary.org/obo/GO_1990110
3579||5502||Clostridium acetobutylicum||http://purl.obolibrary.org/obo/NCBITaxon_1488
3580||1826||Gossypium longicalyx||http://purl.obolibrary.org/obo/NCBITaxon_34280
3581||1826||Musa sp.||http://purl.obolibrary.org/obo/NCBITaxon_46838
3582||9350||Multiple endocrine neoplasia type 2B||http://www.orpha.net/ORDO/Orphanet_247709
3583||2318||Microcephalic primordial dwarfism, Alazami type||http://www.orpha.net/ORDO/Orphanet_319671
3584||770||Ma-Mel-11 cell||http://purl.obolibrary.org/obo/BTO_0005339
3585||5502||Clostridium botulinum||http://purl.obolibrary.org/obo/NCBITaxon_1491
3586||5502||Clostridium butyricum||http://purl.obolibrary.org/obo/NCBITaxon_1492
3587||5502||Clostridium difficile||http://purl.obolibrary.org/obo/NCBITaxon_1496
3588||2318||Microcephalic primordial dwarfism, Dauber type||http://www.orpha.net/ORDO/Orphanet_319675
3589||4266||Encephalopathy - hypertrophic cardiomyopathy - renal tubular disease||http://www.orpha.net/ORDO/Orphanet_319678
3590||10994||famotidine||http://purl.obolibrary.org/obo/CHEBI_4975
3591||1826||Gossypium herbaceum||http://purl.obolibrary.org/obo/NCBITaxon_34274
3592||1826||Gossypium darwinii||http://purl.obolibrary.org/obo/NCBITaxon_34276
3593||1826||Gossypium mustelinum||http://purl.obolibrary.org/obo/NCBITaxon_34275
3594||1826||Gossypium tomentosum||http://purl.obolibrary.org/obo/NCBITaxon_34277
3595||4344||PGM-CDG||http://www.orpha.net/ORDO/Orphanet_319646
3596||5025||Saccharomyces uvarum||http://purl.obolibrary.org/obo/NCBITaxon_230603
3597||9675||Retinal macular dystrophy type 2||http://www.orpha.net/ORDO/Orphanet_319640
3598||13496||Mobala virus||http://purl.obolibrary.org/obo/NCBITaxon_55097
3599||13496||Ippy virus||http://purl.obolibrary.org/obo/NCBITaxon_55096
3600||5025||Kluyveromyces lactis||http://purl.obolibrary.org/obo/NCBITaxon_28985
3601||5843||Constitutional megaloblastic anemia with severe neurologic disease||http://www.orpha.net/ORDO/Orphanet_319651
3602||8191||iron(III) dicitrate||http://purl.obolibrary.org/obo/CHEBI_4991
3603||9332||Niemann-Pick disease type C, adult neurologic onset||http://www.orpha.net/ORDO/Orphanet_216986
3604||9332||Niemann-Pick disease type C, juvenile neurologic onset||http://www.orpha.net/ORDO/Orphanet_216981
3605||6266||Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency||http://www.orpha.net/ORDO/Orphanet_279934
3606||2395||Qualitative or quantitative defects of troponin||http://www.orpha.net/ORDO/Orphanet_284786
3607||3627||X-linked mendelian susceptibility to mycobacterial diseases due to CYBB deficiency||http://www.orpha.net/ORDO/Orphanet_319623
3608||5897||Familial progressive hyper- and hypopigmentation||http://www.orpha.net/ORDO/Orphanet_280628
3609||9332||Niemann-Pick disease type C, severe perinatal form||http://www.orpha.net/ORDO/Orphanet_216972
3611||1022||Mayetiola destructor||http://purl.obolibrary.org/obo/NCBITaxon_39758
3610||10874||Progressive myoclonic epilepsy type 6||http://www.orpha.net/ORDO/Orphanet_280620
3612||9332||Niemann-Pick disease type C, severe early infantile neurologic onset||http://www.orpha.net/ORDO/Orphanet_216975
3613||9332||Niemann-Pick disease type C, late infantile neurologic onset||http://www.orpha.net/ORDO/Orphanet_216978
3614||2345||clozapine||http://purl.obolibrary.org/obo/CHEBI_3766
3615||770||GM15268||http://purl.obolibrary.org/obo/CLO_0027328
3616||10994||clotrimazole||http://purl.obolibrary.org/obo/CHEBI_3764
3617||2395||Qualitative or quantitative defects of tropomyosin||http://www.orpha.net/ORDO/Orphanet_284790
3618||2252||Multiple congenital anomalies - hypotonia - seizures syndrome||http://www.orpha.net/ORDO/Orphanet_280633
3619||4135||Hereditary neutrophilia||http://www.orpha.net/ORDO/Orphanet_279943
3620||10994||amikacin||http://purl.obolibrary.org/obo/CHEBI_2637
3621||10994||amiodarone||http://purl.obolibrary.org/obo/CHEBI_2663
3622||5502||Corynebacterium jeikeium||http://purl.obolibrary.org/obo/NCBITaxon_38289
3624||1826||Avena sativa||http://purl.obolibrary.org/obo/NCBITaxon_4498
3623||1022||Bos indicus||http://purl.obolibrary.org/obo/NCBITaxon_9915
3625||10994||amitriptyline||http://purl.obolibrary.org/obo/CHEBI_2666
3626||1022||Bos taurus||http://purl.obolibrary.org/obo/NCBITaxon_9913
3627||8586||X-linked mendelian susceptibility to mycobacterial diseases||http://www.orpha.net/ORDO/Orphanet_319605
3628||2032||Mendelian susceptibility to mycobacterial diseases due to partial IRF8 deficiency||http://www.orpha.net/ORDO/Orphanet_319600
3629||10994||vincristine||http://purl.obolibrary.org/obo/CHEBI_28445
3630||3627||X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency||http://www.orpha.net/ORDO/Orphanet_319612
3631||15574||Hemoglobinopathy Toms River||http://www.orpha.net/ORDO/Orphanet_280615
3633||13448||mesectoderm||http://purl.obolibrary.org/obo/UBERON_0000927
3632||7782||Fatal infantile hypertonic myofibrillar myopathy||http://www.orpha.net/ORDO/Orphanet_280553
3634||5574||heterocycle biosynthetic process||http://purl.obolibrary.org/obo/GO_0018130
3635||1826||Eucalyptus globulus||http://purl.obolibrary.org/obo/NCBITaxon_34317
3636||2672||embryo||http://purl.obolibrary.org/obo/UBERON_0000922
3637||5967||Warsaw breakage syndrome||http://www.orpha.net/ORDO/Orphanet_280558
3638||1022||Phytophthora sojae||http://purl.obolibrary.org/obo/NCBITaxon_67593
3639||13448||endoderm||http://purl.obolibrary.org/obo/UBERON_0000925
3640||13448||mesoderm||http://purl.obolibrary.org/obo/UBERON_0000926
3641||13448||ectoderm||http://purl.obolibrary.org/obo/UBERON_0000924
3642||3663||Osteochondrosis of genetic origin||http://www.orpha.net/ORDO/Orphanet_399391
3643||1280||abnormality of the skin||http://purl.obolibrary.org/obo/HP_0000951
3644||7158||Infantile hypophosphatasia||http://www.orpha.net/ORDO/Orphanet_247651
3645||2670||meristem||http://www.ebi.ac.uk/efo/EFO_0000990
3646||2670||seed structure||http://www.ebi.ac.uk/efo/EFO_0000991
3647||5864||2q23.1 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_228402
3648||2670||vascular tissue||http://www.ebi.ac.uk/efo/EFO_0000996
3649||2670||storage organ||http://www.ebi.ac.uk/efo/EFO_0000997
3651||2670||plant reproductive system structure||http://www.ebi.ac.uk/efo/EFO_0000998
3650||5502||Francisella tularensis subsp. tularensis SCHU S4||http://purl.obolibrary.org/obo/NCBITaxon_177416
3653||2670||plant developmental tissue||http://www.ebi.ac.uk/efo/EFO_0000999
3652||1022||Capra hircus||http://purl.obolibrary.org/obo/NCBITaxon_9925
3654||2670||shoot||http://www.ebi.ac.uk/efo/EFO_0000992
3655||2670||leaf||http://www.ebi.ac.uk/efo/EFO_0000993
3656||2670||plant fluid||http://www.ebi.ac.uk/efo/EFO_0000994
3657||2670||gall tissue||http://www.ebi.ac.uk/efo/EFO_0000995
3658||1022||Ovis aries||http://purl.obolibrary.org/obo/NCBITaxon_9940
3659||3663||Avascular necrosis of genetic origin||http://www.orpha.net/ORDO/Orphanet_399388
3660||2670||root structure||http://www.ebi.ac.uk/efo/EFO_0000989
3661||8846||Autosomal dominant optic atrophy and late-onset deafness||http://www.orpha.net/ORDO/Orphanet_255117
3662||2672||ventral nerve cord||http://purl.obolibrary.org/obo/UBERON_0000934
3664||3643||Eczema||http://purl.obolibrary.org/obo/HP_0000964
3663||4734||Osteonecrosis of genetic origin||http://www.orpha.net/ORDO/Orphanet_399380
3665||762||Microcephaly - seizures - developmental delay||http://www.orpha.net/ORDO/Orphanet_228418
3666||10652||obsolete_endometrium||http://www.ebi.ac.uk/efo/EFO_0000980
3667||10287||5q35 microduplication syndrome||http://www.orpha.net/ORDO/Orphanet_228415
3668||5306||Polyvalvular heart disease syndrome||http://www.orpha.net/ORDO/Orphanet_228410
3669||10652||obsolete_penis||http://www.ebi.ac.uk/efo/EFO_0000987
3670||2670||gametophyte||http://www.ebi.ac.uk/efo/EFO_0000988
3671||7158||Childhood-onset hypophosphatasia||http://www.orpha.net/ORDO/Orphanet_247667
3672||10652||obsolete_ejaculatory duct||http://www.ebi.ac.uk/efo/EFO_0000985
3673||10652||obsolete_seminal vesicle||http://www.ebi.ac.uk/efo/EFO_0000986
3674||10652||obsolete_testis||http://www.ebi.ac.uk/efo/EFO_0000984
3675||10652||obsolete_ductus deferens||http://www.ebi.ac.uk/efo/EFO_0000981
3676||10652||obsolete_epididymus||http://www.ebi.ac.uk/efo/EFO_0000982
3677||2672||cervix||http://www.ebi.ac.uk/efo/EFO_0000979
3678||2672||vulva||http://www.ebi.ac.uk/efo/EFO_0000978
3679||7158||Prenatal benign hypophosphatasia||http://www.orpha.net/ORDO/Orphanet_247638
3680||2672||abdominal aorta||http://purl.obolibrary.org/obo/UBERON_0001516
3681||2672||thoracic aorta||http://purl.obolibrary.org/obo/UBERON_0001515
3682||3731||osteopenia||http://purl.obolibrary.org/obo/HP_0000938
3683||5295||establishment of localization||http://purl.obolibrary.org/obo/GO_0051234
3684||2252||Syndromic multisystem autoimmune disease due to Itch deficiency||http://www.orpha.net/ORDO/Orphanet_228426
3687||1826||Populus deltoides||http://purl.obolibrary.org/obo/NCBITaxon_3696
3685||15||Generalized congenital lipodystrophy with myopathy||http://www.orpha.net/ORDO/Orphanet_228429
3686||10898||Ehlers-Danlos syndrome, dermatosparaxis type||http://www.orpha.net/ORDO/Orphanet_1901
3689||1826||Populus trichocarpa x Populus deltoides||http://purl.obolibrary.org/obo/NCBITaxon_3695
3688||10503||Ehlers-Danlos syndrome, kyphoscoliotic type||http://www.orpha.net/ORDO/Orphanet_1900
3691||1022||Tetrahymena thermophila||http://purl.obolibrary.org/obo/NCBITaxon_5911
3690||10652||obsolete_male reproductive system||http://www.ebi.ac.uk/efo/EFO_0000970
3692||10652||obsolete_hermaphrodite gonad||http://www.ebi.ac.uk/efo/EFO_0000971
3694||10994||estradiol||http://purl.obolibrary.org/obo/CHEBI_23965
3695||3866||Autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome||http://www.orpha.net/ORDO/Orphanet_391487
3693||10652||obsolete_unfertilized egg||http://www.ebi.ac.uk/efo/EFO_0000972
3696||2672||animal ovary||http://www.ebi.ac.uk/efo/EFO_0000973
3697||4994||Monocytopenia with susceptibility to infections||http://www.orpha.net/ORDO/Orphanet_228423
3698||10652||obsolete_oviduct||http://www.ebi.ac.uk/efo/EFO_0000974
3699||10652||obsolete_uterus||http://www.ebi.ac.uk/efo/EFO_0000975
3700||10652||obsolete_vagina||http://www.ebi.ac.uk/efo/EFO_0000976
3701||10652||obsolete_spermathecum||http://www.ebi.ac.uk/efo/EFO_0000977
3703||10994||novobiocin||http://purl.obolibrary.org/obo/CHEBI_28368
3702||10652||obsolete_female reproductive system||http://www.ebi.ac.uk/efo/EFO_0000969
3704||10652||obsolete_abdomen||http://www.ebi.ac.uk/efo/EFO_0000968
3705||10652||obsolete_neck||http://www.ebi.ac.uk/efo/EFO_0000967
3706||2672||abdomen||http://purl.obolibrary.org/obo/UBERON_0000916
3707||8190||all-cis-icosa-5,8,11,14,17-pentaenoic acid||http://purl.obolibrary.org/obo/CHEBI_28364
3708||1826||Populus nigra||http://purl.obolibrary.org/obo/NCBITaxon_3691
3709||1826||Populus tremuloides||http://purl.obolibrary.org/obo/NCBITaxon_3693
3710||1826||Populus trichocarpa||http://purl.obolibrary.org/obo/NCBITaxon_3694
3711||3072||brachiocephalic artery||http://purl.obolibrary.org/obo/UBERON_0001529
3712||1826||Populus||http://purl.obolibrary.org/obo/NCBITaxon_3689
3713||3072||internal carotid artery||http://purl.obolibrary.org/obo/UBERON_0001532
3714||2672||adult segment||http://www.ebi.ac.uk/efo/EFO_0000961
3715||2672||skin||http://www.ebi.ac.uk/efo/EFO_0000962
3716||10652||obsolete_scale||http://www.ebi.ac.uk/efo/EFO_0000960
3717||10652||obsolete_thorax||http://www.ebi.ac.uk/efo/EFO_0000965
3718||10652||obsolete_trunk||http://www.ebi.ac.uk/efo/EFO_0000966
3719||10652||obsolete_tail||http://www.ebi.ac.uk/efo/EFO_0000963
3720||10652||obsolete_head||http://www.ebi.ac.uk/efo/EFO_0000964
3721||1852||Qualitative or quantitative defects of protein O-mannosyltransferase 2||http://www.orpha.net/ORDO/Orphanet_209033
3722||1852||Qualitative or quantitative defects of protein O-mannosyltransferase 1||http://www.orpha.net/ORDO/Orphanet_209030
3723||6912||Hereditary sensorimotor neuropathy with hyperelastic skin||http://www.orpha.net/ORDO/Orphanet_280598
3724||5053||Congenital lobar emphysema||http://www.orpha.net/ORDO/Orphanet_1928
3725||1022||Daphnia pulex||http://purl.obolibrary.org/obo/NCBITaxon_6669
3726||1022||Ichthyophthirius multifiliis||http://purl.obolibrary.org/obo/NCBITaxon_5932
3727||1852||Qualitative or quantitative defects of protein glycosyltransferase-like||http://www.orpha.net/ORDO/Orphanet_209027
3730||2032||Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency||http://www.orpha.net/ORDO/Orphanet_319595
3728||1852||Qualitative or quantitative defects of protein O-mannose beta1,2N-acetylglucosaminyltransferase||http://www.orpha.net/ORDO/Orphanet_209024
3729||6246||Emery-Nelson syndrome||http://www.orpha.net/ORDO/Orphanet_1927
3731||2063||abnormality of the skeletal system||http://purl.obolibrary.org/obo/HP_0000924
3732||7949||Chondrodysplasia with joint dislocations, gPAPP type||http://www.orpha.net/ORDO/Orphanet_280586
3733||2063||abnormality of metabolism/homeostasis||http://purl.obolibrary.org/obo/HP_0001939
3735||1022||Oryctolagus cuniculus||http://purl.obolibrary.org/obo/NCBITaxon_9986
3734||5502||Caldicellulosiruptor hydrothermalis||http://purl.obolibrary.org/obo/NCBITaxon_413888
3736||1826||Aegilops tauschii x Triticum turgidum||http://purl.obolibrary.org/obo/NCBITaxon_285950
3737||7158||Perinatal lethal hypophosphatasia||http://www.orpha.net/ORDO/Orphanet_247623
3738||10140||Frontorhiny||http://www.orpha.net/ORDO/Orphanet_391474
3739||2032||Autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency||http://www.orpha.net/ORDO/Orphanet_319589
3740||15464||masseter muscle||http://purl.obolibrary.org/obo/UBERON_0001597
3741||3777||Qualitative or quantitative defects of protein ZASP||http://www.orpha.net/ORDO/Orphanet_209050
3742||10272||Juvenile absence epilepsy||http://www.orpha.net/ORDO/Orphanet_1941
3743||6244||Shoulder and thorax deformity - congenital heart disease||http://www.orpha.net/ORDO/Orphanet_1940
3745||2395||Qualitative or quantitative defects of titin||http://www.orpha.net/ORDO/Orphanet_209053
3744||4981||cellular component||http://purl.obolibrary.org/obo/GO_0005575
3746||2032||Autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency||http://www.orpha.net/ORDO/Orphanet_319581
3747||382||Nestor-Guillermo progeria syndrome||http://www.orpha.net/ORDO/Orphanet_280576
3748||1022||Heliconius erato etylus x Heliconius himera||http://purl.obolibrary.org/obo/NCBITaxon_529916
3749||1022||Marmota monax||http://purl.obolibrary.org/obo/NCBITaxon_9995
3750||4430||enzyme inhibitor||http://purl.obolibrary.org/obo/CHEBI_23924
3751||5502||Shewanella oneidensis||http://purl.obolibrary.org/obo/NCBITaxon_70863
3752||1022||Penaeus monodon||http://purl.obolibrary.org/obo/NCBITaxon_6687
3753||4830||Primary glomerular disease||http://www.orpha.net/ORDO/Orphanet_102373
3754||1022||Litopenaeus vannamei||http://purl.obolibrary.org/obo/NCBITaxon_6689
3756||3777||Qualitative or quantitative defects of filamin C||http://www.orpha.net/ORDO/Orphanet_209047
3755||306||Amelo-cerebro-hypohidrotic syndrome||http://www.orpha.net/ORDO/Orphanet_1946
3757||762||Progressive epilepsy - intellectual disability, Finnish type||http://www.orpha.net/ORDO/Orphanet_1947
3759||2252||Epilepsy - microcephaly - skeletal dysplasia||http://www.orpha.net/ORDO/Orphanet_1948
3758||1998||Autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency||http://www.orpha.net/ORDO/Orphanet_319574
3760||10272||Benign familial neonatal seizures||http://www.orpha.net/ORDO/Orphanet_1949
3761||10860||Myoclonic-astastic epilepsy||http://www.orpha.net/ORDO/Orphanet_1942
3762||10272||Rolandic epilepsy||http://www.orpha.net/ORDO/Orphanet_1945
3764||4994||Herpetic encephalitis||http://www.orpha.net/ORDO/Orphanet_1930
3763||8835||Adult-onset autosomal recessive sideroblastic anemia||http://www.orpha.net/ORDO/Orphanet_255132
3765||5025||Leptosphaerulina chartarum||http://purl.obolibrary.org/obo/NCBITaxon_55173
3766||3777||Qualitative or quantitative defects of desmin||http://www.orpha.net/ORDO/Orphanet_209041
3768||3777||Qualitative or quantitative defects of alphaB-cristallin||http://www.orpha.net/ORDO/Orphanet_209044
3767||3753||Rapidly progressive glomerulonephritis||http://www.orpha.net/ORDO/Orphanet_280569
3769||8736||Pyruvate dehydrogenase E1-beta deficiency||http://www.orpha.net/ORDO/Orphanet_255138
3770||5025||Trichophyton violaceum||http://purl.obolibrary.org/obo/NCBITaxon_34388
3771||1022||Spermophilus parryii||http://purl.obolibrary.org/obo/NCBITaxon_9999
3772||5025||Trichophyton schoenleinii||http://purl.obolibrary.org/obo/NCBITaxon_34386
3773||3851||HSD10 disease, neonatal type||http://www.orpha.net/ORDO/Orphanet_391457
3774||9869||Juvenile primary lateral sclerosis||http://www.orpha.net/ORDO/Orphanet_247604
3775||2003||Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency||http://www.orpha.net/ORDO/Orphanet_319563
3776||8835||Early myoclonic encephalopathy||http://www.orpha.net/ORDO/Orphanet_1935
3777||2395||Qualitative or quantitative defects of myofibrillar proteins||http://www.orpha.net/ORDO/Orphanet_209038
3778||8775||Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria||http://www.orpha.net/ORDO/Orphanet_1933
3779||4713||Early infantile epileptic encephalopathy||http://www.orpha.net/ORDO/Orphanet_1934
3780||14124||Frontal encephalocele||http://www.orpha.net/ORDO/Orphanet_1931
3781||1998||Autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency||http://www.orpha.net/ORDO/Orphanet_319569
3782||3851||HSD10 disease, infantile type||http://www.orpha.net/ORDO/Orphanet_391428
3783||321||Alopecia-intellectual disability syndrome||http://www.orpha.net/ORDO/Orphanet_2850
3784||10652||obsolete_thalamus||http://www.ebi.ac.uk/efo/EFO_0000910
3785||10652||obsolete_diencephalon||http://www.ebi.ac.uk/efo/EFO_0000911
3786||5300||Fuhrmann syndrome||http://www.orpha.net/ORDO/Orphanet_2854
3787||6277||Proximal renal tubular acidosis||http://www.orpha.net/ORDO/Orphanet_47159
3788||10652||obsolete_midbrain||http://www.ebi.ac.uk/efo/EFO_0000919
3790||5461||Primary hemophagocytic lymphohistiocytosis||http://www.orpha.net/ORDO/Orphanet_158038
3789||10652||obsolete_epithalamus||http://www.ebi.ac.uk/efo/EFO_0000918
3792||1528||Perrault syndrome||http://www.orpha.net/ORDO/Orphanet_2855
3791||10652||obsolete_temporal lobe||http://www.ebi.ac.uk/efo/EFO_0000917
3794||12009||Persistent M llerian duct syndrome||http://www.orpha.net/ORDO/Orphanet_2856
3793||10652||obsolete_visual cortex||http://www.ebi.ac.uk/efo/EFO_0000916
3795||10652||obsolete_occipital lobe||http://www.ebi.ac.uk/efo/EFO_0000915
3796||10652||obsolete_parietal lobe||http://www.ebi.ac.uk/efo/EFO_0000914
3797||10652||obsolete_frontal lobe||http://www.ebi.ac.uk/efo/EFO_0000913
3798||10652||obsolete_telencephalon||http://www.ebi.ac.uk/efo/EFO_0000912
3799||7966||Exostoses - anetodermia - brachydactyly type E||http://www.orpha.net/ORDO/Orphanet_1962
3800||375||Congenital lethal erythroderma||http://www.orpha.net/ORDO/Orphanet_1954
3802||4259||response to corticosteroid||http://purl.obolibrary.org/obo/GO_0031960
3801||375||Erythromelalgia||http://www.orpha.net/ORDO/Orphanet_1956
3803||5985||Spinocerebellar ataxia type 34||http://www.orpha.net/ORDO/Orphanet_1955
3804||2395||Qualitative or quantitative defects of alpha-actin||http://www.orpha.net/ORDO/Orphanet_209059
3805||14376||mesenchyme derived from head neural crest||http://purl.obolibrary.org/obo/UBERON_0007213
3806||2395||Qualitative or quantitative defects of telethonin||http://www.orpha.net/ORDO/Orphanet_209056
3807||10652||obsolete_dorsal root ganglion||http://www.ebi.ac.uk/efo/EFO_0000900
3808||5965||Familial benign chronic pemphigus||http://www.orpha.net/ORDO/Orphanet_2841
3809||7963||Pelvic dysplasia - arthrogryposis of lower limbs||http://www.orpha.net/ORDO/Orphanet_2840
3810||6270||Pentosuria||http://www.orpha.net/ORDO/Orphanet_2843
3811||10652||obsolete_accumbens nucleus||http://www.ebi.ac.uk/efo/EFO_0000906
3812||10652||obsolete_globus pallidus||http://www.ebi.ac.uk/efo/EFO_0000905
3813||10652||obsolete_central nervous system||http://www.ebi.ac.uk/efo/EFO_0000908
3814||4717||Pericardial and diaphragmatic defect||http://www.orpha.net/ORDO/Orphanet_2847
3815||10652||obsolete_caudate nucleus||http://www.ebi.ac.uk/efo/EFO_0000907
3816||13496||Sabia virus||http://purl.obolibrary.org/obo/NCBITaxon_45709
3817||10652||obsolete_cranial ganglion||http://www.ebi.ac.uk/efo/EFO_0000902
3819||14513||body ganglion||http://www.ebi.ac.uk/efo/EFO_0000901
3818||4812||Perlman syndrome||http://www.orpha.net/ORDO/Orphanet_2849
3820||10652||obsolete_basal ganglion||http://www.ebi.ac.uk/efo/EFO_0000904
3821||10652||obsolete_trigeminal ganglion||http://www.ebi.ac.uk/efo/EFO_0000903
3822||1561||organelle envelope||http://purl.obolibrary.org/obo/GO_0031967
3823||1524||chloroplast membrane||http://purl.obolibrary.org/obo/GO_0031969
3824||10652||obsolete_forebrain||http://www.ebi.ac.uk/efo/EFO_0000909
3825||613||Epilepsy telangiectasia||http://www.orpha.net/ORDO/Orphanet_1951
3826||7939||Pacman dysplasia||http://www.orpha.net/ORDO/Orphanet_1952
3827||4139||Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome||http://www.orpha.net/ORDO/Orphanet_391408
3828||5300||Femoral-facial syndrome||http://www.orpha.net/ORDO/Orphanet_1988
3829||7957||Femoral agenesis/hypoplasia||http://www.orpha.net/ORDO/Orphanet_1987
3831||1561||organelle envelope lumen||http://purl.obolibrary.org/obo/GO_0031970
3830||6244||Gollop-Wolfgang complex||http://www.orpha.net/ORDO/Orphanet_1986
3833||13999||Genetic intestinal polyposis||http://www.orpha.net/ORDO/Orphanet_363314
3832||12769||PHAVER syndrome||http://www.orpha.net/ORDO/Orphanet_2876
3834||5912||Phakomatosis pigmentovascularis||http://www.orpha.net/ORDO/Orphanet_2875
3835||4180||response to doxorubicin||http://purl.obolibrary.org/obo/GO_1902520
3836||5877||Phakomatosis pigmentokeratotica||http://www.orpha.net/ORDO/Orphanet_2874
3837||4180||response to epirubicin||http://purl.obolibrary.org/obo/GO_1902522
3838||2252||Cardiocranial syndrome, Pfeiffer type||http://www.orpha.net/ORDO/Orphanet_2872
3839||2252||Pfeiffer-Palm-Teller syndrome||http://www.orpha.net/ORDO/Orphanet_2871
3840||12151||giardiasis||http://purl.obolibrary.org/obo/DOID_10718
3841||9762||Hypoglycemia||http://purl.obolibrary.org/obo/HP_0001943
3842||14683||fever||http://purl.obolibrary.org/obo/HP_0001945
3843||8736||Pyruvate dehydrogenase E3-binding protein deficiency||http://www.orpha.net/ORDO/Orphanet_255182
3844||6244||Phocomelia, Schinzel type||http://www.orpha.net/ORDO/Orphanet_2879
3845||5700||Phocomelia - ectrodactyly - deafness - sinus arrhythmia||http://www.orpha.net/ORDO/Orphanet_2878
3846||3744||membrane-enclosed lumen||http://purl.obolibrary.org/obo/GO_0031974
3847||3854||Methanobrevibacter smithii||http://purl.obolibrary.org/obo/NCBITaxon_2173
3848||9899||Bilateral striopallidodentate calcinosis||http://www.orpha.net/ORDO/Orphanet_1980
3849||12747||response to cyclophosphamide||http://purl.obolibrary.org/obo/GO_1902518
3850||12432||Lipodystrophy due to peptidic growth factors deficiency||http://www.orpha.net/ORDO/Orphanet_1979
3851||6371||HSD10 disease||http://www.orpha.net/ORDO/Orphanet_391417
3852||1533||nuclear lumen||http://purl.obolibrary.org/obo/GO_0031981
3853||4188||response to docetaxel||http://purl.obolibrary.org/obo/GO_1902519
3854||5005||Archaea||http://purl.obolibrary.org/obo/NCBITaxon_2157
3855||13306||Short stature - wormian bones - dextrocardia||http://www.orpha.net/ORDO/Orphanet_2863
3856||13999||Genetic intestinal disease due to fat malabsorption||http://www.orpha.net/ORDO/Orphanet_363306
3857||2252||Short stature - webbed neck - heart disease||http://www.orpha.net/ORDO/Orphanet_2865
3858||9898||Atypical juvenile parkinsonism||http://www.orpha.net/ORDO/Orphanet_391411
3859||1826||Vitis aestivalis||http://purl.obolibrary.org/obo/NCBITaxon_3605
3860||4575||Porphyria cutanea tarda||http://www.orpha.net/ORDO/Orphanet_101330
3861||1732||Sea-blue histiocytosis||http://www.orpha.net/ORDO/Orphanet_158029
3862||5502||Staphylococcus aureus subsp. aureus NCTC 8325||http://purl.obolibrary.org/obo/NCBITaxon_93061
3863||5700||Short stature - deafness - neutrophil dysfunction - dysmorphism||http://www.orpha.net/ORDO/Orphanet_2866
3865||5502||Staphylococcus aureus subsp. aureus COL||http://purl.obolibrary.org/obo/NCBITaxon_93062
3864||7966||Short stature, Brussels type||http://www.orpha.net/ORDO/Orphanet_2867
3866||13999||Genetic intractable diarrhea of infancy||http://www.orpha.net/ORDO/Orphanet_363300
3867||12769||Short stature - valvular heart disease - characteristic facies||http://www.orpha.net/ORDO/Orphanet_2868
3868||3833||Peutz-Jeghers syndrome||http://www.orpha.net/ORDO/Orphanet_2869
3869||6244||Lethal faciocardiomelic dysplasia||http://www.orpha.net/ORDO/Orphanet_1972
3870||2252||Faciocardiorenal syndrome||http://www.orpha.net/ORDO/Orphanet_1973
3871||4785||Autosomal recessive facio-digito-genital syndrome||http://www.orpha.net/ORDO/Orphanet_1974
3872||3854||Methanobacterium||http://purl.obolibrary.org/obo/NCBITaxon_2160
3873||2252||Facial dysmorphism - macrocephaly - myopia - Dandy-Walker malformation||http://www.orpha.net/ORDO/Orphanet_1970
3874||10652||obsolete_feather||http://www.ebi.ac.uk/efo/EFO_0000955
3875||10652||obsolete_epidermis||http://www.ebi.ac.uk/efo/EFO_0000954
3876||10652||obsolete_dermis||http://www.ebi.ac.uk/efo/EFO_0000953
3877||2672||paired fin skeleton||http://www.ebi.ac.uk/efo/EFO_0000951
3879||2672||median fin skeleton||http://www.ebi.ac.uk/efo/EFO_0000950
3878||10994||iodoform||http://purl.obolibrary.org/obo/CHEBI_37758
3880||9350||Multiple endocrine neoplasia type 2A||http://www.orpha.net/ORDO/Orphanet_247698
3881||1826||Gossypium barbadense||http://purl.obolibrary.org/obo/NCBITaxon_3634
3882||1826||Gossypium hirsutum||http://purl.obolibrary.org/obo/NCBITaxon_3635
3883||4705||Retinal vasculopathy and cerebral leukodystrophy||http://www.orpha.net/ORDO/Orphanet_247691
3884||13501||Spastic paraplegia - facial-cutaneous lesions||http://www.orpha.net/ORDO/Orphanet_2819
3885||1357||pyoderma||http://purl.obolibrary.org/obo/HP_0000999
3886||375||Parana hard-skin syndrome||http://www.orpha.net/ORDO/Orphanet_2812
3888||4139||Spastic paraplegia - glaucoma - intellectual disability||http://www.orpha.net/ORDO/Orphanet_2818
3887||2672||hair||http://www.ebi.ac.uk/efo/EFO_0000958
3889||10652||obsolete_pharyngeal arch||http://www.ebi.ac.uk/efo/EFO_0000959
3891||4139||Spastic paraplegia - epilepsy - intellectual disability||http://www.orpha.net/ORDO/Orphanet_2816
3890||10652||obsolete_nail||http://www.ebi.ac.uk/efo/EFO_0000956
3892||5700||Spastic paraparesis - deafness||http://www.orpha.net/ORDO/Orphanet_2815
3893||2672||axial skeleton structure||http://www.ebi.ac.uk/efo/EFO_0000942
3894||10652||obsolete_lateral line system||http://www.ebi.ac.uk/efo/EFO_0000941
3895||2672||exoskeleton||http://www.ebi.ac.uk/efo/EFO_0000944
3896||10652||obsolete_craniofacial skeleton bone||http://www.ebi.ac.uk/efo/EFO_0000943
3897||5502||Synechococcus sp. WH 8102||http://purl.obolibrary.org/obo/NCBITaxon_84588
3898||10652||obsolete_chordotonal organ||http://www.ebi.ac.uk/efo/EFO_0000940
3899||306||Blepharo-cheilo-odontic syndrome||http://www.orpha.net/ORDO/Orphanet_1997
3900||6904||Familial isolated congenital asplenia||http://www.orpha.net/ORDO/Orphanet_101351
3901||11842||Familial recurrent peripheral facial palsy||http://www.orpha.net/ORDO/Orphanet_2809
3902||5300||Pai syndrome||http://www.orpha.net/ORDO/Orphanet_1993
3903||5300||Cleft lip - retinopathy||http://www.orpha.net/ORDO/Orphanet_1995
3904||2672||cartilage||http://www.ebi.ac.uk/efo/EFO_0000949
3905||7943||Juvenile Paget disease||http://www.orpha.net/ORDO/Orphanet_2801
3906||3114||X-linked sideroblastic anemia with ataxia||http://www.orpha.net/ORDO/Orphanet_2802
3908||6904||Partial pancreatic agenesis||http://www.orpha.net/ORDO/Orphanet_2805
3907||10652||obsolete_limb bone||http://www.ebi.ac.uk/efo/EFO_0000945
3910||2672||pectoral girdle||http://www.ebi.ac.uk/efo/EFO_0000946
3909||613||W syndrome||http://www.orpha.net/ORDO/Orphanet_2804
3911||10926||pelvic girdle||http://www.ebi.ac.uk/efo/EFO_0000947
3912||2672||joint||http://www.ebi.ac.uk/efo/EFO_0000948
3913||7989||Rhizomelic dysplasia, Patterson-Lowry type||http://www.orpha.net/ORDO/Orphanet_2831
3914||12769||Short tarsus - absence of lower eyelashes||http://www.orpha.net/ORDO/Orphanet_2832
3915||7158||Adult hypophosphatasia||http://www.orpha.net/ORDO/Orphanet_247676
3918||14207||gill||http://www.ebi.ac.uk/efo/EFO_0000933
3917||3750||cholinesterase inhibitor||http://purl.obolibrary.org/obo/CHEBI_37733
3916||1826||Cucumis sativus||http://purl.obolibrary.org/obo/NCBITaxon_3659
3919||10652||obsolete_bronchus||http://www.ebi.ac.uk/efo/EFO_0000932
3920||3841||Hypoketotic hypoglycemia||http://purl.obolibrary.org/obo/HP_0001985
3921||10652||obsolete_urethra||http://www.ebi.ac.uk/efo/EFO_0000931
3922||10652||obsolete_ureter||http://www.ebi.ac.uk/efo/EFO_0000930
3923||1826||Cucumis melo||http://purl.obolibrary.org/obo/NCBITaxon_3656
3924||5502||Clostridium tetani||http://purl.obolibrary.org/obo/NCBITaxon_1513
3925||1826||Citrullus lanatus||http://purl.obolibrary.org/obo/NCBITaxon_3654
3926||1826||Cucurbita maxima||http://purl.obolibrary.org/obo/NCBITaxon_3661
3927||14207||spiracle||http://www.ebi.ac.uk/efo/EFO_0000936
3928||6244||Pelvis-shoulder dysplasia||http://www.orpha.net/ORDO/Orphanet_2839
3929||10652||obsolete_diaphragm||http://www.ebi.ac.uk/efo/EFO_0000937
3930||10652||obsolete_lung||http://www.ebi.ac.uk/efo/EFO_0000934
3931||5880||Pellagra-like skin rash - neurological manifestations||http://www.orpha.net/ORDO/Orphanet_2837
3932||10652||obsolete_trachea||http://www.ebi.ac.uk/efo/EFO_0000935
3933||613||PEHO syndrome||http://www.orpha.net/ORDO/Orphanet_2836
3934||15081||Wrinkly skin syndrome||http://www.orpha.net/ORDO/Orphanet_2834
3935||14107||sensory bristle||http://www.ebi.ac.uk/efo/EFO_0000938
3936||14107||sensillum||http://www.ebi.ac.uk/efo/EFO_0000939
3937||375||Stiff skin syndrome||http://www.orpha.net/ORDO/Orphanet_2833
3938||10994||ethyl nitrosourea||http://purl.obolibrary.org/obo/CHEBI_23995
3940||5700||Spastic paraplegia - nephritis - deafness||http://www.orpha.net/ORDO/Orphanet_2820
3939||7158||Odontohypophosphatasia||http://www.orpha.net/ORDO/Orphanet_247685
3941||13501||Spastic paraplegia - neuropathy - poikiloderma||http://www.orpha.net/ORDO/Orphanet_2821
3942||3043||tectum||http://www.ebi.ac.uk/efo/EFO_0000920
3944||5502||Clostridium sporogenes||http://purl.obolibrary.org/obo/NCBITaxon_1509
3943||10652||obsolete_substantia nigra||http://www.ebi.ac.uk/efo/EFO_0000922
3946||3043||tegmentum||http://www.ebi.ac.uk/efo/EFO_0000921
3945||1826||Carica papaya||http://purl.obolibrary.org/obo/NCBITaxon_3649
3948||1826||Theobroma cacao||http://purl.obolibrary.org/obo/NCBITaxon_3641
3947||5502||Clostridium perfringens||http://purl.obolibrary.org/obo/NCBITaxon_1502
3949||3643||Pruritus||http://purl.obolibrary.org/obo/HP_0000989
3950||10652||obsolete_hindbrain||http://www.ebi.ac.uk/efo/EFO_0000923
3953||13501||Spastic paraplegia - precocious puberty||http://www.orpha.net/ORDO/Orphanet_2826
3952||1826||Lotus japonicus||http://purl.obolibrary.org/obo/NCBITaxon_34305
3951||10652||obsolete_medulla oblongata||http://www.ebi.ac.uk/efo/EFO_0000924
3954||10652||obsolete_mushroom body||http://www.ebi.ac.uk/efo/EFO_0000925
3956||9898||Young adult-onset Parkinsonism||http://www.orpha.net/ORDO/Orphanet_2828
3955||10652||obsolete_pars intercerebralis||http://www.ebi.ac.uk/efo/EFO_0000926
3957||2021||Paraplegia - brachydactyly - cone-shaped epiphysis||http://www.orpha.net/ORDO/Orphanet_2823
3958||10652||obsolete_pronephros||http://www.ebi.ac.uk/efo/EFO_0000927
3960||583||Autosomal recessive spastic paraplegia type 11||http://www.orpha.net/ORDO/Orphanet_2822
3959||10652||obsolete_mesonephros||http://www.ebi.ac.uk/efo/EFO_0000928
3962||5300||PARC syndrome||http://www.orpha.net/ORDO/Orphanet_2825
3961||10652||obsolete_kidney||http://www.ebi.ac.uk/efo/EFO_0000929
3964||2252||Paraplegia - intellectual disability - hyperkeratosis||http://www.orpha.net/ORDO/Orphanet_2824
3963||4706||Mohr-Tranebjaerg syndrome||http://www.orpha.net/ORDO/Orphanet_52368
3965||3854||Metallosphaera sedula||http://purl.obolibrary.org/obo/NCBITaxon_43687
3966||10414||Citrin deficiency||http://www.orpha.net/ORDO/Orphanet_247582
3967||3966||Citrullinemia type II||http://www.orpha.net/ORDO/Orphanet_247585
3968||5025||Penicillium corylophilum||http://purl.obolibrary.org/obo/NCBITaxon_70792
3969||14989||gene list||http://purl.obolibrary.org/obo/OBI_0000118
3970||1826||Chara corallina||http://purl.obolibrary.org/obo/NCBITaxon_43696
3971||4108||Adult-onset citrullinemia type I||http://www.orpha.net/ORDO/Orphanet_247573
3972||5025||Komagataella pastoris||http://purl.obolibrary.org/obo/NCBITaxon_4922
3973||1022||Calypte anna||http://purl.obolibrary.org/obo/NCBITaxon_9244
3974||10886||glycoprotein||http://purl.obolibrary.org/obo/CHEBI_17089
3975||583||Autosomal recessive spastic paraplegia type 30||http://www.orpha.net/ORDO/Orphanet_101010
3976||6650||Isolated brachycephaly||http://www.orpha.net/ORDO/Orphanet_35099
3977||6650||Isolated plagiocephaly||http://www.orpha.net/ORDO/Orphanet_35098
3978||5025||Saccharomyces bayanus||http://purl.obolibrary.org/obo/NCBITaxon_4931
3979||8737||Romano-Ward syndrome||http://www.orpha.net/ORDO/Orphanet_101016
3980||5025||Saccharomyces cerevisiae||http://purl.obolibrary.org/obo/NCBITaxon_4932
3981||586||Autosomal dominant spastic paraplegia type 31||http://www.orpha.net/ORDO/Orphanet_101011
3982||1022||Aptenodytes patagonicus||http://purl.obolibrary.org/obo/NCBITaxon_9234
3983||13480||Autosomal recessive spastic paraplegia type 28||http://www.orpha.net/ORDO/Orphanet_101008
3984||13501||Autosomal dominant spastic paraplegia type 29||http://www.orpha.net/ORDO/Orphanet_101009
3985||6650||Isolated scaphocephaly||http://www.orpha.net/ORDO/Orphanet_35093
3986||5502||Caldicellulosiruptor owensensis||http://purl.obolibrary.org/obo/NCBITaxon_55205
3987||5502||Streptosporangium roseum||http://purl.obolibrary.org/obo/NCBITaxon_2001
3988||13470||Autosomal recessive spastic paraplegia type 27||http://www.orpha.net/ORDO/Orphanet_101007
3989||13470||Autosomal recessive spastic paraplegia type 26||http://www.orpha.net/ORDO/Orphanet_101006
3991||13470||Autosomal recessive spastic paraplegia type 25||http://www.orpha.net/ORDO/Orphanet_101005
3990||10994||drug||http://purl.obolibrary.org/obo/CHEBI_23888
3992||13470||Autosomal recessive spastic paraplegia type 24||http://www.orpha.net/ORDO/Orphanet_101004
3993||13470||Autosomal recessive spastic paraplegia type 23||http://www.orpha.net/ORDO/Orphanet_101003
3994||583||Autosomal recessive spastic paraplegia type 21||http://www.orpha.net/ORDO/Orphanet_101001
3995||13470||Autosomal recessive spastic paraplegia type 20||http://www.orpha.net/ORDO/Orphanet_101000
3996||5025||Yarrowia lipolytica||http://purl.obolibrary.org/obo/NCBITaxon_4952
3997||799||osmotic diuretic||http://purl.obolibrary.org/obo/CHEBI_50504
3998||6573||sweetening agent role||http://purl.obolibrary.org/obo/CHEBI_50505
3999||5025||Debaryomyces hansenii||http://purl.obolibrary.org/obo/NCBITaxon_4959
4000||6766||T-B  severe combined immunodeficiency due to JAK3 deficiency||http://www.orpha.net/ORDO/Orphanet_35078
4001||4017||Disorder of O-mannosylglycan synthesis||http://www.orpha.net/ORDO/Orphanet_309469
4002||10994||5-azacytidine||http://purl.obolibrary.org/obo/CHEBI_2038
4003||6238||vasoconstrictor agent||http://purl.obolibrary.org/obo/CHEBI_50514
4004||11842||Infantile neuroaxonal dystrophy||http://www.orpha.net/ORDO/Orphanet_35069
4005||259||cell cycle||http://purl.obolibrary.org/obo/GO_0007049
4006||4017||Disorder of O-xylosyl/N-acetylgalactosaminylglycan synthesis||http://www.orpha.net/ORDO/Orphanet_309463
4007||14970||longitude||http://purl.obolibrary.org/obo/OBI_0001621
4008||14970||latitude||http://purl.obolibrary.org/obo/OBI_0001620
4009||4017||Disorder of O-N-acetylgalactosaminylglycan synthesis||http://www.orpha.net/ORDO/Orphanet_309458
4010||2884||spindle organization||http://purl.obolibrary.org/obo/GO_0007051
4011||4010||mitotic spindle organization||http://purl.obolibrary.org/obo/GO_0007052
4012||10994||3-dehydroteasterone||http://purl.obolibrary.org/obo/CHEBI_20000
4013||10994||arsenic oxide||http://purl.obolibrary.org/obo/CHEBI_50527
4014||4017||Disorder of O-xylosylglycan synthesis||http://www.orpha.net/ORDO/Orphanet_309450
4015||1022||Julidochromis transcriptus||http://purl.obolibrary.org/obo/NCBITaxon_70784
4016||3966||Neonatal intrahepatic cholestasis due to citrin deficiency||http://www.orpha.net/ORDO/Orphanet_247598
4017||10577||Disorder of protein O-glycosylation||http://www.orpha.net/ORDO/Orphanet_309447
4018||7424||Unilateral hemispheric polymicrogyria||http://www.orpha.net/ORDO/Orphanet_101071
4019||7426||Bilateral frontoparietal polymicrogyria||http://www.orpha.net/ORDO/Orphanet_101070
4020||2996||X-linked Charcot-Marie-Tooth disease type 2||http://www.orpha.net/ORDO/Orphanet_101076
4021||2252||Atelosteogenesis type II||http://www.orpha.net/ORDO/Orphanet_56304
4024||2996||X-linked Charcot-Marie-Tooth disease type 1||http://www.orpha.net/ORDO/Orphanet_101075
4023||2252||Atelosteogenesis type III||http://www.orpha.net/ORDO/Orphanet_56305
4022||7142||Genetic transient congenital hypothyroidism||http://www.orpha.net/ORDO/Orphanet_226316
4025||2996||X-linked Charcot-Marie-Tooth disease type 4||http://www.orpha.net/ORDO/Orphanet_101078
4026||2996||X-linked Charcot-Marie-Tooth disease type 3||http://www.orpha.net/ORDO/Orphanet_101077
4027||10994||steroid||http://purl.obolibrary.org/obo/CHEBI_35341
4028||7001||Peripheral hypothyroidism||http://www.orpha.net/ORDO/Orphanet_226310
4029||4738||RIP-seq||http://www.ebi.ac.uk/efo/EFO_0005310
4030||11067||picomole per microliter||http://www.ebi.ac.uk/efo/EFO_0005313
4031||5681||SERKAL syndrome||http://www.orpha.net/ORDO/Orphanet_139466
4032||11067||femtomole per nanogram||http://www.ebi.ac.uk/efo/EFO_0005314
4033||1766||induced mutation||http://www.ebi.ac.uk/efo/EFO_0005315
4034||13883||sample pooling||http://www.ebi.ac.uk/efo/EFO_0005316
4035||14970||axial length measurement||http://www.ebi.ac.uk/efo/EFO_0005318
4036||11563||contact dermatitis||http://www.ebi.ac.uk/efo/EFO_0005319
4037||5502||Granulibacter bethesdensis||http://purl.obolibrary.org/obo/NCBITaxon_364410
4038||6087||Situs inversus totalis||http://www.orpha.net/ORDO/Orphanet_101063
4039||6989||Hypothyroidism due to deficient transcription factors involved in pituitary development or function||http://www.orpha.net/ORDO/Orphanet_226307
4040||5502||Pantoea stewartii||http://purl.obolibrary.org/obo/NCBITaxon_66269
4042||6573||alkylating agent role||http://purl.obolibrary.org/obo/CHEBI_22333
4041||9624||Congenital stromal corneal dystrophy||http://www.orpha.net/ORDO/Orphanet_101068
4043||4254||Autosomal recessive spastic paraplegia type 39||http://www.orpha.net/ORDO/Orphanet_139480
4044||4036||contact dermatitis due to nickel||http://www.ebi.ac.uk/efo/EFO_0005320
4045||1814||molar-incisor hypomineralization||http://www.ebi.ac.uk/efo/EFO_0005321
4046||6899||Microphthalmia with brain and digit anomalies||http://www.orpha.net/ORDO/Orphanet_139471
4047||4050||post-operative sensory disturbance||http://www.ebi.ac.uk/efo/EFO_0005324
4048||4259||response to angiotensin-converting enzyme inhibitor||http://www.ebi.ac.uk/efo/EFO_0005325
4049||3068||callous-unemotional behaviour||http://www.ebi.ac.uk/efo/EFO_0005322
4050||11618||post-operative sign or symptom||http://www.ebi.ac.uk/efo/EFO_0005323
4051||4139||17q11.2 microduplication syndrome||http://www.orpha.net/ORDO/Orphanet_139474
4053||1319||tyrosine||http://purl.obolibrary.org/obo/CHEBI_18186
4052||5002||Bile acid synthesis defect with cholestasis and malabsorption||http://www.orpha.net/ORDO/Orphanet_163631
4054||4740||Maffucci syndrome||http://www.orpha.net/ORDO/Orphanet_163634
4055||12715||Autosomal recessive Charcot-Marie-Tooth disease with hoarseness||http://www.orpha.net/ORDO/Orphanet_101097
4056||5110||Hyper-IgM syndrome type 5||http://www.orpha.net/ORDO/Orphanet_101092
4057||5110||Hyper-IgM syndrome type 4||http://www.orpha.net/ORDO/Orphanet_101091
4058||805||Hemochromatosis type 4||http://www.orpha.net/ORDO/Orphanet_139491
4059||7139||COG8-CDG||http://www.orpha.net/ORDO/Orphanet_95428
4060||5928||Angioma serpiginosum||http://www.orpha.net/ORDO/Orphanet_95429
4061||6543||Autosomal recessive ataxia due to ubiquinone deficiency||http://www.orpha.net/ORDO/Orphanet_139485
4062||2307||aromatic compound biosynthetic process||http://purl.obolibrary.org/obo/GO_0019438
4064||4027||cholesterol ester||http://purl.obolibrary.org/obo/CHEBI_17002
4063||9134||Primary hypomagnesemia with secondary hypocalcemia||http://www.orpha.net/ORDO/Orphanet_30924
4065||303||Hereditary central diabetes insipidus||http://www.orpha.net/ORDO/Orphanet_30925
4066||612||Charcot-Marie-Tooth disease type 1F||http://www.orpha.net/ORDO/Orphanet_101085
4067||612||Charcot-Marie-Tooth disease type 1D||http://www.orpha.net/ORDO/Orphanet_101084
4068||612||Charcot-Marie-Tooth disease type 1A||http://www.orpha.net/ORDO/Orphanet_101081
4069||612||Charcot-Marie-Tooth disease type 1C||http://www.orpha.net/ORDO/Orphanet_101083
4070||612||Charcot-Marie-Tooth disease type 1B||http://www.orpha.net/ORDO/Orphanet_101082
4071||5110||Hyper-IgM syndrome type 2||http://www.orpha.net/ORDO/Orphanet_101089
4072||5115||X-linked hyper-IgM syndrome||http://www.orpha.net/ORDO/Orphanet_101088
4073||4738||ChIP-exo||http://www.ebi.ac.uk/efo/EFO_0005302
4074||6927||Congenital tracheomalacia||http://www.orpha.net/ORDO/Orphanet_95430
4075||1391||sudden infant death syndrome||http://www.ebi.ac.uk/efo/EFO_0005303
4076||4225||word reading||http://www.ebi.ac.uk/efo/EFO_0005300
4077||4225||reading and spelling ability||http://www.ebi.ac.uk/efo/EFO_0005301
4078||11827||Autosomal recessive cerebellar ataxia - saccadic intrusion||http://www.orpha.net/ORDO/Orphanet_95434
4079||11827||Autosomal recessive cerebellar ataxia - blindness - deafness||http://www.orpha.net/ORDO/Orphanet_95433
4080||10994||streptozotocin||http://purl.obolibrary.org/obo/CHEBI_9288
4081||8292||atrial tachycardia||http://www.ebi.ac.uk/efo/EFO_0005308
4083||12996||Ta stage||http://www.ebi.ac.uk/efo/EFO_0005309
4082||5115||Hyper-IgM syndrome type 3||http://www.orpha.net/ORDO/Orphanet_101090
4084||8292||ventricular tachycardia||http://www.ebi.ac.uk/efo/EFO_0005306
4085||4084||torsades de pointes||http://www.ebi.ac.uk/efo/EFO_0005307
4086||5116||atrial conduction disease||http://www.ebi.ac.uk/efo/EFO_0005304
4088||5116||atrioventricular node disease||http://www.ebi.ac.uk/efo/EFO_0005305
4087||5893||Genetic muscular channelopathy||http://www.orpha.net/ORDO/Orphanet_352298
4089||4108||Acute neonatal citrullinemia type I||http://www.orpha.net/ORDO/Orphanet_247546
4090||8530||Peters anomaly - cataract||http://www.orpha.net/ORDO/Orphanet_101033
4091||5632||Female restricted epilepsy with intellectual disability||http://www.orpha.net/ORDO/Orphanet_101039
4092||10143||Spondyloepiphyseal dysplasia, Reardon type||http://www.orpha.net/ORDO/Orphanet_163662
4093||5502||Lactobacillus reuteri 100-23||http://purl.obolibrary.org/obo/NCBITaxon_349123
4094||8715||Leydig cell hypoplasia due to LHB deficiency||http://www.orpha.net/ORDO/Orphanet_325448
4095||5972||Subependymal nodular heterotopia||http://www.orpha.net/ORDO/Orphanet_101030
4096||5700||Spondyloepiphyseal dysplasia, MacDermot type||http://www.orpha.net/ORDO/Orphanet_163668
4097||10994||progesterone||http://purl.obolibrary.org/obo/CHEBI_17026
4098||10994||ethene||http://purl.obolibrary.org/obo/CHEBI_18153
4100||4139||Spondyloepiphyseal dysplasia tarda, Kohn type||http://www.orpha.net/ORDO/Orphanet_163665
4099||7874||polysaccharide||http://purl.obolibrary.org/obo/CHEBI_18154
4101||10994||chitin||http://purl.obolibrary.org/obo/CHEBI_17029
4102||1022||Micropterus salmoides||http://purl.obolibrary.org/obo/NCBITaxon_27706
4103||426||Mediterranean macrothrombocytopenia||http://www.orpha.net/ORDO/Orphanet_101022
4104||6270||Transaldolase deficiency||http://www.orpha.net/ORDO/Orphanet_101028
4105||5972||Sub-cortical nodular heterotopia||http://www.orpha.net/ORDO/Orphanet_101029
4106||10994||( )-alpha-tocopherol||http://purl.obolibrary.org/obo/CHEBI_18145
4107||9676||Primary ciliary dyskinesia - retinitis pigmentosa||http://www.orpha.net/ORDO/Orphanet_247522
4108||10414||Citrullinemia type I||http://www.orpha.net/ORDO/Orphanet_247525
4109||14893||Microlissencephaly type B||http://www.orpha.net/ORDO/Orphanet_101052
4110||10994||gamma-tocopherol||http://purl.obolibrary.org/obo/CHEBI_18185
4111||8074||Familial hypocalciuric hypercalcemia type 3||http://www.orpha.net/ORDO/Orphanet_101050
4112||4139||Spondyloepiphyseal dysplasia, Nishimura type||http://www.orpha.net/ORDO/Orphanet_163649
4113||8074||Familial hypocalciuric hypercalcemia type 2||http://www.orpha.net/ORDO/Orphanet_101049
4114||8147||Autosomal dominant secondary polycythemia||http://www.orpha.net/ORDO/Orphanet_247511
4115||10272||Autosomal dominant epilepsy with auditory features||http://www.orpha.net/ORDO/Orphanet_101046
4116||7817||Familial hypofibrinogenemia||http://www.orpha.net/ORDO/Orphanet_101041
4117||7023||Taussig-Bing syndrome||http://www.orpha.net/ORDO/Orphanet_101042
4118||10143||Spondyloepiphyseal dysplasia, Cantu type||http://www.orpha.net/ORDO/Orphanet_163654
4119||1307||Combined pituitary hormone deficiencies, genetic forms||http://www.orpha.net/ORDO/Orphanet_95494
4120||8937||mural granulosa cell||http://www.ebi.ac.uk/efo/EFO_0005289
4121||4142||Pituitary stalk interruption syndrome||http://www.orpha.net/ORDO/Orphanet_95496
4122||7120||Disease associated with non-acquired combined pituitary hormone deficiency||http://www.orpha.net/ORDO/Orphanet_95495
4123||770||A20||http://www.ebi.ac.uk/efo/EFO_0005285
4124||13587||BALB/cAnN||http://www.ebi.ac.uk/efo/EFO_0005286
4125||2002||reticulum cell sarcoma||http://www.ebi.ac.uk/efo/EFO_0005287
4126||120||non-small cell lung adenocarcinoma||http://www.ebi.ac.uk/efo/EFO_0005288
4127||5502||Streptomyces venezuelae||http://purl.obolibrary.org/obo/NCBITaxon_54571
4128||770||AG06237||http://purl.obolibrary.org/obo/CLO_0035254
4129||1529||Glycogen storage disease due to lactate dehydrogenase H-subunit deficiency||http://www.orpha.net/ORDO/Orphanet_284435
4130||1492||B-lymphoblast||http://www.ebi.ac.uk/efo/EFO_0005293
4131||10994||chlorpromazine||http://purl.obolibrary.org/obo/CHEBI_3647
4132||770||lymphoblastoid cell line||http://www.ebi.ac.uk/efo/EFO_0005292
4133||11202||migraine with aura||http://www.ebi.ac.uk/efo/EFO_0005295
4134||770||chronic myelogenous leukemia cell line||http://www.ebi.ac.uk/efo/EFO_0005294
4135||1732||Rare genetic immune disease||http://www.orpha.net/ORDO/Orphanet_183770
4136||14235||Dark agouti||http://www.ebi.ac.uk/efo/EFO_0005291
4137||14235||Brown Norway||http://www.ebi.ac.uk/efo/EFO_0005290
4138||14970||cardiovascular disease biomarker measurement||http://www.ebi.ac.uk/efo/EFO_0005278
4139||4228||Rare genetic intellectual disability with developmental anomaly||http://www.orpha.net/ORDO/Orphanet_183763
4140||1814||temporomandibular joint disorder||http://www.ebi.ac.uk/efo/EFO_0005279
4141||14602||hydroxy-leucine measurement||http://www.ebi.ac.uk/efo/EFO_0005276
4142||303||Non-acquired pituitary hormone deficiency||http://www.orpha.net/ORDO/Orphanet_95488
4143||13659||sleep time||http://www.ebi.ac.uk/efo/EFO_0005274
4144||14602||dihydroxy docosatrienoic acid measurement||http://www.ebi.ac.uk/efo/EFO_0005275
4145||8193||chlorpropamide||http://purl.obolibrary.org/obo/CHEBI_3650
4146||1529||Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency||http://www.orpha.net/ORDO/Orphanet_284426
4147||770||L-1210||http://www.ebi.ac.uk/efo/EFO_0005284
4148||770||HS-27A||http://www.ebi.ac.uk/efo/EFO_0005283
4149||770||HS-5||http://www.ebi.ac.uk/efo/EFO_0005282
4150||5502||Desulfotomaculum reducens MI-1||http://purl.obolibrary.org/obo/NCBITaxon_349161
4151||7902||Behavioral variant of frontotemporal dementia||http://www.orpha.net/ORDO/Orphanet_275864
4152||13659||sleep latency||http://www.ebi.ac.uk/efo/EFO_0005280
4153||770||TOV-112D||http://www.ebi.ac.uk/efo/EFO_0005263
4154||770||Ect1||http://www.ebi.ac.uk/efo/EFO_0005264
4155||7902||Frontotemporal dementia with motor neuron disease||http://www.orpha.net/ORDO/Orphanet_275872
4156||770||MOLT-3||http://www.ebi.ac.uk/efo/EFO_0005265
4157||14970||serum selenium measurement||http://www.ebi.ac.uk/efo/EFO_0005266
4159||14970||serum copper measurement||http://www.ebi.ac.uk/efo/EFO_0005267
4158||2672||umbilical cord blood||http://purl.obolibrary.org/obo/UBERON_0012168
4160||14970||serum zinc measurement||http://www.ebi.ac.uk/efo/EFO_0005268
4161||2897||Carney triad||http://www.orpha.net/ORDO/Orphanet_139411
4162||1732||congenital heart malformation||http://www.ebi.ac.uk/efo/EFO_0005269
4163||4254||Congenital ichthyosis - intellectual disability - spastic quadriplegia||http://www.orpha.net/ORDO/Orphanet_352333
4164||613||Action myoclonus - renal failure syndrome||http://www.orpha.net/ORDO/Orphanet_163696
4165||8184||2p21 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_163693
4166||6174||Phosphoserine aminotransferase deficiency||http://www.orpha.net/ORDO/Orphanet_284417
4167||8093||Glycerol kinase deficiency, juvenile form||http://www.orpha.net/ORDO/Orphanet_284411
4168||8093||Glycerol kinase deficiency, adult form||http://www.orpha.net/ORDO/Orphanet_284414
4169||8184||Hypotonia - cystinuria syndrome||http://www.orpha.net/ORDO/Orphanet_163690
4170||10994||aluminium hydroxide||http://purl.obolibrary.org/obo/CHEBI_33130
4171||13659||sleep duration||http://www.ebi.ac.uk/efo/EFO_0005271
4172||13659||sleep depth||http://www.ebi.ac.uk/efo/EFO_0005273
4173||10994||organic heterocyclic compound||http://purl.obolibrary.org/obo/CHEBI_24532
4174||13659||sleep quality||http://www.ebi.ac.uk/efo/EFO_0005272
4175||4204||neurally mediated hypotension||http://www.ebi.ac.uk/efo/EFO_0005254
4177||4204||orthostatic hypotension||http://www.ebi.ac.uk/efo/EFO_0005252
4176||3854||Halobacterium sp. NRC-1||http://purl.obolibrary.org/obo/NCBITaxon_64091
4178||4204||postprandial hypotension||http://www.ebi.ac.uk/efo/EFO_0005253
4180||12747||response to anthracycline-based chemotherapy||http://www.ebi.ac.uk/efo/EFO_0005257
4179||5838||molecular quality||http://purl.obolibrary.org/obo/PATO_0002182
4181||6625||Encephalopathy due to prosaposin deficiency||http://www.orpha.net/ORDO/Orphanet_139406
4182||1022||Strombus gigas||http://purl.obolibrary.org/obo/NCBITaxon_291982
4183||6276||Leukoencephalopathy - dystonia - motor neuropathy||http://www.orpha.net/ORDO/Orphanet_163684
4184||5502||Escherichia coli DH1||http://purl.obolibrary.org/obo/NCBITaxon_536056
4185||10994||vanadyl sulfate||http://purl.obolibrary.org/obo/CHEBI_33146
4186||613||Cortical dysplasia - focal epilepsy syndrome||http://www.orpha.net/ORDO/Orphanet_163681
4187||11618||mitral annular calcification||http://www.ebi.ac.uk/efo/EFO_0005262
4188||12747||response to antimicrotubule agent||http://www.ebi.ac.uk/efo/EFO_0005260
4190||4727||Glycerol kinase deficiency, infantile form||http://www.orpha.net/ORDO/Orphanet_284408
4189||8193||pentamidine||http://purl.obolibrary.org/obo/CHEBI_45081
4191||4245||Disorder of phospholipids, sphingolipids and fatty acids biosynthesis with skeletal muscle predominant involvement||http://www.orpha.net/ORDO/Orphanet_352312
4192||2165||hypersomnia||http://www.ebi.ac.uk/efo/EFO_0005246
4194||1732||Rare genetic gynecological and obstetrical diseases||http://www.orpha.net/ORDO/Orphanet_183731
4195||5295||body weight loss||http://www.ebi.ac.uk/efo/EFO_0005245
4193||7479||ribonucleoside biosynthetic process||http://purl.obolibrary.org/obo/GO_0042455
4196||7488||anti-Heliobacter pylori serum IgG measurement||http://www.ebi.ac.uk/efo/EFO_0005247
4198||15363||Genetic gynecological tumor||http://www.orpha.net/ORDO/Orphanet_183734
4197||2102||methamphetamine-induced psychosis||http://www.ebi.ac.uk/efo/EFO_0005242
4200||14970||employment status||http://www.ebi.ac.uk/efo/EFO_0005241
4199||4854||purine nucleoside biosynthetic process||http://purl.obolibrary.org/obo/GO_0042451
4201||14780||gastric bypass||http://www.ebi.ac.uk/efo/EFO_0005244
4202||14970||myeloperoxidase measurement||http://www.ebi.ac.uk/efo/EFO_0005243
4203||2102||occupation-related stress disorder||http://www.ebi.ac.uk/efo/EFO_0005250
4204||1015||hypotension||http://www.ebi.ac.uk/efo/EFO_0005251
4205||2672||shell of nucleus accumbens||http://purl.obolibrary.org/obo/UBERON_0012171
4206||2672||core of nucleus accumbens||http://purl.obolibrary.org/obo/UBERON_0012170
4207||1015||aortic valve calcification||http://www.ebi.ac.uk/efo/EFO_0005239
4208||4571||breed||http://www.ebi.ac.uk/efo/EFO_0005238
4209||770||U-87 MG||http://www.ebi.ac.uk/efo/EFO_0005237
4211||770||NT2/D1||http://www.ebi.ac.uk/efo/EFO_0005236
4210||9649||phosphatidylcholine||http://purl.obolibrary.org/obo/CHEBI_49183
4212||2162||primitive neuroectodermal tumor||http://www.ebi.ac.uk/efo/EFO_0005235
4213||770||PFSK-1||http://www.ebi.ac.uk/efo/EFO_0005234
4214||770||CH12.LX||http://www.ebi.ac.uk/efo/EFO_0005233
4215||120||endometrium adenocarcinoma||http://www.ebi.ac.uk/efo/EFO_0005232
4216||770||ECC-1||http://www.ebi.ac.uk/efo/EFO_0005231
4217||2102||anxiety||http://www.ebi.ac.uk/efo/EFO_0005230
4218||5279||rhegmatogenous retinal detachment||http://www.ebi.ac.uk/efo/EFO_0005240
4219||10994||1-4-dioxane||http://purl.obolibrary.org/obo/CHEBI_47032
4220||10994||cimetidine||http://purl.obolibrary.org/obo/CHEBI_3699
4221||4254||MEGDEL syndrome||http://www.orpha.net/ORDO/Orphanet_352328
4222||4571||plant population||http://www.ebi.ac.uk/efo/EFO_0005228
4223||4263||GRO-seq||http://www.ebi.ac.uk/efo/EFO_0005227
4224||10851||Syndrome associated with hypertrophic cardiomyopathy||http://www.orpha.net/ORDO/Orphanet_217595
4225||12543||reading||http://www.ebi.ac.uk/efo/EFO_0005229
4226||5025||Gibberella moniliformis||http://purl.obolibrary.org/obo/NCBITaxon_117187
4227||12136||pulmonary neuroendocrine tumor||http://www.ebi.ac.uk/efo/EFO_0005220
4228||9918||Rare genetic intellectual disability||http://www.orpha.net/ORDO/Orphanet_183757
4230||2714||avian influenza||http://www.ebi.ac.uk/efo/EFO_0005222
4229||6899||Microtia - eye coloboma - imperforation of the nasolacrimal duct||http://www.orpha.net/ORDO/Orphanet_139450
4231||1006||cholangiocarcinoma||http://www.ebi.ac.uk/efo/EFO_0005221
4232||2700||Q fever||http://www.ebi.ac.uk/efo/EFO_0005224
4233||5295||odontogenesis||http://purl.obolibrary.org/obo/GO_0042476
4234||2102||acute stress reaction||http://www.ebi.ac.uk/efo/EFO_0005223
4235||2714||swine influenza||http://www.ebi.ac.uk/efo/EFO_0005226
4236||11124||human african trypanosomiasis||http://www.ebi.ac.uk/efo/EFO_0005225
4237||9965||Autosomal recessive bestrophinopathy||http://www.orpha.net/ORDO/Orphanet_139455
4238||5113||Isolated agammaglobulinemia||http://www.orpha.net/ORDO/Orphanet_229717
4240||15549||Progressive cavitating leukoencephalopathy||http://www.orpha.net/ORDO/Orphanet_139447
4239||13883||TraDIS sequencing||http://www.ebi.ac.uk/efo/EFO_0005219
4241||770||cervical carcinoma cell line||http://www.ebi.ac.uk/efo/EFO_0005218
4242||770||cervical adenocarcinoma cell line||http://www.ebi.ac.uk/efo/EFO_0005217
4243||770||hepatoma cell line||http://www.ebi.ac.uk/efo/EFO_0005216
4244||3744||bacterial nucleoid||http://purl.obolibrary.org/obo/GO_0043590
4245||5267||Disorder of phospholipids, sphingolipids and fatty acids biosynthesis||http://www.orpha.net/ORDO/Orphanet_352301
4246||14970||aspirin hydrolysis measurement||http://www.ebi.ac.uk/efo/EFO_0005211
4247||8644||brain connectivity measurement||http://www.ebi.ac.uk/efo/EFO_0005210
4248||770||breast adenocarcinoma cell line||http://www.ebi.ac.uk/efo/EFO_0005215
4249||15549||Leukoencephalopathy with bilateral anterior temporal lobe cysts||http://www.orpha.net/ORDO/Orphanet_139444
4250||770||neuroblastoma cell line||http://www.ebi.ac.uk/efo/EFO_0005214
4251||15549||Hypomyelination with atrophy of basal ganglia and cerebellum||http://www.orpha.net/ORDO/Orphanet_139441
4252||14970||central corneal thickness||http://www.ebi.ac.uk/efo/EFO_0005213
4253||10946||atmosphere unit||http://www.ebi.ac.uk/efo/EFO_0005212
4254||4245||Disorder of phospholipids, sphingolipids and fatty acids biosynthesis with central nervous system predominant involvement||http://www.orpha.net/ORDO/Orphanet_352306
4255||5113||Syndromic agammaglobulinemia||http://www.orpha.net/ORDO/Orphanet_229720
4256||4245||Disorder of phospholipids, sphingolipids and fatty acids biosynthesis with peripheral nerves predominant involvement||http://www.orpha.net/ORDO/Orphanet_352309
4257||5502||Staphylococcus saprophyticus subsp. saprophyticus||http://purl.obolibrary.org/obo/NCBITaxon_147452
4258||1022||Cryptococcus neoformans var. neoformans JEC21||http://purl.obolibrary.org/obo/NCBITaxon_214684
4259||6476||response to drug||http://purl.obolibrary.org/obo/GO_0042493
4260||2299||hemorrhage||http://purl.obolibrary.org/obo/MP_0001914
4261||10851||Glycogen storage disease with hypertrophic cardiomyopathy||http://www.orpha.net/ORDO/Orphanet_217572
4262||12750||quantitative confidence value||http://purl.obolibrary.org/obo/OBI_0000071
4263||13883||assay||http://purl.obolibrary.org/obo/OBI_0000070
4264||10851||Fatty acid oxidation and ketogenesis disorder with hypertrophic cardiomyopathy||http://www.orpha.net/ORDO/Orphanet_217591
4265||770||ND00051||http://purl.obolibrary.org/obo/CLO_0029732
4266||10851||Mitochondrial disease with hypertrophic cardiomyopathy||http://www.orpha.net/ORDO/Orphanet_217587
4267||10851||Lysosomal disease with hypertrophic cardiomyopathy||http://www.orpha.net/ORDO/Orphanet_217581
4268||259||cellular response to stimulus||http://purl.obolibrary.org/obo/GO_0051716
4269||5502||Mycoplasma hyopneumoniae||http://purl.obolibrary.org/obo/NCBITaxon_2099
4270||5502||Mycoplasma genitalium||http://purl.obolibrary.org/obo/NCBITaxon_2097
4271||5502||Mycoplasma gallisepticum||http://purl.obolibrary.org/obo/NCBITaxon_2096
4272||4488||Alpha-thalassemia-related diseases||http://www.orpha.net/ORDO/Orphanet_232288
4273||2802||Neonatal acute respiratory distress with surfactant metabolism deficiency||http://www.orpha.net/ORDO/Orphanet_217563
4274||5025||Fusarium incarnatum||http://purl.obolibrary.org/obo/NCBITaxon_298378
4275||9826||Chronic respiratory distress with surfactant metabolism deficiency||http://www.orpha.net/ORDO/Orphanet_217566
4276||4017||Disorder of fucoglycosan synthesis||http://www.orpha.net/ORDO/Orphanet_309505
4277||10994||chlorhexidine||http://purl.obolibrary.org/obo/CHEBI_3614
4278||10577||Disorder of glycosphingolipid and glycosylphosphatidylinositol anchor glycosylation||http://www.orpha.net/ORDO/Orphanet_309515
4279||1585||interaction with host||http://purl.obolibrary.org/obo/GO_0051701
4280||5502||Shewanella oneidensis MR-1||http://purl.obolibrary.org/obo/NCBITaxon_211586
4281||7354||Isolated focal cortical dysplasia type IIb||http://www.orpha.net/ORDO/Orphanet_269008
4282||5103||Wegener s granulomatosis||http://www.ebi.ac.uk/efo/EFO_0005297
4283||11202||migraine without aura||http://www.ebi.ac.uk/efo/EFO_0005296
4284||7354||Isolated focal cortical dysplasia type IIa||http://www.orpha.net/ORDO/Orphanet_269001
4285||4225||non-word reading||http://www.ebi.ac.uk/efo/EFO_0005299
4286||14970||allergic sensitization measurement||http://www.ebi.ac.uk/efo/EFO_0005298
4288||10994||chloroquine||http://purl.obolibrary.org/obo/CHEBI_3638
4287||6572||Glycogen storage disease due to glycogenin deficiency||http://www.orpha.net/ORDO/Orphanet_263297
4289||1022||Dasypus novemcinctus||http://purl.obolibrary.org/obo/NCBITaxon_9361
4290||10994||3,3 ,5-triiodo-L-thyronine||http://purl.obolibrary.org/obo/CHEBI_18258
4291||5855||3q26q27 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_356947
4292||10994||dopamine||http://purl.obolibrary.org/obo/CHEBI_18243
4293||8801||Ethylmalonic encephalopathy||http://www.orpha.net/ORDO/Orphanet_51188
4295||4454||iron||http://purl.obolibrary.org/obo/CHEBI_18248
4294||5918||Familial primary localized cutaneous amyloidosis||http://www.orpha.net/ORDO/Orphanet_353220
4296||1125||organization||http://purl.obolibrary.org/obo/OBI_0000245
4297||5959||SLC35A2-CDG||http://www.orpha.net/ORDO/Orphanet_356961
4298||9856||Spinocerebellar ataxia type 25||http://www.orpha.net/ORDO/Orphanet_101111
4299||9856||Spinocerebellar ataxia type 20||http://www.orpha.net/ORDO/Orphanet_101110
4300||9853||Spinocerebellar ataxia type 26||http://www.orpha.net/ORDO/Orphanet_101112
4301||8814||Mucopolysaccharidosis type 4B||http://www.orpha.net/ORDO/Orphanet_309310
4302||15572||Disorder of sialic acid metabolism||http://www.orpha.net/ORDO/Orphanet_309319
4303||2672||body proper||http://purl.obolibrary.org/obo/UBERON_0013702
4304||10994||xylose||http://purl.obolibrary.org/obo/CHEBI_18222
4305||10994||isoflavone||http://purl.obolibrary.org/obo/CHEBI_18220
4306||6432||Spinocerebellar ataxia type 28||http://www.orpha.net/ORDO/Orphanet_101109
4307||9856||Spinocerebellar ataxia type 23||http://www.orpha.net/ORDO/Orphanet_101108
4308||12715||Charcot-Marie-Tooth disease type 2H||http://www.orpha.net/ORDO/Orphanet_101102
4309||12715||Charcot-Marie-Tooth disease type 2B2||http://www.orpha.net/ORDO/Orphanet_101101
4310||15601||Marin-Amat syndrome||http://www.orpha.net/ORDO/Orphanet_101104
4311||7966||Mazabraud syndrome||http://www.orpha.net/ORDO/Orphanet_57782
4312||15571||Disorder of lysosomal-related organelles||http://www.orpha.net/ORDO/Orphanet_309340
4313||10994||teasterone||http://purl.obolibrary.org/obo/CHEBI_26863
4314||10994||selenite(2-)||http://purl.obolibrary.org/obo/CHEBI_18212
4316||5502||Synechococcus elongatus||http://purl.obolibrary.org/obo/NCBITaxon_32046
4315||8684||Rubinstein-Taybi syndrome due to CREBBP mutations||http://www.orpha.net/ORDO/Orphanet_353277
4317||4268||signal transduction||http://purl.obolibrary.org/obo/GO_0007165
4319||3389||skeletal muscle||http://purl.obolibrary.org/obo/UBERON_0014892
4318||10994||9-cis-retinoic acid||http://purl.obolibrary.org/obo/CHEBI_50648
4320||799||bone density conservation agent||http://purl.obolibrary.org/obo/CHEBI_50646
4321||6314||Salla disease||http://www.orpha.net/ORDO/Orphanet_309334
4322||15572||Lysosomal glycogen storage disease||http://www.orpha.net/ORDO/Orphanet_309337
4323||10994||benzylpenicillin||http://purl.obolibrary.org/obo/CHEBI_18208
4324||1022||Macropus eugenii||http://purl.obolibrary.org/obo/NCBITaxon_9315
4325||5502||Bartonella koehlerae||http://purl.obolibrary.org/obo/NCBITaxon_92181
4326||6314||Intermediate severe Salla disease||http://www.orpha.net/ORDO/Orphanet_309331
4327||259||cell communication||http://purl.obolibrary.org/obo/GO_0007154
4328||1826||Salix viminalis||http://purl.obolibrary.org/obo/NCBITaxon_40686
4329||1022||Sarcophilus harrisii||http://purl.obolibrary.org/obo/NCBITaxon_9305
4330||6314||Free sialic acid storage disease, infantile form||http://www.orpha.net/ORDO/Orphanet_309324
4331||5502||Xanthomonas oryzae pv. oryzae PXO99A||http://purl.obolibrary.org/obo/NCBITaxon_360094
4332||5502||Helicobacter hepaticus||http://purl.obolibrary.org/obo/NCBITaxon_32025
4333||7248||Roifman syndrome||http://www.orpha.net/ORDO/Orphanet_353298
4334||6573||analyte role||http://purl.obolibrary.org/obo/OBI_0000275
4335||15538||protocol||http://purl.obolibrary.org/obo/OBI_0000272
4336||1826||Elodea nuttallii||http://purl.obolibrary.org/obo/NCBITaxon_55313
4337||5984||Encephaloclastic disorder||http://www.orpha.net/ORDO/Orphanet_269190
4338||6473||cyclooxygenase 2 inhibitor||http://purl.obolibrary.org/obo/CHEBI_50629
4339||8684||Rubinstein-Taybi syndrome due to 16p13.3 microdeletion||http://www.orpha.net/ORDO/Orphanet_353281
4340||8684||Rubinstein-Taybi syndrome due to EP300 haploinsufficiency||http://www.orpha.net/ORDO/Orphanet_353284
4341||1022||Dreissena polymorpha||http://purl.obolibrary.org/obo/NCBITaxon_45954
4342||6473||cyclooxygenase 1 inhibitor||http://purl.obolibrary.org/obo/CHEBI_50630
4343||10230||Naxos disease||http://www.orpha.net/ORDO/Orphanet_34217
4344||10577||Disorder of protein N-glycosylation||http://www.orpha.net/ORDO/Orphanet_309347
4345||10994||polychlorinated biphenyls||http://purl.obolibrary.org/obo/CHEBI_35446
4346||799||antinematodal drug||http://purl.obolibrary.org/obo/CHEBI_35444
4347||14970||serum dimethylarginine measurement||http://www.ebi.ac.uk/efo/EFO_0005418
4348||14970||contrast sensitivity measurement||http://www.ebi.ac.uk/efo/EFO_0005419
4349||11618||airway hyperresponsiveness||http://www.ebi.ac.uk/efo/EFO_0005414
4350||14970||serum alpha-1-antitrypsin measurement||http://www.ebi.ac.uk/efo/EFO_0005415
4351||14970||serum ST2 measurement||http://www.ebi.ac.uk/efo/EFO_0005416
4353||10994||cocaine||http://purl.obolibrary.org/obo/CHEBI_27958
4352||4430||folic acid reductase inhibitor||http://purl.obolibrary.org/obo/CHEBI_50683
4354||12747||response to mTOR inhibitor||http://www.ebi.ac.uk/efo/EFO_0005417
4355||1814||tooth agenesis||http://www.ebi.ac.uk/efo/EFO_0005410
4356||4139||Alacrimia-choreoathetosis-liver dysfunction syndrome||http://www.orpha.net/ORDO/Orphanet_404454
4357||2102||schizoaffective disorder||http://www.ebi.ac.uk/efo/EFO_0005411
4358||14970||functional impairment measurement||http://www.ebi.ac.uk/efo/EFO_0005412
4359||14970||joint damage measurement||http://www.ebi.ac.uk/efo/EFO_0005413
4360||2252||FBLN1-related developmental delay-central nervous system anomaly-syndactyly syndrome||http://www.orpha.net/ORDO/Orphanet_404451
4361||11618||borderline personality disorder symptom||http://www.ebi.ac.uk/efo/EFO_0005429
4364||4366||social communication impairment||http://www.ebi.ac.uk/efo/EFO_0005427
4362||2252||ADNP-related multiple congenital anomalies-intellectual disability-autism spectrum disorder||http://www.orpha.net/ORDO/Orphanet_404448
4363||10994||minocycline||http://purl.obolibrary.org/obo/CHEBI_50694
4365||2102||language impairment||http://www.ebi.ac.uk/efo/EFO_0005425
4366||11618||autism spectrum disorder symptom||http://www.ebi.ac.uk/efo/EFO_0005426
4367||8261||adolescent idiopathic scoliosis||http://www.ebi.ac.uk/efo/EFO_0005423
4368||2102||dyslexia||http://www.ebi.ac.uk/efo/EFO_0005424
4369||14970||serum homoarginine measurement||http://www.ebi.ac.uk/efo/EFO_0005421
4370||2827||skin aging||http://www.ebi.ac.uk/efo/EFO_0005422
4371||2252||Tall stature-intellectual disability-facial dysmorphism syndrome||http://www.orpha.net/ORDO/Orphanet_404443
4372||2252||Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency||http://www.orpha.net/ORDO/Orphanet_404440
4373||14970||grey matter volume measurement||http://www.ebi.ac.uk/efo/EFO_0005420
4374||5502||Staphylococcus aureus subsp. aureus MRSA252||http://purl.obolibrary.org/obo/NCBITaxon_282458
4375||5502||Staphylococcus aureus subsp. aureus MSSA476||http://purl.obolibrary.org/obo/NCBITaxon_282459
4376||10994||mercaptopurine||http://purl.obolibrary.org/obo/CHEBI_50667
4377||799||antidepressant||http://purl.obolibrary.org/obo/CHEBI_35469
4379||4401||array control genomic DNA||http://www.ebi.ac.uk/efo/EFO_0005436
4378||6928||Distal hereditary motor neuropathy type 7||http://www.orpha.net/ORDO/Orphanet_139589
4380||4401||array control hybridization quality||http://www.ebi.ac.uk/efo/EFO_0005437
4381||760||Diffuse cerebral and cerebellar atrophy-intractable seizures-progressive microcephaly syndrome||http://www.orpha.net/ORDO/Orphanet_404437
4382||4401||array control label||http://www.ebi.ac.uk/efo/EFO_0005438
4383||4401||array control reporter size||http://www.ebi.ac.uk/efo/EFO_0005439
4384||3068||nicotine use||http://www.ebi.ac.uk/efo/EFO_0005430
4385||6889||X-linked hereditary sensory and autonomic neuropathy with deafness||http://www.orpha.net/ORDO/Orphanet_139583
4386||3068||illegal drug consumption||http://www.ebi.ac.uk/efo/EFO_0005431
4387||3068||non-substance related disinhibited behaviour||http://www.ebi.ac.uk/efo/EFO_0005432
4388||4401||array control biosequence||http://www.ebi.ac.uk/efo/EFO_0005433
4389||4401||array control buffer||http://www.ebi.ac.uk/efo/EFO_0005434
4390||4401||array control empty||http://www.ebi.ac.uk/efo/EFO_0005435
4391||10994||1-naphthyl isothiocyanate||http://purl.obolibrary.org/obo/CHEBI_35455
4392||8191||cadmium dichloride||http://purl.obolibrary.org/obo/CHEBI_35456
4393||799||angiotensin-converting enzyme inhibitor||http://purl.obolibrary.org/obo/CHEBI_35457
4394||6036||chlorosome||http://purl.obolibrary.org/obo/GO_0046858
4395||770||PEO6||http://www.ebi.ac.uk/efo/EFO_0005449
4396||10994||methimazole||http://purl.obolibrary.org/obo/CHEBI_50673
4397||770||PEO23||http://www.ebi.ac.uk/efo/EFO_0005447
4398||770||PEO4||http://www.ebi.ac.uk/efo/EFO_0005448
4399||770||DU 145||http://www.ebi.ac.uk/efo/EFO_0005441
4400||770||OVCAR4||http://www.ebi.ac.uk/efo/EFO_0005442
4401||69||array control design||http://www.ebi.ac.uk/efo/EFO_0005440
4402||770||PEO1||http://www.ebi.ac.uk/efo/EFO_0005445
4403||770||PEO14||http://www.ebi.ac.uk/efo/EFO_0005446
4404||770||OVCAR5||http://www.ebi.ac.uk/efo/EFO_0005443
4405||770||OVCAR8||http://www.ebi.ac.uk/efo/EFO_0005444
4406||1024||Rare hemorrhagic disorder due to a constitutional thrombocytopenia||http://www.orpha.net/ORDO/Orphanet_275729
4407||799||non-narcotic analgesic||http://purl.obolibrary.org/obo/CHEBI_35481
4408||1022||Eubalaena glacialis||http://purl.obolibrary.org/obo/NCBITaxon_27606
4409||4424||Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to KIAA0226 deficiency||http://www.orpha.net/ORDO/Orphanet_404499
4410||4424||Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to TUD deficiency||http://www.orpha.net/ORDO/Orphanet_404493
4411||10994||3-methylbenzyl alcohol||http://purl.obolibrary.org/obo/CHEBI_27995
4412||4430||vitamin||http://purl.obolibrary.org/obo/CHEBI_33229
4413||10994||tolbutamide||http://purl.obolibrary.org/obo/CHEBI_27999
4414||2063||abnormality of the central nervous system||http://purl.obolibrary.org/obo/HP_0000707
4415||799||antipsychotic drug||http://purl.obolibrary.org/obo/CHEBI_35476
4416||10994||bisphenol A||http://purl.obolibrary.org/obo/CHEBI_33216
4418||508||jasmonic acid||http://purl.obolibrary.org/obo/CHEBI_18292
4417||799||non-steroidal anti-inflammatory drug||http://purl.obolibrary.org/obo/CHEBI_35475
4420||10994||17alpha-estradiol||http://purl.obolibrary.org/obo/CHEBI_17160
4419||799||antimanic drug||http://purl.obolibrary.org/obo/CHEBI_35477
4421||799||anti-inflammatory drug||http://purl.obolibrary.org/obo/CHEBI_35472
4422||10994||methyl glyoxal||http://purl.obolibrary.org/obo/CHEBI_17158
4423||1839||Autosomal recessive dopa-responsive dystonia||http://www.orpha.net/ORDO/Orphanet_101150
4424||762||Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome||http://www.orpha.net/ORDO/Orphanet_404481
4425||2252||Severe intellectual disability-progressive spastic diplegia syndrome||http://www.orpha.net/ORDO/Orphanet_404473
4426||4812||Global developmental delay-lung cysts-overgrowth-Wilms tumor syndrome||http://www.orpha.net/ORDO/Orphanet_404476
4427||5715||protein metabolic process||http://purl.obolibrary.org/obo/GO_0019538
4428||10994||sulindac||http://purl.obolibrary.org/obo/CHEBI_9352
4429||799||antipyretic||http://purl.obolibrary.org/obo/CHEBI_35493
4430||6573||biological role||http://purl.obolibrary.org/obo/CHEBI_24432
4431||1125||chemical entity||http://purl.obolibrary.org/obo/CHEBI_24431
4432||4705||Multisystemic smooth muscle dysfunction syndrome||http://www.orpha.net/ORDO/Orphanet_404463
4433||6476||response to low sodium diet||http://www.ebi.ac.uk/efo/EFO_0005402
4434||4439||Female infertility due to zona pellucida defect||http://www.orpha.net/ORDO/Orphanet_404466
4435||6476||response to high sodium diet||http://www.ebi.ac.uk/efo/EFO_0005401
4436||1391||chemotherapy-induced alopecia||http://www.ebi.ac.uk/efo/EFO_0005400
4437||8840||colorectal adenoma||http://www.ebi.ac.uk/efo/EFO_0005406
4438||4259||response to antihypertensive drug||http://www.ebi.ac.uk/efo/EFO_0005405
4439||12014||Female infertility due to fertilization defect||http://www.orpha.net/ORDO/Orphanet_404469
4440||6476||response to cold pressor test||http://www.ebi.ac.uk/efo/EFO_0005404
4441||6476||response to dietary potassium supplementation||http://www.ebi.ac.uk/efo/EFO_0005403
4442||5502||Bifidobacterium longum||http://purl.obolibrary.org/obo/NCBITaxon_216816
4443||8579||fat body mass||http://www.ebi.ac.uk/efo/EFO_0005409
4444||14602||pyroglutamine measurement||http://www.ebi.ac.uk/efo/EFO_0005408
4445||2102||psychosis||http://www.ebi.ac.uk/efo/EFO_0005407
4446||6928||Distal hereditary motor neuropathy type 5||http://www.orpha.net/ORDO/Orphanet_139536
4447||770||HuH-7||http://www.ebi.ac.uk/efo/EFO_0005384
4448||770||IGROV-1||http://www.ebi.ac.uk/efo/EFO_0005385
4449||15574||Sickle cell disease and related diseases||http://www.orpha.net/ORDO/Orphanet_275752
4450||770||INA-6||http://www.ebi.ac.uk/efo/EFO_0005386
4451||770||JeKo-1||http://www.ebi.ac.uk/efo/EFO_0005387
4452||770||JIMT-1||http://www.ebi.ac.uk/efo/EFO_0005388
4453||770||KARPAS 231||http://www.ebi.ac.uk/efo/EFO_0005389
4454||4431||element||http://purl.obolibrary.org/obo/CHEBI_33250
4455||770||KARPAS 299||http://www.ebi.ac.uk/efo/EFO_0005390
4456||770||LAPC-4||http://www.ebi.ac.uk/efo/EFO_0005392
4457||770||LA-N-1||http://www.ebi.ac.uk/efo/EFO_0005391
4458||770||MLO-Y4||http://www.ebi.ac.uk/efo/EFO_0005394
4459||770||LAPC-9||http://www.ebi.ac.uk/efo/EFO_0005393
4460||6928||Distal hereditary motor neuropathy type 2||http://www.orpha.net/ORDO/Orphanet_139525
4461||10994||sulfasalazine||http://purl.obolibrary.org/obo/CHEBI_9334
4462||770||HCC2935||http://www.ebi.ac.uk/efo/EFO_0005375
4463||770||UACC-257||http://www.ebi.ac.uk/efo/EFO_0005376
4464||1754||Lysosomal acid lipase deficiency||http://www.orpha.net/ORDO/Orphanet_275761
4465||770||HCC1806||http://www.ebi.ac.uk/efo/EFO_0005373
4466||770||HCC227||http://www.ebi.ac.uk/efo/EFO_0005374
4467||770||UACC-62||http://www.ebi.ac.uk/efo/EFO_0005377
4468||5502||Salmonella enterica subsp. enterica serovar Emek||http://purl.obolibrary.org/obo/NCBITaxon_286784
4469||770||HMEC1||http://www.ebi.ac.uk/efo/EFO_0005383
4470||770||HepG3||http://www.ebi.ac.uk/efo/EFO_0005382
4471||8146||Idiopathic pulmonary arterial hypertension||http://www.orpha.net/ORDO/Orphanet_275766
4472||3148||Sex chromosome disorder of sex development||http://www.orpha.net/ORDO/Orphanet_325546
4473||2999||Charcot-Marie-Tooth disease type 4J||http://www.orpha.net/ORDO/Orphanet_139515
4474||6928||Distal hereditary motor neuropathy type 1||http://www.orpha.net/ORDO/Orphanet_139518
4475||5700||Neuropathy with hearing impairment||http://www.orpha.net/ORDO/Orphanet_139512
4476||12319||hyperosmotic salinity response||http://purl.obolibrary.org/obo/GO_0042538
4478||1826||Bruguiera gymnorhiza||http://purl.obolibrary.org/obo/NCBITaxon_39984
4477||1024||Rare hemorrhagic disorder due to a platelet receptor defect||http://www.orpha.net/ORDO/Orphanet_275736
4479||6310||Hb Bart s hydrops fetalis||http://www.orpha.net/ORDO/Orphanet_163596
4480||266||African iron overload||http://www.orpha.net/ORDO/Orphanet_139507
4481||5534||Non-classic congenital lipoid adrenal hyperplasia due to STAR deficency||http://www.orpha.net/ORDO/Orphanet_325529
4482||4483||high content analysis of cells by morphological and physical properties||http://www.ebi.ac.uk/efo/EFO_0005399
4483||13883||high content analysis of cells||http://www.ebi.ac.uk/efo/EFO_0005397
4484||1732||Genetic infertility||http://www.orpha.net/ORDO/Orphanet_275742
4485||4483||high content analysis of cells by molecular content||http://www.ebi.ac.uk/efo/EFO_0005398
4486||770||MUTZ-3||http://www.ebi.ac.uk/efo/EFO_0005395
4487||13297||exome sequencing||http://www.ebi.ac.uk/efo/EFO_0005396
4488||15574||Alpha-thalassemia and related diseases||http://www.orpha.net/ORDO/Orphanet_275745
4489||1813||nutrient||http://purl.obolibrary.org/obo/CHEBI_33284
4490||15574||Beta-thalassemia and related diseases||http://www.orpha.net/ORDO/Orphanet_275749
4491||6573||agrochemical role||http://purl.obolibrary.org/obo/CHEBI_33286
4492||4491||fertilizer||http://purl.obolibrary.org/obo/CHEBI_33287
4493||7008||Classic congenital lipoid adrenal hyperplasia due to STAR deficency||http://www.orpha.net/ORDO/Orphanet_325524
4494||770||GM12868||http://www.ebi.ac.uk/efo/EFO_0005341
4495||4499||glucose homeostasis||http://purl.obolibrary.org/obo/GO_0042593
4496||770||GM12867||http://www.ebi.ac.uk/efo/EFO_0005340
4497||770||GM12870||http://www.ebi.ac.uk/efo/EFO_0005343
4498||770||GM12869||http://www.ebi.ac.uk/efo/EFO_0005342
4499||5295||homeostatic process||http://purl.obolibrary.org/obo/GO_0042592
4500||770||GM13976||http://www.ebi.ac.uk/efo/EFO_0005345
4501||6900||Hereditary sensory and autonomic neuropathy with deafness and global delay||http://www.orpha.net/ORDO/Orphanet_139573
4502||770||GM12871||http://www.ebi.ac.uk/efo/EFO_0005344
4503||770||GM15510||http://www.ebi.ac.uk/efo/EFO_0005347
4504||770||GM13977||http://www.ebi.ac.uk/efo/EFO_0005346
4505||770||GM18951||http://www.ebi.ac.uk/efo/EFO_0005349
4506||770||GM18526||http://www.ebi.ac.uk/efo/EFO_0005348
4507||6900||Hereditary sensory and autonomic neuropathy with spastic paraplegia||http://www.orpha.net/ORDO/Orphanet_139578
4508||1826||Volvox carteri||http://purl.obolibrary.org/obo/NCBITaxon_3067
4509||2454||Acute hepatic porphyria||http://www.orpha.net/ORDO/Orphanet_95157
4510||4575||Hepatoerythropoietic porphyria||http://www.orpha.net/ORDO/Orphanet_95159
4511||5502||Xylella fastidiosa Temecula1||http://purl.obolibrary.org/obo/NCBITaxon_183190
4512||5346||46,XY disorder of sex development due to cholesterol synthesis defect||http://www.orpha.net/ORDO/Orphanet_325511
4513||4142||Congenital hypogonadotropic hypogonadism||http://www.orpha.net/ORDO/Orphanet_174590
4514||770||GM19099||http://www.ebi.ac.uk/efo/EFO_0005350
4515||770||GM18505||http://www.ebi.ac.uk/efo/EFO_0005332
4517||770||GM10847||http://www.ebi.ac.uk/efo/EFO_0005336
4516||6888||Hereditary sensory and autonomic neuropathy type 1B||http://www.orpha.net/ORDO/Orphanet_139564
4518||770||GM10266||http://www.ebi.ac.uk/efo/EFO_0005335
4519||770||GM10248||http://www.ebi.ac.uk/efo/EFO_0005334
4520||770||GM08714||http://www.ebi.ac.uk/efo/EFO_0005333
4521||10994||L-proline||http://purl.obolibrary.org/obo/CHEBI_17203
4522||770||GM12866||http://www.ebi.ac.uk/efo/EFO_0005339
4523||770||GM12865||http://www.ebi.ac.uk/efo/EFO_0005338
4524||770||GM12864||http://www.ebi.ac.uk/efo/EFO_0005337
4525||1826||Chlamydomonas reinhardtii||http://purl.obolibrary.org/obo/NCBITaxon_3055
4526||4259||response to interferon beta||http://purl.obolibrary.org/obo/GO_0035456
4527||4139||Spondylocostal dysostosis - anal and genitourinary malformations||http://www.orpha.net/ORDO/Orphanet_94095
4528||7114||Pseudohypoparathyroidism type 2||http://www.orpha.net/ORDO/Orphanet_94090
4529||770||CCD-8Lu||http://www.ebi.ac.uk/efo/EFO_0005367
4531||770||CCD-33Lu||http://www.ebi.ac.uk/efo/EFO_0005366
4530||6930||Distal hereditary motor neuropathy, Jerash type||http://www.orpha.net/ORDO/Orphanet_139552
4532||770||Granta-519||http://www.ebi.ac.uk/efo/EFO_0005369
4533||770||HFL1||http://www.ebi.ac.uk/efo/EFO_0005368
4534||770||CCD-19Lu||http://www.ebi.ac.uk/efo/EFO_0005363
4535||770||CCD-16Lu||http://www.ebi.ac.uk/efo/EFO_0005362
4536||770||CCD-29Lu||http://www.ebi.ac.uk/efo/EFO_0005365
4537||770||CCD-25Lu||http://www.ebi.ac.uk/efo/EFO_0005364
4539||2380||X-linked distal spinal muscular atrophy||http://www.orpha.net/ORDO/Orphanet_139557
4538||10994||tetracycline||http://purl.obolibrary.org/obo/CHEBI_27902
4540||4810||Hereditary renal hypouricemia||http://www.orpha.net/ORDO/Orphanet_94088
4541||6305||Blue diaper syndrome||http://www.orpha.net/ORDO/Orphanet_94086
4542||7114||Pseudohypoparathyroidism type 1B||http://www.orpha.net/ORDO/Orphanet_94089
4543||770||HCC2998||http://www.ebi.ac.uk/efo/EFO_0005370
4544||8146||Heritable pulmonary arterial hypertension||http://www.orpha.net/ORDO/Orphanet_275777
4545||770||HCC1195||http://www.ebi.ac.uk/efo/EFO_0005371
4546||770||HCC1419||http://www.ebi.ac.uk/efo/EFO_0005372
4547||4736||Partington syndrome||http://www.orpha.net/ORDO/Orphanet_94083
4548||770||CAL51||http://www.ebi.ac.uk/efo/EFO_0005358
4549||770||CAL148||http://www.ebi.ac.uk/efo/EFO_0005357
4550||770||CAL120||http://www.ebi.ac.uk/efo/EFO_0005356
4551||770||HUES1||http://www.ebi.ac.uk/efo/EFO_0005355
4552||11067||milligram per kilogram body weight||http://www.ebi.ac.uk/efo/EFO_0005354
4553||770||GM12801||http://www.ebi.ac.uk/efo/EFO_0005353
4554||770||GM20000||http://www.ebi.ac.uk/efo/EFO_0005352
4555||770||GM19193||http://www.ebi.ac.uk/efo/EFO_0005351
4556||6930||Distal spinal muscular atrophy type 3||http://www.orpha.net/ORDO/Orphanet_139547
4557||5502||Shigella flexneri 2a str. 301||http://purl.obolibrary.org/obo/NCBITaxon_198214
4558||770||CAL851||http://www.ebi.ac.uk/efo/EFO_0005359
4559||770||CCD-11Lu||http://www.ebi.ac.uk/efo/EFO_0005360
4560||770||CCD-13Lu||http://www.ebi.ac.uk/efo/EFO_0005361
4561||11802||Coronary artery disease - hyperlipidemia - hypertension - diabetes - osteoporosis||http://www.orpha.net/ORDO/Orphanet_94062
4562||201||Macrocephaly - immune deficiency - anemia||http://www.orpha.net/ORDO/Orphanet_94061
4563||7981||Spondyloepiphyseal dysplasia congenita||http://www.orpha.net/ORDO/Orphanet_94068
4564||1591||Deafness-infertility syndrome||http://www.orpha.net/ORDO/Orphanet_94064
4565||4139||12q14 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_94063
4566||2252||Severe intellectual disability - epilepsy - anal anomalies - distal phalangeal hypoplasia||http://www.orpha.net/ORDO/Orphanet_94066
4567||2252||15q24 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_94065
4568||12407||Multiple acyl-CoA dehydrogenation deficiency, severe neonatal type||http://www.orpha.net/ORDO/Orphanet_394529
4569||13735||Humero-ulnar synostosis||http://www.orpha.net/ORDO/Orphanet_94056
4570||12407||Multiple acyl-CoA dehydrogenation deficiency, mild type||http://www.orpha.net/ORDO/Orphanet_394532
4571||1125||population||http://purl.obolibrary.org/obo/OBI_0000181
4572||1247||Rare hereditary thrombophilia||http://www.orpha.net/ORDO/Orphanet_217454
4573||9940||intracellular region of host||http://purl.obolibrary.org/obo/GO_0043656
4574||1537||extracellular space of host||http://purl.obolibrary.org/obo/GO_0043655
4575||8566||Chronic hepatic porphyria||http://www.orpha.net/ORDO/Orphanet_95161
4576||6004||host cell||http://purl.obolibrary.org/obo/GO_0043657
4577||5838||has extra parts of type||http://purl.obolibrary.org/obo/PATO_0002002
4578||4572||Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency||http://www.orpha.net/ORDO/Orphanet_217467
4579||970||Hereditary breast cancer||http://www.orpha.net/ORDO/Orphanet_227535
4580||5170||Pyruvate carboxylase deficiency, infantile form||http://www.orpha.net/ORDO/Orphanet_353308
4581||5502||Staphylococcus lentus||http://purl.obolibrary.org/obo/NCBITaxon_42858
4582||10994||cefuroxime||http://purl.obolibrary.org/obo/CHEBI_3515
4583||321||Hereditary hypotrichosis with recurrent skin vesicles||http://www.orpha.net/ORDO/Orphanet_217407
4584||5170||Pyruvate carboxylase deficiency, severe neonatal type||http://www.orpha.net/ORDO/Orphanet_353314
4585||5502||Lactobacillus casei str. Zhang||http://purl.obolibrary.org/obo/NCBITaxon_498216
4587||770||GM06944||http://purl.obolibrary.org/obo/CLO_0036460
4586||5025||Aspergillus multicolor||http://purl.obolibrary.org/obo/NCBITaxon_41759
4588||4344||Congenital myasthenic syndromes with glycosylation defect||http://www.orpha.net/ORDO/Orphanet_353327
4590||15||Torsade-de-pointes syndrome with short coupling interval||http://www.orpha.net/ORDO/Orphanet_51084
4589||1022||Ornithorhynchus anatinus||http://purl.obolibrary.org/obo/NCBITaxon_9258
4591||15||Familial short QT syndrome||http://www.orpha.net/ORDO/Orphanet_51083
4592||5502||Ureaplasma parvum||http://purl.obolibrary.org/obo/NCBITaxon_134821
4593||5170||Pyruvate carboxylase deficiency, benign type||http://www.orpha.net/ORDO/Orphanet_353320
4594||1022||Tachyglossus aculeatus||http://purl.obolibrary.org/obo/NCBITaxon_9261
4595||6293||Tay-Sachs disease, B1 variant||http://www.orpha.net/ORDO/Orphanet_309239
4596||5502||Collinsella||http://purl.obolibrary.org/obo/NCBITaxon_102106
4597||8147||Autosomal recessive secondary polycythemia not associated with VHL gene||http://www.orpha.net/ORDO/Orphanet_247378
4598||8190||(9R,13R)-12-oxo-phytodienoic acid||http://purl.obolibrary.org/obo/CHEBI_34005
4599||1532||membrane raft||http://purl.obolibrary.org/obo/GO_0045121
4600||1022||Gephyrocapsa oceanica||http://purl.obolibrary.org/obo/NCBITaxon_38817
4601||5985||Erythrokeratoderma variabilis progressiva||http://www.orpha.net/ORDO/Orphanet_308166
4602||4424||Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to WWOX deficiency||http://www.orpha.net/ORDO/Orphanet_284282
4603||14145||Adult-onset autosomal recessive cerebellar ataxia||http://www.orpha.net/ORDO/Orphanet_284289
4604||5025||Magnaporthe oryzae||http://purl.obolibrary.org/obo/NCBITaxon_318829
4605||6573||surfactant role||http://purl.obolibrary.org/obo/CHEBI_35195
4606||325||Generalized pustular psoriasis||http://www.orpha.net/ORDO/Orphanet_247353
4607||10994||1,4-dithiothreitol||http://purl.obolibrary.org/obo/CHEBI_18320
4608||5502||Pseudomonas syringae pv. tomato str. DC3000||http://purl.obolibrary.org/obo/NCBITaxon_223283
4609||4027||steroid hormone||http://purl.obolibrary.org/obo/CHEBI_26764
4610||8191||zinc sulfate||http://purl.obolibrary.org/obo/CHEBI_35176
4611||1826||Ophrys fusca||http://purl.obolibrary.org/obo/NCBITaxon_145942
4612||1022||Callithrix jacchus||http://purl.obolibrary.org/obo/NCBITaxon_9483
4613||8001||Metaphyseal chondrodysplasia, Jansen type||http://www.orpha.net/ORDO/Orphanet_33067
4614||4713||Dravet syndrome||http://www.orpha.net/ORDO/Orphanet_33069
4615||3683||establishment of protein localization||http://purl.obolibrary.org/obo/GO_0045184
4616||3341||Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures||http://www.orpha.net/ORDO/Orphanet_209341
4617||4262||p-value||http://purl.obolibrary.org/obo/OBI_0001442
4618||8035||Adult-onset proximal spinal muscular atrophy, autosomal dominant||http://www.orpha.net/ORDO/Orphanet_209335
4619||5502||Collimonas||http://purl.obolibrary.org/obo/NCBITaxon_202907
4620||2997||Autosomal dominant Charcot-Marie-Tooth disease type 2O||http://www.orpha.net/ORDO/Orphanet_284232
4621||5129||Medullar aplasia||http://www.orpha.net/ORDO/Orphanet_182040
4622||5502||Listeria monocytogenes EGD-e||http://purl.obolibrary.org/obo/NCBITaxon_169963
4623||5502||Salmonella enterica subsp. enterica serovar Typhi str. Ty2||http://purl.obolibrary.org/obo/NCBITaxon_209261
4624||5129||Rare constitutional hemolytic anemia||http://www.orpha.net/ORDO/Orphanet_182043
4625||1826||Ginkgo biloba||http://purl.obolibrary.org/obo/NCBITaxon_3311
4626||1826||Picea glauca||http://purl.obolibrary.org/obo/NCBITaxon_3330
4627||2366||organophosphate metabolic process||http://purl.obolibrary.org/obo/GO_0019637
4628||426||MYH9-related disease||http://www.orpha.net/ORDO/Orphanet_182050
4629||1732||Rare genetic vascular disease||http://www.orpha.net/ORDO/Orphanet_233655
4630||1826||Picea abies||http://purl.obolibrary.org/obo/NCBITaxon_3329
4631||5700||Autosomal dominant cerebellar ataxia, deafness and narcolepsy||http://www.orpha.net/ORDO/Orphanet_314404
4632||1826||Larix laricina||http://purl.obolibrary.org/obo/NCBITaxon_3326
4633||6202||Silver-Russell syndrome due to a point mutation||http://www.orpha.net/ORDO/Orphanet_397590
4635||762||Severe neonatal-onset encephalopathy with microcephaly||http://www.orpha.net/ORDO/Orphanet_209370
4634||799||parasympatholytic||http://purl.obolibrary.org/obo/CHEBI_50370
4636||6595||Sialidosis||http://www.orpha.net/ORDO/Orphanet_309294
4637||5025||Dactylellina haptotyla||http://purl.obolibrary.org/obo/NCBITaxon_430498
4638||4987||Severe neonatal lactic acidosis due to NFS1-ISD11 complex deficiency||http://www.orpha.net/ORDO/Orphanet_397593
4639||8814||Mucopolysaccharidosis type 4A||http://www.orpha.net/ORDO/Orphanet_309297
4640||238||Activated PIK3-delta syndrome||http://www.orpha.net/ORDO/Orphanet_397596
4641||2496||Alpha-mannosidosis, adult form||http://www.orpha.net/ORDO/Orphanet_309288
4642||1826||Picea sitchensis||http://purl.obolibrary.org/obo/NCBITaxon_3332
4644||1826||Picea mariana||http://purl.obolibrary.org/obo/NCBITaxon_3335
4643||10994||salmeterol||http://purl.obolibrary.org/obo/CHEBI_9011
4645||2496||Alpha-mannosidosis, infantile form||http://www.orpha.net/ORDO/Orphanet_309282
4646||2364||ribose phosphate metabolic process||http://purl.obolibrary.org/obo/GO_0019693
4647||10994||cytochalasin D||http://purl.obolibrary.org/obo/CHEBI_529996
4648||1826||Pinus sylvestris||http://purl.obolibrary.org/obo/NCBITaxon_3349
4649||1826||Pinus strobus||http://purl.obolibrary.org/obo/NCBITaxon_3348
4650||1826||Pinus radiata||http://purl.obolibrary.org/obo/NCBITaxon_3347
4651||15572||Glycoproteinosis||http://www.orpha.net/ORDO/Orphanet_309279
4652||7377||Autosomal dominant medullary cystic kidney disease with or without hyperuricemia||http://www.orpha.net/ORDO/Orphanet_34149
4653||7501||Metachromatic leukodystrophy, adult form||http://www.orpha.net/ORDO/Orphanet_309271
4654||11827||Autosomal recessive cerebellar ataxia - psychomotor retardation||http://www.orpha.net/ORDO/Orphanet_284271
4655||4981||specimen with known storage state||http://purl.obolibrary.org/obo/OBI_0001472
4657||5478||Lymphedema - distichiasis||http://www.orpha.net/ORDO/Orphanet_33001
4656||5843||Formiminoglutamic aciduria||http://www.orpha.net/ORDO/Orphanet_51208
4658||7501||Metachromatic leukodystrophy, juvenile form||http://www.orpha.net/ORDO/Orphanet_309263
4659||238||Omenn syndrome||http://www.orpha.net/ORDO/Orphanet_39041
4660||9607||Familial retinal arterial macroaneurysm||http://www.orpha.net/ORDO/Orphanet_284247
4661||781||antibiotic||http://purl.obolibrary.org/obo/CHEBI_22582
4662||4256||Hereditary sensory and autonomic neuropathy type 1||http://www.orpha.net/ORDO/Orphanet_36386
4663||10272||Generalized epilepsy with febrile seizures-plus||http://www.orpha.net/ORDO/Orphanet_36387
4664||4705||Familial cervical artery dissections||http://www.orpha.net/ORDO/Orphanet_36382
4665||4705||Familial vascular leukoencephalopathy||http://www.orpha.net/ORDO/Orphanet_36383
4666||7501||Metachromatic leukodystrophy, late infantile form||http://www.orpha.net/ORDO/Orphanet_309256
4667||799||antiviral||http://purl.obolibrary.org/obo/CHEBI_22587
4668||6573||antioxidant||http://purl.obolibrary.org/obo/CHEBI_22586
4671||10994||antimycin A||http://purl.obolibrary.org/obo/CHEBI_22584
4670||2770||snRNA||http://purl.obolibrary.org/obo/SO_0000274
4669||5502||Burkholderia lata||http://purl.obolibrary.org/obo/NCBITaxon_482957
4672||7638||Atypical Gaucher disease due to saposin C deficiency||http://www.orpha.net/ORDO/Orphanet_309252
4673||10994||carbaryl||http://purl.obolibrary.org/obo/CHEBI_3390
4674||10994||carbamazepine||http://purl.obolibrary.org/obo/CHEBI_3387
4675||10994||captopril||http://purl.obolibrary.org/obo/CHEBI_3380
4676||5023||GM2-gangliosidosis, AB variant||http://www.orpha.net/ORDO/Orphanet_309246
4677||1022||Phytophthora infestans||http://purl.obolibrary.org/obo/NCBITaxon_4787
4678||5344||Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency||http://www.orpha.net/ORDO/Orphanet_95699
4679||4477||P2Y12 defect||http://www.orpha.net/ORDO/Orphanet_36355
4680||10994||carvacrol||http://purl.obolibrary.org/obo/CHEBI_3440
4681||4652||Autosomal dominant medullary cystic kidney disease with hyperuricemia||http://www.orpha.net/ORDO/Orphanet_88950
4682||14970||leptin measurement||http://www.ebi.ac.uk/efo/EFO_0005000
4683||14970||lysine measurement||http://www.ebi.ac.uk/efo/EFO_0005002
4684||14970||phenylalanine measurement||http://www.ebi.ac.uk/efo/EFO_0005001
4685||5502||Salmonella enterica subsp. enterica serovar Paratyphi A||http://purl.obolibrary.org/obo/NCBITaxon_54388
4686||5849||Distal monosomy 1q||http://www.orpha.net/ORDO/Orphanet_36367
4687||6610||Familial scaphocephaly syndrome||http://www.orpha.net/ORDO/Orphanet_169163
4688||6766||T-B  severe combined immunodeficiency due to CD3delta/CD3epsilon/CD3zeta||http://www.orpha.net/ORDO/Orphanet_169160
4689||4454||aluminium||http://purl.obolibrary.org/obo/CHEBI_28984
4690||1309||Growth delay due to insulin-like growth factor I resistance||http://www.orpha.net/ORDO/Orphanet_73273
4691||204||Immunodeficiency due to a late component of complements deficiency||http://www.orpha.net/ORDO/Orphanet_169150
4692||9918||Rare hereditary ataxia||http://www.orpha.net/ORDO/Orphanet_183518
4693||6766||T-B  severe combined immunodeficiency due to IL-7Ralpha deficiency||http://www.orpha.net/ORDO/Orphanet_169154
4694||6766||T-B  severe combined immunodeficiency due to CD45 deficiency||http://www.orpha.net/ORDO/Orphanet_169157
4695||9918||Rare genetic medullar disease||http://www.orpha.net/ORDO/Orphanet_183515
4696||9918||Rare genetic epilepsy||http://www.orpha.net/ORDO/Orphanet_183512
4697||4477||Bleeding diathesis due to a collagen receptor defect||http://www.orpha.net/ORDO/Orphanet_73271
4698||1309||Growth delay due to insulin-like growth factor type 1 deficiency||http://www.orpha.net/ORDO/Orphanet_73272
4699||6930||Young adult-onset distal hereditary motor neuropathy||http://www.orpha.net/ORDO/Orphanet_314485
4700||9918||Rare genetic headache||http://www.orpha.net/ORDO/Orphanet_183509
4701||15257||Syndromic obesity||http://www.orpha.net/ORDO/Orphanet_240371
4702||4717||Genetic central nervous system malformation||http://www.orpha.net/ORDO/Orphanet_183506
4703||5191||Recurrent infection due to specific granule deficiency||http://www.orpha.net/ORDO/Orphanet_169142
4704||204||Immunodeficiency due to an early component of complement deficiency||http://www.orpha.net/ORDO/Orphanet_169147
4705||9918||Genetic central nervous system and retinal vascular disease||http://www.orpha.net/ORDO/Orphanet_183503
4706||9918||Genetic neurodegenerative disease||http://www.orpha.net/ORDO/Orphanet_183500
4707||2498||X-linked Alport syndrome||http://www.orpha.net/ORDO/Orphanet_88917
4708||2498||Autosomal dominant Alport syndrome||http://www.orpha.net/ORDO/Orphanet_88918
4709||2498||Autosomal recessive Alport syndrome||http://www.orpha.net/ORDO/Orphanet_88919
4710||8918||454 GS 20 standard manufacturer s protocol||http://www.ebi.ac.uk/efo/EFO_0005051
4711||14970||internal carotid intimal medial thickness||http://www.ebi.ac.uk/efo/EFO_0005053
4712||14970||nervous system measurement||http://www.ebi.ac.uk/efo/EFO_0005052
4713||762||Channelopathy with epilepsy||http://www.orpha.net/ORDO/Orphanet_182083
4714||8190||hypochlorous acid||http://purl.obolibrary.org/obo/CHEBI_24757
4715||4717||Genetic multiple congenital anomalies/dysmorphic syndrome||http://www.orpha.net/ORDO/Orphanet_183533
4716||7330||erythrocyte measurement||http://www.ebi.ac.uk/efo/EFO_0005047
4717||1732||Rare genetic developmental defect during embryogenesis||http://www.orpha.net/ORDO/Orphanet_183530
4718||14970||cardiac troponin T measurement||http://www.ebi.ac.uk/efo/EFO_0005043
4720||12151||Leishmaniasis||http://www.ebi.ac.uk/efo/EFO_0005044
4719||4717||Genetic congenital limb malformation||http://www.orpha.net/ORDO/Orphanet_183536
4721||4720||visceral Leishmaniasis||http://www.ebi.ac.uk/efo/EFO_0005045
4722||4720||cutaneous Leishmaniasis||http://www.ebi.ac.uk/efo/EFO_0005046
4723||4717||Genetic renal or urinary tract malformation||http://www.orpha.net/ORDO/Orphanet_183539
4724||3750||topoisomerase I inhibitor||http://purl.obolibrary.org/obo/CHEBI_50276
4725||7377||Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis||http://www.orpha.net/ORDO/Orphanet_88924
4726||10652||obsolete_response to temozolomide||http://www.ebi.ac.uk/efo/EFO_0005040
4727||11899||Syndromic neurometabolic disease with X-linked intellectual disability||http://www.orpha.net/ORDO/Orphanet_182076
4728||4139||Syndromic neurometabolic disease with non-X-linked intellectual disability||http://www.orpha.net/ORDO/Orphanet_182073
4729||2063||hair morphology||http://www.ebi.ac.uk/efo/EFO_0005038
4730||1391||hippocampal atrophy||http://www.ebi.ac.uk/efo/EFO_0005039
4731||14970||platelet measurement||http://www.ebi.ac.uk/efo/EFO_0005036
4733||14970||aortic root size||http://www.ebi.ac.uk/efo/EFO_0005037
4732||9918||Rare genetic movement disorder||http://www.orpha.net/ORDO/Orphanet_183521
4735||1788||anti-CTCF||http://www.ebi.ac.uk/efo/EFO_0005034
4734||1732||Rare genetic bone disease||http://www.orpha.net/ORDO/Orphanet_183524
4737||14970||hippocampal volume||http://www.ebi.ac.uk/efo/EFO_0005035
4736||762||ARX-related epileptic encephalopathy||http://www.orpha.net/ORDO/Orphanet_182079
4738||13883||IP-seq||http://www.ebi.ac.uk/efo/EFO_0005032
4739||13883||RIP||http://www.ebi.ac.uk/efo/EFO_0005033
4740||15363||Genetic bone tumor||http://www.orpha.net/ORDO/Orphanet_183527
4741||6573||prodrug role||http://purl.obolibrary.org/obo/CHEBI_50266
4742||8713||Pseudohypoaldosteronism type 2A||http://www.orpha.net/ORDO/Orphanet_88938
4743||8713||Pseudohypoaldosteronism type 2B||http://www.orpha.net/ORDO/Orphanet_88939
4744||1433||Lissencephaly due to LIS1 mutation||http://www.orpha.net/ORDO/Orphanet_95232
4745||5025||Eurotium chevalieri||http://purl.obolibrary.org/obo/NCBITaxon_41411
4746||1788||input DNA||http://www.ebi.ac.uk/efo/EFO_0005031
4747||1788||anti-IgG||http://www.ebi.ac.uk/efo/EFO_0005030
4748||4007||collection longitude||http://www.ebi.ac.uk/efo/EFO_0005021
4750||2415||Genetic developmental defect of the eye||http://www.orpha.net/ORDO/Orphanet_183557
4749||1483||adipose tissue derived mesenchymal stem cell||http://www.ebi.ac.uk/efo/EFO_0005023
4751||7549||placental pericyte||http://www.ebi.ac.uk/efo/EFO_0005024
4752||4717||Genetic respiratory or mediastinal malformation||http://www.orpha.net/ORDO/Orphanet_183554
4753||1788||anti-Bcl11a||http://www.ebi.ac.uk/efo/EFO_0005027
4754||1788||anti-H3K27-3Me||http://www.ebi.ac.uk/efo/EFO_0005028
4755||1788||anti-H3k4-3Me||http://www.ebi.ac.uk/efo/EFO_0005029
4756||8191||cadmium sulfate||http://purl.obolibrary.org/obo/CHEBI_50292
4757||10994||1,9-dideoxyforskolin||http://purl.obolibrary.org/obo/CHEBI_50295
4758||4652||Autosomal dominant medullary cystic kidney disease without hyperuricemia||http://www.orpha.net/ORDO/Orphanet_88949
4759||5502||Vibrio vulnificus CMCP6||http://purl.obolibrary.org/obo/NCBITaxon_216895
4760||4008||collection latitude||http://www.ebi.ac.uk/efo/EFO_0005020
4761||15511||dorsal closure stage||http://purl.obolibrary.org/obo/FBdv_00005331
4762||4717||Genetic digestive tract malformation||http://www.orpha.net/ORDO/Orphanet_183545
4763||4717||Genetic visceral malformation of the liver, biliary tract, pancreas or spleen||http://www.orpha.net/ORDO/Orphanet_183548
4764||8909||Autosomal dominant centronuclear myopathy||http://www.orpha.net/ORDO/Orphanet_169189
4765||4263||454 Sequencing||http://www.ebi.ac.uk/efo/EFO_0005016
4766||4717||Genetic cranial malformation||http://www.orpha.net/ORDO/Orphanet_183542
4767||2770||non polyA RNA||http://www.ebi.ac.uk/efo/EFO_0005017
4768||4767||long non poly RNA||http://www.ebi.ac.uk/efo/EFO_0005018
4769||10248||long poly A RNA||http://www.ebi.ac.uk/efo/EFO_0005019
4770||8713||Pseudohypoaldosteronism type 2C||http://www.orpha.net/ORDO/Orphanet_88940
4771||3745||Autosomal recessive centronuclear myopathy||http://www.orpha.net/ORDO/Orphanet_169186
4772||10083||Isolated Dandy-Walker malformation with hydrocephalus||http://www.orpha.net/ORDO/Orphanet_269212
4773||10083||Isolated Dandy-Walker malformation without hydrocephalus||http://www.orpha.net/ORDO/Orphanet_269215
4774||4139||Intellectual disability - hypotonia - spasticity - sleep disorder||http://www.orpha.net/ORDO/Orphanet_356996
4775||4717||Genetic branchial arch or oral-acral syndrome||http://www.orpha.net/ORDO/Orphanet_183576
4776||14970||whole-brain volume||http://www.ebi.ac.uk/efo/EFO_0005089
4777||1006||testicular carcinoma||http://www.ebi.ac.uk/efo/EFO_0005088
4778||8918||Illumina MiSeq standard manufacturer s protocol||http://www.ebi.ac.uk/efo/EFO_0005087
4779||2672||abdomenal wall||http://www.ebi.ac.uk/efo/EFO_0005096
4780||2672||bronchiole||http://www.ebi.ac.uk/efo/EFO_0005097
4781||14970||P wave duration||http://www.ebi.ac.uk/efo/EFO_0005094
4782||14970||PR segment||http://www.ebi.ac.uk/efo/EFO_0005095
4783||14970||entorhinal cortical volume||http://www.ebi.ac.uk/efo/EFO_0005092
4785||4717||Genetic malformation syndrome with short stature||http://www.orpha.net/ORDO/Orphanet_183570
4784||8700||hip circumference||http://www.ebi.ac.uk/efo/EFO_0005093
4787||14970||basophil count||http://www.ebi.ac.uk/efo/EFO_0005090
4786||4717||Genetic overgrowth/obesity syndrome||http://www.orpha.net/ORDO/Orphanet_183573
4788||14970||monocyte count||http://www.ebi.ac.uk/efo/EFO_0005091
4789||4194||M llerian aplasia||http://www.orpha.net/ORDO/Orphanet_73217
4790||4815||spotted protein reporter||http://www.ebi.ac.uk/efo/EFO_0005077
4791||4815||spotted double stranded DNA reporter||http://www.ebi.ac.uk/efo/EFO_0005076
4792||4815||spotted single stranded oligo reporter||http://www.ebi.ac.uk/efo/EFO_0005079
4793||4815||spotted single stranded DNA PCR amplicon reporter||http://www.ebi.ac.uk/efo/EFO_0005078
4794||8918||Illumina Genome Analyzer II standard manufacturer s protocol||http://www.ebi.ac.uk/efo/EFO_0005083
4795||8918||Illumina Genome Analyzer IIx standard manufacturer s protocol||http://www.ebi.ac.uk/efo/EFO_0005084
4796||8918||Illumina HiSeq 1000 standard manufacturer s protocol||http://www.ebi.ac.uk/efo/EFO_0005085
4797||8918||Illumina HiSeq 2000 standard manufacturer s protocol||http://www.ebi.ac.uk/efo/EFO_0005086
4798||14970||CC16 measurement||http://www.ebi.ac.uk/efo/EFO_0005080
4799||14970||surfactant protein D measurement||http://www.ebi.ac.uk/efo/EFO_0005081
4800||3352||Arabidopsis arenosa||http://purl.obolibrary.org/obo/NCBITaxon_38785
4801||8918||Illumina Genome Analyzer standard manufacturer s protocol||http://www.ebi.ac.uk/efo/EFO_0005082
4802||5025||Lodderomyces elongisporus NRRL YB-4239||http://purl.obolibrary.org/obo/NCBITaxon_379508
4803||1732||Inherited cancer-predisposing syndrome||http://www.orpha.net/ORDO/Orphanet_140162
4804||4805||block||http://www.ebi.ac.uk/efo/EFO_0005067
4805||1125||collection of material||http://www.ebi.ac.uk/efo/EFO_0005066
4806||4835||silicon substrate||http://www.ebi.ac.uk/efo/EFO_0005065
4807||2415||Rare genetic palpebral, lacrimal system and conjunctival disease||http://www.orpha.net/ORDO/Orphanet_183598
4808||4833||array surface coating||http://www.ebi.ac.uk/efo/EFO_0005069
4809||4808||aminosilane substrate coating||http://www.ebi.ac.uk/efo/EFO_0005070
4810||11809||Genetic renal tubular disease||http://www.orpha.net/ORDO/Orphanet_183592
4811||4808||polylysine substrate coating||http://www.ebi.ac.uk/efo/EFO_0005071
4812||15363||Genetic renal tumor||http://www.orpha.net/ORDO/Orphanet_183595
4813||4790||spotted antibody reporter||http://www.ebi.ac.uk/efo/EFO_0005074
4814||4815||spotted colony reporter||http://www.ebi.ac.uk/efo/EFO_0005075
4815||4833||array reporter||http://www.ebi.ac.uk/efo/EFO_0005072
4816||4815||in situ oligo||http://www.ebi.ac.uk/efo/EFO_0005073
4817||10994||ammonium||http://purl.obolibrary.org/obo/CHEBI_28938
4818||10994||N-acetyl-L-cysteine||http://purl.obolibrary.org/obo/CHEBI_28939
4819||2594||D,L-2-hydroxyglutaric aciduria||http://www.orpha.net/ORDO/Orphanet_356978
4820||10994||3-aminophenol||http://purl.obolibrary.org/obo/CHEBI_28924
4821||2842||QRS duration||http://www.ebi.ac.uk/efo/EFO_0005055
4822||14970||QRS complex||http://www.ebi.ac.uk/efo/EFO_0005054
4824||14970||myoglobin measurement||http://www.ebi.ac.uk/efo/EFO_0005057
4823||11809||Genetic thrombotic microangiopathy||http://www.orpha.net/ORDO/Orphanet_183589
4825||27||age at death||http://www.ebi.ac.uk/efo/EFO_0005056
4826||14970||acylcarnitine measurement||http://www.ebi.ac.uk/efo/EFO_0005059
4828||14970||tyrosine measurement||http://www.ebi.ac.uk/efo/EFO_0005058
4827||13496||Lagos bat virus||http://purl.obolibrary.org/obo/NCBITaxon_38766
4829||13496||Duvenhage virus||http://purl.obolibrary.org/obo/NCBITaxon_38767
4830||11809||Genetic glomerular disease||http://www.orpha.net/ORDO/Orphanet_183586
4831||5502||Streptococcus pyogenes NZ131||http://purl.obolibrary.org/obo/NCBITaxon_471876
4832||4717||Genetic head and neck malformation||http://www.orpha.net/ORDO/Orphanet_183583
4833||1125||instrument part||http://www.ebi.ac.uk/efo/EFO_0005060
4834||4717||Genetic malformation syndrome with odontal and/or periodontal component||http://www.orpha.net/ORDO/Orphanet_183580
4835||4833||substrate||http://www.ebi.ac.uk/efo/EFO_0005061
4836||4835||glass substrate||http://www.ebi.ac.uk/efo/EFO_0005062
4837||4835||nylon substrate||http://www.ebi.ac.uk/efo/EFO_0005063
4838||4835||nitrocellulose substrate||http://www.ebi.ac.uk/efo/EFO_0005064
4839||10994||AACOCF3||http://purl.obolibrary.org/obo/CHEBI_2341
4840||11456||Partial duplication of the long arm of chromosome 22||http://www.orpha.net/ORDO/Orphanet_263004
4841||260||Transient hypogammaglobulinemia of infancy||http://www.orpha.net/ORDO/Orphanet_169139
4842||3744||synapse||http://purl.obolibrary.org/obo/GO_0045202
4843||4762||Esophageal malformation||http://www.orpha.net/ORDO/Orphanet_88993
4844||1562||increased rate||http://purl.obolibrary.org/obo/PATO_0000912
4845||3352||Arabidopsis arenosa x Arabidopsis thaliana||http://purl.obolibrary.org/obo/NCBITaxon_378006
4846||10994||calciol||http://purl.obolibrary.org/obo/CHEBI_28940
4847||2450||Spinal muscular atrophy - Dandy-Walker malformation - cataracts||http://www.orpha.net/ORDO/Orphanet_73245
4848||2252||Visceral neuropathy - brain anomalies - facial dysmorphism - developmental delay||http://www.orpha.net/ORDO/Orphanet_73246
4849||10994||praziquantel||http://purl.obolibrary.org/obo/CHEBI_45267
4850||2063||abnormality of the nose||http://purl.obolibrary.org/obo/HP_0000366
4851||3990||abacavir||http://purl.obolibrary.org/obo/CHEBI_2360
4852||8190||( )-abscisic acid||http://purl.obolibrary.org/obo/CHEBI_2365
4853||10994||5-amino-1-(5-phospho-D-ribosyl)imidazole-4-carboxamide||http://purl.obolibrary.org/obo/CHEBI_18406
4855||10994||ampicillin||http://purl.obolibrary.org/obo/CHEBI_28971
4854||7481||purine nucleoside metabolic process||http://purl.obolibrary.org/obo/GO_0042278
4856||4139||Ossification anomalies - psychomotor development delay||http://www.orpha.net/ORDO/Orphanet_73230
4857||1513||Dentinogenesis imperfecta||http://www.orpha.net/ORDO/Orphanet_49042
4858||7234||Immunoglobulin heavy chain deficiency||http://www.orpha.net/ORDO/Orphanet_169110
4859||8191||sodium chloride||http://purl.obolibrary.org/obo/CHEBI_26710
4860||8191||sodium cholate||http://purl.obolibrary.org/obo/CHEBI_26711
4861||10994||acarbose||http://purl.obolibrary.org/obo/CHEBI_2376
4862||13986||cortical collecting duct||http://www.ebi.ac.uk/efo/EFO_0005098
4863||2670||stele||http://www.ebi.ac.uk/efo/EFO_0005099
4864||6914||X-linked intellectual disability - hypotonic face||http://www.orpha.net/ORDO/Orphanet_73220
4865||4139||Global developmental delay - osteopenia - ectodermal defect||http://www.orpha.net/ORDO/Orphanet_73223
4866||5486||Immunodeficiency due to CD25 deficiency||http://www.orpha.net/ORDO/Orphanet_169100
4867||4951||Tubular renal disease - cardiomyopathy||http://www.orpha.net/ORDO/Orphanet_73224
4868||4705||Autosomal dominant familial hematuria - retinal arteriolar tortuosity - contractures||http://www.orpha.net/ORDO/Orphanet_73229
4869||10994||ozone||http://purl.obolibrary.org/obo/CHEBI_25812
4870||2252||Intellectual disability - short stature - hypertelorism||http://www.orpha.net/ORDO/Orphanet_3074
4871||11899||X-linked intellectual disability - psychosis - macroorchidism||http://www.orpha.net/ORDO/Orphanet_3077
4872||2252||Costello syndrome||http://www.orpha.net/ORDO/Orphanet_3071
4873||6287||X-linked dominant chondrodysplasia punctata||http://www.orpha.net/ORDO/Orphanet_35173
4874||11326||X and Y chromosomal anomaly||http://www.orpha.net/ORDO/Orphanet_263749
4875||805||Hemochromatosis type 3||http://www.orpha.net/ORDO/Orphanet_225123
4876||11326||Y chromosome number anomaly||http://www.orpha.net/ORDO/Orphanet_263746
4877||2252||Intellectual disability, Buenos-Aires type||http://www.orpha.net/ORDO/Orphanet_3079
4878||7989||Short stature-auditory canal atresia-mandibular hypoplasia-skeletal anomalies syndrome||http://www.orpha.net/ORDO/Orphanet_397623
4879||9709||Severe X-linked intellectual disability, Gustavson type||http://www.orpha.net/ORDO/Orphanet_3078
4880||2252||Intellectual disability, Wolff type||http://www.orpha.net/ORDO/Orphanet_3080
4881||9965||Revesz syndrome||http://www.orpha.net/ORDO/Orphanet_3088
4882||5146||Retinohepatoendocrinologic syndrome||http://www.orpha.net/ORDO/Orphanet_3087
4883||9719||Autosomal dominant vitreoretinochoroidopathy||http://www.orpha.net/ORDO/Orphanet_3086
4884||5700||Retinitis pigmentosa - intellectual disability - deafness - hypogenitalism||http://www.orpha.net/ORDO/Orphanet_3085
4885||2252||Intellectual disability - polydactyly - uncombable hair||http://www.orpha.net/ORDO/Orphanet_3082
4886||1022||Macaca radiata||http://purl.obolibrary.org/obo/NCBITaxon_9548
4887||4904||Partial monosomy of the short arm of chromosome X||http://www.orpha.net/ORDO/Orphanet_263731
4888||4891||Papio hamadryas||http://purl.obolibrary.org/obo/NCBITaxon_9557
4889||4891||Papio anubis||http://purl.obolibrary.org/obo/NCBITaxon_9555
4890||5010||Autosomal recessive disease associated with punctate palmoplantar keratoderma as a major feature||http://www.orpha.net/ORDO/Orphanet_308041
4891||1022||Papio||http://purl.obolibrary.org/obo/NCBITaxon_9554
4892||5025||Aspergillus fumigatus||http://purl.obolibrary.org/obo/NCBITaxon_746128
4893||2252||intellectual disability - sparse hair - brachydactyly||http://www.orpha.net/ORDO/Orphanet_3051
4894||4139||Intellectual disability - hypotonia - skin hyperpigmentation||http://www.orpha.net/ORDO/Orphanet_3050
4895||11899||X-linked intellectual disability - seizures - psoriasis||http://www.orpha.net/ORDO/Orphanet_3052
4896||11899||X-linked intellectual disability - short stature - obesity||http://www.orpha.net/ORDO/Orphanet_3055
4897||2021||Hyperphosphatasia-intellectual disability syndrome||http://www.orpha.net/ORDO/Orphanet_247262
4899||4727||Monoamine oxidase A deficiency||http://www.orpha.net/ORDO/Orphanet_3057
4898||4912||Polysomy of X chromosome||http://www.orpha.net/ORDO/Orphanet_263723
4900||11899||X-linked intellectual disability, Brooks type||http://www.orpha.net/ORDO/Orphanet_3056
4901||11899||X-linked intellectual disability, Gu type||http://www.orpha.net/ORDO/Orphanet_3059
4903||508||cytokinins||http://purl.obolibrary.org/obo/CHEBI_23530
4902||4919||X chromosome number anomaly with male phenotype||http://www.orpha.net/ORDO/Orphanet_263720
4904||11327||Partial deletion of chromosome X||http://www.orpha.net/ORDO/Orphanet_263726
4905||6326||Disorder of mitochondrial fatty acid oxidation||http://www.orpha.net/ORDO/Orphanet_309115
4906||1022||Macaca mulatta||http://purl.obolibrary.org/obo/NCBITaxon_9544
4907||4905||Acyl-CoA dehydrogenase deficiency||http://www.orpha.net/ORDO/Orphanet_309120
4908||1022||Macaca nemestrina||http://purl.obolibrary.org/obo/NCBITaxon_9545
4909||1022||Macaca fascicularis||http://purl.obolibrary.org/obo/NCBITaxon_9541
4910||10860||Cryptogenic late-onset epileptic spasms||http://www.orpha.net/ORDO/Orphanet_163708
4911||11899||X-linked intellectual disability, Schutz type||http://www.orpha.net/ORDO/Orphanet_3062
4913||11899||X-linked intellectual disability, Raynaud type||http://www.orpha.net/ORDO/Orphanet_3061
4912||4919||X chromosome number anomaly with female phenotype||http://www.orpha.net/ORDO/Orphanet_263717
4914||11899||X-linked intellectual disability, Wittner type||http://www.orpha.net/ORDO/Orphanet_3064
4915||11899||X-linked intellectual disability, Snyder type||http://www.orpha.net/ORDO/Orphanet_3063
4916||4139||Intellectual disability - myopathy - short stature - endocrine defect||http://www.orpha.net/ORDO/Orphanet_3068
4917||4139||Intellectual disability - microcephaly - phalangeal - facial abnormalities||http://www.orpha.net/ORDO/Orphanet_3067
4918||5235||Pancreatic colipase deficiency||http://www.orpha.net/ORDO/Orphanet_309108
4919||11326||X chromosome number anomaly||http://www.orpha.net/ORDO/Orphanet_263714
4920||1022||Chlorocebus aethiops||http://purl.obolibrary.org/obo/NCBITaxon_9534
4921||5235||Combined pancreatic lipase-colipase deficiency||http://www.orpha.net/ORDO/Orphanet_309111
4922||1022||Cercocebus atys||http://purl.obolibrary.org/obo/NCBITaxon_9531
4923||10272||Benign familial mesial temporal lobe epilepsy||http://www.orpha.net/ORDO/Orphanet_163717
4924||10994||sulphur dioxide||http://purl.obolibrary.org/obo/CHEBI_18422
4925||212||Cytomegalic congenital adrenal hypoplasia||http://www.orpha.net/ORDO/Orphanet_95702
4926||212||Familial adrenal hypoplasia with absent pituitary luteinizing hormone||http://www.orpha.net/ORDO/Orphanet_95700
4927||770||GM15144||http://purl.obolibrary.org/obo/CLO_0029916
4928||11443||Complex chromosomal rearrangement||http://www.orpha.net/ORDO/Orphanet_263708
4929||11802||Familial dilated cardiomyopathy||http://www.orpha.net/ORDO/Orphanet_217607
4930||1826||Panicum virgatum||http://purl.obolibrary.org/obo/NCBITaxon_38727
4931||10159||Non-acquired premature ovarian failure||http://www.orpha.net/ORDO/Orphanet_95710
4932||6986||Congenital hypothyroidism due to developmental anomaly||http://www.orpha.net/ORDO/Orphanet_95711
4933||4932||Thyroid ectopia||http://www.orpha.net/ORDO/Orphanet_95712
4934||4932||Athyreosis||http://www.orpha.net/ORDO/Orphanet_95713
4935||6986||Primary congenital hypothyroidism without thyroid developmental anomaly||http://www.orpha.net/ORDO/Orphanet_95714
4936||4935||Familial thyroid dyshormonogenesis||http://www.orpha.net/ORDO/Orphanet_95716
4937||4932||Thyroid hemiagenesis||http://www.orpha.net/ORDO/Orphanet_95719
4938||1022||Gorilla gorilla||http://purl.obolibrary.org/obo/NCBITaxon_9593
4939||1022||Pan paniscus||http://purl.obolibrary.org/obo/NCBITaxon_9597
4940||4938||Gorilla gorilla gorilla||http://purl.obolibrary.org/obo/NCBITaxon_9595
4941||10994||cytochalasin B||http://purl.obolibrary.org/obo/CHEBI_23527
4942||1022||Pan troglodytes||http://purl.obolibrary.org/obo/NCBITaxon_9598
4943||6888||Chronic diarrhea with hereditary sensory and autonomic neuropathy||http://www.orpha.net/ORDO/Orphanet_397606
4944||3651||cob||http://purl.obolibrary.org/obo/ZEA_0015075
4945||561||Atypical Rett syndrome||http://www.orpha.net/ORDO/Orphanet_3095
4946||3019||Meacham syndrome||http://www.orpha.net/ORDO/Orphanet_3097
4947||7989||Rhizomelic syndrome, Urbach type||http://www.orpha.net/ORDO/Orphanet_3098
4948||4951||Sensorineural deafness with dilated cardiomyopathy||http://www.orpha.net/ORDO/Orphanet_217622
4949||1826||Ostreococcus tauri||http://purl.obolibrary.org/obo/NCBITaxon_70448
4951||4929||Syndrome associated with dilated cardiomyopathy||http://www.orpha.net/ORDO/Orphanet_217619
4950||10876||Obesity due to CEP19 deficiency||http://www.orpha.net/ORDO/Orphanet_397615
4952||2252||Macrocephaly-developmental delay syndrome||http://www.orpha.net/ORDO/Orphanet_397612
4953||9690||Foveal hypoplasia-optic nerve decussation defect-anterior segment dysgenesis syndrome||http://www.orpha.net/ORDO/Orphanet_397618
4954||10994||16-ketoestradiol||http://purl.obolibrary.org/obo/CHEBI_34165
4955||1022||Blastocladiella emersonii||http://purl.obolibrary.org/obo/NCBITaxon_4808
4956||5502||Dehalobacter restrictus||http://purl.obolibrary.org/obo/NCBITaxon_55583
4957||4929||Neuromuscular disease with dilated cardiomyopathy||http://www.orpha.net/ORDO/Orphanet_217610
4958||4929||Mitochondrial disease with dilated cardiomyopathy||http://www.orpha.net/ORDO/Orphanet_217613
4959||4929||Fatty acid oxidation and ketogenesis disorder with dilated cardiomyopathy||http://www.orpha.net/ORDO/Orphanet_217616
4960||6293||Tay-Sachs disease, B variant, juvenile form||http://www.orpha.net/ORDO/Orphanet_309185
4961||5025||Emericella nidulans||http://purl.obolibrary.org/obo/NCBITaxon_162425
4962||14145||Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia||http://www.orpha.net/ORDO/Orphanet_284324
4963||5670||46,XY ovotesticular disorder of sex development||http://www.orpha.net/ORDO/Orphanet_325345
4964||6293||Tay-Sachs disease, B variant, infantile form||http://www.orpha.net/ORDO/Orphanet_309178
4965||8191||sertraline hydrochloride||http://purl.obolibrary.org/obo/CHEBI_9124
4967||14145||Infantile-onset autosomal recessive nonprogressive cerebellar ataxia||http://www.orpha.net/ORDO/Orphanet_284332
4966||4259||response to antibiotic||http://purl.obolibrary.org/obo/GO_0046677
4968||3575||46,XY disorder of sex development due to impaired androgen production||http://www.orpha.net/ORDO/Orphanet_325357
4969||1826||Physcomitrella patens||http://purl.obolibrary.org/obo/NCBITaxon_3218
4970||770||AG05416||http://purl.obolibrary.org/obo/CLO_0035232
4971||10994||sevoflurane||http://purl.obolibrary.org/obo/CHEBI_9130
4972||9894||Pontocerebellar hypoplasia type 7||http://www.orpha.net/ORDO/Orphanet_284339
4973||6422||Sandhoff disease, adult form||http://www.orpha.net/ORDO/Orphanet_309169
4974||4932||Thyroid hypoplasia||http://www.orpha.net/ORDO/Orphanet_95720
4975||1826||Pachycladon novaezelandiae||http://purl.obolibrary.org/obo/NCBITaxon_106788
4976||4430||phospholipase A2 inhibitor||http://purl.obolibrary.org/obo/CHEBI_50469
4977||1826||Pachycladon||http://purl.obolibrary.org/obo/NCBITaxon_106787
4978||10994||1-benzofuran||http://purl.obolibrary.org/obo/CHEBI_35260
4979||6293||Tay-Sachs disease, B variant, adult form||http://www.orpha.net/ORDO/Orphanet_309192
4980||1022||Pinctada maxima||http://purl.obolibrary.org/obo/NCBITaxon_104660
4981||1125||specimen||http://purl.obolibrary.org/obo/OBI_0100051
4982||1826||Pachycladon cheesemanii||http://purl.obolibrary.org/obo/NCBITaxon_106773
4983||10860||Rolandic epilepsy - speech dyspraxia||http://www.orpha.net/ORDO/Orphanet_163721
4984||5191||Neutrophil immunodeficiency syndrome||http://www.orpha.net/ORDO/Orphanet_183707
4985||10860||Rolandic epilepsy - paroxysmal exercise-induced dystonia - writer s cramp||http://www.orpha.net/ORDO/Orphanet_163727
4986||6625||Gangliosidosis||http://www.orpha.net/ORDO/Orphanet_309144
4987||288||Mitochondrial disorder due to a defect in assembly or maturation of the respiratory chain complexes||http://www.orpha.net/ORDO/Orphanet_309136
4988||5025||Schizosaccharomyces pombe||http://purl.obolibrary.org/obo/NCBITaxon_4896
4989||5025||Schizosaccharomyces japonicus||http://purl.obolibrary.org/obo/NCBITaxon_4897
4990||13883||PCR||http://purl.obolibrary.org/obo/OBI_0000415
4991||1826||Selaginella||http://purl.obolibrary.org/obo/NCBITaxon_3246
4992||10994||rapamycin||http://purl.obolibrary.org/obo/CHEBI_9168
4993||1826||Vitis amurensis||http://purl.obolibrary.org/obo/NCBITaxon_103351
4994||194||Genetic susceptibility to infections due to particular pathogens||http://www.orpha.net/ORDO/Orphanet_183710
4995||6326||Metabolic disease due to other fatty acid oxidation disorder||http://www.orpha.net/ORDO/Orphanet_309133
4997||4994||Pyogenic bacterial infections due to MyD88 deficiency||http://www.orpha.net/ORDO/Orphanet_183713
4996||6326||Disorder of carnitine cycle and carnitine transport||http://www.orpha.net/ORDO/Orphanet_309130
4998||1022||Puccinia graminis f. sp. tritici||http://purl.obolibrary.org/obo/NCBITaxon_56615
4999||4905||3-hydroxyacyl-CoA dehydrogenase deficiency||http://www.orpha.net/ORDO/Orphanet_309127
5000||10994||alpha-tocopherol_5000||http://purl.obolibrary.org/obo/CHEBI_22470
5001||1826||Vitis rotundifolia||http://purl.obolibrary.org/obo/NCBITaxon_103349
5002||266||Familial intrahepatic cholestasis||http://www.orpha.net/ORDO/Orphanet_284385
5003||5700||Neurologic Waardenburg-Shah syndrome||http://www.orpha.net/ORDO/Orphanet_163746
5004||5010||Autosomal dominant disease associated with punctate palmoplantar keratoderma as a major feature||http://www.orpha.net/ORDO/Orphanet_308031
5005||1125||organism||http://purl.obolibrary.org/obo/OBI_0100026
5007||5061||Familial  hyperprolactinemia||http://www.orpha.net/ORDO/Orphanet_397685
5006||6422||Sandhoff disease, juvenile form||http://www.orpha.net/ORDO/Orphanet_309162
5008||6573||antimetabolite role||http://purl.obolibrary.org/obo/CHEBI_35221
5010||13988||Disease with punctate palmoplantar keratoderma as a major feature||http://www.orpha.net/ORDO/Orphanet_308023
5009||1022||Glomus intraradices||http://purl.obolibrary.org/obo/NCBITaxon_4876
5012||5025||Fusarium cerealis||http://purl.obolibrary.org/obo/NCBITaxon_56641
5011||6573||inhibitor role||http://purl.obolibrary.org/obo/CHEBI_35222
5013||11549||congenital heart disease||http://www.ebi.ac.uk/efo/EFO_0005207
5015||14970||glomerular filtration rate||http://www.ebi.ac.uk/efo/EFO_0005208
5014||507||plant growth retardant||http://purl.obolibrary.org/obo/CHEBI_35219
5017||14451||response to dabigatran etexilate||http://www.ebi.ac.uk/efo/EFO_0005205
5016||1022||Gasterosteus aculeatus||http://purl.obolibrary.org/obo/NCBITaxon_69293
5018||14970||oligoclonal band measurement||http://www.ebi.ac.uk/efo/EFO_0005206
5021||15519||Hereditary isolated aplastic anemia||http://www.orpha.net/ORDO/Orphanet_397692
5019||14970||antiphospholipid antibody measurement||http://www.ebi.ac.uk/efo/EFO_0005200
5020||6422||Sandhoff disease, infantile form||http://www.orpha.net/ORDO/Orphanet_309155
5022||2252||3q27.3 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_397695
5023||4706||GM2 gangliosidosis||http://www.orpha.net/ORDO/Orphanet_309152
5024||2102||eating disorder||http://www.ebi.ac.uk/efo/EFO_0005203
5025||1022||Ascomycota||http://purl.obolibrary.org/obo/NCBITaxon_4890
5026||5024||bulimia nervosa||http://www.ebi.ac.uk/efo/EFO_0005204
5027||8700||height growth measurement||http://www.ebi.ac.uk/efo/EFO_0005201
5028||9052||response to hydrochlorothiazide||http://www.ebi.ac.uk/efo/EFO_0005202
5029||14158||Focal acral hyperkeratosis||http://www.orpha.net/ORDO/Orphanet_308013
5030||6264||Hyper-beta-alaninemia||http://www.orpha.net/ORDO/Orphanet_309147
5031||5502||Bacillus anthracis str. Ames||http://purl.obolibrary.org/obo/NCBITaxon_198094
5032||10994||apratoxin A||http://purl.obolibrary.org/obo/CHEBI_35212
5033||10994||simvastatin||http://purl.obolibrary.org/obo/CHEBI_9150
5034||10994||candesartan||http://purl.obolibrary.org/obo/CHEBI_3347
5035||5414||Diarrhea-vomiting due to trehalase deficiency||http://www.orpha.net/ORDO/Orphanet_103909
5036||12165||anther||http://www.ebi.ac.uk/efo/EFO_0005101
5038||3655||flag leaf||http://www.ebi.ac.uk/efo/EFO_0005100
5037||10682||Rare genetic parathyroid disease and phosphocalcic metabolism disorder||http://www.orpha.net/ORDO/Orphanet_183634
5040||13448||antennal disc||http://www.ebi.ac.uk/efo/EFO_0005103
5039||10682||Rare genetic thyroid disease||http://www.orpha.net/ORDO/Orphanet_183631
5041||12165||filament||http://www.ebi.ac.uk/efo/EFO_0005102
5042||14970||lipid or lipoprotein measurement||http://www.ebi.ac.uk/efo/EFO_0005105
5043||13448||eye disc||http://www.ebi.ac.uk/efo/EFO_0005104
5044||2670||collective leaf structure||http://www.ebi.ac.uk/efo/EFO_0005107
5045||8700||body composition measurement||http://www.ebi.ac.uk/efo/EFO_0005106
5046||5295||energy expenditure||http://www.ebi.ac.uk/efo/EFO_0005109
5047||8700||arm span||http://www.ebi.ac.uk/efo/EFO_0005108
5049||15170||Congenital sodium diarrhea||http://www.orpha.net/ORDO/Orphanet_103908
5048||10682||Rare genetic adrenal disease||http://www.orpha.net/ORDO/Orphanet_183637
5050||5414||Chronic diarrhea due to glucoamylase deficiency||http://www.orpha.net/ORDO/Orphanet_103907
5051||15177||Congenital enterocyte heparan sulfate deficiency||http://www.orpha.net/ORDO/Orphanet_103910
5052||10874||Progressive myoclonic epilepsy type 5||http://www.orpha.net/ORDO/Orphanet_402082
5053||10732||Genetic respiratory malformation||http://www.orpha.net/ORDO/Orphanet_183622
5054||3683||establishment of localization in cell||http://purl.obolibrary.org/obo/GO_0051649
5055||10682||Rare genetic diabetes mellitus||http://www.orpha.net/ORDO/Orphanet_183625
5056||10994||butan-1-ol||http://purl.obolibrary.org/obo/CHEBI_28885
5057||6087||Familial bicuspid aortic valve||http://www.orpha.net/ORDO/Orphanet_402075
5058||259||cellular localization||http://purl.obolibrary.org/obo/GO_0051641
5059||15177||Epithelio-exfoliative colitis - deafness||http://www.orpha.net/ORDO/Orphanet_103912
5060||5058||mitochondrion localization||http://purl.obolibrary.org/obo/GO_0051646
5061||10682||Rare genetic hypothalamic or pituitary disease||http://www.orpha.net/ORDO/Orphanet_183628
5062||15174||Chronic diarrhea due to guanylate cyclase 2C overactivity||http://www.orpha.net/ORDO/Orphanet_314373
5063||15174||Intestinal obstruction in the newborn due to guanylate cyclase 2C deficiency||http://www.orpha.net/ORDO/Orphanet_314376
5064||14970||thyroxine measurement||http://www.ebi.ac.uk/efo/EFO_0005130
5065||4981||RNAlater specimen||http://www.ebi.ac.uk/efo/EFO_0005125
5067||14970||cancer biomarker measurement||http://www.ebi.ac.uk/efo/EFO_0005127
5066||2593||Autosomal recessive distal renal tubular acidosis||http://www.orpha.net/ORDO/Orphanet_402041
5068||14970||arylesterase enzyme measurement||http://www.ebi.ac.uk/efo/EFO_0005126
5069||4981||freeze dried specimen||http://www.ebi.ac.uk/efo/EFO_0005121
5070||2415||Genetic neuro-ophthalmological disease||http://www.orpha.net/ORDO/Orphanet_183616
5071||14915||hepatitis C induced liver cirrhosis||http://www.ebi.ac.uk/efo/EFO_0005129
5072||7330||albumin:globulin ratio measurement||http://www.ebi.ac.uk/efo/EFO_0005128
5073||15363||Genetic eye tumor||http://www.orpha.net/ORDO/Orphanet_183619
5074||6900||Hereditary sensory and autonomic neuropathy type 6||http://www.orpha.net/ORDO/Orphanet_314381
5075||10994||fluroanthene||http://purl.obolibrary.org/obo/CHEBI_33083
5076||5085||Xq12-q13.3 duplication syndrome||http://www.orpha.net/ORDO/Orphanet_314389
5077||14602||urinary metabolite measurement||http://www.ebi.ac.uk/efo/EFO_0005116
5078||14970||metabolic rate measurement||http://www.ebi.ac.uk/efo/EFO_0005115
5079||8700||head circumference||http://www.ebi.ac.uk/efo/EFO_0005114
5080||27||gestational age||http://www.ebi.ac.uk/efo/EFO_0005112
5082||14970||folic acid measurement||http://www.ebi.ac.uk/efo/EFO_0005111
5081||2415||Rare genetic refraction anomaly||http://www.orpha.net/ORDO/Orphanet_183601
5083||14970||fatty acid measurement||http://www.ebi.ac.uk/efo/EFO_0005110
5084||2415||Genetic lens and zonula anomaly||http://www.orpha.net/ORDO/Orphanet_183607
5085||561||Rare disease with autism||http://www.orpha.net/ORDO/Orphanet_180772
5086||14970||antioxidant measurement||http://www.ebi.ac.uk/efo/EFO_0005119
5087||14970||IGFBP-1 measurement||http://www.ebi.ac.uk/efo/EFO_0005118
5089||14970||CCL5 measurement||http://www.ebi.ac.uk/efo/EFO_0005117
5088||10994||tobramycin||http://purl.obolibrary.org/obo/CHEBI_28864
5090||1022||Limanda limanda||http://purl.obolibrary.org/obo/NCBITaxon_27771
5091||5098||Col-2||http://www.ebi.ac.uk/efo/EFO_0005150
5092||5098||Col-4||http://www.ebi.ac.uk/efo/EFO_0005152
5093||5098||Col-3||http://www.ebi.ac.uk/efo/EFO_0005151
5094||15289||Malformative syndrome with dentinogenesis imperfecta||http://www.orpha.net/ORDO/Orphanet_180766
5095||238||Cernunnos-XLF deficiency||http://www.orpha.net/ORDO/Orphanet_169079
5096||990||Hermansky-Pudlak syndrome with neutropenia||http://www.orpha.net/ORDO/Orphanet_183678
5098||3349||Columbia ecotype||http://www.ebi.ac.uk/efo/EFO_0005147
5097||7234||Recurrent infections associated with rare immunoglobulin isotypes deficiency||http://www.orpha.net/ORDO/Orphanet_183675
5099||5098||Col-0||http://www.ebi.ac.uk/efo/EFO_0005148
5100||5098||Col-1||http://www.ebi.ac.uk/efo/EFO_0005149
5101||8191||calcium chloride||http://purl.obolibrary.org/obo/CHEBI_3312
5102||238||Severe combined immunodeficiency||http://www.orpha.net/ORDO/Orphanet_183660
5103||1790||autoimmune disease||http://www.ebi.ac.uk/efo/EFO_0005140
5104||5502||Escherichia coli UTI89||http://purl.obolibrary.org/obo/NCBITaxon_364106
5105||5502||Salmonella enterica subsp. enterica serovar Typhisuis||http://purl.obolibrary.org/obo/NCBITaxon_41529
5106||5502||Salmonella enterica subsp. enterica serovar Typhimurium str. LT2||http://purl.obolibrary.org/obo/NCBITaxon_99287
5107||14970||serum ceruloplasmin measurement||http://www.ebi.ac.uk/efo/EFO_0005139
5108||14970||MHPG measurement||http://www.ebi.ac.uk/efo/EFO_0005133
5109||10994||calicheamicin gamma1(I)||http://purl.obolibrary.org/obo/CHEBI_3319
5111||14970||amino acid measurement||http://www.ebi.ac.uk/efo/EFO_0005134
5110||7256||Hyper-IgM syndrome without susceptibility to opportunistic infections||http://www.orpha.net/ORDO/Orphanet_183666
5112||14970||HVA measurement||http://www.ebi.ac.uk/efo/EFO_0005131
5113||260||Agammaglobulinemia||http://www.orpha.net/ORDO/Orphanet_183669
5114||14970||5-HIAA measurement||http://www.ebi.ac.uk/efo/EFO_0005132
5115||238||Hyper-IgM syndrome with susceptibility to opportunistic infections||http://www.orpha.net/ORDO/Orphanet_183663
5116||1391||conduction system disorder||http://www.ebi.ac.uk/efo/EFO_0005137
5117||1336||acquired long QT syndrome||http://www.ebi.ac.uk/efo/EFO_0005138
5118||4571||strain||http://www.ebi.ac.uk/efo/EFO_0005135
5119||4571||cultivar||http://www.ebi.ac.uk/efo/EFO_0005136
5120||5121||Bl-0||http://www.ebi.ac.uk/efo/EFO_0005172
5121||3349||Bologna ecotype||http://www.ebi.ac.uk/efo/EFO_0005171
5122||3349||Bayreuth ecotype||http://www.ebi.ac.uk/efo/EFO_0005174
5123||5121||Bl-1||http://www.ebi.ac.uk/efo/EFO_0005173
5124||5128||Bur-0||http://www.ebi.ac.uk/efo/EFO_0005170
5125||238||Alymphoid cystic thymic dysgenesis||http://www.orpha.net/ORDO/Orphanet_169095
5126||12461||Rare genetic coagulation disorder||http://www.orpha.net/ORDO/Orphanet_183654
5127||1760||wild type genotype||http://www.ebi.ac.uk/efo/EFO_0005168
5128||3349||Burren ecotype||http://www.ebi.ac.uk/efo/EFO_0005169
5129||12461||Rare constitutional anemia||http://www.orpha.net/ORDO/Orphanet_183651
5130||3349||Calver ecotype||http://www.ebi.ac.uk/efo/EFO_0005164
5131||13304||Autosomal dominant focal non-epidermolytic palmoplantar keratoderma with plantar blistering||http://www.orpha.net/ORDO/Orphanet_402003
5132||5130||Cal-0||http://www.ebi.ac.uk/efo/EFO_0005165
5133||3349||Blanes ecotype||http://www.ebi.ac.uk/efo/EFO_0005166
5134||5133||Bla-1||http://www.ebi.ac.uk/efo/EFO_0005167
5135||5139||Uk-3||http://www.ebi.ac.uk/efo/EFO_0005163
5136||5139||Uk-2||http://www.ebi.ac.uk/efo/EFO_0005162
5137||10994||hormone||http://purl.obolibrary.org/obo/CHEBI_24621
5138||5139||Uk-1||http://www.ebi.ac.uk/efo/EFO_0005161
5139||3349||Umkirch ecotype||http://www.ebi.ac.uk/efo/EFO_0005160
5140||238||Combined immunodeficiency due to CRAC channel dysfunction||http://www.orpha.net/ORDO/Orphanet_169090
5141||5502||Thiomonas sp. 3As||http://purl.obolibrary.org/obo/NCBITaxon_426114
5142||238||Susceptibility to respiratory infections associated with CD8alpha chain mutation||http://www.orpha.net/ORDO/Orphanet_169085
5144||10994||hemin||http://purl.obolibrary.org/obo/CHEBI_50385
5143||238||Combined immunodeficiency due to CD3gamma deficiency||http://www.orpha.net/ORDO/Orphanet_169082
5145||5150||Ws-3||http://www.ebi.ac.uk/efo/EFO_0005159
5147||5150||Ws-1||http://www.ebi.ac.uk/efo/EFO_0005157
5146||10682||Genetic polyendocrinopathy||http://www.orpha.net/ORDO/Orphanet_183643
5148||5150||Ws-2||http://www.ebi.ac.uk/efo/EFO_0005158
5149||5152||Ler-1||http://www.ebi.ac.uk/efo/EFO_0005155
5150||3349||Wassilewskija ecotype||http://www.ebi.ac.uk/efo/EFO_0005156
5151||5098||Col-5||http://www.ebi.ac.uk/efo/EFO_0005153
5152||3349||Landsberg ecotype||http://www.ebi.ac.uk/efo/EFO_0005154
5153||14970||respiratory quotient||http://www.ebi.ac.uk/efo/EFO_0005189
5154||14970||CCL11 measurement||http://www.ebi.ac.uk/efo/EFO_0005188
5155||11802||Familial restrictive cardiomyopathy||http://www.orpha.net/ORDO/Orphanet_217635
5156||14970||C-peptide measurement||http://www.ebi.ac.uk/efo/EFO_0005187
5157||2672||uterus fundus||http://www.ebi.ac.uk/efo/EFO_0005186
5158||5155||Lysosomal disease with restrictive cardiomyopathy||http://www.orpha.net/ORDO/Orphanet_217638
5159||5502||Enterococcus mundtii||http://purl.obolibrary.org/obo/NCBITaxon_53346
5160||14970||waist height ratio||http://www.ebi.ac.uk/efo/EFO_0005191
5161||7330||red blood cell distribution width||http://www.ebi.ac.uk/efo/EFO_0005192
5162||13770||Mirror polydactyly - vertebral segmentation - limbs defects||http://www.orpha.net/ORDO/Orphanet_3004
5164||14970||urinary nitrogen measurement||http://www.ebi.ac.uk/efo/EFO_0005190
5163||8026||Pyknoachondrogenesis||http://www.orpha.net/ORDO/Orphanet_3003
5166||4259||response to cholinesterase inhibitor||http://www.ebi.ac.uk/efo/EFO_0005195
5165||6265||Pyridoxine-dependent epilepsy||http://www.orpha.net/ORDO/Orphanet_3006
5168||14970||vasoactive peptide measurement||http://www.ebi.ac.uk/efo/EFO_0005196
5167||7943||Pyle disease||http://www.orpha.net/ORDO/Orphanet_3005
5170||6321||Pyruvate carboxylase deficiency||http://www.orpha.net/ORDO/Orphanet_3008
5169||7488||serum IgG glycosylation measurement||http://www.ebi.ac.uk/efo/EFO_0005193
5171||14970||amyloid-beta measurement||http://www.ebi.ac.uk/efo/EFO_0005194
5172||3349||Coimbra ecotype||http://www.ebi.ac.uk/efo/EFO_0005176
5173||5122||Bay-0||http://www.ebi.ac.uk/efo/EFO_0005175
5174||3349||San Eleno ecotype||http://www.ebi.ac.uk/efo/EFO_0005178
5175||5172||Co-1||http://www.ebi.ac.uk/efo/EFO_0005177
5176||5502||Cyanothece||http://purl.obolibrary.org/obo/NCBITaxon_43988
5177||5174||Se-0||http://www.ebi.ac.uk/efo/EFO_0005179
5178||5502||Cyanothece sp. ATCC 51142||http://purl.obolibrary.org/obo/NCBITaxon_43989
5179||13587||CD1 mus strain||http://www.ebi.ac.uk/efo/EFO_0005180
5180||13587||C57BL||http://www.ebi.ac.uk/efo/EFO_0005181
5181||3626||N Dama||http://www.ebi.ac.uk/efo/EFO_0005182
5182||3626||Boran cattle||http://www.ebi.ac.uk/efo/EFO_0005183
5183||13587||DBA/2J||http://www.ebi.ac.uk/efo/EFO_0005184
5184||2672||terminal ileum||http://www.ebi.ac.uk/efo/EFO_0005185
5185||11327||Uniparental disomy of chromosome X||http://www.orpha.net/ORDO/Orphanet_263793
5186||10230||Familial isolated arrhythmogenic right ventricular dysplasia||http://www.orpha.net/ORDO/Orphanet_217656
5187||6287||Desmosterolosis||http://www.orpha.net/ORDO/Orphanet_35107
5188||14970||transplant outcome measurement||http://www.ebi.ac.uk/efo/EFO_0005198
5189||14970||beta-2 microglobulin measurement||http://www.ebi.ac.uk/efo/EFO_0005197
5190||5188||renal transplant outcome measurement||http://www.ebi.ac.uk/efo/EFO_0005199
5191||194||Functional neutrophil defect||http://www.orpha.net/ORDO/Orphanet_183681
5192||8190||(2,4-dichlorophenoxy)acetic acid||http://purl.obolibrary.org/obo/CHEBI_28854
5193||10994||organochlorine pesticides||http://purl.obolibrary.org/obo/CHEBI_25705
5194||10994||P-nitrotoluene||http://purl.obolibrary.org/obo/CHEBI_33097
5195||10994||O-nitrotoluene||http://purl.obolibrary.org/obo/CHEBI_33098
5196||5220||Partial duplication of the short arm of chromosome X||http://www.orpha.net/ORDO/Orphanet_263775
5197||7074||Blepharophimosis-intellectual disability syndrome, SBBYS type||http://www.orpha.net/ORDO/Orphanet_3047
5198||9742||Epidermal nevus syndrome||http://www.orpha.net/ORDO/Orphanet_35125
5199||11801||Familial infantile bilateral striatal necrosis||http://www.orpha.net/ORDO/Orphanet_225154
5200||6264||Hemolytic anemia due to pyrimidine 5  nucleotidase deficiency||http://www.orpha.net/ORDO/Orphanet_35120
5201||15519||Autosomal dominant aplasia and myelodysplasia||http://www.orpha.net/ORDO/Orphanet_314399
5202||2252||Intellectual disability - balding - patella luxation - acromicria||http://www.orpha.net/ORDO/Orphanet_3041
5203||4139||Intellectual disability - cataracts - calcified pinnae - myopathy||http://www.orpha.net/ORDO/Orphanet_3042
5204||5414||Congenital sucrase-isomaltase deficiency||http://www.orpha.net/ORDO/Orphanet_35122
5205||7948||Short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome||http://www.orpha.net/ORDO/Orphanet_314394
5207||15572||Acid phosphatase deficiency||http://www.orpha.net/ORDO/Orphanet_35121
5206||2252||Intellectual disability - dysmorphism - hypogonadism - diabetes mellitus||http://www.orpha.net/ORDO/Orphanet_3044
5208||10994||5-amino-1-(5-phospho-D-ribosyl)imidazole||http://purl.obolibrary.org/obo/CHEBI_28843
5209||5220||Partial duplication of the long arm of chromosome X||http://www.orpha.net/ORDO/Orphanet_263783
5210||4766||Delayed membranous cranial ossification||http://www.orpha.net/ORDO/Orphanet_3034
5211||5053||Growth delay - hydrocephaly - lung hypoplasia||http://www.orpha.net/ORDO/Orphanet_3035
5212||2252||Delayed speech - facial asymmetry - strabismus - ear lobe creases||http://www.orpha.net/ORDO/Orphanet_3038
5213||5955||NPHP3-related Meckel-like syndrome||http://www.orpha.net/ORDO/Orphanet_3032
5214||10994||gibberellin A3||http://purl.obolibrary.org/obo/CHEBI_28833
5215||7319||Caudal regression sequence||http://www.orpha.net/ORDO/Orphanet_3027
5216||4904||Partial deletion of the long arm of chromosome X||http://www.orpha.net/ORDO/Orphanet_263756
5217||9919||Ramsay-Hunt syndrome||http://www.orpha.net/ORDO/Orphanet_3020
5218||5300||RAPADILINO syndrome||http://www.orpha.net/ORDO/Orphanet_3021
5219||4027||phytosterol||http://purl.obolibrary.org/obo/CHEBI_28824
5220||11327||Partial duplication of chromosome X||http://www.orpha.net/ORDO/Orphanet_263768
5221||4834||Ramon syndrome||http://www.orpha.net/ORDO/Orphanet_3019
5222||6244||Radius absent - anogenital anomalies||http://www.orpha.net/ORDO/Orphanet_3016
5223||6244||Radio-renal syndrome||http://www.orpha.net/ORDO/Orphanet_3015
5224||4139||Qazi-Markouizos syndrome||http://www.orpha.net/ORDO/Orphanet_3010
5225||4139||Spastic tetraplegia - retinitis pigmentosa - intellectual disability||http://www.orpha.net/ORDO/Orphanet_3011
5226||11801||Sporadic infantile bilateral striatal necrosis||http://www.orpha.net/ORDO/Orphanet_225147
5227||12769||Multinodular goiter - cystic kidney - polydactyly||http://www.orpha.net/ORDO/Orphanet_2091
5228||306||Focal dermal hypoplasia||http://www.orpha.net/ORDO/Orphanet_2092
5230||6202||Silver-Russell syndrome due to imprinting defect of 11p15||http://www.orpha.net/ORDO/Orphanet_231140
5229||7942||Grant syndrome||http://www.orpha.net/ORDO/Orphanet_2097
5231||7990||Acromesomelic dysplasia, Grebe type||http://www.orpha.net/ORDO/Orphanet_2098
5232||306||Gorlin-Chaudhry-Moss syndrome||http://www.orpha.net/ORDO/Orphanet_2095
5234||1560||monolayer-surrounded lipid storage body||http://purl.obolibrary.org/obo/GO_0012511
5233||6202||Silver-Russell syndrome due to 11p15 microduplication||http://www.orpha.net/ORDO/Orphanet_231144
5235||5267||Disorder of lipid absorption and transport||http://www.orpha.net/ORDO/Orphanet_309028
5236||6202||Silver-Russell syndrome due to maternal uniparental disomy of chromosome 11||http://www.orpha.net/ORDO/Orphanet_231147
5237||6287||Mevalonate kinase deficiency||http://www.orpha.net/ORDO/Orphanet_309025
5238||5235||Pancreatic triacylglycerol lipase deficiency||http://www.orpha.net/ORDO/Orphanet_309031
5239||1327||Prelingual non-syndromic genetic deafness||http://www.orpha.net/ORDO/Orphanet_216445
5240||6043||cellular nitrogen compound biosynthetic process||http://purl.obolibrary.org/obo/GO_0044271
5241||5295||protein localization||http://purl.obolibrary.org/obo/GO_0008104
5242||2252||Prominent glabella - microcephaly - hypogenitalism||http://www.orpha.net/ORDO/Orphanet_2083
5243||6899||Glaucoma - ectopia - microspherophakia - stiff joints - short stature||http://www.orpha.net/ORDO/Orphanet_2084
5244||6899||Glaucoma - sleep apnea||http://www.orpha.net/ORDO/Orphanet_2085
5245||3753||Glomerulonephritis - sparse hair - telangiectasis||http://www.orpha.net/ORDO/Orphanet_2087
5246||3121||CANDLE syndrome||http://www.orpha.net/ORDO/Orphanet_325004
5247||266||Glycogen storage disease due to GLUT2 deficiency||http://www.orpha.net/ORDO/Orphanet_2088
5249||4928||Beckwith-Wiedemann syndrome due to 11p15 translocation/inversion||http://www.orpha.net/ORDO/Orphanet_231130
5248||9403||Glycogen storage disease due to hepatic glycogen synthase deficiency||http://www.orpha.net/ORDO/Orphanet_2089
5250||10994||bleomycin A2||http://purl.obolibrary.org/obo/CHEBI_3139
5252||6202||Silver-Russell syndrome due to 7p11.2p13 microduplication||http://www.orpha.net/ORDO/Orphanet_231137
5251||7404||Duplication of the pituitary gland||http://www.orpha.net/ORDO/Orphanet_314621
5253||10652||obsolete_Arabidopsis Growth Stage 6.10||http://www.ebi.ac.uk/efo/EFO_0005792
5254||2607||ER to Golgi transport vesicle membrane||http://purl.obolibrary.org/obo/GO_0012507
5255||11088||FL.01 1/4 of flowers open stage||http://www.ebi.ac.uk/efo/EFO_0005793
5256||1491||endomembrane system||http://purl.obolibrary.org/obo/GO_0012505
5257||5502||Streptomyces reticuliscabiei||http://purl.obolibrary.org/obo/NCBITaxon_146821
5259||1491||vesicle membrane||http://purl.obolibrary.org/obo/GO_0012506
5258||5715||cellular macromolecule metabolic process||http://purl.obolibrary.org/obo/GO_0044260
5260||6825||CLN11 disease||http://www.orpha.net/ORDO/Orphanet_314629
5261||1327||Postlingual non-syndromic genetic deafness||http://www.orpha.net/ORDO/Orphanet_216452
5262||5800|| neonatal abstinence syndrome ||http://www.ebi.ac.uk/efo/EFO_0005799
5263||5502||Escherichia coli BL21(DE3)||http://purl.obolibrary.org/obo/NCBITaxon_469008
5264||4427||cellular protein metabolic process||http://purl.obolibrary.org/obo/GO_0044267
5265||4139||GMS syndrome||http://www.orpha.net/ORDO/Orphanet_2090
5266||4705||Familial cerebral saccular aneurysm||http://www.orpha.net/ORDO/Orphanet_231160
5267||15571||Disorder of lipid metabolism||http://www.orpha.net/ORDO/Orphanet_309005
5268||6379||Usher syndrome type 1||http://www.orpha.net/ORDO/Orphanet_231169
5269||5270||blastoma||http://www.ebi.ac.uk/efo/EFO_0005785
5270||2162||embryonal neoplasm||http://www.ebi.ac.uk/efo/EFO_0005784
5271||1006||NUT midline carcinoma||http://www.ebi.ac.uk/efo/EFO_0005783
5272||9380||age-related hearing impairment||http://www.ebi.ac.uk/efo/EFO_0005782
5273||8110||Familial lipoprotein lipase deficiency||http://www.orpha.net/ORDO/Orphanet_309015
5274||6432||Autosomal recessive spastic ataxia with leukoencephalopathy||http://www.orpha.net/ORDO/Orphanet_314603
5275||238||Combined immunodeficiency T  B  due to partial RAG1 deficiency||http://www.orpha.net/ORDO/Orphanet_231154
5276||1391||brain disease||http://www.ebi.ac.uk/efo/EFO_0005774
5279||12497||retinal detachment||http://www.ebi.ac.uk/efo/EFO_0005773
5277||1826||Solanum phureja||http://purl.obolibrary.org/obo/NCBITaxon_172790
5280||5937||Severe combined immunodeficiency due to IKK2 deficiency||http://www.orpha.net/ORDO/Orphanet_397787
5278||7111||material property||http://www.ifomis.org/bfo/1.1/snap#SpecificallyDependentContinuant
5281||2509||Proximal spinal muscular atrophy type 1||http://www.orpha.net/ORDO/Orphanet_83330
5282||1391||aortic disease||http://www.ebi.ac.uk/efo/EFO_0005775
5283||3866||Syndromic diarrhea||http://www.orpha.net/ORDO/Orphanet_84064
5284||8110||Familial apolipoprotein C-II deficiency||http://www.orpha.net/ORDO/Orphanet_309020
5285||2165||neurodegenerative disease||http://www.ebi.ac.uk/efo/EFO_0005772
5286||1761||ovarian disease||http://www.ebi.ac.uk/efo/EFO_0005771
5287||4717||Developmental anomaly of metabolic origin||http://www.orpha.net/ORDO/Orphanet_139009
5288||1022||Fenneropenaeus merguiensis||http://purl.obolibrary.org/obo/NCBITaxon_71412
5289||2252||5q31.3 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_314655
5290||6054||Autosomal dominant beta2-microglobulinic amyloidosis||http://www.orpha.net/ORDO/Orphanet_314652
5291||6379||Usher syndrome type 3||http://www.orpha.net/ORDO/Orphanet_231183
5292||5295||metabolic process||http://purl.obolibrary.org/obo/GO_0008152
5293||4609||estrogen||http://purl.obolibrary.org/obo/CHEBI_50114
5294||10994||androgen||http://purl.obolibrary.org/obo/CHEBI_50113
5295||1014||biological process||http://purl.obolibrary.org/obo/GO_0008150
5296||4259||response to rate control therapy||http://www.ebi.ac.uk/efo/EFO_0005768
5297||920||sex hormone||http://purl.obolibrary.org/obo/CHEBI_50112
5298||1391||calcium metabolic disease||http://www.ebi.ac.uk/efo/EFO_0005769
5299||14970||skin fluorescence measurement||http://www.ebi.ac.uk/efo/EFO_0005766
5300||12083||Orofacial clefting syndrome||http://www.orpha.net/ORDO/Orphanet_139039
5301||14970||rheumatoid factor measurement||http://www.ebi.ac.uk/efo/EFO_0005767
5302||6732||extra or missing processual parts||http://purl.obolibrary.org/obo/PATO_0001564
5303||5302||having extra processual parts||http://purl.obolibrary.org/obo/PATO_0001561
5304||14970||serum carcinoembryonic antigen measurement||http://www.ebi.ac.uk/efo/EFO_0005760
5305||8970||lupus nephritis||http://www.ebi.ac.uk/efo/EFO_0005761
5306||4717||Malformation syndrome with connective tissue involvement||http://www.orpha.net/ORDO/Orphanet_139030
5307||13516||response to haloperidol||http://www.ebi.ac.uk/efo/EFO_0005765
5308||10929||neuropathic pain||http://www.ebi.ac.uk/efo/EFO_0005762
5309||14970||pulse pressure measurement||http://www.ebi.ac.uk/efo/EFO_0005763
5310||10994||bromobenzene||http://purl.obolibrary.org/obo/CHEBI_3179
5311||6379||Usher syndrome type 2||http://www.orpha.net/ORDO/Orphanet_231178
5312||4344||TMEM165-CDG||http://www.orpha.net/ORDO/Orphanet_314667
5313||8024||Segmental progressive overgrowth syndrome with fibroadipose hyperplasia||http://www.orpha.net/ORDO/Orphanet_314662
5314||799||excitatory amino acid agonist||http://purl.obolibrary.org/obo/CHEBI_50103
5315||15526||rheumatic disease||http://www.ebi.ac.uk/efo/EFO_0005755
5316||11618||skin wound||http://www.ebi.ac.uk/efo/EFO_0005756
5317||4717||Malformation syndrome with skin/mucosae involvement||http://www.orpha.net/ORDO/Orphanet_139027
5320||10994||monensin A||http://purl.obolibrary.org/obo/CHEBI_27617
5318||6867||vaginal inflammation||http://www.ebi.ac.uk/efo/EFO_0005757
5319||7377||Senior-Boichis syndrome||http://www.orpha.net/ORDO/Orphanet_84081
5321||12497||cycloplegia||http://www.ebi.ac.uk/efo/EFO_0005758
5322||11563||eye allergy||http://www.ebi.ac.uk/efo/EFO_0005751
5323||6867||eye inflammation||http://www.ebi.ac.uk/efo/EFO_0005752
5324||1391||ocular vascular disease||http://www.ebi.ac.uk/efo/EFO_0005753
5325||1391||parathyroid disease||http://www.ebi.ac.uk/efo/EFO_0005754
5326||9898||Parkinsonim due to ATP13A2 deficiency||http://www.orpha.net/ORDO/Orphanet_314632
5327||4266||Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency||http://www.orpha.net/ORDO/Orphanet_314637
5328||8190||1-(2,4-dichlorobenzyl)-1H-indazole-3-carboxylic acid||http://purl.obolibrary.org/obo/CHEBI_50138
5329||8798||Mucopolysaccharidosis type 2, severe form||http://www.orpha.net/ORDO/Orphanet_217085
5330||10994||bromocriptine methanesulfonate||http://purl.obolibrary.org/obo/CHEBI_3182
5331||15549||Unknown leukodystrophy||http://www.orpha.net/ORDO/Orphanet_84096
5332||6910||Hereditary thermosensitive neuropathy||http://www.orpha.net/ORDO/Orphanet_84093
5333||770||G2||http://www.ebi.ac.uk/efo/EFO_0005746
5334||770||GM2||http://www.ebi.ac.uk/efo/EFO_0005747
5335||3753||Fibronectin glomerulopathy||http://www.orpha.net/ORDO/Orphanet_84090
5337||770||CME-W2||http://www.ebi.ac.uk/efo/EFO_0005744
5336||10994||5-aza-2 -deoxycytidine||http://purl.obolibrary.org/obo/CHEBI_50131
5338||770||fGS/OSS||http://www.ebi.ac.uk/efo/EFO_0005745
5339||770||lung fibroblast derived cell line||http://www.ebi.ac.uk/efo/EFO_0005742
5340||770||CME-W1-Cl.8 ||http://www.ebi.ac.uk/efo/EFO_0005743
5341||3023||46,XY disorder of sex development due to testicular steroidogenesis defect||http://www.orpha.net/ORDO/Orphanet_90787
5342||770||iPSC derived cell line||http://www.ebi.ac.uk/efo/EFO_0005740
5344||3023||46,XY disorder of sex development due to adrenal and testicular steroidogenesis defect||http://www.orpha.net/ORDO/Orphanet_90786
5343||1391||infectious disease||http://www.ebi.ac.uk/efo/EFO_0005741
5345||10994||cycloheximide||http://purl.obolibrary.org/obo/CHEBI_27641
5346||4968||46,XY disorder of sex development due to testosterone synthesis defect||http://www.orpha.net/ORDO/Orphanet_90783
5347||9856||Non-progressive cerebellar ataxia with intellectual disability||http://www.orpha.net/ORDO/Orphanet_314647
5348||8798||Mucopolysaccharidosis type 2, attenuated form||http://www.orpha.net/ORDO/Orphanet_217093
5349||770||ESC derived cell line||http://www.ebi.ac.uk/efo/EFO_0005738
5350||5502||Campylobacter jejuni subsp. jejuni 81-176||http://purl.obolibrary.org/obo/NCBITaxon_354242
5351||10652||obsolete_induced pluripotent stem cell||http://www.ebi.ac.uk/efo/EFO_0005739
5352||770||muscle cell derived cell line||http://www.ebi.ac.uk/efo/EFO_0005734
5353||770||smooth muscle cell derived cell line||http://www.ebi.ac.uk/efo/EFO_0005735
5354||10994||rosiglitazone||http://purl.obolibrary.org/obo/CHEBI_50122
5355||770||bronchial smooth muscle cell derived cell line||http://www.ebi.ac.uk/efo/EFO_0005736
5356||3042||46,XX disorder of sex development induced by fetal androgens excess||http://www.orpha.net/ORDO/Orphanet_90776
5358||770||endothelial cell derived cell line||http://www.ebi.ac.uk/efo/EFO_0005730
5357||6299||Rhabditis remanei||http://purl.obolibrary.org/obo/NCBITaxon_446304
5359||770||cardiac myocyte cell derived cell line||http://www.ebi.ac.uk/efo/EFO_0005731
5360||5502||uncultured Acidobacteria bacterium||http://purl.obolibrary.org/obo/NCBITaxon_171953
5361||770||SK-N-DZ||http://www.ebi.ac.uk/efo/EFO_0005721
5362||770||SK-MEL-5||http://www.ebi.ac.uk/efo/EFO_0005720
5363||770||GM23248||http://www.ebi.ac.uk/efo/EFO_0005723
5364||770||SJCRH30||http://www.ebi.ac.uk/efo/EFO_0005722
5365||770||BE(2)-C||http://www.ebi.ac.uk/efo/EFO_0005725
5367||770||MM.1S||http://www.ebi.ac.uk/efo/EFO_0005724
5366||8190||retinoic acid||http://purl.obolibrary.org/obo/CHEBI_26536
5368||10994||actinomycin D||http://purl.obolibrary.org/obo/CHEBI_27666
5369||770||LNCaP clone FGC||http://www.ebi.ac.uk/efo/EFO_0005726
5370||1681||bronchial epithelial cell derived cell line||http://www.ebi.ac.uk/efo/EFO_0005728
5371||10994||gefitinib||http://purl.obolibrary.org/obo/CHEBI_49668
5372||2997||Autosomal dominant Charcot-Marie-Tooth disease type 2 due to MARS mutation||http://www.orpha.net/ORDO/Orphanet_397735
5373||10994||indomethacin||http://purl.obolibrary.org/obo/CHEBI_49662
5374||1826||Vitis sp. cv.  Norton ||http://purl.obolibrary.org/obo/NCBITaxon_171960
5375||770||HFF-Myc||http://www.ebi.ac.uk/efo/EFO_0005710
5376||770||LHCN-M2||http://www.ebi.ac.uk/efo/EFO_0005714
5377||770||8988T||http://www.ebi.ac.uk/efo/EFO_0005713
5378||770||RPMI-7951||http://www.ebi.ac.uk/efo/EFO_0005712
5379||770||HPDE6-E6E7||http://www.ebi.ac.uk/efo/EFO_0005711
5381||10994||camptothecin||http://purl.obolibrary.org/obo/CHEBI_27656
5380||770||Ishikawa||http://www.ebi.ac.uk/efo/EFO_0005718
5382||5383||retinoblastoma (nonhereditary)||http://www.ebi.ac.uk/efo/EFO_0005717
5383||766||retinal cancer||http://www.ebi.ac.uk/efo/EFO_0005716
5384||770||WERI-Rb-1||http://www.ebi.ac.uk/efo/EFO_0005715
5385||770||Karpas 422||http://www.ebi.ac.uk/efo/EFO_0005719
5386||7675||COASY protein-associated neurodegeneration||http://www.orpha.net/ORDO/Orphanet_397725
5387||5502||Anaplasma phagocytophilum HZ||http://purl.obolibrary.org/obo/NCBITaxon_212042
5388||770||olfactory neurosphere cell line||http://www.ebi.ac.uk/efo/EFO_0005705
5389||770||HuH-7.5||http://www.ebi.ac.uk/efo/EFO_0005704
5390||770||786-0||http://www.ebi.ac.uk/efo/EFO_0005707
5391||770||Mel-2183||http://www.ebi.ac.uk/efo/EFO_0005706
5392||2162||malignant rhabdoid tumour||http://www.ebi.ac.uk/efo/EFO_0005701
5393||770||TTC549||http://www.ebi.ac.uk/efo/EFO_0005700
5394||770||G401.6||http://www.ebi.ac.uk/efo/EFO_0005703
5395||770||A204.1||http://www.ebi.ac.uk/efo/EFO_0005702
5396||120||renal cell adenocarcinoma||http://www.ebi.ac.uk/efo/EFO_0005708
5397||770||HTR8/SVneo||http://www.ebi.ac.uk/efo/EFO_0005709
5398||5025||Neurospora tetrasperma||http://purl.obolibrary.org/obo/NCBITaxon_40127
5399||13496||Acanthamoeba polyphaga mimivirus||http://purl.obolibrary.org/obo/NCBITaxon_212035
5400||1721||Joubert syndrome with Jeune asphyxiating thoracic dystrophy||http://www.orpha.net/ORDO/Orphanet_397715
5401||2252||Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome||http://www.orpha.net/ORDO/Orphanet_397709
5402||2299||disseminated intravascular coagulation||http://purl.obolibrary.org/obo/HP_0005521
5403||1022||Harpagifer antarcticus||http://purl.obolibrary.org/obo/NCBITaxon_43256
5404||3042||46,XX disorder of sex development induced by fetoplacental androgens excess||http://www.orpha.net/ORDO/Orphanet_325061
5405||6347||Macrodactyly of fingers, unilateral||http://www.orpha.net/ORDO/Orphanet_295239
5406||6330||Congenital patella dislocation, bilateral||http://www.orpha.net/ORDO/Orphanet_295237
5407||6330||Congenital patella dislocation, unilateral||http://www.orpha.net/ORDO/Orphanet_295234
5409||3150||46,XX disorder of gonadal development||http://www.orpha.net/ORDO/Orphanet_325055
5408||6331||Congenital genu flexum||http://www.orpha.net/ORDO/Orphanet_295232
5410||7984||Spondylocamptodactyly syndrome||http://www.orpha.net/ORDO/Orphanet_3180
5411||2252||Holoprosencephaly - radial heart renal anomalies||http://www.orpha.net/ORDO/Orphanet_3186
5412||4834||Steatocystoma multiplex - natal teeth||http://www.orpha.net/ORDO/Orphanet_3184
5413||4454||Vanadium||http://purl.obolibrary.org/obo/CHEBI_27698
5414||6309||Disorder of carbohydrate absorption and transport||http://www.orpha.net/ORDO/Orphanet_309001
5415||10994||acetazolamide||http://purl.obolibrary.org/obo/CHEBI_27690
5417||4692||Corneal-cerebellar syndrome||http://www.orpha.net/ORDO/Orphanet_3177
5416||6354||Macrodactyly of toes, unilateral||http://www.orpha.net/ORDO/Orphanet_295243
5418||6354||Macrodactyly of toes, bilateral||http://www.orpha.net/ORDO/Orphanet_295245
5419||8191||copper(2 ) sulfate||http://purl.obolibrary.org/obo/CHEBI_23414
5420||6347||Macrodactyly of fingers, bilateral||http://www.orpha.net/ORDO/Orphanet_295241
5421||13770||Eyebrow duplication - syndactyly||http://www.orpha.net/ORDO/Orphanet_3172
5422||613||Infantile spasms - broad thumbs||http://www.orpha.net/ORDO/Orphanet_3173
5424||770||GM07029||http://purl.obolibrary.org/obo/CLO_0036870
5423||4736||Spasticity - intellectual disability - X-linked epilepsy||http://www.orpha.net/ORDO/Orphanet_3175
5425||11882||Spina bifida - hypospadias||http://www.orpha.net/ORDO/Orphanet_3176
5426||4569||Humero-ulnar synostosis, bilateral||http://www.orpha.net/ORDO/Orphanet_295215
5427||4569||Humero-ulnar synostosis, unilateral||http://www.orpha.net/ORDO/Orphanet_295213
5428||5005||human oral metagenome||http://purl.obolibrary.org/obo/NCBITaxon_447426
5430||5881||Radio-ulnar synostosis, bilateral||http://www.orpha.net/ORDO/Orphanet_295219
5429||9560||Periodic paralysis with later-onset distal motor neuropathy||http://www.orpha.net/ORDO/Orphanet_397750
5431||5881||Radio-ulnar synostosis, unilateral||http://www.orpha.net/ORDO/Orphanet_295217
5433||5884||Humero-radial synostosis, bilateral||http://www.orpha.net/ORDO/Orphanet_295211
5432||9965||Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies||http://www.orpha.net/ORDO/Orphanet_397758
5434||4087||Periodic paralysis with transient compartment-like syndrome||http://www.orpha.net/ORDO/Orphanet_397755
5435||10994||lapatinib||http://purl.obolibrary.org/obo/CHEBI_49603
5436||6332||Congenital elbow dislocation, unilateral||http://www.orpha.net/ORDO/Orphanet_295225
5437||6332||Congenital elbow dislocation, bilateral||http://www.orpha.net/ORDO/Orphanet_295227
5438||6331||Congenital genu recurvatum||http://www.orpha.net/ORDO/Orphanet_295229
5439||2252||Stimmler syndrome||http://www.orpha.net/ORDO/Orphanet_3199
5441||5700||Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome||http://www.orpha.net/ORDO/Orphanet_397744
5440||6438||Madelung deformity, unilateral||http://www.orpha.net/ORDO/Orphanet_295221
5442||6438||Madelung deformity, bilateral||http://www.orpha.net/ORDO/Orphanet_295223
5443||266||Steroid dehydrogenase deficiency - dental anomalies||http://www.orpha.net/ORDO/Orphanet_3196
5444||4732||Hereditary hyperekplexia||http://www.orpha.net/ORDO/Orphanet_3197
5445||9622||Subaortic stenosis - short stature||http://www.orpha.net/ORDO/Orphanet_3191
5446||6087||Supravalvular aortic stenosis||http://www.orpha.net/ORDO/Orphanet_3193
5447||306||Stern-Lubinsky-Durrie syndrome||http://www.orpha.net/ORDO/Orphanet_3194
5448||2252||Say-Barber-Miller syndrome||http://www.orpha.net/ORDO/Orphanet_3132
5449||4701||Ulnar-mammary syndrome||http://www.orpha.net/ORDO/Orphanet_3138
5450||6595||Alpha-N-acetylgalactosaminidase deficiency||http://www.orpha.net/ORDO/Orphanet_3137
5451||3642||Familial Scheuermann disease||http://www.orpha.net/ORDO/Orphanet_3135
5452||9994||Congenital vertical talus, unilateral||http://www.orpha.net/ORDO/Orphanet_295201
5453||2252||SCARF syndrome||http://www.orpha.net/ORDO/Orphanet_3134
5454||13770||Say-Field-Coldwell syndrome||http://www.orpha.net/ORDO/Orphanet_3133
5455||5883||Humero-radio-ulnar synostosis, unilateral||http://www.orpha.net/ORDO/Orphanet_295205
5457||11472||Partial deletion of the long arm of chromosome 13||http://www.orpha.net/ORDO/Orphanet_262101
5456||1022||Agrotis segetum||http://purl.obolibrary.org/obo/NCBITaxon_47767
5458||9994||Congenital vertical talus, bilateral||http://www.orpha.net/ORDO/Orphanet_295203
5459||5884||Humero-radial synostosis, unilateral||http://www.orpha.net/ORDO/Orphanet_295209
5460||5883||Humero-radio-ulnar synostosis, bilateral||http://www.orpha.net/ORDO/Orphanet_295207
5461||8386||Immune dysregulation disease with immunodeficiency||http://www.orpha.net/ORDO/Orphanet_169361
5462||11472||Partial deletion of the long arm of chromosome 15||http://www.orpha.net/ORDO/Orphanet_262119
5463||5502||Lactobacillus crispatus||http://purl.obolibrary.org/obo/NCBITaxon_47770
5464||4810||Nephrogenic diabetes insipidus - intracranial calcification||http://www.orpha.net/ORDO/Orphanet_3145
5465||4006||Schneckenbecken dysplasia||http://www.orpha.net/ORDO/Orphanet_3144
5466||11472||Partial deletion of the long arm of chromosome 14||http://www.orpha.net/ORDO/Orphanet_262110
5467||8126||polyuria||http://purl.obolibrary.org/obo/HP_0000103
5468||12736||KRT14-related epidermolysis bullosa simplex||http://www.orpha.net/ORDO/Orphanet_89838
5469||12748||Epidermolysis bullosa simplex superficialis||http://www.orpha.net/ORDO/Orphanet_89839
5470||7943||Sclerosteosis||http://www.orpha.net/ORDO/Orphanet_3152
5471||14891||Multiple sclerosis - ichthyosis - factor VIII deficiency||http://www.orpha.net/ORDO/Orphanet_3151
5473||2957||Septo-optic dysplasia||http://www.orpha.net/ORDO/Orphanet_3157
5472||10658||Partial deletion of the long arm of chromosome 16||http://www.orpha.net/ORDO/Orphanet_262128
5474||7377||Senior-Loken syndrome||http://www.orpha.net/ORDO/Orphanet_3156
5475||7175||DNA repair defect other than combined T-cell and B-cell immunodeficiencies||http://www.orpha.net/ORDO/Orphanet_169346
5476||9923||host cell nucleus||http://purl.obolibrary.org/obo/GO_0042025
5477||7175||Immuno-osseous dysplasia||http://www.orpha.net/ORDO/Orphanet_169349
5478||372||Syndromic lymphedema||http://www.orpha.net/ORDO/Orphanet_89832
5479||1393||SHORT syndrome||http://www.orpha.net/ORDO/Orphanet_3163
5480||2252||Omphalocele syndrome, Shprintzen-Goldberg type||http://www.orpha.net/ORDO/Orphanet_3164
5481||10732||Siegler-Brewer-Carey syndrome||http://www.orpha.net/ORDO/Orphanet_3167
5482||4302||Sialuria||http://www.orpha.net/ORDO/Orphanet_3166
5483||10640||Partial deletion of the long arm of chromosome 17||http://www.orpha.net/ORDO/Orphanet_262137
5484||6246||Sirenomelia||http://www.orpha.net/ORDO/Orphanet_3169
5485||13770||Sillence syndrome||http://www.orpha.net/ORDO/Orphanet_3168
5486||5461||Immunodeficiency syndrome with autoimmunity||http://www.orpha.net/ORDO/Orphanet_169355
5487||508||jasmonic acids||http://purl.obolibrary.org/obo/CHEBI_24937
5488||6912||Autosomal recessive intermediate Charcot-Marie-Tooth disease||http://www.orpha.net/ORDO/Orphanet_268337
5489||4430||immunosuppressive agent||http://purl.obolibrary.org/obo/CHEBI_35705
5490||4430||xenobiotic||http://purl.obolibrary.org/obo/CHEBI_35703
5491||5300||Robin sequence - oligodactyly||http://www.orpha.net/ORDO/Orphanet_3104
5492||13306||Robinow-like syndrome||http://www.orpha.net/ORDO/Orphanet_3105
5493||8361||Autosomal dominant Robinow syndrome||http://www.orpha.net/ORDO/Orphanet_3107
5494||5502||Pseudomonas stutzeri A1501||http://purl.obolibrary.org/obo/NCBITaxon_379731
5495||10143||Richieri Costa-da Silva syndrome||http://www.orpha.net/ORDO/Orphanet_3101
5496||5300||Richieri Costa-Pereira syndrome||http://www.orpha.net/ORDO/Orphanet_3102
5497||5300||Roberts syndrome||http://www.orpha.net/ORDO/Orphanet_3103
5498||5502||Clostridium beijerinckii NCIMB 8052||http://purl.obolibrary.org/obo/NCBITaxon_290402
5499||4406||Hereditary thrombocytopenia with normal platelets||http://www.orpha.net/ORDO/Orphanet_268322
5500||5502||Buchnera aphidicola||http://purl.obolibrary.org/obo/NCBITaxon_9
5501||5747||Mayer-Rokitansky-K ster-Hauser syndrome||http://www.orpha.net/ORDO/Orphanet_3109
5502||5005||Bacteria||http://purl.obolibrary.org/obo/NCBITaxon_2
5503||266||Rotor syndrome||http://www.orpha.net/ORDO/Orphanet_3111
5504||12553||Generalized isolated dystonia||http://www.orpha.net/ORDO/Orphanet_376724
5505||6910||Roussy-L vy syndrome||http://www.orpha.net/ORDO/Orphanet_3115
5506||5877||Rombo syndrome||http://www.orpha.net/ORDO/Orphanet_3110
5507||12460||wound healing||http://purl.obolibrary.org/obo/GO_0042060
5508||6464||Neural tube closure defect||http://www.orpha.net/ORDO/Orphanet_268357
5509||13972||Saccharopinuria||http://www.orpha.net/ORDO/Orphanet_3124
5510||6610||Sakati-Nyhan syndrome||http://www.orpha.net/ORDO/Orphanet_3128
5511||6285||Sarcosinemia||http://www.orpha.net/ORDO/Orphanet_3129
5512||5959||Progressive cerebello-cerebral atrophy||http://www.orpha.net/ORDO/Orphanet_247198
5513||5502||Actinobacillus pleuropneumoniae serovar 7||http://purl.obolibrary.org/obo/NCBITaxon_209841
5514||5025||Saccharomyces paradoxus||http://purl.obolibrary.org/obo/NCBITaxon_27291
5516||2252||Ruvalcaba syndrome||http://www.orpha.net/ORDO/Orphanet_3121
5515||5025||Saccharomyces pastorianus||http://purl.obolibrary.org/obo/NCBITaxon_27292
5517||2874||dorsal anterior lateral line ganglion||http://purl.obolibrary.org/obo/UBERON_2001312
5518||1826||Spartina x townsendii||http://purl.obolibrary.org/obo/NCBITaxon_198504
5519||5520||Rare male infertility due to hypothalamic-pituitary-gonadal axis disorder of genetic origin||http://www.orpha.net/ORDO/Orphanet_399983
5520||4484||Rare genetic male infertility||http://www.orpha.net/ORDO/Orphanet_399980
5521||4142||Isolated thyroid-stimulating hormone deficiency||http://www.orpha.net/ORDO/Orphanet_90674
5523||2252||Acro-cardio-facial syndrome||http://www.orpha.net/ORDO/Orphanet_2008
5522||4935||Hypothyroidism due to TSH receptor mutations||http://www.orpha.net/ORDO/Orphanet_90673
5524||11472||Partial deletion of the long arm of chromosome 22||http://www.orpha.net/ORDO/Orphanet_262182
5526||5541||Total spina bifida aperta||http://www.orpha.net/ORDO/Orphanet_268377
5525||10994||triazolam||http://purl.obolibrary.org/obo/CHEBI_9674
5527||10994||tribenuron methyl||http://purl.obolibrary.org/obo/CHEBI_9678
5528||5025||Aspergillus fumigatus Af293||http://purl.obolibrary.org/obo/NCBITaxon_330879
5529||12769||Alar cartilages hypoplasia - coloboma - telecanthus||http://www.orpha.net/ORDO/Orphanet_2007
5530||6927||Laryngo-tracheo-esophageal cleft - pulmonary hypoplasia||http://www.orpha.net/ORDO/Orphanet_2005
5531||5300||Cleft lip/palate - deafness - sacral lipoma||http://www.orpha.net/ORDO/Orphanet_2003
5532||5300||Cleft lip/palate - intestinal malrotation - cardiopathy||http://www.orpha.net/ORDO/Orphanet_2001
5533||3058||outer membrane||http://purl.obolibrary.org/obo/GO_0019867
5534||5519||Rare male infertility due to adrenal disorder of genetic origin||http://www.orpha.net/ORDO/Orphanet_399994
5535||13769||Femur-fibula-ulna complex||http://www.orpha.net/ORDO/Orphanet_2019
5536||11456||Partial duplication of chromosome 2||http://www.orpha.net/ORDO/Orphanet_262196
5537||3330||Open iniencephaly||http://www.orpha.net/ORDO/Orphanet_268363
5538||5520||Male infertility due to obstructive azoospermia of genetic origin||http://www.orpha.net/ORDO/Orphanet_399998
5539||3330||Closed iniencephaly||http://www.orpha.net/ORDO/Orphanet_268366
5540||11456||Partial duplication of chromosome 1||http://www.orpha.net/ORDO/Orphanet_262191
5541||6197||Spina bifida aperta||http://www.orpha.net/ORDO/Orphanet_268369
5542||5502||Streptomyces avermitilis||http://purl.obolibrary.org/obo/NCBITaxon_33903
5544||10994||( )-catechin monohydrate||http://purl.obolibrary.org/obo/CHEBI_58994
5543||4834||Cleft palate - stapes fixation - oligodontia||http://www.orpha.net/ORDO/Orphanet_2010
5545||2252||Cleft palate - short stature - vertebral anomalies||http://www.orpha.net/ORDO/Orphanet_2015
5546||5300||Cleft palate-lateral synechia syndrome||http://www.orpha.net/ORDO/Orphanet_2016
5547||2302||Acquired porencephaly||http://www.orpha.net/ORDO/Orphanet_314697
5548||5300||Cleft palate - large ears - small head||http://www.orpha.net/ORDO/Orphanet_2013
5549||5541||Cervicothoracic spina bifida aperta||http://www.orpha.net/ORDO/Orphanet_268397
5550||1307||Panhypopituitarism||http://www.orpha.net/ORDO/Orphanet_90695
5551||5541||Cervical spina bifida aperta||http://www.orpha.net/ORDO/Orphanet_268392
5552||2390||Congenital fiber-type disproportion myopathy||http://www.orpha.net/ORDO/Orphanet_2020
5553||7971||Fibrochondrogenesis||http://www.orpha.net/ORDO/Orphanet_2021
5554||1619||Hereditary gingival fibromatosis||http://www.orpha.net/ORDO/Orphanet_2024
5555||4834||Gingival fibromatosis - facial dysmorphism||http://www.orpha.net/ORDO/Orphanet_2025
5556||4929||Endomyocardial fibroelastosis||http://www.orpha.net/ORDO/Orphanet_2022
5557||4834||Juvenile hyaline fibromatosis||http://www.orpha.net/ORDO/Orphanet_2028
5558||7966||Multiple non-ossifying fibromatosis||http://www.orpha.net/ORDO/Orphanet_2029
5559||306||Gingival fibromatosis-hypertrichosis syndrome||http://www.orpha.net/ORDO/Orphanet_2026
5560||238||Combined immunodeficiency due to STK4 deficiency||http://www.orpha.net/ORDO/Orphanet_314689
5561||4834||Gingival fibromatosis - progressive deafness||http://www.orpha.net/ORDO/Orphanet_2027
5562||5541||Thoracolumbosacral spina bifida aperta||http://www.orpha.net/ORDO/Orphanet_268384
5563||799||sedative drug||http://purl.obolibrary.org/obo/CHEBI_35717
5564||5541||Lumbosacral spina bifida aperta||http://www.orpha.net/ORDO/Orphanet_268388
5565||799||antifungal drug||http://purl.obolibrary.org/obo/CHEBI_35718
5566||10994||imidazole||http://purl.obolibrary.org/obo/CHEBI_50059
5567||4139||Hepatic fibrosis - renal cysts - intellectual disability||http://www.orpha.net/ORDO/Orphanet_2031
5568||2252||Cerebro-facio-articular syndrome||http://www.orpha.net/ORDO/Orphanet_314679
5569||306||Scalp-ear-nipple syndrome||http://www.orpha.net/ORDO/Orphanet_2036
5570||10994||vitamin A||http://purl.obolibrary.org/obo/CHEBI_12777
5571||10994||tomatine||http://purl.obolibrary.org/obo/CHEBI_9630
5572||5502||Lactobacillus johnsonii||http://purl.obolibrary.org/obo/NCBITaxon_33959
5573||10639||Partial deletion of the long arm of chromosome 18||http://www.orpha.net/ORDO/Orphanet_262146
5574||6085||heterocycle metabolic process||http://purl.obolibrary.org/obo/GO_0046483
5575||6307||Beta-thalassemia major||http://www.orpha.net/ORDO/Orphanet_231214
5576||382||Flynn-Aird syndrome||http://www.orpha.net/ORDO/Orphanet_2047
5577||307||FLOTCH syndrome||http://www.orpha.net/ORDO/Orphanet_2045
5578||9739||Hereditary epidermolysis bullosa associated with ocular features||http://www.orpha.net/ORDO/Orphanet_263676
5579||2252||Floating-Harbor syndrome||http://www.orpha.net/ORDO/Orphanet_2044
5580||5053||Tracheo-esophageal fistula - hypospadias||http://www.orpha.net/ORDO/Orphanet_2042
5581||15026||validation by reverse transcription PCR design||http://purl.obolibrary.org/obo/OBI_0001162
5582||15026||validation by real time PCR design||http://purl.obolibrary.org/obo/OBI_0001166
5583||10275||Centripetalis recessive dystrophic epidermolysis bullosa||http://www.orpha.net/ORDO/Orphanet_89841
5584||5578||Recessive dystrophic epidermolysis bullosa-generalized other||http://www.orpha.net/ORDO/Orphanet_89842
5585||10278||Junctional epidermolysis bullosa, non-Herlitz type||http://www.orpha.net/ORDO/Orphanet_89840
5586||10275||Dystrophic epidermolysis bullosa pruriginosa||http://www.orpha.net/ORDO/Orphanet_89843
5587||5478||Lissencephaly syndrome, Norman-Roberts type||http://www.orpha.net/ORDO/Orphanet_89844
5588||10628||Partial deletion of the long arm of chromosome 19||http://www.orpha.net/ORDO/Orphanet_262155
5589||6307||Dominant beta-thalassemia||http://www.orpha.net/ORDO/Orphanet_231226
5590||4027||tomatidine||http://purl.obolibrary.org/obo/CHEBI_9629
5591||6307||Beta-thalassemia intermedia||http://www.orpha.net/ORDO/Orphanet_231222
5592||2252||Fryns syndrome||http://www.orpha.net/ORDO/Orphanet_2059
5593||5502||Prochlorococcus marinus str. MIT 9515||http://purl.obolibrary.org/obo/NCBITaxon_167542
5594||9775||Essential fructosuria||http://www.orpha.net/ORDO/Orphanet_2056
5595||6899||Blepharophimosis - ptosis - esotropia - syndactyly - short stature||http://www.orpha.net/ORDO/Orphanet_2057
5596||5700||Fraser syndrome||http://www.orpha.net/ORDO/Orphanet_2052
5597||12769||Freeman-Sheldon syndrome||http://www.orpha.net/ORDO/Orphanet_2053
5598||7942||Cole-Carpenter syndrome||http://www.orpha.net/ORDO/Orphanet_2050
5599||770||KMS-11||http://www.ebi.ac.uk/efo/EFO_0005694
5600||15011||transposable element identification design||http://www.ebi.ac.uk/efo/EFO_0005692
5601||15011||mobile element identification design||http://www.ebi.ac.uk/efo/EFO_0005693
5603||5611||Delta-beta-thalassemia||http://www.orpha.net/ORDO/Orphanet_231237
5602||10631||Partial deletion of the long arm of chromosome 20||http://www.orpha.net/ORDO/Orphanet_262164
5604||770||Daoy||http://www.ebi.ac.uk/efo/EFO_0005698
5605||2597||desmoplastic medulloblastoma||http://www.ebi.ac.uk/efo/EFO_0005699
5606||770||D721Med||http://www.ebi.ac.uk/efo/EFO_0005696
5607||770||M059J||http://www.ebi.ac.uk/efo/EFO_0005697
5608||5912||Gastrocutaneous syndrome||http://www.orpha.net/ORDO/Orphanet_2069
5609||10994||butein||http://purl.obolibrary.org/obo/CHEBI_3237
5610||306||GAPO syndrome||http://www.orpha.net/ORDO/Orphanet_2067
5611||4490||Beta-thalassemia associated with another hemoglobin anomaly||http://www.orpha.net/ORDO/Orphanet_231230
5612||6328||Gamma-aminobutyric acid transaminase deficiency||http://www.orpha.net/ORDO/Orphanet_2066
5613||1022||Pristionchus pacificus||http://purl.obolibrary.org/obo/NCBITaxon_54126
5614||3753||Galloway-Mowat syndrome||http://www.orpha.net/ORDO/Orphanet_2065
5615||12769||Posterior fusion of lumbosacral vertebrae - blepharoptosis||http://www.orpha.net/ORDO/Orphanet_2064
5616||4775||Splenogonadal fusion - limb defects - micrognathia||http://www.orpha.net/ORDO/Orphanet_2063
5617||7963||Progressive non-infectious anterior vertebral fusion||http://www.orpha.net/ORDO/Orphanet_2062
5618||5025||Stenocarpella maydis||http://purl.obolibrary.org/obo/NCBITaxon_238245
5619||5502||Leuconostoc pseudomesenteroides||http://purl.obolibrary.org/obo/NCBITaxon_33968
5620||10994||bucladesine||http://purl.obolibrary.org/obo/CHEBI_50095
5621||5611||Hemoglobin E - beta-thalassemia||http://www.orpha.net/ORDO/Orphanet_231249
5622||10994||S-nitrosoglutathione||http://purl.obolibrary.org/obo/CHEBI_50091
5623||11472||Partial deletion of the long arm of chromosome 21||http://www.orpha.net/ORDO/Orphanet_262173
5625||5502||Leuconostoc citreum||http://purl.obolibrary.org/obo/NCBITaxon_33964
5624||5502||Lactobacillus rhamnosus||http://purl.obolibrary.org/obo/NCBITaxon_47715
5626||7942||Geroderma osteodysplastica||http://www.orpha.net/ORDO/Orphanet_2078
5628||5478||German syndrome||http://www.orpha.net/ORDO/Orphanet_2077
5627||5502||Lactobacillus plantarum WCFS1||http://purl.obolibrary.org/obo/NCBITaxon_220668
5629||5611||Hemoglobin C - beta-thalassemia||http://www.orpha.net/ORDO/Orphanet_231242
5630||7638||Gaucher disease - ophthalmoplegia - cardiovascular calcification||http://www.orpha.net/ORDO/Orphanet_2072
5631||5502||Pseudomonas fluorescens Pf-5||http://purl.obolibrary.org/obo/NCBITaxon_220664
5632||762||X-linked intellectual disability - epilepsy||http://www.orpha.net/ORDO/Orphanet_2076
5633||5300||Genito-palato-cardiac syndrome||http://www.orpha.net/ORDO/Orphanet_2075
5634||4014||Larsen-like syndrome, B3GAT3 type||http://www.orpha.net/ORDO/Orphanet_284139
5635||5912||Familial generalized lentiginosis||http://www.orpha.net/ORDO/Orphanet_231040
5636||10994||benzbromarone||http://purl.obolibrary.org/obo/CHEBI_3023
5637||1767||X-linked intellectual disability, Cilliers type||http://www.orpha.net/ORDO/Orphanet_163971
5638||1767||X-linked intellectual disability, Van Esch type||http://www.orpha.net/ORDO/Orphanet_163976
5639||5239||X-linked non-syndromic sensorineural deafness type DFN||http://www.orpha.net/ORDO/Orphanet_90625
5640||11899||X-linked intellectual disability - craniofacioskeletal syndrome||http://www.orpha.net/ORDO/Orphanet_163979
5641||5317||Ichthyosis-short stature-brachydactyly-microspherophakia syndrome||http://www.orpha.net/ORDO/Orphanet_363992
5642||375||Erythema palmaris hereditarium||http://www.orpha.net/ORDO/Orphanet_231031
5643||9965||Familial benign flecked retina||http://www.orpha.net/ORDO/Orphanet_363989
5644||5961||X-linked intellectual disability, Kroes type||http://www.orpha.net/ORDO/Orphanet_163961
5645||11899||X-linked dominant chondrodysplasia, Chassaing-Lacombe type||http://www.orpha.net/ORDO/Orphanet_163966
5646||5502||Mycobacterium bovis BCG||http://purl.obolibrary.org/obo/NCBITaxon_33892
5647||2999||Charcot-Marie-Tooth disease type 4B3||http://www.orpha.net/ORDO/Orphanet_363981
5648||2465||Familial amyloid polyneuropathy||http://www.orpha.net/ORDO/Orphanet_85447
5649||2465||Familial amyloidosis, Finnish type||http://www.orpha.net/ORDO/Orphanet_85448
5650||13496||Cyanophage S-BnM1||http://purl.obolibrary.org/obo/NCBITaxon_65016
5651||5502||Listeria monocytogenes 10403S||http://purl.obolibrary.org/obo/NCBITaxon_393133
5652||5502||Listeria monocytogenes J0161||http://purl.obolibrary.org/obo/NCBITaxon_393130
5653||4122||Short stature - pituitary and cerebellar defects - small sella turcica||http://www.orpha.net/ORDO/Orphanet_85442
5654||10851||AL amyloidosis||http://www.orpha.net/ORDO/Orphanet_85443
5655||1022||Chlamydotis undulata||http://purl.obolibrary.org/obo/NCBITaxon_172680
5656||5670||Testicular agenesis||http://www.orpha.net/ORDO/Orphanet_325124
5657||4705||Hereditary cerebral hemorrhage with amyloidosis||http://www.orpha.net/ORDO/Orphanet_85458
5658||10994||benomyl||http://purl.obolibrary.org/obo/CHEBI_3015
5659||5070||Congenital trigeminal anesthesia||http://www.orpha.net/ORDO/Orphanet_231013
5660||11899||X-linked intellectual disability - spastic quadriparesis||http://www.orpha.net/ORDO/Orphanet_163982
5661||4834||Craniosynostosis and dental anomalies||http://www.orpha.net/ORDO/Orphanet_284149
5663||2683||Cobblestone lissencephaly||http://www.orpha.net/ORDO/Orphanet_51577
5662||5700||Developmental delay - deafness, Hildebrand type||http://www.orpha.net/ORDO/Orphanet_163988
5664||4732||Hyperekplexia - epilepsy||http://www.orpha.net/ORDO/Orphanet_163985
5665||5912||X-linked reticulate pigmentary disorder with systemic manifestations||http://www.orpha.net/ORDO/Orphanet_85453
5666||5155||Transthyretin-related familial amyloid cardiomyopathy||http://www.orpha.net/ORDO/Orphanet_85451
5668||1231||abnormal||http://purl.obolibrary.org/obo/PATO_0000460
5667||4830||Familial renal amyloidosis||http://www.orpha.net/ORDO/Orphanet_85450
5669||1231||normal||http://purl.obolibrary.org/obo/PATO_0000461
5670||3556||46,XY disorder of gonadal development||http://www.orpha.net/ORDO/Orphanet_325118
5672||6291||Central polydactyly of fingers, unilateral||http://www.orpha.net/ORDO/Orphanet_295171
5671||7139||COG1-CDG||http://www.orpha.net/ORDO/Orphanet_263508
5673||1552||dead||http://purl.obolibrary.org/obo/PATO_0001422
5674||6291||Central polydactyly of fingers, bilateral||http://www.orpha.net/ORDO/Orphanet_295173
5675||6292||Preaxial polydactyly of toes, unilateral||http://www.orpha.net/ORDO/Orphanet_295175
5676||6292||Preaxial polydactyly of toes, bilateral||http://www.orpha.net/ORDO/Orphanet_295177
5677||5483||17q21.31 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_363958
5678||6286||Postaxial polydactyly of toes, unilateral||http://www.orpha.net/ORDO/Orphanet_295179
5679||7139||COG4-CDG||http://www.orpha.net/ORDO/Orphanet_263501
5680||1552||alive||http://purl.obolibrary.org/obo/PATO_0001421
5681||3150||Syndrome with 46,XX disorder of sex development||http://www.orpha.net/ORDO/Orphanet_325109
5682||799||anticoagulant||http://purl.obolibrary.org/obo/CHEBI_50249
5683||6286||Postaxial polydactyly of toes, bilateral||http://www.orpha.net/ORDO/Orphanet_295181
5684||6377||Central polydactyly of toes, bilateral||http://www.orpha.net/ORDO/Orphanet_295185
5685||8191||copper(II) chloride||http://purl.obolibrary.org/obo/CHEBI_49553
5686||6377||Central polydactyly of toes, unilateral||http://www.orpha.net/ORDO/Orphanet_295183
5687||8181||Zygodactyly type 2||http://www.orpha.net/ORDO/Orphanet_295189
5688||8181||Zygodactyly type 1||http://www.orpha.net/ORDO/Orphanet_295187
5689||6180||Stickler syndrome type 2||http://www.orpha.net/ORDO/Orphanet_90654
5690||5502||Lactobacillus mindensis||http://purl.obolibrary.org/obo/NCBITaxon_167481
5691||9374||Otopalatodigital syndrome type 1||http://www.orpha.net/ORDO/Orphanet_90650
5692||6180||Stickler syndrome type 1||http://www.orpha.net/ORDO/Orphanet_90653
5693||9374||Otopalatodigital syndrome type 2||http://www.orpha.net/ORDO/Orphanet_90652
5694||612||Charcot-Marie-Tooth disease type 1E||http://www.orpha.net/ORDO/Orphanet_90658
5695||8181||Zygodactyly type 3||http://www.orpha.net/ORDO/Orphanet_295191
5696||8181||Zygodactyly type 4||http://www.orpha.net/ORDO/Orphanet_295193
5697||8183||Synpolydactyly type 3||http://www.orpha.net/ORDO/Orphanet_295199
5698||8183||Synpolydactyly type 1||http://www.orpha.net/ORDO/Orphanet_295195
5699||8183||Synpolydactyly type 2||http://www.orpha.net/ORDO/Orphanet_295197
5700||8303||Syndromic genetic deafness||http://www.orpha.net/ORDO/Orphanet_90642
5701||5239||Mitochondrial non-syndromic sensorineural deafness||http://www.orpha.net/ORDO/Orphanet_90641
5702||5967||Noonan syndrome-like disorder with juvenile myelomonocytic leukemia||http://www.orpha.net/ORDO/Orphanet_363972
5703||1767||Deafness - hypogonadism||http://www.orpha.net/ORDO/Orphanet_90646
5704||11460||obstructive lung disease||http://purl.obolibrary.org/obo/HP_0006536
5705||1022||Camponotus floridanus||http://purl.obolibrary.org/obo/NCBITaxon_104421
5707||10994||mitomycin C||http://purl.obolibrary.org/obo/CHEBI_27504
5706||5700||Jervell and Lange-Nielsen syndrome||http://www.orpha.net/ORDO/Orphanet_90647
5708||10994||( )-dexrazoxane||http://purl.obolibrary.org/obo/CHEBI_50223
5709||4706||Autosomal recessive cerebral atrophy||http://www.orpha.net/ORDO/Orphanet_363969
5710||9044||Koolen-De Vries syndrome due to a point mutation||http://www.orpha.net/ORDO/Orphanet_363965
5711||10994||diazepam||http://purl.obolibrary.org/obo/CHEBI_49575
5712||1826||Miscanthus x giganteus||http://purl.obolibrary.org/obo/NCBITaxon_183674
5713||5239||Autosomal dominant non-syndromic sensorineural deafness type DFNA||http://www.orpha.net/ORDO/Orphanet_90635
5714||5239||Autosomal recessive non-syndromic sensorineural deafness type DFNB||http://www.orpha.net/ORDO/Orphanet_90636
5715||14860||macromolecule metabolic process||http://purl.obolibrary.org/obo/GO_0043170
5716||770||ML-DmD17-c3||http://www.ebi.ac.uk/efo/EFO_0005826
5717||770||ML-DmD16-c3||http://www.ebi.ac.uk/efo/EFO_0005825
5718||770||ML-DmD20-c5||http://www.ebi.ac.uk/efo/EFO_0005828
5719||4454||selenium||http://purl.obolibrary.org/obo/CHEBI_27568
5720||770||ML-DmD20-c2||http://www.ebi.ac.uk/efo/EFO_0005827
5721||770||ML-DmBG2-c2||http://www.ebi.ac.uk/efo/EFO_0005822
5722||770||ML-DmBG1-c1||http://www.ebi.ac.uk/efo/EFO_0005821
5723||5502||Escherichia coli CFT073||http://purl.obolibrary.org/obo/NCBITaxon_199310
5724||770||ML-DmD11||http://www.ebi.ac.uk/efo/EFO_0005824
5725||770||ML-DmBG3-c2||http://www.ebi.ac.uk/efo/EFO_0005823
5726||11808||Symbrachydactyly of hand and foot, bilateral||http://www.orpha.net/ORDO/Orphanet_295138
5727||770||mbn2||http://www.ebi.ac.uk/efo/EFO_0005820
5729||11808||Symbrachydactyly of hand and foot, unilateral||http://www.orpha.net/ORDO/Orphanet_295136
5728||10994||oxirane||http://purl.obolibrary.org/obo/CHEBI_27561
5730||4454||arsenic||http://purl.obolibrary.org/obo/CHEBI_27563
5731||13668||Brachydactyly of fingers, bilateral||http://www.orpha.net/ORDO/Orphanet_295130
5732||13662||Brachydactyly of toes, bilateral||http://www.orpha.net/ORDO/Orphanet_295134
5733||13662||Brachydactyly of toes, unilateral||http://www.orpha.net/ORDO/Orphanet_295132
5734||770||ML-DmD21||http://www.ebi.ac.uk/efo/EFO_0005829
5735||10886||microtubule-associated protein tau||http://www.ebi.ac.uk/efo/EFO_0005816
5736||5285||tauopathy||http://www.ebi.ac.uk/efo/EFO_0005815
5737||5744||Pseudounicornuate uterus||http://www.orpha.net/ORDO/Orphanet_180079
5738||8563||Polydactyly of a triphalangeal thumb, unilateral||http://www.orpha.net/ORDO/Orphanet_295148
5739||6281||Hyperphalangy, unilateral||http://www.orpha.net/ORDO/Orphanet_295140
5740||6281||Hyperphalangy, bilateral||http://www.orpha.net/ORDO/Orphanet_295142
5741||8557||Polydactyly of a biphalangeal thumb, unilateral||http://www.orpha.net/ORDO/Orphanet_295144
5742||8557||Polydactyly of a biphalangeal thumb, bilateral||http://www.orpha.net/ORDO/Orphanet_295146
5743||5744||True unicornuate uterus||http://www.orpha.net/ORDO/Orphanet_180074
5744||4789||Unilateral aplasia of the M llerian ducts||http://www.orpha.net/ORDO/Orphanet_180071
5745||770||Kc167||http://www.ebi.ac.uk/efo/EFO_0005819
5746||1826||Populus alba||http://purl.obolibrary.org/obo/NCBITaxon_43335
5747||4789||Partial bilateral aplasia of the M llerian ducts||http://www.orpha.net/ORDO/Orphanet_180068
5748||10994||bicuculline||http://purl.obolibrary.org/obo/CHEBI_3092
5749||8193||bicalutamide||http://purl.obolibrary.org/obo/CHEBI_3090
5750||3514||Syndrome associated with Pierre Robin syndrome||http://www.orpha.net/ORDO/Orphanet_138063
5751||8558||Polysyndactyly, unilateral||http://www.orpha.net/ORDO/Orphanet_295159
5753||3514||Pierre Robin syndrome associated with miscellaneous anomalies||http://www.orpha.net/ORDO/Orphanet_138066
5752||8024||Simpson-Golabi-Behmel syndrome type 2||http://www.orpha.net/ORDO/Orphanet_79022
5754||8562||Polydactyly of an index finger, bilateral||http://www.orpha.net/ORDO/Orphanet_295154
5755||8562||Polydactyly of an index finger, unilateral||http://www.orpha.net/ORDO/Orphanet_295152
5756||8563||Polydactyly of a triphalangeal thumb, bilateral||http://www.orpha.net/ORDO/Orphanet_295150
5757||770||OSS||http://www.ebi.ac.uk/efo/EFO_0005835
5758||770||OSC||http://www.ebi.ac.uk/efo/EFO_0005834
5759||770||ML-DmD9||http://www.ebi.ac.uk/efo/EFO_0005833
5760||770||ML-DmD8||http://www.ebi.ac.uk/efo/EFO_0005832
5761||770||Sg4||http://www.ebi.ac.uk/efo/EFO_0005839
5762||770||S3||http://www.ebi.ac.uk/efo/EFO_0005838
5763||770||S2R ||http://www.ebi.ac.uk/efo/EFO_0005837
5764||770||S2-DRSC||http://www.ebi.ac.uk/efo/EFO_0005836
5765||770||ML-DmD4-c1||http://www.ebi.ac.uk/efo/EFO_0005831
5767||3514||Pierre Robin syndrome associated with bone disease||http://www.orpha.net/ORDO/Orphanet_138055
5768||770||ML-DmD32||http://www.ebi.ac.uk/efo/EFO_0005830
5766||8560||Postaxial polydactyly type B, bilateral||http://www.orpha.net/ORDO/Orphanet_295169
5769||8561||Postaxial polydactyly type A, bilateral||http://www.orpha.net/ORDO/Orphanet_295165
5770||8560||Postaxial polydactyly type B, unilateral||http://www.orpha.net/ORDO/Orphanet_295167
5771||8558||Polysyndactyly, bilateral||http://www.orpha.net/ORDO/Orphanet_295161
5772||8561||Postaxial polydactyly type A, unilateral||http://www.orpha.net/ORDO/Orphanet_295163
5773||3514||Pierre Robin syndrome associated with a chromosomal anomaly||http://www.orpha.net/ORDO/Orphanet_138047
5775||1022||Pythium ultimum||http://purl.obolibrary.org/obo/NCBITaxon_65071
5774||5961||X-linked intellectual disability, Najm type||http://www.orpha.net/ORDO/Orphanet_163937
5776||5502||Listeria monocytogenes FSL J1-208||http://purl.obolibrary.org/obo/NCBITaxon_393119
5777||3514||Pierre Robin syndrome associated with collagen disease||http://www.orpha.net/ORDO/Orphanet_138041
5778||375||Acrodermatitis continua suppurativa of Hallopeau||http://www.orpha.net/ORDO/Orphanet_163931
5779||3514||Pierre Robin syndrome associated with branchial archs anomalies||http://www.orpha.net/ORDO/Orphanet_138050
5780||13631||Acheiria, bilateral||http://www.orpha.net/ORDO/Orphanet_295103
5781||4454||carbon||http://purl.obolibrary.org/obo/CHEBI_27594
5782||13630||Apodia, unilateral||http://www.orpha.net/ORDO/Orphanet_295105
5783||375||Pustulosis palmaris et plantaris||http://www.orpha.net/ORDO/Orphanet_163927
5784||13630||Apodia, bilateral||http://www.orpha.net/ORDO/Orphanet_295107
5785||259||cell death||http://purl.obolibrary.org/obo/GO_0008219
5786||2252||8q21.11 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_284160
5787||5502||Listeria monocytogenes FSL J2-071||http://purl.obolibrary.org/obo/NCBITaxon_393121
5788||11029||10p11.21p12.31 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_284169
5789||10994||HC toxin||http://purl.obolibrary.org/obo/CHEBI_48028
5790||5502||Borrelia burgdorferi||http://purl.obolibrary.org/obo/NCBITaxon_139
5791||13631||Acheiria, unilateral||http://www.orpha.net/ORDO/Orphanet_295101
5792||5502||Treponema pallidum||http://purl.obolibrary.org/obo/NCBITaxon_160
5793||10994||aldosterone||http://purl.obolibrary.org/obo/CHEBI_27584
5795||15571||Disorder of amino acid and other organic acid metabolism||http://www.orpha.net/ORDO/Orphanet_79062
5794||6731||Adactyly of foot, bilateral||http://www.orpha.net/ORDO/Orphanet_295118
5796||5005||uncultured microorganism||http://purl.obolibrary.org/obo/NCBITaxon_358574
5797||6731||Adactyly of foot, unilateral||http://www.orpha.net/ORDO/Orphanet_295116
5798||13670||Congenital absence/hypoplasia of fingers excluding thumb, bilateral||http://www.orpha.net/ORDO/Orphanet_295114
5799||11899||X-linked intellectual disability, Nascimento type||http://www.orpha.net/ORDO/Orphanet_163956
5800||2102|| substance withdrawal syndrome ||http://www.ebi.ac.uk/efo/EFO_0005800
5801||1015||cholesterol embolism||http://www.ebi.ac.uk/efo/EFO_0005801
5802||15526||cartilage disease||http://www.ebi.ac.uk/efo/EFO_0005802
5803||1022||Julidochromis marlieri||http://purl.obolibrary.org/obo/NCBITaxon_32499
5804||1391||hematological system disease||http://www.ebi.ac.uk/efo/EFO_0005803
5805||1391||polycythemia||http://www.ebi.ac.uk/efo/EFO_0005804
5806||5805||polycythemia due to hypoxia||http://www.ebi.ac.uk/efo/EFO_0005805
5807||1790||type II hypersensitivity reaction disease||http://www.ebi.ac.uk/efo/EFO_0005809
5808||770||GM17172||http://purl.obolibrary.org/obo/CLO_0014025
5809||770||GM17171||http://purl.obolibrary.org/obo/CLO_0014024
5810||770||GM17170||http://purl.obolibrary.org/obo/CLO_0014022
5811||770||GM17178||http://purl.obolibrary.org/obo/CLO_0014029
5813||13627||Congenital absence/hypoplasia of thumb, bilateral||http://www.orpha.net/ORDO/Orphanet_295112
5812||770||GM17179||http://purl.obolibrary.org/obo/CLO_0014028
5815||13627||Congenital absence/hypoplasia of thumb, unilateral||http://www.orpha.net/ORDO/Orphanet_295110
5814||770||GM17173||http://purl.obolibrary.org/obo/CLO_0014026
5816||2327||Juvenile polyposis of infancy||http://www.orpha.net/ORDO/Orphanet_79076
5817||2252||Xp22.13p22.2 duplication syndrome||http://www.orpha.net/ORDO/Orphanet_284180
5818||4454||silicon||http://purl.obolibrary.org/obo/CHEBI_27573
5819||13667||Split foot, bilateral||http://www.orpha.net/ORDO/Orphanet_295126
5820||13668||Brachydactyly of fingers, unilateral||http://www.orpha.net/ORDO/Orphanet_295128
5821||1022||Melampsora larici-populina||http://purl.obolibrary.org/obo/NCBITaxon_203908
5822||5502||Candidatus Blochmannia floridanus||http://purl.obolibrary.org/obo/NCBITaxon_203907
5823||1022||Masticophis||http://purl.obolibrary.org/obo/NCBITaxon_94898
5824||5502||Caulobacter crescentus CB15||http://purl.obolibrary.org/obo/NCBITaxon_190650
5825||306||Teebi-Shaltout syndrome||http://www.orpha.net/ORDO/Orphanet_3291
5826||12322||Tel Hashomer camptodactyly syndrome||http://www.orpha.net/ORDO/Orphanet_3292
5827||2252||Telecanthus - hypertelorism - strabismus - pes cavus||http://www.orpha.net/ORDO/Orphanet_3293
5828||770||GM17174||http://purl.obolibrary.org/obo/CLO_0014034
5829||6246||Extensor tendons of finger anomalies||http://www.orpha.net/ORDO/Orphanet_3294
5830||770||GM17175||http://purl.obolibrary.org/obo/CLO_0014033
5831||13676||Split hand, bilateral||http://www.orpha.net/ORDO/Orphanet_295122
5832||770||GM17177||http://purl.obolibrary.org/obo/CLO_0014037
5834||13667||Split foot, unilateral||http://www.orpha.net/ORDO/Orphanet_295124
5833||5502||Treponema denticola||http://purl.obolibrary.org/obo/NCBITaxon_158
5835||770||GM17176||http://purl.obolibrary.org/obo/CLO_0014039
5836||13676||Split hand, unilateral||http://www.orpha.net/ORDO/Orphanet_295120
5837||12439||Familial partial lipodystrophy associated with PPARG mutations||http://www.orpha.net/ORDO/Orphanet_79083
5838||5278||quality||http://www.ifomis.org/bfo/1.1/snap#Quality
5839||4430||coenzyme||http://purl.obolibrary.org/obo/CHEBI_23354
5840||10994||colchicine||http://purl.obolibrary.org/obo/CHEBI_23359
5841||4001||Congenital muscular dystrophy without intellectual disability||http://www.orpha.net/ORDO/Orphanet_370980
5842||2252||Radio-ulnar synostosis - intellectual disability - hypotonia||http://www.orpha.net/ORDO/Orphanet_3270
5843||8681||Disorder of folate metabolism and transport||http://www.orpha.net/ORDO/Orphanet_285657
5844||7968||Spondylocarpotarsal synostosis||http://www.orpha.net/ORDO/Orphanet_3275
5845||5861||regulation of cellular process||http://purl.obolibrary.org/obo/GO_0050794
5846||6591||Folinic acid-responsive seizures||http://www.orpha.net/ORDO/Orphanet_79097
5847||6265||Pyridoxal phosphate-responsive seizures||http://www.orpha.net/ORDO/Orphanet_79096
5848||2454||Congenital bile acid synthesis defect type 4||http://www.orpha.net/ORDO/Orphanet_79095
5849||10368||Partial deletion of the long arm of chromosome 1||http://www.orpha.net/ORDO/Orphanet_262001
5850||5502||Leptospira interrogans||http://purl.obolibrary.org/obo/NCBITaxon_173
5851||6573||compatible osmolytes role||http://purl.obolibrary.org/obo/CHEBI_23366
5852||5502||Neisseria gonorrhoeae F62||http://purl.obolibrary.org/obo/NCBITaxon_528351
5853||1619||Taurodontism||http://www.orpha.net/ORDO/Orphanet_3289
5854||12372||Hereditary inclusion body myopathy - joint contractures - ophthalmoplegia||http://www.orpha.net/ORDO/Orphanet_79091
5855||10312||Partial deletion of the long arm of chromosome 3||http://www.orpha.net/ORDO/Orphanet_262019
5856||1491||myelin sheath||http://purl.obolibrary.org/obo/GO_0043209
5857||5306||Grange syndrome||http://www.orpha.net/ORDO/Orphanet_79094
5858||8846||Autosomal recessive optic atrophy, OPA7 type||http://www.orpha.net/ORDO/Orphanet_227976
5859||15||His bundle tachycardia||http://www.orpha.net/ORDO/Orphanet_3283
5860||15||Catecholaminergic polymorphic ventricular tachycardia||http://www.orpha.net/ORDO/Orphanet_3286
5861||5295||regulation of biological process||http://purl.obolibrary.org/obo/GO_0050789
5862||12439||Familial partial lipodystrophy due to AKT2 mutations||http://www.orpha.net/ORDO/Orphanet_79085
5863||12439||Familial partial lipodystrophy, K bberling type||http://www.orpha.net/ORDO/Orphanet_79084
5864||10314||Partial deletion of the long arm of chromosome 2||http://www.orpha.net/ORDO/Orphanet_262010
5865||5918||Genetic mixed dermis disorder||http://www.orpha.net/ORDO/Orphanet_183481
5866||13770||Syndactyly-polydactyly-ear lobe syndrome||http://www.orpha.net/ORDO/Orphanet_3259
5867||13770||Cenani-Lenz syndrome||http://www.orpha.net/ORDO/Orphanet_3258
5868||15383||Genetic subcutaneous tissue disorder||http://www.orpha.net/ORDO/Orphanet_183484
5869||2252||Filippi syndrome||http://www.orpha.net/ORDO/Orphanet_3255
5871||590||Zlotogora-Ogur syndrome||http://www.orpha.net/ORDO/Orphanet_3253
5870||7159||Autosomal dominant hypophosphatemic rickets||http://www.orpha.net/ORDO/Orphanet_89937
5872||5700||Infantile Bartter syndrome with sensorineural deafness||http://www.orpha.net/ORDO/Orphanet_89938
5873||7159||X-linked hypophosphatemia||http://www.orpha.net/ORDO/Orphanet_89936
5874||7953||Proximal symphalangism||http://www.orpha.net/ORDO/Orphanet_3250
5875||4001||Congenital muscular dystrophy with intellectual disability||http://www.orpha.net/ORDO/Orphanet_370968
5876||5502||Campylobacter jejuni||http://purl.obolibrary.org/obo/NCBITaxon_197
5877||15363||Genetic skin tumor||http://www.orpha.net/ORDO/Orphanet_183487
5878||5502||Campylobacter coli||http://purl.obolibrary.org/obo/NCBITaxon_195
5879||5502||Campylobacter||http://purl.obolibrary.org/obo/NCBITaxon_194
5880||15383||Genetic photodermatosis||http://www.orpha.net/ORDO/Orphanet_183490
5881||13735||Radio-ulnar synostosis||http://www.orpha.net/ORDO/Orphanet_3269
5882||15383||Genetic immune deficiency with skin involvement||http://www.orpha.net/ORDO/Orphanet_183494
5883||13735||Humero-radio-ulnar synostosis||http://www.orpha.net/ORDO/Orphanet_3266
5884||13735||Humero-radial synostosis||http://www.orpha.net/ORDO/Orphanet_3265
5885||7953||Synostosis - microcephaly - scoliosis||http://www.orpha.net/ORDO/Orphanet_3268
5886||6650||Familial lambdoid synostosis||http://www.orpha.net/ORDO/Orphanet_3267
5887||7962||Syngnathia multiple anomalies||http://www.orpha.net/ORDO/Orphanet_3262
5888||5486||Autoimmune lymphoproliferative syndrome||http://www.orpha.net/ORDO/Orphanet_3261
5890||5300||Syngnathia - cleft palate||http://www.orpha.net/ORDO/Orphanet_3263
5889||9918||Paroxysmal extreme pain disorder||http://www.orpha.net/ORDO/Orphanet_46348
5891||4001||Congenital muscular dystrophy with cerebellar involvement||http://www.orpha.net/ORDO/Orphanet_370959
5892||5295||leukocyte activation||http://purl.obolibrary.org/obo/GO_0045321
5893||9918||Genetic neuromuscular disease||http://www.orpha.net/ORDO/Orphanet_183497
5894||8793||Congenital muscular dystrophy due to dystroglycanopathy||http://www.orpha.net/ORDO/Orphanet_370953
5895||4834||Deafness - oligodontia||http://www.orpha.net/ORDO/Orphanet_3230
5896||306||Deafness-onychodystrophy syndrome||http://www.orpha.net/ORDO/Orphanet_3231
5897||15383||Genetic pigmentation anomaly of the skin||http://www.orpha.net/ORDO/Orphanet_183463
5898||5700||Progressive deafness with stapes fixation||http://www.orpha.net/ORDO/Orphanet_3235
5899||5700||Deafness - ear malformation - facial palsy||http://www.orpha.net/ORDO/Orphanet_3232
5900||5942||Genetic sebaceous gland anomaly||http://www.orpha.net/ORDO/Orphanet_183460
5901||7749||GTP cyclohydrolase I deficiency||http://www.orpha.net/ORDO/Orphanet_2102
5903||4139||Grubben-de Cock-Borghgraef syndrome||http://www.orpha.net/ORDO/Orphanet_2101
5902||5700||Cochleosaccular degeneration - cataract||http://www.orpha.net/ORDO/Orphanet_3233
5904||5700||Cardiospondylocarpofacial syndrome||http://www.orpha.net/ORDO/Orphanet_3238
5905||5700||Deafness - vitiligo - achalasia||http://www.orpha.net/ORDO/Orphanet_3239
5906||306||Conductive deafness - ptosis - skeletal anomalies||http://www.orpha.net/ORDO/Orphanet_3236
5907||5700||Multiple synostoses syndrome||http://www.orpha.net/ORDO/Orphanet_3237
5908||2252||Hall-Riggs syndrome||http://www.orpha.net/ORDO/Orphanet_2107
5909||1826||Populus tremula x Populus tremuloides||http://purl.obolibrary.org/obo/NCBITaxon_47664
5910||306||Hallermann-Streiff syndrome||http://www.orpha.net/ORDO/Orphanet_2108
5911||5897||Genetic hypopigmentation of the skin||http://www.orpha.net/ORDO/Orphanet_183469
5912||5897||Genetic hyperpigmentation of the skin||http://www.orpha.net/ORDO/Orphanet_183466
5913||4344||Autism spectrum disorder-epilepsy-arthrogryposis syndrome||http://www.orpha.net/ORDO/Orphanet_370943
5914||8193||N-nitrosodimethylamine||http://purl.obolibrary.org/obo/CHEBI_35807
5915||4139||Central nervous system calcification - deafness - tubular acidosis - anemia||http://www.orpha.net/ORDO/Orphanet_3240
5916||5700||Deafness-craniofacial syndrome||http://www.orpha.net/ORDO/Orphanet_3241
5917||2252||Renpenning syndrome||http://www.orpha.net/ORDO/Orphanet_3242
5918||15383||Genetic dermis disorder||http://www.orpha.net/ORDO/Orphanet_183472
5919||13770||Hallux varus - preaxial polysyndactyly||http://www.orpha.net/ORDO/Orphanet_2110
5920||7953||Symphalangism with multiple anomalies of hands and feet||http://www.orpha.net/ORDO/Orphanet_3246
5921||5300||Hartsfield-Bixler-Demyer syndrome||http://www.orpha.net/ORDO/Orphanet_2117
5923||13735||Distal symphalangism||http://www.orpha.net/ORDO/Orphanet_3248
5922||5880||Hartnup disease||http://www.orpha.net/ORDO/Orphanet_2116
5924||2252||Harrod syndrome||http://www.orpha.net/ORDO/Orphanet_2115
5925||7972||Hip dysplasia, Beukes type||http://www.orpha.net/ORDO/Orphanet_2114
5926||1839||Hawkinsinuria||http://www.orpha.net/ORDO/Orphanet_2118
5927||4254||ST3GAL5-CDG||http://www.orpha.net/ORDO/Orphanet_370933
5928||5918||Genetic skin vascular disorder||http://www.orpha.net/ORDO/Orphanet_183478
5929||2252||XYLT1-CDG||http://www.orpha.net/ORDO/Orphanet_370930
5930||5927||Salt-and-pepper syndrome||http://www.orpha.net/ORDO/Orphanet_370938
5931||799||anticholesteremic drug||http://purl.obolibrary.org/obo/CHEBI_35821
5932||10994||acetoacetate||http://purl.obolibrary.org/obo/CHEBI_13705
5933||5700||Deafness -  small bowel diverticulosis - neuropathy||http://www.orpha.net/ORDO/Orphanet_3217
5934||5700||Deaf blind hypopigmentation syndrome, Yemenite type||http://www.orpha.net/ORDO/Orphanet_3214
5936||5025||Penicillium italicum||http://purl.obolibrary.org/obo/NCBITaxon_40296
5937||5102||T  B  severe combined immunodeficiency||http://www.orpha.net/ORDO/Orphanet_397802
5935||5965||Genetic acrokeratoderma||http://www.orpha.net/ORDO/Orphanet_183441
5938||6610||Summitt syndrome||http://www.orpha.net/ORDO/Orphanet_3210
5939||5965||Genetic porokeratosis||http://www.orpha.net/ORDO/Orphanet_183444
5940||4344||STT3A-CDG||http://www.orpha.net/ORDO/Orphanet_370921
5942||15383||Genetic epidermal appendage anomaly||http://www.orpha.net/ORDO/Orphanet_183447
5941||2252||Fountain syndrome||http://www.orpha.net/ORDO/Orphanet_3219
5943||5700||Deafness - epiphyseal dysplasia - short stature||http://www.orpha.net/ORDO/Orphanet_3218
5944||2252||SSR4-CDG||http://www.orpha.net/ORDO/Orphanet_370927
5945||4344||STT3B-CDG||http://www.orpha.net/ORDO/Orphanet_370924
5946||5502||Dehalococcoides sp. BAV1||http://purl.obolibrary.org/obo/NCBITaxon_216389
5947||306||Deafness - enamel hypoplasia - nail defects||http://www.orpha.net/ORDO/Orphanet_3220
5948||5700||Hearing loss - familial salivary gland insensitivity to aldosterone||http://www.orpha.net/ORDO/Orphanet_3225
5949||5478||Deafness - lymphedema - leukemia||http://www.orpha.net/ORDO/Orphanet_3226
5950||1313||Generalized resistance to thyroid hormone||http://www.orpha.net/ORDO/Orphanet_3221
5952||4727||Phosphoribosylpyrophosphate synthetase superactivity||http://www.orpha.net/ORDO/Orphanet_3222
5951||5942||Genetic hair anomaly||http://www.orpha.net/ORDO/Orphanet_183450
5953||2252||Deafness - genital anomalies - metacarpal and metatarsal synostosis||http://www.orpha.net/ORDO/Orphanet_3224
5954||5942||Genetic nail anomaly||http://www.orpha.net/ORDO/Orphanet_183454
5955||5961||Genetic syndrome with a Dandy-Walker malformation as major feature||http://www.orpha.net/ORDO/Orphanet_269570
5956||5959||Genetic syndrome with corpus callosum agenesis/dysgenesis as a major feature||http://www.orpha.net/ORDO/Orphanet_269573
5957||1523||plastid membrane||http://purl.obolibrary.org/obo/GO_0042170
5958||9655||Rare non-syndromic cataract||http://www.orpha.net/ORDO/Orphanet_217049
5959||4702||Genetic syndrome with a central nervous system malformation as major feature||http://www.orpha.net/ORDO/Orphanet_269564
5961||5959||Genetic syndrome with a cerebellar malformation as major feature||http://www.orpha.net/ORDO/Orphanet_269567
5962||10672||Partial monosomy of the long arm of chromosome 10||http://www.orpha.net/ORDO/Orphanet_262083
5960||10994||motexafin gadolinium||http://purl.obolibrary.org/obo/CHEBI_50161
5963||5977||Autosomal recessive childhood-onset cortical cataract||http://www.orpha.net/ORDO/Orphanet_217046
5964||5981||Genetic cerebellar malformation||http://www.orpha.net/ORDO/Orphanet_269560
5965||15383||Genetic epidermal disorder||http://www.orpha.net/ORDO/Orphanet_183426
5966||2967||response to morphine||http://purl.obolibrary.org/obo/GO_0043278
5967||4803||Polymalformative genetic syndrome with increased risk of developing cancer||http://www.orpha.net/ORDO/Orphanet_183422
5968||6610||Craniosynostosis, Herrmann-Opitz type||http://www.orpha.net/ORDO/Orphanet_2145
5969||13306||Donnai-Barrow syndrome||http://www.orpha.net/ORDO/Orphanet_2143
5970||6212||Acral peeling skin syndrome||http://www.orpha.net/ORDO/Orphanet_263534
5971||15363||Genetic endocrine tumor||http://www.orpha.net/ORDO/Orphanet_271847
5972||1902||Nodular neuronal heterotopia||http://www.orpha.net/ORDO/Orphanet_2149
5973||1433||Lissencephaly type 1 due to doublecortin gene mutation||http://www.orpha.net/ORDO/Orphanet_2148
5974||15363||Genetic cardiac tumor||http://www.orpha.net/ORDO/Orphanet_271841
5975||15363||Genetic urogenital tumor||http://www.orpha.net/ORDO/Orphanet_271844
5976||12769||Diaphragmatic defect - limb deficiency - skull defect||http://www.orpha.net/ORDO/Orphanet_2141
5977||5958||Early-onset non-syndromic cataract||http://www.orpha.net/ORDO/Orphanet_217052
5978||10994||antirheumatic drug||http://purl.obolibrary.org/obo/CHEBI_35842
5979||3854||Sulfolobus acidocaldarius DSM 639||http://purl.obolibrary.org/obo/NCBITaxon_330779
5980||10876||Obesity due to MC3R deficiency||http://www.orpha.net/ORDO/Orphanet_217031
5982||799||dermatologic drug||http://purl.obolibrary.org/obo/CHEBI_50177
5981||5987||Genetic posterior fossa malformation||http://www.orpha.net/ORDO/Orphanet_269557
5983||10671||Partial deletion of the long arm of chromosome 11||http://www.orpha.net/ORDO/Orphanet_262092
5984||5987||Genetic cerebral malformation||http://www.orpha.net/ORDO/Orphanet_269553
5985||5965||Genetic erythrokeratoderma||http://www.orpha.net/ORDO/Orphanet_183438
5988||4139||White matter hypoplasia - corpus callosum agenesis - intellectual disability||http://www.orpha.net/ORDO/Orphanet_3207
5987||4702||Genetic non-syndromic central nervous system malformation||http://www.orpha.net/ORDO/Orphanet_269550
5986||5965||Inherited ichthyosis||http://www.orpha.net/ORDO/Orphanet_183435
5989||8910||Isolated succinate-CoQ reductase deficiency||http://www.orpha.net/ORDO/Orphanet_3208
5990||6212||Generalized peeling skin syndrome||http://www.orpha.net/ORDO/Orphanet_263543
5991||15363||Genetic digestive tract tumor||http://www.orpha.net/ORDO/Orphanet_271835
5992||12329||Dehydrated hereditary stomatocytosis||http://www.orpha.net/ORDO/Orphanet_3202
5993||843||Myoclonus-dystonia syndrome||http://www.orpha.net/ORDO/Orphanet_36899
5994||5300||Ventricular extrasystoles with syncopal episodes - perodactyly - Robin sequence||http://www.orpha.net/ORDO/Orphanet_3201
5995||5700||Hirschsprung disease - deafness - polydactyly||http://www.orpha.net/ORDO/Orphanet_2155
5996||2252||Hirsutism-skeletal dysplasia-intellectual disability syndrome||http://www.orpha.net/ORDO/Orphanet_2156
5997||6315||Histidinemia||http://www.orpha.net/ORDO/Orphanet_2157
5998||7991||St ve-Wiedemann syndrome||http://www.orpha.net/ORDO/Orphanet_3206
5999||616||Sturge-Weber syndrome||http://www.orpha.net/ORDO/Orphanet_3205
6000||5990||Peeling skin syndrome type A||http://www.orpha.net/ORDO/Orphanet_263548
6001||4406||Stormorken-Sjaastad-Langslet syndrome||http://www.orpha.net/ORDO/Orphanet_3204
6002||4766||Craniofacial dysplasia-osteopenia syndrome||http://www.orpha.net/ORDO/Orphanet_314555
6003||12329||Overhydrated hereditary stomatocytosis||http://www.orpha.net/ORDO/Orphanet_3203
6004||1537||other organism part||http://purl.obolibrary.org/obo/GO_0044217
6005||6770||Hirschsprung disease - type D brachydactyly||http://www.orpha.net/ORDO/Orphanet_2150
6007||15363||Genetic soft tissue tumor||http://www.orpha.net/ORDO/Orphanet_271832
6006||6770||Hirschsprung disease - ganglioneuroblastoma||http://www.orpha.net/ORDO/Orphanet_2151
6008||2252||Mowat-Wilson syndrome||http://www.orpha.net/ORDO/Orphanet_2152
6009||6770||Hirschsprung disease - nail hypoplasia - dysmorphism||http://www.orpha.net/ORDO/Orphanet_2153
6010||10994||sodium pyruvate||http://purl.obolibrary.org/obo/CHEBI_50144
6011||10683||Partial deletion of the long arm of chromosome 8||http://www.orpha.net/ORDO/Orphanet_262065
6012||6017||Distal tetrasomy 15q||http://www.orpha.net/ORDO/Orphanet_314588
6013||5967||Hemihypertrophy||http://www.orpha.net/ORDO/Orphanet_2128
6014||7333||Progressive myoclonic epilepsy type 3||http://www.orpha.net/ORDO/Orphanet_263516
6015||5317||Cavernous hemangiomas of face - supraumbilical midline raphe||http://www.orpha.net/ORDO/Orphanet_2124
6016||10994||fenpropimorph||http://purl.obolibrary.org/obo/CHEBI_50148
6017||2252||15q overgrowth syndrome||http://www.orpha.net/ORDO/Orphanet_314585
6018||331||Isolated congenital digital clubbing||http://www.orpha.net/ORDO/Orphanet_217059
6019||10994||1,1-bis(2-aminoethyl)-2-hydroxy-3-oxotriazane||http://purl.obolibrary.org/obo/CHEBI_50154
6020||1022||Postia placenta||http://purl.obolibrary.org/obo/NCBITaxon_104341
6021||5488||Autosomal recessive intermediate Charcot-Marie-Tooth disease type A||http://www.orpha.net/ORDO/Orphanet_217055
6022||10684||Partial monosomy of the long arm of chromosome 9||http://www.orpha.net/ORDO/Orphanet_262074
6023||2252||Hennekam syndrome||http://www.orpha.net/ORDO/Orphanet_2136
6024||1528||46,XX ovotesticular disorder of sex development||http://www.orpha.net/ORDO/Orphanet_2138
6025||2252||Hern ndez-Aguirre Negrete syndrome||http://www.orpha.net/ORDO/Orphanet_2139
6026||15574||Hemoglobin C disease||http://www.orpha.net/ORDO/Orphanet_2132
6027||15574||Hemoglobin E disease||http://www.orpha.net/ORDO/Orphanet_2133
6028||4624||Atypical hemolytic-uremic syndrome||http://www.orpha.net/ORDO/Orphanet_2134
6029||13306||Hennekam-Beemer syndrome||http://www.orpha.net/ORDO/Orphanet_2135
6031||10994||canrenoate||http://purl.obolibrary.org/obo/CHEBI_50159
6030||7957||Hemimelia||http://www.orpha.net/ORDO/Orphanet_2130
6032||6969||Alternating hemiplegia of childhood||http://www.orpha.net/ORDO/Orphanet_2131
6033||2252||Intellectual disability-hypotonia-brachycephaly-pyloric stenosis-cryptorchidism syndrome||http://www.orpha.net/ORDO/Orphanet_314575
6034||4705||Autosomal recessive leukoencephalopathy with ischemic stroke-retinitis pigmentosa syndrome||http://www.orpha.net/ORDO/Orphanet_314572
6035||6092||intracellular membrane-bounded organelle||http://purl.obolibrary.org/obo/GO_0043231
6036||6096||intracellular non-membrane-bounded organelle||http://purl.obolibrary.org/obo/GO_0043232
6037||10547||Beckwith-Wiedemann syndrome due to imprinting defect of 11p15||http://www.orpha.net/ORDO/Orphanet_231117
6038||1537||extracellular organelle||http://purl.obolibrary.org/obo/GO_0043230
6039||10348||Partial deletion of the long arm of chromosome 6||http://www.orpha.net/ORDO/Orphanet_262047
6040||1022||environmental samples||http://purl.obolibrary.org/obo/NCBITaxon_33858
6041||7380||Hydrocephalus with stenosis of the aqueduct of Sylvius||http://www.orpha.net/ORDO/Orphanet_2182
6042||12769||Hydrocephaly - tall stature - joint laxity||http://www.orpha.net/ORDO/Orphanet_2181
6044||13306||Hydrocephalus - costovertebral dysplasia - Sprengel anomaly||http://www.orpha.net/ORDO/Orphanet_2180
6043||6085||cellular biosynthetic process||http://purl.obolibrary.org/obo/GO_0044249
6045||7319||Hydrocephalus - blue sclerae - nephropathy||http://www.orpha.net/ORDO/Orphanet_2186
6046||5959||Syndrome with microcephaly as major feature||http://www.orpha.net/ORDO/Orphanet_269528
6047||5987||Congenital hydrocephalus||http://www.orpha.net/ORDO/Orphanet_2185
6048||1767||Hydrocephalus - obesity - hypogonadism||http://www.orpha.net/ORDO/Orphanet_2183
6049||5300||Hydrolethalus||http://www.orpha.net/ORDO/Orphanet_2189
6050||10547||Beckwith-Wiedemann syndrome due to 11p15 microdeletion||http://www.orpha.net/ORDO/Orphanet_231127
6051||3454||ribose phosphate biosynthetic process||http://purl.obolibrary.org/obo/GO_0046390
6052||10335||Partial deletion of the long arm of chromosome 7||http://www.orpha.net/ORDO/Orphanet_262056
6054||1732||Rare genetic systemic or rheumatologic disease||http://www.orpha.net/ORDO/Orphanet_271870
6053||6047||Congenital non-communicating hydrocephalus||http://www.orpha.net/ORDO/Orphanet_269510
6055||742||Congenital hydronephrosis||http://www.orpha.net/ORDO/Orphanet_2190
6056||5700||Chudley-McCullough syndrome||http://www.orpha.net/ORDO/Orphanet_314597
6057||6305||Dicarboxylic aminoaciduria||http://www.orpha.net/ORDO/Orphanet_2195
6058||4810||Idiopathic hypercalciuria||http://www.orpha.net/ORDO/Orphanet_2197
6059||9104||Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis with severe ocular involvement||http://www.orpha.net/ORDO/Orphanet_2196
6060||12401||Epidermolytic palmoplantar keratoderma||http://www.orpha.net/ORDO/Orphanet_2199
6062||12316||Palmoplantar keratoderma-esophageal carcinoma syndrome||http://www.orpha.net/ORDO/Orphanet_2198
6061||10547||Beckwith-Wiedemann syndrome due to CDKN1C mutation||http://www.orpha.net/ORDO/Orphanet_231120
6063||5892||macrophage activation||http://purl.obolibrary.org/obo/GO_0042116
6064||4430||insecticide||http://purl.obolibrary.org/obo/CHEBI_24852
6065||5990||Peeling skin syndrome type B||http://www.orpha.net/ORDO/Orphanet_263553
6066||4785||Microcephaly - facio-cardio-skeletal syndrome, Hadziselimovic type||http://www.orpha.net/ORDO/Orphanet_217026
6067||10994||troglitazone||http://purl.obolibrary.org/obo/CHEBI_9753
6068||6028||Atypical hemolytic-uremic syndrome with thrombomodulin anomaly||http://www.orpha.net/ORDO/Orphanet_217023
6070||3854||Ferroglobus placidus||http://purl.obolibrary.org/obo/NCBITaxon_54261
6069||6047||Congenital communicating hydrocephalus||http://www.orpha.net/ORDO/Orphanet_269505
6071||6610||Holoprosencephaly - craniosynostosis||http://www.orpha.net/ORDO/Orphanet_2163
6072||760||Holoprosencephaly||http://www.orpha.net/ORDO/Orphanet_2162
6073||6054||Familial transthyretin-related amyloidosis||http://www.orpha.net/ORDO/Orphanet_271861
6074||1391||Malignant epithelial tumor of ovary||http://www.orpha.net/ORDO/Orphanet_398934
6075||9287||Methylcobalamin deficiency type cblE||http://www.orpha.net/ORDO/Orphanet_2169
6076||6275||Homocarnosinosis||http://www.orpha.net/ORDO/Orphanet_2168
6078||5300||Holzgreve-Wagner-Rehder syndrome||http://www.orpha.net/ORDO/Orphanet_2167
6077||5990||Generalized peeling skin syndrome type C||http://www.orpha.net/ORDO/Orphanet_263558
6080||2252||Holoprosencephaly - postaxial polydactyly||http://www.orpha.net/ORDO/Orphanet_2166
6079||10308||Partial deletion of the long arm of chromosome 4||http://www.orpha.net/ORDO/Orphanet_262029
6081||1839||Tyrosinemia type 2||http://www.orpha.net/ORDO/Orphanet_28378
6082||7349||Muscle-eye-brain disease with bilateral multicystic leucodystrophy||http://www.orpha.net/ORDO/Orphanet_370997
6083||2252||Zechi-Ceide syndrome||http://www.orpha.net/ORDO/Orphanet_217017
6084||6007||Familial rhabdoid tumor||http://www.orpha.net/ORDO/Orphanet_231108
6085||5292||cellular metabolic process||http://purl.obolibrary.org/obo/GO_0044237
6086||9853||Spinocerebellar ataxia type 31||http://www.orpha.net/ORDO/Orphanet_217012
6088||2252||Microcephaly - glomerulonephritis - marfanoid habitus||http://www.orpha.net/ORDO/Orphanet_2172
6087||4717||Genetic cardiac anomaly||http://www.orpha.net/ORDO/Orphanet_271853
6089||1826||Phalaenopsis aphrodite subsp. formosana||http://purl.obolibrary.org/obo/NCBITaxon_308872
6090||5292||primary metabolic process||http://purl.obolibrary.org/obo/GO_0044238
6091||4823||Methylcobalamin deficiency type cblG||http://www.orpha.net/ORDO/Orphanet_2170
6093||4337||Hydranencephaly||http://www.orpha.net/ORDO/Orphanet_2177
6092||6095||membrane-bounded organelle||http://purl.obolibrary.org/obo/GO_0043227
6095||3744||organelle||http://purl.obolibrary.org/obo/GO_0043226
6094||5317||Infantile systemic hyalinosis||http://www.orpha.net/ORDO/Orphanet_2176
6096||1539||intracellular organelle||http://purl.obolibrary.org/obo/GO_0043229
6097||10306||Partial deletion of the long arm of chromosome 5||http://www.orpha.net/ORDO/Orphanet_262038
6098||6476||response to alcohol||http://www.ebi.ac.uk/efo/EFO_0005526
6099||10994||tetrabenazine||http://purl.obolibrary.org/obo/CHEBI_9467
6100||14970||ejection fraction measurement||http://www.ebi.ac.uk/efo/EFO_0005527
6101||2849||large artery stroke||http://www.ebi.ac.uk/efo/EFO_0005524
6102||7941||Eiken syndrome||http://www.orpha.net/ORDO/Orphanet_79106
6103||5700||Developmental malformations - deafness - dystonia||http://www.orpha.net/ORDO/Orphanet_79107
6104||14970||parasitemia measurement||http://www.ebi.ac.uk/efo/EFO_0005528
6105||1016||Chagas cardiomyopathy||http://www.ebi.ac.uk/efo/EFO_0005529
6106||4717||Rare genetic bone development disorder||http://www.orpha.net/ORDO/Orphanet_404584
6107||15538||substrate type||http://www.ebi.ac.uk/efo/EFO_0005522
6108||15538||surface type||http://www.ebi.ac.uk/efo/EFO_0005523
6109||7068||Atrophoderma vermiculata||http://www.orpha.net/ORDO/Orphanet_79100
6110||14179||Hyperprolinemia type 2||http://www.orpha.net/ORDO/Orphanet_79101
6111||4335||conversion protocol||http://www.ebi.ac.uk/efo/EFO_0005520
6113||15538||technology type||http://www.ebi.ac.uk/efo/EFO_0005521
6112||1391||Thyrotoxic periodic paralysis||http://www.orpha.net/ORDO/Orphanet_79102
6114||8537||Tibial hemimelia, unilateral||http://www.orpha.net/ORDO/Orphanet_295077
6115||8537||Tibial hemimelia, bilateral||http://www.orpha.net/ORDO/Orphanet_295079
6116||770||AG07307||http://purl.obolibrary.org/obo/CLO_0035579
6117||8539||Ulnar hemimelia, bilateral||http://www.orpha.net/ORDO/Orphanet_295073
6118||8539||Ulnar hemimelia, unilateral||http://www.orpha.net/ORDO/Orphanet_295075
6119||8536||Radial hemimelia, bilateral||http://www.orpha.net/ORDO/Orphanet_295071
6120||14970||progesterone receptor status||http://www.ebi.ac.uk/efo/EFO_0005513
6121||14970||HER2 status||http://www.ebi.ac.uk/efo/EFO_0005514
6122||9616||RIP-Chip by array||http://www.ebi.ac.uk/efo/EFO_0005517
6123||4335||sample collection protocol||http://www.ebi.ac.uk/efo/EFO_0005518
6124||4335||dissection protocol||http://www.ebi.ac.uk/efo/EFO_0005519
6125||7377||Neonatal diabetes - congenital hypothyroidism - congenital glaucoma - hepatic fibrosis - polycystic kidneys||http://www.orpha.net/ORDO/Orphanet_79118
6127||14544||L2d-dauer molt||http://www.ebi.ac.uk/efo/EFO_0005510
6126||1171||Mandibulofacial dysostosis-microcephaly syndrome||http://www.orpha.net/ORDO/Orphanet_79113
6128||14544||post dauer stage||http://www.ebi.ac.uk/efo/EFO_0005511
6129||14970||estrogen receptor status||http://www.ebi.ac.uk/efo/EFO_0005512
6130||13709||Congenital absence of thigh and lower leg with foot present, unilateral||http://www.orpha.net/ORDO/Orphanet_295089
6131||1826||Pinus pinaster||http://purl.obolibrary.org/obo/NCBITaxon_71647
6132||13708||Congenital absence of upper arm and forearm with hand present, bilateral||http://www.orpha.net/ORDO/Orphanet_295087
6133||13708||Congenital absence of upper arm and forearm with hand present, unilateral||http://www.orpha.net/ORDO/Orphanet_295085
6134||8547||Fibular hemimelia, bilateral||http://www.orpha.net/ORDO/Orphanet_295083
6135||8547||Fibular hemimelia, unilateral||http://www.orpha.net/ORDO/Orphanet_295081
6136||4344||DPAGT1-CDG||http://www.orpha.net/ORDO/Orphanet_86309
6137||14544||L1 larva||http://www.ebi.ac.uk/efo/EFO_0005508
6138||14544||L4 larva||http://www.ebi.ac.uk/efo/EFO_0005509
6139||15511||elongating embryo||http://www.ebi.ac.uk/efo/EFO_0005506
6141||14544||dauer larva||http://www.ebi.ac.uk/efo/EFO_0005507
6140||5502||Porphyromonas gingivalis ATCC 33277||http://purl.obolibrary.org/obo/NCBITaxon_431947
6142||15511||fully-elongated embryo||http://www.ebi.ac.uk/efo/EFO_0005504
6143||6148||enclosing embryo||http://www.ebi.ac.uk/efo/EFO_0005505
6144||6148||late cleavage stage embryo||http://www.ebi.ac.uk/efo/EFO_0005502
6145||6148||gastrulating embryo||http://www.ebi.ac.uk/efo/EFO_0005503
6146||15511||4-cell embryo||http://www.ebi.ac.uk/efo/EFO_0005500
6147||13697||Amelia of lower limb, bilateral||http://www.orpha.net/ORDO/Orphanet_295059
6148||15511||proliferating embryo||http://www.ebi.ac.uk/efo/EFO_0005501
6149||10994||resveratrol||http://purl.obolibrary.org/obo/CHEBI_27881
6150||13761||Lower limb hypertrophy||http://www.orpha.net/ORDO/Orphanet_295051
6152||13699||Amelia of upper limb, unilateral||http://www.orpha.net/ORDO/Orphanet_295053
6151||4173||isoxazole||http://purl.obolibrary.org/obo/CHEBI_35595
6153||13699||Amelia of upper limb, bilateral||http://www.orpha.net/ORDO/Orphanet_295055
6154||13697||Amelia of lower limb, unilateral||http://www.orpha.net/ORDO/Orphanet_295057
6155||4027||pregnenolone 16alpha-carbonitrile||http://purl.obolibrary.org/obo/CHEBI_35591
6156||6160||sensory perception of bitter taste||http://purl.obolibrary.org/obo/GO_0050913
6157||3829||Femoral agenesis/hypoplasia, unilateral||http://www.orpha.net/ORDO/Orphanet_295065
6158||13707||Humeral agenesis/hypoplasia, bilateral||http://www.orpha.net/ORDO/Orphanet_295063
6159||2252||X-linked intellectual disability - epilepsy - progressive joint contractures - dysmorphism||http://www.orpha.net/ORDO/Orphanet_85319
6162||11899||X-linked intellectual disability - precocious puberty - obesity||http://www.orpha.net/ORDO/Orphanet_85318
6160||3015||sensory perception of taste||http://purl.obolibrary.org/obo/GO_0050909
6161||8536||Radial hemimelia, unilateral||http://www.orpha.net/ORDO/Orphanet_295069
6163||2252||X-linked intellectual disability - hypogammaglobulinemia - progressive neurological deterioration||http://www.orpha.net/ORDO/Orphanet_85317
6164||3829||Femoral agenesis/hypoplasia, bilateral||http://www.orpha.net/ORDO/Orphanet_295067
6165||3787||Autosomal dominant proximal renal tubular acidosis||http://www.orpha.net/ORDO/Orphanet_314889
6166||13707||Humeral agenesis/hypoplasia, unilateral||http://www.orpha.net/ORDO/Orphanet_295061
6168||1485||hypercalcemia||http://www.ebi.ac.uk/efo/EFO_0005563
6167||8663||Aromatic L-amino acid decarboxylase deficiency||http://www.orpha.net/ORDO/Orphanet_35708
6169||8970||hydronephrosis||http://www.ebi.ac.uk/efo/EFO_0005562
6170||2252||Deafness - intellectual disability, Martin-Probst type||http://www.orpha.net/ORDO/Orphanet_85321
6173||2002||histiocytoma||http://www.ebi.ac.uk/efo/EFO_0005561
6171||6854||Stargardt disease||http://www.orpha.net/ORDO/Orphanet_827
6172||8716||Glutaric acidemia type 3||http://www.orpha.net/ORDO/Orphanet_35706
6176||11899||X-linked intellectual disability - macrocephaly - macroorchidism||http://www.orpha.net/ORDO/Orphanet_85320
6174||6285||Neurometabolic disorder due to serine deficiency||http://www.orpha.net/ORDO/Orphanet_35705
6175||8323||hereditary multiple exostoses||http://www.ebi.ac.uk/efo/EFO_0005560
6178||11899||X-linked intellectual disability, Seemanova type||http://www.orpha.net/ORDO/Orphanet_85323
6177||1484||malignant peritoneal mesothelioma||http://www.ebi.ac.uk/efo/EFO_0005567
6179||2252||X-linked intellectual disability, Pai type||http://www.orpha.net/ORDO/Orphanet_85322
6181||4988||Schizosaccharomyces pombe 972h-||http://purl.obolibrary.org/obo/NCBITaxon_284812
6180||5700||Stickler syndrome||http://www.orpha.net/ORDO/Orphanet_828
6183||2252||X-linked intellectual disability, Stevenson type||http://www.orpha.net/ORDO/Orphanet_85325
6182||1790||janus kinase-3 deficiency||http://www.ebi.ac.uk/efo/EFO_0005565
6184||11899||X-linked intellectual disability, Shrimpton type||http://www.orpha.net/ORDO/Orphanet_85324
6185||12497||microphthalmia||http://www.ebi.ac.uk/efo/EFO_0005569
6186||1732||methylmalonic aciduria and homocystinuria type cblE||http://www.ebi.ac.uk/efo/EFO_0005568
6187||3753||Sporadic idiopathic steroid-resistant nephrotic syndrome||http://www.orpha.net/ORDO/Orphanet_84271
6188||2252||X-linked intellectual disability, Stoll type||http://www.orpha.net/ORDO/Orphanet_85326
6189||11899||X-linked intellectual disability - acromegaly - hyperactivity||http://www.orpha.net/ORDO/Orphanet_85327
6190||11899||X-linked intellectual disability, Turner type||http://www.orpha.net/ORDO/Orphanet_85328
6191||2252||X-linked intellectual disability - hypotonia - facial dysmorphism - aggressive behavior||http://www.orpha.net/ORDO/Orphanet_85329
6194||1002||oral cavity cancer||http://www.ebi.ac.uk/efo/EFO_0005570
6192||5967||Sotos syndrome||http://www.orpha.net/ORDO/Orphanet_821
6193||6324||Arginine:glycine amidinotransferase deficiency||http://www.orpha.net/ORDO/Orphanet_35704
6195||12330||Hereditary spherocytosis||http://www.orpha.net/ORDO/Orphanet_822
6196||6272||3-hydroxy-3-methylglutaryl-CoA synthase deficiency||http://www.orpha.net/ORDO/Orphanet_35701
6197||5508||Isolated spina bifida||http://www.orpha.net/ORDO/Orphanet_823
6198||4254||Sj gren-Larsson syndrome||http://www.orpha.net/ORDO/Orphanet_816
6199||4887||X-linked intellectual disability-retinitis pigmentosa syndrome||http://www.orpha.net/ORDO/Orphanet_85332
6200||11899||X-linked intellectual disability - hypogonadism - ichthyosis - obesity - short stature||http://www.orpha.net/ORDO/Orphanet_85331
6201||5956||X-linked intellectual disability - corpus callosum agenesis - spastic quadriparesis||http://www.orpha.net/ORDO/Orphanet_85330
6203||15417||dysembryoplastic neuroepithelial tumor||http://www.ebi.ac.uk/efo/EFO_0005551
6202||4785||Silver-Russell syndrome||http://www.orpha.net/ORDO/Orphanet_813
6204||4706||X-linked neurodegenerative syndrome, Hamel type||http://www.orpha.net/ORDO/Orphanet_85336
6206||2252||Fried syndrome||http://www.orpha.net/ORDO/Orphanet_85335
6205||2252||Smith-Magenis syndrome||http://www.orpha.net/ORDO/Orphanet_819
6207||1002||eccrine sweat gland cancer||http://www.ebi.ac.uk/efo/EFO_0005553
6209||2252||Smith-Lemli-Opitz syndrome||http://www.orpha.net/ORDO/Orphanet_818
6208||1485||Gilbert syndrome||http://www.ebi.ac.uk/efo/EFO_0005556
6210||4706||X-linked neurodegenerative syndrome, Bertini type||http://www.orpha.net/ORDO/Orphanet_85334
6212||11037||Peeling skin syndrome||http://www.orpha.net/ORDO/Orphanet_817
6211||1790||gamma chain deficiency||http://www.ebi.ac.uk/efo/EFO_0005555
6213||8298||hemolytic anemia||http://www.ebi.ac.uk/efo/EFO_0005558
6214||1002||gum cancer||http://www.ebi.ac.uk/efo/EFO_0005557
6215||11899||X-linked intellectual disability, Zorick type||http://www.orpha.net/ORDO/Orphanet_85337
6216||6322||Glucose-galactose malabsorption||http://www.orpha.net/ORDO/Orphanet_35710
6217||3114||X-linked intellectual disability - ataxia - apraxia||http://www.orpha.net/ORDO/Orphanet_85338
6218||5191||Shwachman-Diamond syndrome||http://www.orpha.net/ORDO/Orphanet_811
6219||4636||Sialidosis type 1||http://www.orpha.net/ORDO/Orphanet_812
6220||1732||congenital disorder of glycosylation type I||http://www.ebi.ac.uk/efo/EFO_0005545
6221||4477||Scott syndrome||http://www.orpha.net/ORDO/Orphanet_806
6222||11614||brain glioma||http://www.ebi.ac.uk/efo/EFO_0005543
6224||2700||botulism||http://www.ebi.ac.uk/efo/EFO_0005542
6223||2318||Seckel syndrome||http://www.orpha.net/ORDO/Orphanet_808
6225||8323||bone development disease||http://www.ebi.ac.uk/efo/EFO_0005541
6226||1006||bile duct carcinoma||http://www.ebi.ac.uk/efo/EFO_0005540
6228||616||Tuberous sclerosis||http://www.orpha.net/ORDO/Orphanet_805
6227||5877||Familial atypical multiple mole melanoma syndrome||http://www.orpha.net/ORDO/Orphanet_404560
6229||2700||diphtheria||http://www.ebi.ac.uk/efo/EFO_0005549
6230||2102||developmental disorder of mental health||http://www.ebi.ac.uk/efo/EFO_0005548
6232||2714||dengue disease||http://www.ebi.ac.uk/efo/EFO_0005547
6231||4734||Dysostosis of genetic origin||http://www.orpha.net/ORDO/Orphanet_404568
6233||1732||congenital disorder of glycosylation type II||http://www.ebi.ac.uk/efo/EFO_0005546
6234||10994||furan||http://purl.obolibrary.org/obo/CHEBI_35559
6236||13709||Congenital absence of thigh and lower leg with foot present, bilateral||http://www.orpha.net/ORDO/Orphanet_295091
6235||10994||perhexiline||http://purl.obolibrary.org/obo/CHEBI_35553
6237||13705||Congenital absence of both forearm and hand, unilateral||http://www.orpha.net/ORDO/Orphanet_295093
6238||799||cardiovascular drug||http://purl.obolibrary.org/obo/CHEBI_35554
6239||13705||Congenital absence of both forearm and hand, bilateral||http://www.orpha.net/ORDO/Orphanet_295095
6240||13633||Congenital absence of both lower leg and foot, unilateral||http://www.orpha.net/ORDO/Orphanet_295097
6241||1882||Schwartz-Jampel syndrome||http://www.orpha.net/ORDO/Orphanet_800
6242||13633||Congenital absence of both lower leg and foot, bilateral||http://www.orpha.net/ORDO/Orphanet_295099
6243||2866||angioedema||http://www.ebi.ac.uk/efo/EFO_0005532
6245||2866||urticaria||http://www.ebi.ac.uk/efo/EFO_0005531
6244||6246||Genetic syndrome with limb reduction defects||http://www.orpha.net/ORDO/Orphanet_404574
6247||1391||delayed encephalopathy after acute carbon monoxide poisoning||http://www.ebi.ac.uk/efo/EFO_0005534
6246||4719||Genetic syndrome with limb malformations as a major feature||http://www.orpha.net/ORDO/Orphanet_404577
6248||4259||response to non-steroidal anti-inflammatory||http://www.ebi.ac.uk/efo/EFO_0005533
6249||6231||Dysostosis of genetic origin with limb anomaly as a major feature||http://www.orpha.net/ORDO/Orphanet_404571
6250||5868||Primary lipodystrophy||http://www.orpha.net/ORDO/Orphanet_90970
6251||14970||Trypanosoma cruzi seropositivity||http://www.ebi.ac.uk/efo/EFO_0005530
6252||15416||adrenal gland disease||http://www.ebi.ac.uk/efo/EFO_0005539
6253||14970||nitric oxide exhalation measurement||http://www.ebi.ac.uk/efo/EFO_0005536
6255||3072||primitive mesencephalic artery||http://purl.obolibrary.org/obo/UBERON_2001062
6254||4981||specimen vial||http://www.ebi.ac.uk/efo/EFO_0005535
6256||14970||thrombin generation potential measurement||http://www.ebi.ac.uk/efo/EFO_0005538
6257||970||triple-negative breast cancer||http://www.ebi.ac.uk/efo/EFO_0005537
6258||1022||Trypanosoma brucei TREU927||http://purl.obolibrary.org/obo/NCBITaxon_185431
6259||3990||alpha-adrenergic agonist||http://purl.obolibrary.org/obo/CHEBI_35569
6260||4142||Short stature due to GHSR deficiency||http://www.orpha.net/ORDO/Orphanet_314811
6261||4775||Treacher-Collins syndrome||http://www.orpha.net/ORDO/Orphanet_861
6262||6087||Congenitally uncorrected transposition of the great arteries||http://www.orpha.net/ORDO/Orphanet_860
6263||899||Familial multiple trichoepithelioma||http://www.orpha.net/ORDO/Orphanet_867
6264||6621||Disorder of pyrimidine metabolism||http://www.orpha.net/ORDO/Orphanet_79193
6265||6600||Disorder of pyridoxine metabolism||http://www.orpha.net/ORDO/Orphanet_79192
6266||6621||Disorder of purine metabolism||http://www.orpha.net/ORDO/Orphanet_79191
6267||5795||Disorder of phenylalanin or tyrosine metabolism||http://www.orpha.net/ORDO/Orphanet_79190
6268||12386||Gyps africanus||http://purl.obolibrary.org/obo/NCBITaxon_43490
6269||5795||Disorder of ornithine or proline metabolism||http://www.orpha.net/ORDO/Orphanet_79185
6270||6309||Disorder of pentose phosphate metabolism||http://www.orpha.net/ORDO/Orphanet_79186
6272||6326||Disorder of ketone body metabolism||http://www.orpha.net/ORDO/Orphanet_79183
6271||9760||Triose phosphate-isomerase deficiency||http://www.orpha.net/ORDO/Orphanet_868
6273||212||Triple A syndrome||http://www.orpha.net/ORDO/Orphanet_869
6274||266||Peroxisome biogenesis disorder-Zellweger syndrome spectrum||http://www.orpha.net/ORDO/Orphanet_79189
6275||5795||Disorder of peptide metabolism||http://www.orpha.net/ORDO/Orphanet_79187
6276||8716||Peroxisomal beta-oxidation disorder||http://www.orpha.net/ORDO/Orphanet_79188
6277||4810||Primary renal tubular acidosis||http://www.orpha.net/ORDO/Orphanet_314822
6278||14954||Constriction rings syndrome||http://www.orpha.net/ORDO/Orphanet_295000
6279||5499||X-linked thrombocytopenia with normal platelets||http://www.orpha.net/ORDO/Orphanet_852
6280||4406||Paris-Trousseau thrombocytopenia||http://www.orpha.net/ORDO/Orphanet_851
6281||7956||Hyperphalangy||http://www.orpha.net/ORDO/Orphanet_295002
6282||5502||Aliivibrio salmonicida LFI1238||http://purl.obolibrary.org/obo/NCBITaxon_316275
6283||10994||N-methyl-N -nitro-N-nitrosoguanidine||http://purl.obolibrary.org/obo/CHEBI_21759
6286||2169||Postaxial polydactyly of toes||http://www.orpha.net/ORDO/Orphanet_295008
6284||4775||Townes-Brocks syndrome||http://www.orpha.net/ORDO/Orphanet_857
6285||5795||Disorder of serine or glycine metabolism||http://www.orpha.net/ORDO/Orphanet_79194
6287||5287||Sterol biosynthesis disorder||http://www.orpha.net/ORDO/Orphanet_79195
6288||5795||Disorder of the gamma-glutamyl cycle||http://www.orpha.net/ORDO/Orphanet_79196
6289||6294||Transcobalamin deficiency||http://www.orpha.net/ORDO/Orphanet_859
6290||5795||Disorder of branched-chain amino acid metabolism||http://www.orpha.net/ORDO/Orphanet_79197
6291||2169||Central polydactyly of fingers||http://www.orpha.net/ORDO/Orphanet_295004
6292||2169||Preaxial polydactyly of toes||http://www.orpha.net/ORDO/Orphanet_295006
6293||2454||Tay-Sachs disease||http://www.orpha.net/ORDO/Orphanet_845
6294||8681||Disorder of cobalamin metabolism and transport||http://www.orpha.net/ORDO/Orphanet_79171
6295||15||Atrial tachyarrhythmia with short PR interval||http://www.orpha.net/ORDO/Orphanet_844
6296||5900||Sebocystomatosis||http://www.orpha.net/ORDO/Orphanet_841
6297||6039||6q terminal deletion syndrome||http://www.orpha.net/ORDO/Orphanet_75857
6298||4701||MORM syndrome||http://www.orpha.net/ORDO/Orphanet_75858
6299||1022||Rhabditinae||http://purl.obolibrary.org/obo/NCBITaxon_55887
6300||5502||Stenotrophomonas maltophilia||http://purl.obolibrary.org/obo/NCBITaxon_40324
6301||6600||Disorder of neurotransmitter metabolism and transport||http://www.orpha.net/ORDO/Orphanet_79169
6302||5795||Disorder of urea cycle metabolism and ammonia detoxification||http://www.orpha.net/ORDO/Orphanet_79167
6303||6626||Disorder of bile acid synthesis||http://www.orpha.net/ORDO/Orphanet_79168
6304||6318||Spinal muscular atrophy with respiratory distress type 2||http://www.orpha.net/ORDO/Orphanet_404521
6305||5795||Disorder of amino acid absorption and transport||http://www.orpha.net/ORDO/Orphanet_79166
6306||14261||Classic organic aciduria||http://www.orpha.net/ORDO/Orphanet_79163
6307||4490||Beta-thalassemia||http://www.orpha.net/ORDO/Orphanet_848
6308||4406||Glanzmann thrombasthenia||http://www.orpha.net/ORDO/Orphanet_849
6309||15571||Disorder of carbohydrate metabolism||http://www.orpha.net/ORDO/Orphanet_79161
6310||4488||Alpha-thalassemia||http://www.orpha.net/ORDO/Orphanet_846
6311||3019||Alpha-thalassemia - X-linked intellectual disability syndrome||http://www.orpha.net/ORDO/Orphanet_847
6312||6272||Succinyl-CoA:3-ketoacid CoA transferase deficiency||http://www.orpha.net/ORDO/Orphanet_832
6313||7353||Ehlers-Danlos syndrome with periventricular heterotopia||http://www.orpha.net/ORDO/Orphanet_82004
6314||6575||Free sialic acid storage disease||http://www.orpha.net/ORDO/Orphanet_834
6316||5287||Encephalopathy due to sulfite oxidase deficiency||http://www.orpha.net/ORDO/Orphanet_833
6315||5795||Disorder of histidine metabolism||http://www.orpha.net/ORDO/Orphanet_79181
6317||1309||Short stature due to partial GHR deficiency||http://www.orpha.net/ORDO/Orphanet_314802
6318||13153||X-linked distal hereditary motor neuropathy||http://www.orpha.net/ORDO/Orphanet_404538
6319||2313||Congenital muscular dystrophy, Ullrich type||http://www.orpha.net/ORDO/Orphanet_75840
6320||7172||Congenital nephrotic syndrome, Finnish type||http://www.orpha.net/ORDO/Orphanet_839
6321||6309||Gluconeogenesis disorder||http://www.orpha.net/ORDO/Orphanet_79177
6322||5414||Glucose transport disorder||http://www.orpha.net/ORDO/Orphanet_79178
6323||6309||Disorder of glycerol metabolism||http://www.orpha.net/ORDO/Orphanet_79179
6324||6570||Disorder of creatine biosynthesis||http://www.orpha.net/ORDO/Orphanet_79172
6325||5795||Disorder of methionine cycle and sulfur amino acid metabolism||http://www.orpha.net/ORDO/Orphanet_79173
6327||11867||supraorbital lateral line neuromast||http://purl.obolibrary.org/obo/UBERON_2001026
6326||6570||Disorder of fatty acid oxidation and ketone body metabolism||http://www.orpha.net/ORDO/Orphanet_79174
6329||11867||occipital lateral line neuromast||http://purl.obolibrary.org/obo/UBERON_2001025
6328||6600||Disorder of gamma-aminobutyric acid metabolism||http://www.orpha.net/ORDO/Orphanet_79175
6330||13764||Congenital patella dislocation||http://www.orpha.net/ORDO/Orphanet_295036
6331||13764||Congenital knee dislocation||http://www.orpha.net/ORDO/Orphanet_295034
6332||13764||Congenital elbow dislocation||http://www.orpha.net/ORDO/Orphanet_295032
6333||13764||Congenital shoulder dislocation||http://www.orpha.net/ORDO/Orphanet_295030
6334||325||Familial Dupuytren contracture||http://www.orpha.net/ORDO/Orphanet_79142
6335||13304||Hereditary painful callosities||http://www.orpha.net/ORDO/Orphanet_79141
6336||2252||Intellectual disability-obesity-prognathism-eye and skin anomalies syndrome||http://www.orpha.net/ORDO/Orphanet_397973
6337||5912||Familial progressive hyperpigmentation||http://www.orpha.net/ORDO/Orphanet_79146
6338||4276||Dowling-Degos disease||http://www.orpha.net/ORDO/Orphanet_79145
6340||307||Congenital onychodysplasia||http://www.orpha.net/ORDO/Orphanet_79144
6339||1377||Patella aplasia/hypoplasia, unilateral||http://www.orpha.net/ORDO/Orphanet_295038
6341||331||Congenital anonychia||http://www.orpha.net/ORDO/Orphanet_79143
6342||5918||Dermochondrocorneal dystrophy||http://www.orpha.net/ORDO/Orphanet_79149
6343||2681||Familial reactive perforating collagenosis||http://www.orpha.net/ORDO/Orphanet_79147
6344||6287||Lathosterolosis||http://www.orpha.net/ORDO/Orphanet_46059
6345||4705||Familial exudative vitreoretinopathy||http://www.orpha.net/ORDO/Orphanet_891
6346||2713||Von Hippel-Lindau disease||http://www.orpha.net/ORDO/Orphanet_892
6347||13761||Macrodactyly of fingers||http://www.orpha.net/ORDO/Orphanet_295044
6348||3019||WAGR syndrome||http://www.orpha.net/ORDO/Orphanet_893
6350||238||Combined immunodeficiency due to MALT1 deficiency||http://www.orpha.net/ORDO/Orphanet_397964
6349||6996||Waardenburg syndrome type 1||http://www.orpha.net/ORDO/Orphanet_894
6351||6996||Waardenburg syndrome type 2||http://www.orpha.net/ORDO/Orphanet_895
6354||13761||Macrodactyly of toes||http://www.orpha.net/ORDO/Orphanet_295047
6352||10994||but-1-ene||http://purl.obolibrary.org/obo/CHEBI_48362
6353||6996||Waardenburg syndrome type 3||http://www.orpha.net/ORDO/Orphanet_896
6355||5700||Waardenburg-Shah syndrome||http://www.orpha.net/ORDO/Orphanet_897
6358||12715||Charcot-Marie-Tooth disease type 2R||http://www.orpha.net/ORDO/Orphanet_397968
6357||1377||Patella aplasia/hypoplasia, bilateral||http://www.orpha.net/ORDO/Orphanet_295041
6356||9625||Wagner disease||http://www.orpha.net/ORDO/Orphanet_898
6359||1843||Walker-Warburg syndrome||http://www.orpha.net/ORDO/Orphanet_899
6360||5935||Acrokeratosis verruciformis of Hopf||http://www.orpha.net/ORDO/Orphanet_79151
6361||5912||Linear and whorled nevoid hypermelanosis||http://www.orpha.net/ORDO/Orphanet_79150
6362||331||Autosomal dominant nail dysplasia||http://www.orpha.net/ORDO/Orphanet_79153
6363||5939||Disseminated superficial actinic porokeratosis||http://www.orpha.net/ORDO/Orphanet_79152
6364||14068||Encephalopathy due to hydroxykynureninuria||http://www.orpha.net/ORDO/Orphanet_79155
6365||13761||Upper limb hypertrophy||http://www.orpha.net/ORDO/Orphanet_295049
6366||13972||2-aminoadipic 2-oxoadipic aciduria||http://www.orpha.net/ORDO/Orphanet_79154
6367||13543||Drosophila montana||http://purl.obolibrary.org/obo/NCBITaxon_40370
6368||6306||2-methylbutyryl-CoA dehydrogenase deficiency||http://www.orpha.net/ORDO/Orphanet_79157
6369||13972||Seizures - intellectual disability due to hydroxylysinuria||http://www.orpha.net/ORDO/Orphanet_79156
6370||4951||Isobutyryl-CoA dehydrogenase deficiency||http://www.orpha.net/ORDO/Orphanet_79159
6371||14261||Cerebral organic aciduria||http://www.orpha.net/ORDO/Orphanet_79158
6372||10994||cisplatin||http://purl.obolibrary.org/obo/CHEBI_27899
6373||1528||Turner syndrome||http://www.orpha.net/ORDO/Orphanet_881
6374||6573||polar aprotic solvent role||http://purl.obolibrary.org/obo/CHEBI_48358
6375||12083||Van der Woude syndrome||http://www.orpha.net/ORDO/Orphanet_888
6376||6573||polar solvent role||http://purl.obolibrary.org/obo/CHEBI_48354
6377||2169||Central polydactyly of toes||http://www.orpha.net/ORDO/Orphanet_295010
6378||5486||TCR-alpha-beta-positive T-cell deficiency||http://www.orpha.net/ORDO/Orphanet_397959
6379||5700||Usher syndrome||http://www.orpha.net/ORDO/Orphanet_886
6380||7319||VACTERL/VATER association||http://www.orpha.net/ORDO/Orphanet_887
6381||7518||Tetrasomy 12p||http://www.orpha.net/ORDO/Orphanet_884
6382||13736||Familial isolated clinodactyly of fingers||http://www.orpha.net/ORDO/Orphanet_295014
6383||266||Tyrosinemia type 1||http://www.orpha.net/ORDO/Orphanet_882
6384||10567||Syndactyly type 6||http://www.orpha.net/ORDO/Orphanet_295012
6387||2252||Microcephaly-thin corpus callosum-intellectual disability syndrome||http://www.orpha.net/ORDO/Orphanet_397951
6385||7175||Hepatic veno-occlusive disease - immunodeficiency||http://www.orpha.net/ORDO/Orphanet_79124
6386||10292||Congenital pseudoarthrosis of the tibia||http://www.orpha.net/ORDO/Orphanet_295018
6388||13736||Camptodactyly of fingers||http://www.orpha.net/ORDO/Orphanet_295016
6389||306||Trichodysplasia - amelogenesis imperfecta||http://www.orpha.net/ORDO/Orphanet_79129
6390||13470||Autosomal recessive spastic paraplegia type 58||http://www.orpha.net/ORDO/Orphanet_397946
6391||10292||Congenital pseudoarthrosis of the femur||http://www.orpha.net/ORDO/Orphanet_295020
6392||15||Familial progressive cardiac conduction defect||http://www.orpha.net/ORDO/Orphanet_871
6393||10292||Congenital pseudoarthrosis of the fibula||http://www.orpha.net/ORDO/Orphanet_295022
6394||10292||Congenital pseudoarthrosis of the radius||http://www.orpha.net/ORDO/Orphanet_295024
6395||1325||Focal facial dermal dysplasia type I||http://www.orpha.net/ORDO/Orphanet_79133
6397||306||Sparse hair - short stature - skin anomalies||http://www.orpha.net/ORDO/Orphanet_79132
6396||10292||Congenital pseudoarthrosis of the ulna||http://www.orpha.net/ORDO/Orphanet_295026
6398||7944||Episodic ataxia type 3||http://www.orpha.net/ORDO/Orphanet_79135
6399||13735||Tibio-fibular synostosis||http://www.orpha.net/ORDO/Orphanet_295028
6401||4344||MAN1B1-CDG||http://www.orpha.net/ORDO/Orphanet_397941
6400||613||DEND syndrome||http://www.orpha.net/ORDO/Orphanet_79134
6402||10272||Generalized epilepsy - paroxysmal dyskinesia||http://www.orpha.net/ORDO/Orphanet_79137
6403||7944||Episodic ataxia type 4||http://www.orpha.net/ORDO/Orphanet_79136
6404||1022||Callicebus cupreus||http://purl.obolibrary.org/obo/NCBITaxon_202457
6405||306||Toriello-Lacassie-Droste syndrome||http://www.orpha.net/ORDO/Orphanet_3339
6406||4810||Primary Fanconi syndrome||http://www.orpha.net/ORDO/Orphanet_3337
6408||5300||Toriello-Carey syndrome||http://www.orpha.net/ORDO/Orphanet_3338
6407||7992||Sacral agenesis-abnormal ossification of the vertebral bodies-persistent notochordal canal syndrome||http://www.orpha.net/ORDO/Orphanet_397927
6409||4706||Ferro-cerebro-cutaneous syndrome||http://www.orpha.net/ORDO/Orphanet_397922
6410||7942||Bowed tibiae  - radial anomalies - osteopenia - fractures||http://www.orpha.net/ORDO/Orphanet_3331
6411||13769||Hypoplastic tibiae - postaxial polydactyly||http://www.orpha.net/ORDO/Orphanet_3332
6412||8835||Epileptic encephalopathy with global cerebral demyelination||http://www.orpha.net/ORDO/Orphanet_353217
6413||4957||Polyglucosan body myopathy||http://www.orpha.net/ORDO/Orphanet_397937
6414||7353||Arterial tortuosity syndrome||http://www.orpha.net/ORDO/Orphanet_3342
6416||11899||Severe intellectual disability-progressive postnatal microcephaly- midline stereotypic hand movements syndrome||http://www.orpha.net/ORDO/Orphanet_397933
6415||7991||Weismann-Netter syndrome||http://www.orpha.net/ORDO/Orphanet_3344
6417||11882||Torticollis - keloids - cryptorchidism - renal dysplasia||http://www.orpha.net/ORDO/Orphanet_3341
6418||5486||RAS-associated autoimmune leukoproliferative disease||http://www.orpha.net/ORDO/Orphanet_268114
6419||306||Trichoodontoonychial dysplasia||http://www.orpha.net/ORDO/Orphanet_3355
6421||1391||Sarcoidosis||http://www.orpha.net/ORDO/Orphanet_797
6420||9740||Mitochondrial DNA depletion syndrome||http://www.orpha.net/ORDO/Orphanet_35698
6422||2454||Sandhoff disease||http://www.orpha.net/ORDO/Orphanet_796
6423||306||Trichodermodysplasia - dental alterations||http://www.orpha.net/ORDO/Orphanet_3353
6425||306||Tricho-oculo-dermo-vertebral syndrome||http://www.orpha.net/ORDO/Orphanet_3354
6424||5967||Saethre-Chotzen syndrome||http://www.orpha.net/ORDO/Orphanet_794
6426||306||Autosomal dominant trichoodontoonychodysplasia-syndactyly||http://www.orpha.net/ORDO/Orphanet_3357
6427||760||Schizencephaly||http://www.orpha.net/ORDO/Orphanet_799
6428||306||Schinzel-Giedion syndrome||http://www.orpha.net/ORDO/Orphanet_798
6429||306||Trichodental syndrome||http://www.orpha.net/ORDO/Orphanet_3351
6430||306||Tricho-dento-osseous syndrome||http://www.orpha.net/ORDO/Orphanet_3352
6431||6897||X-linked retinoschisis||http://www.orpha.net/ORDO/Orphanet_792
6432||288||Mitochondrial disorder due to a defect in mitochondrial protein synthesis||http://www.orpha.net/ORDO/Orphanet_35696
6433||9965||Retinitis pigmentosa||http://www.orpha.net/ORDO/Orphanet_791
6434||5073||Retinoblastoma||http://www.orpha.net/ORDO/Orphanet_790
6435||5475||Nijmegen breakage syndrome-like disorder||http://www.orpha.net/ORDO/Orphanet_240760
6436||4706||Primary lateral sclerosis||http://www.orpha.net/ORDO/Orphanet_35689
6437||6610||Trigonocephaly - broad thumbs||http://www.orpha.net/ORDO/Orphanet_3365
6438||7989||Madelung deformity||http://www.orpha.net/ORDO/Orphanet_35688
6439||6650||Isolated trigonocephaly||http://www.orpha.net/ORDO/Orphanet_3366
6440||12769||Trigonocephaly - bifid nose - acral anomalies||http://www.orpha.net/ORDO/Orphanet_3368
6441||2252||Trigonocephaly - short stature - developmental delay||http://www.orpha.net/ORDO/Orphanet_3369
6442||4627||organophosphate biosynthetic process||http://purl.obolibrary.org/obo/GO_0090407
6443||330||Trichodysplasia - xeroderma||http://www.orpha.net/ORDO/Orphanet_3361
6444||306||Trichomegaly - cataract - hereditary spherocytosis||http://www.orpha.net/ORDO/Orphanet_3362
6445||306||Trichomegaly - retina pigmentary degeneration - dwarfism||http://www.orpha.net/ORDO/Orphanet_3363
6446||5048||Hereditary pheochromocytoma-paraganglioma||http://www.orpha.net/ORDO/Orphanet_29072
6447||2252||19q13.11 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_217346
6448||2252||17q21.31 microduplication  syndrome||http://www.orpha.net/ORDO/Orphanet_217340
6449||10641||Distal trisomy 17q||http://www.orpha.net/ORDO/Orphanet_3379
6451||5055||Pancreatic beta cell agenesis with neonatal diabetes mellitus||http://www.orpha.net/ORDO/Orphanet_28455
6450||7319||Trisomy 13||http://www.orpha.net/ORDO/Orphanet_3378
6452||13421||Trismus - pseudocamptodactyly||http://www.orpha.net/ORDO/Orphanet_3377
6453||4701||Triploidy||http://www.orpha.net/ORDO/Orphanet_3376
6454||4898||Trisomy X||http://www.orpha.net/ORDO/Orphanet_3375
6455||7139||COG5-CDG||http://www.orpha.net/ORDO/Orphanet_263487
6456||3540||Spondyloepiphyseal dysplasia, Maroteaux type||http://www.orpha.net/ORDO/Orphanet_263482
6457||10138||MACS syndrome||http://www.orpha.net/ORDO/Orphanet_217335
6458||4810||Hyperuricemia - anemia - renal failure||http://www.orpha.net/ORDO/Orphanet_217330
6459||6244||Humerus trochlea aplasia||http://www.orpha.net/ORDO/Orphanet_3383
6460||7319||Trisomy 18||http://www.orpha.net/ORDO/Orphanet_3380
6461||10994||4-nonylphenol||http://purl.obolibrary.org/obo/CHEBI_34440
6462||322||Isolated anterior cervical hypertrichosis||http://www.orpha.net/ORDO/Orphanet_3387
6463||1979||Tuberculosis||http://www.orpha.net/ORDO/Orphanet_3389
6464||5987||Neural tube defect||http://www.orpha.net/ORDO/Orphanet_3388
6465||5894||DPM3-CDG||http://www.orpha.net/ORDO/Orphanet_263494
6466||7407||Proximal tubulopathy - diabetes mellitus - cerebellar ataxia||http://www.orpha.net/ORDO/Orphanet_3390
6467||2670||leaf tip||http://purl.obolibrary.org/obo/PO_0025142
6468||770||416B||http://www.ebi.ac.uk/efo/EFO_0005482
6469||770||Patski||http://www.ebi.ac.uk/efo/EFO_0005481
6470||770||MEL-GATA-1-ER||http://www.ebi.ac.uk/efo/EFO_0005480
6471||10994||perfluorodecanoic acid||http://purl.obolibrary.org/obo/CHEBI_35546
6472||238||Combined immunodeficiency due to DOCK8 deficiency||http://www.orpha.net/ORDO/Orphanet_217390
6473||3750||cyclooxygenase inhibitor||http://purl.obolibrary.org/obo/CHEBI_35544
6475||2252||17p13.3 microduplication syndrome||http://www.orpha.net/ORDO/Orphanet_217385
6476||5295||response to stimulus||http://purl.obolibrary.org/obo/GO_0050896
6474||5502||Staphylococcus aureus subsp. aureus str. Newman||http://purl.obolibrary.org/obo/NCBITaxon_426430
6478||770||U-266||http://www.ebi.ac.uk/efo/EFO_0005478
6477||7494||Intermittent maple syrup urine disease||http://www.orpha.net/ORDO/Orphanet_268173
6479||770||Z-138||http://www.ebi.ac.uk/efo/EFO_0005479
6480||770||JVM-2||http://www.ebi.ac.uk/efo/EFO_0005476
6481||10652||obsolete_KARPAS 422||http://www.ebi.ac.uk/efo/EFO_0005477
6482||770||BL-2||http://www.ebi.ac.uk/efo/EFO_0005475
6483||13202||CB1489||http://www.ebi.ac.uk/efo/EFO_0005491
6484||13202||BA671||http://www.ebi.ac.uk/efo/EFO_0005490
6485||13202||MT10430||http://www.ebi.ac.uk/efo/EFO_0005493
6486||13202||JK1107||http://www.ebi.ac.uk/efo/EFO_0005492
6487||9719||Autosomal dominant rhegmatogenous retinal detachment||http://www.orpha.net/ORDO/Orphanet_209867
6488||4706||Neurodegenerative syndrome due to cerebral folate transport deficiency||http://www.orpha.net/ORDO/Orphanet_217382
6489||2252||Microduplication Xp11.22-p11.23 syndrome||http://www.orpha.net/ORDO/Orphanet_217377
6490||1022||Streptopelia risoria||http://purl.obolibrary.org/obo/NCBITaxon_328808
6491||13202||DZ685||http://www.ebi.ac.uk/efo/EFO_0005487
6492||13202||NW1229||http://www.ebi.ac.uk/efo/EFO_0005488
6493||13202||LX837||http://www.ebi.ac.uk/efo/EFO_0005489
6494||7494||Intermediate maple syrup urine disease||http://www.orpha.net/ORDO/Orphanet_268162
6495||770||ES-Bruce4||http://www.ebi.ac.uk/efo/EFO_0005483
6496||770||46C||http://www.ebi.ac.uk/efo/EFO_0005484
6498||770||TT2||http://www.ebi.ac.uk/efo/EFO_0005485
6497||9899||Neuroacanthocytosis||http://www.orpha.net/ORDO/Orphanet_263440
6499||770||J185a||http://www.ebi.ac.uk/efo/EFO_0005486
6501||798||Nanophthalmia||http://www.orpha.net/ORDO/Orphanet_35612
6500||8870||Hyperinsulinism due to INSR deficiency||http://www.orpha.net/ORDO/Orphanet_263458
6502||770||SKI-DCLC||http://www.ebi.ac.uk/efo/EFO_0005460
6503||799||beta-adrenergic agonist||http://purl.obolibrary.org/obo/CHEBI_35522
6504||266||Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins||http://www.orpha.net/ORDO/Orphanet_217371
6505||5025||Penicillium fellutanum||http://purl.obolibrary.org/obo/NCBITaxon_70095
6506||799||hypoglycemic drug||http://purl.obolibrary.org/obo/CHEBI_35526
6507||770||SK-MM-2||http://www.ebi.ac.uk/efo/EFO_0005458
6508||10652||obsolete_SK-N-F1||http://www.ebi.ac.uk/efo/EFO_0005459
6509||5502||Thermosynechococcus elongatus BP-1||http://purl.obolibrary.org/obo/NCBITaxon_197221
6510||770||SF295||http://www.ebi.ac.uk/efo/EFO_0005452
6511||770||SF539||http://www.ebi.ac.uk/efo/EFO_0005453
6512||770||SF126||http://www.ebi.ac.uk/efo/EFO_0005450
6513||770||SF268||http://www.ebi.ac.uk/efo/EFO_0005451
6515||11347||Hyperinsulinism due to HNF4A deficiency||http://www.orpha.net/ORDO/Orphanet_263455
6514||770||SHEP-2||http://www.ebi.ac.uk/efo/EFO_0005456
6516||770||SK-MM-1||http://www.ebi.ac.uk/efo/EFO_0005457
6517||770||SHEF-1||http://www.ebi.ac.uk/efo/EFO_0005454
6518||770||SHEF-3||http://www.ebi.ac.uk/efo/EFO_0005455
6519||6266||Familial juvenile hyperuricemic nephropathy type 1||http://www.orpha.net/ORDO/Orphanet_209886
6520||8190||abscisic acid_6520||http://purl.obolibrary.org/obo/CHEBI_22152
6521||8191||ammonium sulfate||http://purl.obolibrary.org/obo/CHEBI_62946
6522||770||SUDHL1||http://www.ebi.ac.uk/efo/EFO_0005461
6523||770||SW527||http://www.ebi.ac.uk/efo/EFO_0005462
6524||4014||CHST3-related skeletal dysplasia||http://www.orpha.net/ORDO/Orphanet_263463
6525||7494||Thiamine-responsive maple syrup urine disease||http://www.orpha.net/ORDO/Orphanet_268184
6526||5039||Congenital isolated thyroxine-binding globulin deficiency||http://www.orpha.net/ORDO/Orphanet_209893
6527||13496||Macacine herpesvirus 3||http://purl.obolibrary.org/obo/NCBITaxon_47929
6528||9845||Tetraploidy||http://www.orpha.net/ORDO/Orphanet_3305
6529||2252||Fallot complex - intellectual disability - growth delay||http://www.orpha.net/ORDO/Orphanet_3304
6530||4629||Generalized arterial calcification of infancy||http://www.orpha.net/ORDO/Orphanet_51608
6531||2413||ALDH18A1-related De Barsy syndrome||http://www.orpha.net/ORDO/Orphanet_35664
6532||6244||Tetraamelia - multiple malformations||http://www.orpha.net/ORDO/Orphanet_3301
6533||10817||Tetrasomy 5p||http://www.orpha.net/ORDO/Orphanet_3309
6534||4928||Duplication/inversion 15q11||http://www.orpha.net/ORDO/Orphanet_3306
6535||10370||Tetrasomy 18p||http://www.orpha.net/ORDO/Orphanet_3307
6536||10994||6-deoxycathasterone||http://purl.obolibrary.org/obo/CHEBI_20714
6537||10994||6-deoxotyphasterol||http://purl.obolibrary.org/obo/CHEBI_20717
6538||10994||3-dehydro-6-deoxoteasterone||http://purl.obolibrary.org/obo/CHEBI_20710
6539||10994||6-deoxocastasterone||http://purl.obolibrary.org/obo/CHEBI_20712
6540||2730||Spheroid body myopathy||http://www.orpha.net/ORDO/Orphanet_268129
6541||8896||WHIM syndrome||http://www.orpha.net/ORDO/Orphanet_51636
6542||8050||Tetrasomy 9p||http://www.orpha.net/ORDO/Orphanet_3310
6543||288||Coenzyme Q10 deficiency||http://www.orpha.net/ORDO/Orphanet_35656
6544||3642||Thiemann disease, familial form||http://www.orpha.net/ORDO/Orphanet_3314
6546||1211||Bartter syndrome with hypocalcemia||http://www.orpha.net/ORDO/Orphanet_263417
6545||5300||Thomas syndrome||http://www.orpha.net/ORDO/Orphanet_3316
6547||6266||Thiopurine S-methyltransferase deficiency||http://www.orpha.net/ORDO/Orphanet_3315
6549||15191||pharyngeal muscle cell||http://www.ebi.ac.uk/efo/EFO_0005497
6548||5053||Thoracolaryngopelvic dysplasia||http://www.orpha.net/ORDO/Orphanet_3317
6550||2672||Caenorhabditis component||http://www.ebi.ac.uk/efo/EFO_0005496
6551||15158||NSM||http://www.ebi.ac.uk/efo/EFO_0005495
6552||4406||Congenital amegakaryocytic thrombocytopenia||http://www.orpha.net/ORDO/Orphanet_3319
6553||2672||gonad||http://www.ebi.ac.uk/efo/EFO_0005494
6554||4139||Infantile spams - psychomotor retardation - progressive brain atrophy - basal ganglia disease||http://www.orpha.net/ORDO/Orphanet_263410
6555||15511||3-fold embryo||http://www.ebi.ac.uk/efo/EFO_0005499
6556||13131||newly molted young adult hermaphrodite||http://www.ebi.ac.uk/efo/EFO_0005498
6557||8191||ammonium phosphate||http://purl.obolibrary.org/obo/CHEBI_62982
6558||5300||Thrombocytopenia - Robin sequence||http://www.orpha.net/ORDO/Orphanet_3323
6559||5961||Hoyeraal-Hreidarsson syndrome||http://www.orpha.net/ORDO/Orphanet_3322
6560||4406||Thrombocytopenia - absent radius||http://www.orpha.net/ORDO/Orphanet_3320
6561||7319||Thyrocerebrorenal syndrome||http://www.orpha.net/ORDO/Orphanet_3327
6562||7319||Thymic-renal-anal-lung dysplasia||http://www.orpha.net/ORDO/Orphanet_3326
6563||1247||Familial thrombomodulin anomalies||http://www.orpha.net/ORDO/Orphanet_3324
6564||6244||Absent tibia - polydactyly - arachnoid cyst||http://www.orpha.net/ORDO/Orphanet_3328
6565||5300||Tibial aplasia - ectrodactyly||http://www.orpha.net/ORDO/Orphanet_3329
6566||11842||Progressive demyelinating neuropathy with bilateral striatal necrosis||http://www.orpha.net/ORDO/Orphanet_217396
6568||6889||Congenital insensitivity to pain with hyperhidrosis||http://www.orpha.net/ORDO/Orphanet_217399
6567||7494||Classic maple syrup urine disease||http://www.orpha.net/ORDO/Orphanet_268145
6569||644||Crohn s colitis||http://www.ebi.ac.uk/efo/EFO_0005622
6570||15571||Disorder of energy metabolism||http://www.orpha.net/ORDO/Orphanet_79200
6572||6309||Glycogen storage disease||http://www.orpha.net/ORDO/Orphanet_79201
6571||10826||lung adenocarcinoma grade||http://www.ebi.ac.uk/efo/EFO_0005620
6573||5278||role||http://www.ifomis.org/bfo/1.1/snap#Role
6574||644||small bowel Crohn s disease||http://www.ebi.ac.uk/efo/EFO_0005629
6575||15572||Disorder of lysosomal amino acid transport||http://www.orpha.net/ORDO/Orphanet_79207
6576||644||perianal Crohn s disease||http://www.ebi.ac.uk/efo/EFO_0005627
6577||11620||proctitis||http://www.ebi.ac.uk/efo/EFO_0005628
6578||644||oral Crohn s disease||http://www.ebi.ac.uk/efo/EFO_0005625
6579||2829||pancolitis||http://www.ebi.ac.uk/efo/EFO_0005626
6580||2829||distal colitis||http://www.ebi.ac.uk/efo/EFO_0005623
6581||6625||Lipid storage disease||http://www.orpha.net/ORDO/Orphanet_79204
6582||644||ileocolitis||http://www.ebi.ac.uk/efo/EFO_0005624
6583||238||X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia||http://www.orpha.net/ORDO/Orphanet_317476
6584||10994||L-glutamine||http://purl.obolibrary.org/obo/CHEBI_18050
6586||238||Pancytopenia due to IKZF1 mutations||http://www.orpha.net/ORDO/Orphanet_317473
6585||8190||1-aminocyclopropane-1-carboxylic acid||http://purl.obolibrary.org/obo/CHEBI_18053
6587||1735||Combined hyperlipidemia||http://www.orpha.net/ORDO/Orphanet_79211
6588||4651||Mucolipidosis||http://www.orpha.net/ORDO/Orphanet_79212
6589||11030||opiate dependence||http://www.ebi.ac.uk/efo/EFO_0005611
6590||1326||coronary artery raised atherosclerotic lesion||http://www.ebi.ac.uk/efo/EFO_0005616
6591||6600||Metabolic disease involving other neurotransmitter deficiency||http://www.orpha.net/ORDO/Orphanet_79219
6592||2503||thoracic aortic fatty streak||http://www.ebi.ac.uk/efo/EFO_0005617
6593||2503|| thoracic aortic raised atherosclerotic lesion ||http://www.ebi.ac.uk/efo/EFO_0005618
6595||4651||Oligosaccharidosis||http://www.orpha.net/ORDO/Orphanet_79215
6594||6589||morphine dependence||http://www.ebi.ac.uk/efo/EFO_0005612
6597||5287||Mucopolysaccharidosis||http://www.orpha.net/ORDO/Orphanet_79213
6596||10994||lipid||http://purl.obolibrary.org/obo/CHEBI_18059
6600||15571||Disorder of biogenic amine metabolism and transport||http://www.orpha.net/ORDO/Orphanet_79214
6598||1422||prostate cancer staging||http://www.ebi.ac.uk/efo/EFO_0005615
6599||8190||oxamic acid||http://purl.obolibrary.org/obo/CHEBI_18058
6601||770||GM17736||http://purl.obolibrary.org/obo/CLO_0017043
6602||770||GM17737||http://purl.obolibrary.org/obo/CLO_0017044
6603||770||GM17734||http://purl.obolibrary.org/obo/CLO_0017045
6604||770||GM17735||http://purl.obolibrary.org/obo/CLO_0017046
6605||1826||Saccharum officinarum complex||http://purl.obolibrary.org/obo/NCBITaxon_286192
6606||2420||X-linked cerebral adrenoleukodystrophy||http://www.orpha.net/ORDO/Orphanet_139396
6607||254||Werner syndrome||http://www.orpha.net/ORDO/Orphanet_902
6608||6640||ATC Code J Antiinfectives for systemic use||http://www.ebi.ac.uk/efo/EFO_0005640
6609||15365||Von Willebrand disease||http://www.orpha.net/ORDO/Orphanet_903
6610||11840||Syndromic craniosynostosis||http://www.orpha.net/ORDO/Orphanet_139393
6611||2252||Williams syndrome||http://www.orpha.net/ORDO/Orphanet_904
6613||266||Wilson disease||http://www.orpha.net/ORDO/Orphanet_905
6612||6640||ATC Code N Nervous system||http://www.ebi.ac.uk/efo/EFO_0005643
6615||2420||Adrenomyeloneuropathy||http://www.orpha.net/ORDO/Orphanet_139399
6616||5882||Wiskott-Aldrich syndrome||http://www.orpha.net/ORDO/Orphanet_906
6614||6640||ATC Code P Antiparasitic products, insecticides and repellents||http://www.ebi.ac.uk/efo/EFO_0005644
6617||6640||ATC Code L Antineoplastic and immunomodulating agents||http://www.ebi.ac.uk/efo/EFO_0005641
6619||2252||Fragile X syndrome||http://www.orpha.net/ORDO/Orphanet_908
6618||6640||ATC Code M Musculo-skeletal system||http://www.ebi.ac.uk/efo/EFO_0005642
6621||15571||Disorder of purine or pyrimidine metabolism||http://www.orpha.net/ORDO/Orphanet_79224
6623||10994||ticlopidine||http://purl.obolibrary.org/obo/CHEBI_9588
6620||1754||Cerebrotendinous xanthomatosis||http://www.orpha.net/ORDO/Orphanet_909
6622||6640||ATC Code V Various||http://www.ebi.ac.uk/efo/EFO_0005647
6625||15572||Sphingolipidosis||http://www.orpha.net/ORDO/Orphanet_79225
6624||770||1182-4H||http://www.ebi.ac.uk/efo/EFO_0005648
6626||5267||Sterol metabolism disorder||http://www.orpha.net/ORDO/Orphanet_79226
6627||6640||ATC Code R Respiratory system||http://www.ebi.ac.uk/efo/EFO_0005645
6628||6640||ATC Code S Sensory organs||http://www.ebi.ac.uk/efo/EFO_0005646
6629||10994||glyphosate||http://purl.obolibrary.org/obo/CHEBI_27744
6630||1391||spondylolysis||http://www.ebi.ac.uk/efo/EFO_0005649
6631||799||antiseptic drug||http://purl.obolibrary.org/obo/CHEBI_48218
6632||805||Hemochromatosis type 2||http://www.orpha.net/ORDO/Orphanet_79230
6633||15583||CEL data file format||http://www.ebi.ac.uk/efo/EFO_0005630
6634||11385||Hypoxanthine guanine phosphoribosyltransferase partial deficiency||http://www.orpha.net/ORDO/Orphanet_79233
6635||120||rectal adenocarcinoma||http://www.ebi.ac.uk/efo/EFO_0005631
6636||10126||Crigler-Najjar syndrome type 1||http://www.orpha.net/ORDO/Orphanet_79234
6637||9753||intestinal necrosis||http://www.ebi.ac.uk/efo/EFO_0005632
6638||6640||ATC Code A Alimentary tract and metabolism||http://www.ebi.ac.uk/efo/EFO_0005633
6640||15538||ATC Classification System||http://www.ebi.ac.uk/efo/EFO_0005634
6639||7654||Galactokinase deficiency||http://www.orpha.net/ORDO/Orphanet_79237
6642||6640||ATC Code B Blood and blood forming organs||http://www.ebi.ac.uk/efo/EFO_0005635
6641||7654||Galactose epimerase deficiency||http://www.orpha.net/ORDO/Orphanet_79238
6644||6640||ATC Code C Cardiovascular system||http://www.ebi.ac.uk/efo/EFO_0005636
6643||10126||Crigler-Najjar syndrome type 2||http://www.orpha.net/ORDO/Orphanet_79235
6645||6640||ATC Code D Dermatologicals||http://www.ebi.ac.uk/efo/EFO_0005637
6647||10994||caffeine||http://purl.obolibrary.org/obo/CHEBI_27732
6646||6640||ATC Code G Genito-urinary system and sex hormones||http://www.ebi.ac.uk/efo/EFO_0005638
6648||6640||ATC Code H Systemic hormonal preparations, excluding sex hormones and insulins||http://www.ebi.ac.uk/efo/EFO_0005639
6649||4931||Classic galactosemia||http://www.orpha.net/ORDO/Orphanet_79239
6650||11840||Isolated craniosynostosis||http://www.orpha.net/ORDO/Orphanet_139390
6651||1802||intracerebral hemorrhage||http://www.ebi.ac.uk/efo/EFO_0005669
6652||14970||anterior chamber depth measurement||http://www.ebi.ac.uk/efo/EFO_0005668
6653||1022||Dictyostelium discoideum||http://purl.obolibrary.org/obo/NCBITaxon_44689
6654||5077||urinary albumin excretion rate||http://www.ebi.ac.uk/efo/EFO_0005667
6655||14970||thyroid peroxidase antibody measurement||http://www.ebi.ac.uk/efo/EFO_0005666
6657||14970||white matter hyperintensity measurement||http://www.ebi.ac.uk/efo/EFO_0005665
6656||6302||Hyperammonemia due to N-acetylglutamate synthetase deficiency||http://www.orpha.net/ORDO/Orphanet_927
6659||14602||blood metabolite measurement||http://www.ebi.ac.uk/efo/EFO_0005664
6658||7353||Lethal arteriopathy syndrome due to fibulin-4 deficiency||http://www.orpha.net/ORDO/Orphanet_314718
6660||5077||urinary uromodulin measurement||http://www.ebi.ac.uk/efo/EFO_0005663
6661||9608||Achalasia - microcephaly||http://www.orpha.net/ORDO/Orphanet_929
6662||9293||Recessive hereditary methemoglobinemia type 1||http://www.orpha.net/ORDO/Orphanet_139373
6663||14970||Child Behaviour Checklist assessment||http://www.ebi.ac.uk/efo/EFO_0005661
6665||14970||plasma beta-amyloid 1-42 measurement||http://www.ebi.ac.uk/efo/EFO_0005660
6664||8716||Acatalasemia||http://www.orpha.net/ORDO/Orphanet_926
6666||5300||Ablepharon macrostomia syndrome||http://www.orpha.net/ORDO/Orphanet_920
6667||9293||Recessive hereditary methemoglobinemia type 2||http://www.orpha.net/ORDO/Orphanet_139380
6668||5300||Abruzzo-Erickson syndrome||http://www.orpha.net/ORDO/Orphanet_921
6669||799||antilipemic drug||http://purl.obolibrary.org/obo/CHEBI_35679
6670||5140||Combined immunodeficiency due to STIM1 deficiency||http://www.orpha.net/ORDO/Orphanet_317430
6671||5502||Salmonella enterica subsp. enterica serovar Typhi str. CT18||http://purl.obolibrary.org/obo/NCBITaxon_220341
6672||1826||Rubus idaeus||http://purl.obolibrary.org/obo/NCBITaxon_32247
6673||4259||response to protease inhibitor||http://www.ebi.ac.uk/efo/EFO_0005657
6674||14970||plasma beta-amyloid 1-40 measurement||http://www.ebi.ac.uk/efo/EFO_0005659
6675||9051||response to selective serotonin reuptake inhibitor||http://www.ebi.ac.uk/efo/EFO_0005658
6676||14602||serum metabolite measurement||http://www.ebi.ac.uk/efo/EFO_0005653
6677||12747||response to cytosine arabinoside||http://www.ebi.ac.uk/efo/EFO_0005655
6679||14970||velocity of sound measurement||http://www.ebi.ac.uk/efo/EFO_0005654
6678||5300||Aase-Smith syndrome||http://www.orpha.net/ORDO/Orphanet_916
6680||2252||Aarskog-Scott syndrome||http://www.orpha.net/ORDO/Orphanet_915
6681||618||drosophila developmental stage||http://www.ebi.ac.uk/efo/EFO_0005651
6683||770||CME-L1||http://www.ebi.ac.uk/efo/EFO_0005650
6682||5287||Zellweger syndrome||http://www.orpha.net/ORDO/Orphanet_912
6684||2322||Xeroderma pigmentosum||http://www.orpha.net/ORDO/Orphanet_910
6685||11458||Atypical dentin dysplasia due to SMOC2 deficiency||http://www.orpha.net/ORDO/Orphanet_314721
6686||238||Combined immunodeficiency due to ZAP70 deficiency||http://www.orpha.net/ORDO/Orphanet_911
6687||5025||Fusarium globosum||http://purl.obolibrary.org/obo/NCBITaxon_78864
6688||6768||Severe combined immunodeficiency due to DNA-PKcs deficiency||http://www.orpha.net/ORDO/Orphanet_317425
6689||5140||Combined immunodeficiency due to ORAI1 deficiency||http://www.orpha.net/ORDO/Orphanet_317428
6690||6573||spike-in quality control role||http://purl.obolibrary.org/obo/OBI_0001140
6691||1022||Holothuria glaberrima||http://purl.obolibrary.org/obo/NCBITaxon_31192
6692||6573||dye swap quality control role||http://purl.obolibrary.org/obo/OBI_0001142
6693||14970||non-high density lipoprotein cholesterol measurement||http://www.ebi.ac.uk/efo/EFO_0005689
6694||11475||RNA-seq of coding RNA from single cells||http://www.ebi.ac.uk/efo/EFO_0005684
6695||6610||Acrocephalosyndactyly||http://www.orpha.net/ORDO/Orphanet_946
6696||2670||plant callus||http://www.ebi.ac.uk/efo/EFO_0005683
6697||14970||oxygen saturation measurement||http://www.ebi.ac.uk/efo/EFO_0005682
6698||7963||Ischio-vertebral syndrome||http://www.orpha.net/ORDO/Orphanet_85200
6699||2700||Staphylococcus aureus infection||http://www.ebi.ac.uk/efo/EFO_0005681
6700||2021||Keutel syndrome||http://www.orpha.net/ORDO/Orphanet_85202
6701||10215||NHDL cholesterol||http://www.ebi.ac.uk/efo/EFO_0005688
6703||2252||Genitopatellar syndrome||http://www.orpha.net/ORDO/Orphanet_85201
6704||1171||Acrocraniofacial dysostosis||http://www.orpha.net/ORDO/Orphanet_949
6702||1391||fibromyalgia||http://www.ebi.ac.uk/efo/EFO_0005687
6705||12543||receptive language perception||http://www.ebi.ac.uk/efo/EFO_0005686
6707||13770||Acro-pectoral syndrome||http://www.orpha.net/ORDO/Orphanet_85203
6706||11476||RNA-seq of non coding RNA from single cells||http://www.ebi.ac.uk/efo/EFO_0005685
6709||12543||musical aptitude||http://www.ebi.ac.uk/efo/EFO_0005690
6708||5502||Bacillus subtilis subsp. subtilis str. 168||http://purl.obolibrary.org/obo/NCBITaxon_224308
6710||7200||D-glyceric aciduria||http://www.orpha.net/ORDO/Orphanet_941
6711||14970||plasma trimethylamine N-oxide measurement||http://www.ebi.ac.uk/efo/EFO_0005691
6712||4995||Malonic aciduria||http://www.orpha.net/ORDO/Orphanet_943
6713||8191||cobalt dichloride||http://purl.obolibrary.org/obo/CHEBI_35696
6714||5013||conotruncal heart defect||http://www.ebi.ac.uk/efo/EFO_0005679
6715||2165||hippocampal sclerosis of aging||http://www.ebi.ac.uk/efo/EFO_0005678
6716||14970||smoking behaviour measurement||http://www.ebi.ac.uk/efo/EFO_0005671
6717||3068||smoking initiation||http://www.ebi.ac.uk/efo/EFO_0005670
6719||11618||chronic mucus hypersecretion||http://www.ebi.ac.uk/efo/EFO_0005673
6718||6768||Short-limb skeletal dysplasia with severe combined immunodeficiency||http://www.orpha.net/ORDO/Orphanet_935
6720||1015||acute coronary syndrome||http://www.ebi.ac.uk/efo/EFO_0005672
6721||14970||vitamin D-binding protein measurement||http://www.ebi.ac.uk/efo/EFO_0005675
6722||14970||white matter microstructure measurement||http://www.ebi.ac.uk/efo/EFO_0005674
6723||14970||puberty onset measurement||http://www.ebi.ac.uk/efo/EFO_0005677
6724||6306||3-hydroxyisobutyric aciduria||http://www.orpha.net/ORDO/Orphanet_939
6726||5103||autoimmune hepatits type 1||http://www.ebi.ac.uk/efo/EFO_0005676
6725||7638||Fetal Gaucher disease||http://www.orpha.net/ORDO/Orphanet_85212
6727||1022||Cryptococcus neoformans var. neoformans||http://purl.obolibrary.org/obo/NCBITaxon_40410
6728||7984||Achondrogenesis||http://www.orpha.net/ORDO/Orphanet_932
6729||10994||dasatinib||http://purl.obolibrary.org/obo/CHEBI_49375
6731||13799||Acheiropodia||http://www.orpha.net/ORDO/Orphanet_931
6730||5083||omega-6 polyunsaturated fatty acid measurement||http://www.ebi.ac.uk/efo/EFO_0005680
6732||5838||process quality||http://purl.obolibrary.org/obo/PATO_0001236
6733||799||serotonergic antagonist||http://purl.obolibrary.org/obo/CHEBI_48279
6734||322||Hypertrichosis-acromegaloid facial appearance syndrome||http://www.orpha.net/ORDO/Orphanet_966
6736||799||serotonergic drug||http://purl.obolibrary.org/obo/CHEBI_48278
6737||9357||Fish-eye disease||http://www.orpha.net/ORDO/Orphanet_79292
6735||10886||serum albumin||http://purl.obolibrary.org/obo/PR_000003918
6738||13306||Acromegaloid facial appearance syndrome||http://www.orpha.net/ORDO/Orphanet_965
6739||1783||mass spectrometer||http://purl.obolibrary.org/obo/OBI_0000049
6740||2446||Methylmalonic acidemia with homocystinuria type cblF||http://www.orpha.net/ORDO/Orphanet_79284
6741||7986||Acromicric dysplasia||http://www.orpha.net/ORDO/Orphanet_969
6742||2446||Methylmalonic acidemia with homocystinuria, type cblC||http://www.orpha.net/ORDO/Orphanet_79282
6743||2446||Methylmalonic acidemia with homocystinuria, type cblD||http://www.orpha.net/ORDO/Orphanet_79283
6745||2390||Desmin-related myopathy with Mallory body-like inclusions||http://www.orpha.net/ORDO/Orphanet_84132
6744||7990||Acromesomelic dysplasia, Hunter-Thomson type||http://www.orpha.net/ORDO/Orphanet_968
6746||1687||Primary intraosseous vascular malformation||http://www.orpha.net/ORDO/Orphanet_140436
6747||306||Acrofacial dysostosis, Weyers type||http://www.orpha.net/ORDO/Orphanet_952
6748||7319||Acroosteolysis dominant type||http://www.orpha.net/ORDO/Orphanet_955
6749||7986||Acrodysostosis||http://www.orpha.net/ORDO/Orphanet_950
6750||2252||Christianson syndrome||http://www.orpha.net/ORDO/Orphanet_85278
6752||762||Syndromic X-linked intellectual disability due to JARID1C mutation||http://www.orpha.net/ORDO/Orphanet_85279
6751||9100||Diazoxide-resistant focal hyperinsulinism||http://www.orpha.net/ORDO/Orphanet_79298
6753||9760||Hyperinsulinism due to glucokinase deficiency||http://www.orpha.net/ORDO/Orphanet_79299
6754||2252||Syndromic X-linked intellectual disability 7||http://www.orpha.net/ORDO/Orphanet_85274
6755||4624||Familial LCAT deficiency||http://www.orpha.net/ORDO/Orphanet_79293
6756||7319||Acro-pectoro-renal dysplasia||http://www.orpha.net/ORDO/Orphanet_956
6757||13770||Acropectorovertebral dysplasia||http://www.orpha.net/ORDO/Orphanet_957
6758||2252||Microphthalmia - ankyloblepharon - intellectual disability||http://www.orpha.net/ORDO/Orphanet_85275
6760||12769||Acro-renal-mandibular syndrome||http://www.orpha.net/ORDO/Orphanet_958
6759||2252||X-linked intellectual disability, Armfield type||http://www.orpha.net/ORDO/Orphanet_85276
6762||12769||Acro-renal-ocular syndrome||http://www.orpha.net/ORDO/Orphanet_959
6761||11899||X-linked intellectual disability, Cantagrel type||http://www.orpha.net/ORDO/Orphanet_85277
6763||2252||X-linked intellectual disability, Abidi type||http://www.orpha.net/ORDO/Orphanet_85273
6764||4843||Non-syndromic esophageal malformation||http://www.orpha.net/ORDO/Orphanet_108959
6765||5670||Testicular regression syndrome||http://www.orpha.net/ORDO/Orphanet_983
6766||5102||T-B  severe combined immunodeficiency_6766||http://www.orpha.net/ORDO/Orphanet_317416
6767||6244||Absent tibia - polydactyly||http://www.orpha.net/ORDO/Orphanet_988
6768||5102||T-B- severe combined immunodeficiency_6768||http://www.orpha.net/ORDO/Orphanet_317419
6769||3308||Hypoglossia - hypodactyly||http://www.orpha.net/ORDO/Orphanet_989
6770||9726||Syndromic intestinal malformation||http://www.orpha.net/ORDO/Orphanet_108969
6771||9726||Non-syndromic intestinal malformation||http://www.orpha.net/ORDO/Orphanet_108967
6772||9727||Syndromic gastroduodenal malformation||http://www.orpha.net/ORDO/Orphanet_108965
6774||5654||Primary systemic amyloidosis||http://www.orpha.net/ORDO/Orphanet_314701
6773||7319||Acrorenal syndrome||http://www.orpha.net/ORDO/Orphanet_971
6775||9727||Non-syndromic gastroduodenal malformation||http://www.orpha.net/ORDO/Orphanet_108963
6776||6900||Hereditary sensory and autonomic neuropathy type 2||http://www.orpha.net/ORDO/Orphanet_970
6777||13670||Congenital absence/hypoplasia of fingers excluding thumb, unilateral||http://www.orpha.net/ORDO/Orphanet_973
6778||12348||Hereditary continuous muscle fiber activity||http://www.orpha.net/ORDO/Orphanet_972
6779||5865||Adams-Oliver syndrome||http://www.orpha.net/ORDO/Orphanet_974
6780||212||Adrenomyodystrophy||http://www.orpha.net/ORDO/Orphanet_977
6781||6266||Adenine phosphoribosyltransferase deficiency||http://www.orpha.net/ORDO/Orphanet_976
6782||4834||ADULT syndrome||http://www.orpha.net/ORDO/Orphanet_978
6783||5654||Primary localized amyloidosis||http://www.orpha.net/ORDO/Orphanet_314709
6784||1022||Tetranychus urticae||http://purl.obolibrary.org/obo/NCBITaxon_32264
6785||1274||nucleobase-containing compound biosynthetic process||http://purl.obolibrary.org/obo/GO_0034654
6786||10994||trichlorofluoromethane||http://purl.obolibrary.org/obo/CHEBI_48236
6788||5025||Saccharomyces boulardii||http://purl.obolibrary.org/obo/NCBITaxon_252598
6787||8736||Pyruvate dehydrogenase phosphatase deficiency||http://www.orpha.net/ORDO/Orphanet_79246
6789||8736||Pyruvate dehydrogenase E2 deficiency||http://www.orpha.net/ORDO/Orphanet_79244
6790||8736||Pyruvate dehydrogenase E1-alpha deficiency||http://www.orpha.net/ORDO/Orphanet_79243
6791||10599||Holocarboxylase synthetase deficiency||http://www.orpha.net/ORDO/Orphanet_79242
6792||2454||Biotinidase deficiency||http://www.orpha.net/ORDO/Orphanet_79241
6793||266||Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency||http://www.orpha.net/ORDO/Orphanet_79240
6794||5700||Albinism-deafness syndrome||http://www.orpha.net/ORDO/Orphanet_998
6795||5700||Ermine phenotype||http://www.orpha.net/ORDO/Orphanet_999
6796||6573||material supplier role||http://purl.obolibrary.org/obo/OBI_0000018
6797||6927||Fetal akinesia deformation sequence||http://www.orpha.net/ORDO/Orphanet_994
6798||2252||Agnathia - holoprosencephaly - situs inversus||http://www.orpha.net/ORDO/Orphanet_990
6799||3019||PAGOD syndrome||http://www.orpha.net/ORDO/Orphanet_991
6800||2740||cellular nitrogen compound metabolic process||http://purl.obolibrary.org/obo/GO_0034641
6801||7613||Glycogen storage disease due to glucose-6-phosphatase deficiency type a||http://www.orpha.net/ORDO/Orphanet_79258
6802||7642||GM1 gangliosidosis type 3||http://www.orpha.net/ORDO/Orphanet_79257
6803||7613||Glycogen storage disease due to glucose-6-phosphatase deficiency type b||http://www.orpha.net/ORDO/Orphanet_79259
6804||8611||Classical phenylketonuria||http://www.orpha.net/ORDO/Orphanet_79254
6805||8611||Mild phenylketonuria||http://www.orpha.net/ORDO/Orphanet_79253
6806||7642||GM1 gangliosidosis type 2||http://www.orpha.net/ORDO/Orphanet_79256
6807||7642||GM1 gangliosidosis type 1||http://www.orpha.net/ORDO/Orphanet_79255
6808||770||AG07139||http://purl.obolibrary.org/obo/CLO_0035608
6809||6854||Fundus albipunctatus||http://www.orpha.net/ORDO/Orphanet_227796
6810||8811||Sanfilippo syndrome type B||http://www.orpha.net/ORDO/Orphanet_79270
6812||13174||age at alcohol diagnosis||http://www.ebi.ac.uk/efo/EFO_0005602
6811||2252||X-linked intellectual disability - cubitus valgus - dysmorphism||http://www.orpha.net/ORDO/Orphanet_85280
6813||2503||abdominal aortic raised atherosclerotic lesion||http://www.ebi.ac.uk/efo/EFO_0005601
6814||8811||Sanfilippo syndrome type A||http://www.orpha.net/ORDO/Orphanet_79269
6815||13174||age at breast cancer diagnosis||http://www.ebi.ac.uk/efo/EFO_0005603
6816||2252||BRESEK syndrome||http://www.orpha.net/ORDO/Orphanet_85284
6817||1176||family history of breast cancer||http://www.ebi.ac.uk/efo/EFO_0005606
6818||2252||X-linked intellectual disability, Miles-Carpenter type||http://www.orpha.net/ORDO/Orphanet_85283
6821||14970||cortical opacity measurement||http://www.ebi.ac.uk/efo/EFO_0005608
6819||12317||Mal de Meleda||http://www.orpha.net/ORDO/Orphanet_87503
6820||4701||MEHMO syndrome||http://www.orpha.net/ORDO/Orphanet_85282
6822||1422||breast cancer stage||http://www.ebi.ac.uk/efo/EFO_0005607
6824||11899||X-linked intellectual disability, Stocco Dos Santos type||http://www.orpha.net/ORDO/Orphanet_85288
6823||10080||Infantile neuronal ceroid lipofuscinosis||http://www.orpha.net/ORDO/Orphanet_79263
6826||2252||X-linked intellectual disability, Siderius type||http://www.orpha.net/ORDO/Orphanet_85287
6825||10080||Adult neuronal ceroid lipofuscinosis||http://www.orpha.net/ORDO/Orphanet_79262
6827||2252||X-linked intellectual disability, Shashi type||http://www.orpha.net/ORDO/Orphanet_85286
6828||11899||X-linked intellectual disability, Schimke type||http://www.orpha.net/ORDO/Orphanet_85285
6830||2503||abdominal aortic fatty streak||http://www.ebi.ac.uk/efo/EFO_0005600
6829||6573||detergent role||http://purl.obolibrary.org/obo/CHEBI_27780
6832||2252||X-linked intellectual disability, Vitale type||http://www.orpha.net/ORDO/Orphanet_85289
6831||10080||Juvenile neuronal ceroid lipofuscinosis||http://www.orpha.net/ORDO/Orphanet_79264
6833||5450||Alpha-N-acetylgalactosaminidase deficiency type 2||http://www.orpha.net/ORDO/Orphanet_79280
6834||5450||Alpha-N-acetylgalactosaminidase deficiency type 3||http://www.orpha.net/ORDO/Orphanet_79281
6835||5450||Alpha-N-acetylgalactosaminidase deficiency type 1||http://www.orpha.net/ORDO/Orphanet_79279
6836||10994||griseofulvin||http://purl.obolibrary.org/obo/CHEBI_27779
6837||2252||X-linked intellectual disability, Wittwer type||http://www.orpha.net/ORDO/Orphanet_85291
6838||11899||X-linked intellectual disability, Wilson type||http://www.orpha.net/ORDO/Orphanet_85290
6839||2252||X-linked intellectual disability, Cabezas type||http://www.orpha.net/ORDO/Orphanet_85293
6840||3114||X-linked spinocerebellar ataxia type 4||http://www.orpha.net/ORDO/Orphanet_85292
6841||3851||HSD10 disease, atypical type||http://www.orpha.net/ORDO/Orphanet_85295
6842||762||X-linked epilepsy - learning disabilities - behavior disorders||http://www.orpha.net/ORDO/Orphanet_85294
6844||3114||X-linked spinocerebellar ataxia type 3||http://www.orpha.net/ORDO/Orphanet_85297
6843||8811||Sanfilippo syndrome type D||http://www.orpha.net/ORDO/Orphanet_79272
6845||1022||Meleagris gallopavo||http://purl.obolibrary.org/obo/NCBITaxon_9103
6846||8811||Sanfilippo syndrome type C||http://www.orpha.net/ORDO/Orphanet_79271
6847||4509||Hereditary coproporphyria||http://www.orpha.net/ORDO/Orphanet_79273
6848||4509||Acute intermittent porphyria||http://www.orpha.net/ORDO/Orphanet_79276
6849||8566||Erythropoietic protoporphyria||http://www.orpha.net/ORDO/Orphanet_79278
6850||8566||Congenital erythropoietic porphyria||http://www.orpha.net/ORDO/Orphanet_79277
6851||1022||Pavo cristatus||http://purl.obolibrary.org/obo/NCBITaxon_9049
6852||1022||Lophura nycthemera||http://purl.obolibrary.org/obo/NCBITaxon_9046
6853||11456||Partial duplication of chromosome 3||http://www.orpha.net/ORDO/Orphanet_262201
6855||7961||Yunis-Varon syndrome||http://www.orpha.net/ORDO/Orphanet_3472
6854||9675||Familial flecked retinopathy||http://www.orpha.net/ORDO/Orphanet_227786
6856||2252||Zimmermann-Laband syndrome||http://www.orpha.net/ORDO/Orphanet_3473
6857||10732||Young syndrome||http://www.orpha.net/ORDO/Orphanet_3471
6859||6864||Urinary incontinence||http://purl.obolibrary.org/obo/HP_0000020
6858||8921||T-cell immunodeficiency with epidermodysplasia verruciformis||http://www.orpha.net/ORDO/Orphanet_324294
6860||306||CHIME syndrome||http://www.orpha.net/ORDO/Orphanet_3474
6861||11456||Partial duplication of chromosome 4||http://www.orpha.net/ORDO/Orphanet_262206
6862||11456||Partial trisomy/tetrasomy of chromosome 5||http://www.orpha.net/ORDO/Orphanet_262211
6863||1022||Gallus gallus||http://purl.obolibrary.org/obo/NCBITaxon_9031
6864||2063||Abnormality of the bladder||http://purl.obolibrary.org/obo/HP_0000014
6865||7206||Autosomal recessive hyper-IgE syndrome||http://www.orpha.net/ORDO/Orphanet_169446
6866||260||Specific antibody deficiency with normal immunoglobulin concentrations and normal numbers of B cells||http://www.orpha.net/ORDO/Orphanet_169443
6867||1355||inflammation||http://purl.obolibrary.org/obo/MP_0001845
6868||5300||Weissenbacher- Zweymuller syndrome||http://www.orpha.net/ORDO/Orphanet_3450
6869||4139||West syndrome||http://www.orpha.net/ORDO/Orphanet_3451
6870||4701||Wilson-Turner syndrome||http://www.orpha.net/ORDO/Orphanet_3459
6871||4775||Wildervanck syndrome||http://www.orpha.net/ORDO/Orphanet_3456
6872||11899||Intellectual disability-developmental delay-contractures syndrome||http://www.orpha.net/ORDO/Orphanet_3454
6873||382||Wiedemann-Rautenstrauch syndrome||http://www.orpha.net/ORDO/Orphanet_3455
6874||212||Autoimmune polyendocrinopathy type 1||http://www.orpha.net/ORDO/Orphanet_3453
6875||9918||Childhood apraxia of speech||http://www.orpha.net/ORDO/Orphanet_209908
6876||10874||Early-onset Lafora body disease||http://www.orpha.net/ORDO/Orphanet_324290
6877||1022||Colinus virginianus||http://purl.obolibrary.org/obo/NCBITaxon_9014
6878||5502||Xanthomonas axonopodis pv. citri str. 306||http://purl.obolibrary.org/obo/NCBITaxon_190486
6879||1022||Coturnix japonica||http://purl.obolibrary.org/obo/NCBITaxon_93934
6880||9572||Torg-Winchester syndrome||http://www.orpha.net/ORDO/Orphanet_3460
6881||5502||Thermotoga petrophila||http://purl.obolibrary.org/obo/NCBITaxon_93929
6882||6266||Hereditary xanthinuria||http://www.orpha.net/ORDO/Orphanet_3467
6883||1735||Hypercholesterolemia due to cholesterol 7alpha-hydroxylase deficiency||http://www.orpha.net/ORDO/Orphanet_209902
6884||2802||Brain-lung-thyroid syndrome||http://www.orpha.net/ORDO/Orphanet_209905
6885||5055||Wolfram syndrome||http://www.orpha.net/ORDO/Orphanet_3463
6886||1306||Woodhouse-Sakati syndrome||http://www.orpha.net/ORDO/Orphanet_3464
6887||15519||WT limb-blood syndrome||http://www.orpha.net/ORDO/Orphanet_3466
6888||6889||Autosomal dominant hereditary sensory and autonomic neuropathy||http://www.orpha.net/ORDO/Orphanet_140474
6889||11842||Hereditary sensory and autonomic neuropathy||http://www.orpha.net/ORDO/Orphanet_140471
6890||5005||uncultured prokaryote||http://purl.obolibrary.org/obo/NCBITaxon_198431
6891||11842||Primary CD59 deficiency||http://www.orpha.net/ORDO/Orphanet_169464
6892||10740||Pseudohyperaldosteronism type 2||http://www.orpha.net/ORDO/Orphanet_88660
6893||1619||Amelogenesis imperfecta||http://www.orpha.net/ORDO/Orphanet_88661
6894||204||Recurrent Neisseria infections due to factor D deficiency||http://www.orpha.net/ORDO/Orphanet_169467
6895||1022||Chrysolophus pictus||http://purl.obolibrary.org/obo/NCBITaxon_9089
6896||1022||Chrysolophus amherstiae||http://purl.obolibrary.org/obo/NCBITaxon_9088
6897||4750||Non-syndromic developmental defect of the eye||http://www.orpha.net/ORDO/Orphanet_108985
6898||13470||Autosomal recessive spastic paraplegia type 18||http://www.orpha.net/ORDO/Orphanet_209951
6899||4750||Syndromic developmental defect of the eye||http://www.orpha.net/ORDO/Orphanet_108987
6900||6889||Autosomal recessive hereditary sensory and autonomic neuropathy||http://www.orpha.net/ORDO/Orphanet_140477
6901||6910||Autosomal dominant slowed nerve conduction velocity||http://www.orpha.net/ORDO/Orphanet_140481
6902||5025||Fusarium acuminatum||http://purl.obolibrary.org/obo/NCBITaxon_502705
6903||4763||Syndromic visceral malformation||http://www.orpha.net/ORDO/Orphanet_108973
6904||4763||Non-syndromic visceral malformation||http://www.orpha.net/ORDO/Orphanet_108971
6905||3296||Autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency||http://www.orpha.net/ORDO/Orphanet_324262
6906||7944||Episodic ataxia type 6||http://www.orpha.net/ORDO/Orphanet_209967
6907||10740||Autosomal dominant progressive nephropathy with hypertension||http://www.orpha.net/ORDO/Orphanet_88659
6908||6900||Channelopathy-associated congenital insensitivity to pain||http://www.orpha.net/ORDO/Orphanet_88642
6909||7074||Obesity - colitis - hypothyroidism - cardiac hypertrophy - developmental delay||http://www.orpha.net/ORDO/Orphanet_88643
6911||14145||Autosomal recessive ataxia, Beauce type||http://www.orpha.net/ORDO/Orphanet_88644
6910||6912||Autosomal dominant hereditary demyelinating motor and sensory neuropathy||http://www.orpha.net/ORDO/Orphanet_140453
6912||11842||Hereditary motor and sensory neuropathy||http://www.orpha.net/ORDO/Orphanet_140450
6914||2252||ATR-X-related syndrome||http://www.orpha.net/ORDO/Orphanet_263355
6913||5715||macromolecule modification||http://purl.obolibrary.org/obo/GO_0043412
6915||6913||macromolecule glycosylation||http://purl.obolibrary.org/obo/GO_0043413
6916||5025||Fusarium avenaceum||http://purl.obolibrary.org/obo/NCBITaxon_502741
6917||6912||Autosomal dominant hereditary axonal motor and sensory neuropathy||http://www.orpha.net/ORDO/Orphanet_140456
6918||5502||Salmonella enterica subsp. enterica serovar Typhimurium str. SL1344||http://purl.obolibrary.org/obo/NCBITaxon_216597
6920||9803||mode of inheritance||http://purl.obolibrary.org/obo/HP_0000005
6919||9965||Cone dystrophy with supernormal rod response||http://www.orpha.net/ORDO/Orphanet_209932
6921||6912||Autosomal recessive hereditary demyelinating motor and sensory neuropathy||http://www.orpha.net/ORDO/Orphanet_140459
6922||9625||Achromatopsia||http://www.orpha.net/ORDO/Orphanet_49382
6923||6897||Familial ocular anterior segment mesenchymal dysgenesis||http://www.orpha.net/ORDO/Orphanet_88632
6924||5912||Terminal osseous dysplasia - pigmentary defects||http://www.orpha.net/ORDO/Orphanet_88630
6925||2382||Myopathy due to calsequestrin and SERCA1 protein overload||http://www.orpha.net/ORDO/Orphanet_88635
6926||6912||X-linked recessive hereditary axonal motor and sensory neuropathy||http://www.orpha.net/ORDO/Orphanet_140462
6927||4752||Non-syndromic respiratory or mediastinal malformation||http://www.orpha.net/ORDO/Orphanet_108993
6928||2380||Autosomal dominant distal hereditary motor neuropathy||http://www.orpha.net/ORDO/Orphanet_140465
6929||6306||Neurodegeneration due to 3-hydroxyisobutyryl-CoA hydrolase deficiency||http://www.orpha.net/ORDO/Orphanet_88639
6930||2380||Autosomal recessive distal hereditary motor neuropathy||http://www.orpha.net/ORDO/Orphanet_140468
6931||1306||Hypomyelination - hypogonadotropic hypogonadism - hypodontia||http://www.orpha.net/ORDO/Orphanet_88637
6932||9690||IRVAN syndrome||http://www.orpha.net/ORDO/Orphanet_209943
6933||799||adrenergic uptake inhibitor||http://purl.obolibrary.org/obo/CHEBI_35640
6934||11828||Posterior column ataxia - retinitis pigmentosa||http://www.orpha.net/ORDO/Orphanet_88628
6935||9682||Tritanopia||http://www.orpha.net/ORDO/Orphanet_88629
6936||1732||red-green color blindness||http://www.ebi.ac.uk/efo/EFO_0005581
6937||1732||red color blindness||http://www.ebi.ac.uk/efo/EFO_0005580
6938||6225||osteochondrodysplasia||http://www.ebi.ac.uk/efo/EFO_0005571
6939||1002||pharynx cancer||http://www.ebi.ac.uk/efo/EFO_0005577
6940||11622||pituitary cancer||http://www.ebi.ac.uk/efo/EFO_0005578
6941||1761||penis carcinoma||http://www.ebi.ac.uk/efo/EFO_0005575
6942||12143||pernicious anemia||http://www.ebi.ac.uk/efo/EFO_0005576
6943||1761||pseudohermaphroditism||http://www.ebi.ac.uk/efo/EFO_0005579
6944||14891||Ichthyosis prematurity syndrome||http://www.orpha.net/ORDO/Orphanet_88621
6945||9918||Familial acute necrotizing encephalopathy||http://www.orpha.net/ORDO/Orphanet_88619
6946||1299||Autosomal recessive non-syndromic intellectual disability||http://www.orpha.net/ORDO/Orphanet_88616
6947||4139||Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency||http://www.orpha.net/ORDO/Orphanet_88618
6948||9654||MRCS syndrome||http://www.orpha.net/ORDO/Orphanet_263347
6949||5502||Bacillus thuringiensis Bt407||http://purl.obolibrary.org/obo/NCBITaxon_527021
6950||1485||steroid inherited metabolic disorder||http://www.ebi.ac.uk/efo/EFO_0005590
6951||2252||Ulbright-Hodes syndrome||http://www.orpha.net/ORDO/Orphanet_3404
6952||5025||Penicillium expansum||http://purl.obolibrary.org/obo/NCBITaxon_27334
6953||8393||T-cell leukemia||http://www.ebi.ac.uk/efo/EFO_0005592
6954||1839||Transient tyrosinemia of the newborn||http://www.orpha.net/ORDO/Orphanet_3402
6955||1006||sweat gland carcinoma||http://www.ebi.ac.uk/efo/EFO_0005591
6956||1006||renal pelvis carcinoma||http://www.ebi.ac.uk/efo/EFO_0005582
6957||7966||Upington disease||http://www.orpha.net/ORDO/Orphanet_3408
6958||8323||rickets||http://www.ebi.ac.uk/efo/EFO_0005583
6960||2866||seborrheic keratosis||http://www.ebi.ac.uk/efo/EFO_0005584
6959||7068||Ulerythema ophryogenesis||http://www.orpha.net/ORDO/Orphanet_3406
6962||2700||shigellosis||http://www.ebi.ac.uk/efo/EFO_0005585
6961||6770||Umbilical cord ulceration - intestinal atresia||http://www.orpha.net/ORDO/Orphanet_3405
6963||1006||small intestine carcinoma||http://www.ebi.ac.uk/efo/EFO_0005588
6964||2252||Urban-Rogers-Meyer syndrome||http://www.orpha.net/ORDO/Orphanet_3409
6966||10994||thiopurines||http://purl.obolibrary.org/obo/CHEBI_35666
6965||7944||Episodic ataxia type 7||http://www.orpha.net/ORDO/Orphanet_209970
6967||6969||Benign familial nocturnal alternating hemiplegia of childhood||http://www.orpha.net/ORDO/Orphanet_209973
6968||1086||concentrated||http://purl.obolibrary.org/obo/PATO_0001159
6969||9918||Alternating hemiplegia||http://www.orpha.net/ORDO/Orphanet_209978
6970||1022||Lagopus lagopus scotica||http://purl.obolibrary.org/obo/NCBITaxon_359986
6971||10994||thapsigargin||http://purl.obolibrary.org/obo/CHEBI_9516
6972||1732||methylmalonic aciduria and homocystinuria type cblG||http://www.ebi.ac.uk/efo/EFO_0005597
6973||5025||Paracoccidioides brasiliensis Pb01||http://purl.obolibrary.org/obo/NCBITaxon_502779
6974||2165||toxic encephalopathy||http://www.ebi.ac.uk/efo/EFO_0005595
6975||1485||vitamin metabolic disorder||http://www.ebi.ac.uk/efo/EFO_0005596
6976||2700||tetanus||http://www.ebi.ac.uk/efo/EFO_0005593
6977||7319||BNAR syndrome||http://www.orpha.net/ORDO/Orphanet_217266
6979||10994||thalidomide||http://purl.obolibrary.org/obo/CHEBI_9513
6978||4193||purine ribonucleoside biosynthetic process||http://purl.obolibrary.org/obo/GO_0046129
6980||4854||purine ribonucleoside metabolic process||http://purl.obolibrary.org/obo/GO_0046128
6981||12332||IRIDA syndrome||http://www.orpha.net/ORDO/Orphanet_209981
6982||10252||Symptomatic form of hemophilia B in female carriers||http://www.orpha.net/ORDO/Orphanet_177929
6983||10253||Symptomatic form of hemophilia A in female carriers||http://www.orpha.net/ORDO/Orphanet_177926
6984||6968||increased concentration||http://purl.obolibrary.org/obo/PATO_0001162
6985||4179||decreased concentration||http://purl.obolibrary.org/obo/PATO_0001163
6986||7001||Primary congenital hypothyroidism||http://www.orpha.net/ORDO/Orphanet_226295
6987||2021||Microcephaly - brachydactyly - kyphoscoliosis||http://www.orpha.net/ORDO/Orphanet_3433
6988||2252||MMEP syndrome||http://www.orpha.net/ORDO/Orphanet_3434
6989||7001||Central congenital hypothyroidism||http://www.orpha.net/ORDO/Orphanet_226298
6990||1826||Eucalyptus camaldulensis x Eucalyptus grandis||http://purl.obolibrary.org/obo/NCBITaxon_538997
6991||8565||Prader-Willi syndrome due to imprinting mutation||http://www.orpha.net/ORDO/Orphanet_177910
6992||12769||Von Voss-Cherstvoy syndrome||http://www.orpha.net/ORDO/Orphanet_3439
6993||2252||Weaver-Williams syndrome||http://www.orpha.net/ORDO/Orphanet_3448
6994||2252||Weaver syndrome||http://www.orpha.net/ORDO/Orphanet_3447
6995||7989||SHOX-related short stature||http://www.orpha.net/ORDO/Orphanet_314795
6996||5317||Waardenburg syndrome||http://www.orpha.net/ORDO/Orphanet_3440
6997||10800||Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2||http://www.orpha.net/ORDO/Orphanet_177904
6998||10994||thioridazine||http://purl.obolibrary.org/obo/CHEBI_9566
6999||10800||Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1||http://www.orpha.net/ORDO/Orphanet_177901
7000||2021||Weill-Marchesani syndrome||http://www.orpha.net/ORDO/Orphanet_3449
7001||7142||Permanent congenital hypothyroidism||http://www.orpha.net/ORDO/Orphanet_226292
7002||8565||Prader-Willi syndrome due to translocation||http://www.orpha.net/ORDO/Orphanet_177907
7003||5623||21q22.13q22.2 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_268261
7004||770||GM17743||http://purl.obolibrary.org/obo/CLO_0017024
7006||2252||VACTERL with hydrocephalus||http://www.orpha.net/ORDO/Orphanet_3412
7007||770||GM17738||http://purl.obolibrary.org/obo/CLO_0017023
7005||5344||Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency||http://www.orpha.net/ORDO/Orphanet_90791
7009||770||GM17739||http://purl.obolibrary.org/obo/CLO_0017022
7008||4931||Congenital lipoid adrenal hyperplasia due to STAR deficency||http://www.orpha.net/ORDO/Orphanet_90790
7010||770||GM17740||http://purl.obolibrary.org/obo/CLO_0017021
7011||7319||Double uterus - hemivagina - renal agenesis||http://www.orpha.net/ORDO/Orphanet_3411
7012||770||GM17742||http://purl.obolibrary.org/obo/CLO_0017025
7013||3990||anticonvulsant||http://purl.obolibrary.org/obo/CHEBI_35623
7014||5502||Anaeromyxobacter dehalogenans 2CP-C||http://purl.obolibrary.org/obo/NCBITaxon_290397
7015||6238||vasodilator agent||http://purl.obolibrary.org/obo/CHEBI_35620
7016||8718||Partial androgen insensitivity syndrome||http://www.orpha.net/ORDO/Orphanet_90797
7018||5356||Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency||http://www.orpha.net/ORDO/Orphanet_90795
7017||7943||Hyperostosis corticalis generalisata||http://www.orpha.net/ORDO/Orphanet_3416
7020||5341||46,XY disorder of sex development due to isolated 17,20 lyase deficiency||http://www.orpha.net/ORDO/Orphanet_90796
7019||5935||Van den Bosch syndrome||http://www.orpha.net/ORDO/Orphanet_3417
7021||4931||Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency||http://www.orpha.net/ORDO/Orphanet_90793
7022||5356||Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency||http://www.orpha.net/ORDO/Orphanet_90794
7023||6087||Double outlet right ventricle||http://www.orpha.net/ORDO/Orphanet_3426
7024||5300||Velo-facial-skeletal syndrome||http://www.orpha.net/ORDO/Orphanet_3424
7025||3883||Cerebroretinal vasculopathy||http://www.orpha.net/ORDO/Orphanet_3421
7026||799||antineoplastic agent||http://purl.obolibrary.org/obo/CHEBI_35610
7027||1022||Cervus elaphus hispanicus||http://purl.obolibrary.org/obo/NCBITaxon_141655
7028||5300||Verloove Vanhorick-Brubakk syndrome||http://www.orpha.net/ORDO/Orphanet_3429
7029||770||GM17741||http://purl.obolibrary.org/obo/CLO_0017020
7030||5462||15q11.2 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_261183
7032||10994||promethazine||http://purl.obolibrary.org/obo/CHEBI_8461
7031||772||photosynthetic cell||http://purl.obolibrary.org/obo/CL_0000628
7033||10994||prostaglandin E2||http://purl.obolibrary.org/obo/CHEBI_15551
7034||15148||acinar cell||http://purl.obolibrary.org/obo/CL_0000622
7035||9294||natural killer cell||http://purl.obolibrary.org/obo/CL_0000623
7036||8205||CD4-positive, alpha-beta T cell||http://purl.obolibrary.org/obo/CL_0000624
7037||8205||CD8-positive, alpha-beta T cell||http://purl.obolibrary.org/obo/CL_0000625
7038||3349||CS57622||http://www.ebi.ac.uk/efo/EFO_0000039
7039||3349||CS57620||http://www.ebi.ac.uk/efo/EFO_0000037
7040||3349||CS57621||http://www.ebi.ac.uk/efo/EFO_0000038
7041||3349||CS57618||http://www.ebi.ac.uk/efo/EFO_0000035
7042||3349||CS57619||http://www.ebi.ac.uk/efo/EFO_0000036
7043||3349||CS57615||http://www.ebi.ac.uk/efo/EFO_0000033
7044||3349||CS57616||http://www.ebi.ac.uk/efo/EFO_0000034
7045||3349||CS57606||http://www.ebi.ac.uk/efo/EFO_0000031
7046||3349||CS57610||http://www.ebi.ac.uk/efo/EFO_0000032
7047||6573||explosive role||http://purl.obolibrary.org/obo/CHEBI_63490
7048||3349||CS57603||http://www.ebi.ac.uk/efo/EFO_0000030
7049||6917||Hereditary motor and sensory neuropathy type 6||http://www.orpha.net/ORDO/Orphanet_90120
7050||6912||Autosomal dominant intermediate Charcot-Marie-Tooth disease||http://www.orpha.net/ORDO/Orphanet_90114
7051||6917||Hereditary motor and sensory neuropathy, Okinawa type||http://www.orpha.net/ORDO/Orphanet_90117
7052||6912||Severe early-onset axonal neuropathy due to MFN2 deficiency||http://www.orpha.net/ORDO/Orphanet_90118
7053||8190||(15Z)-12-oxophyto-10,15-dienoic acid||http://purl.obolibrary.org/obo/CHEBI_15560
7054||6912||Axonal Charcot-Marie-Tooth disease with acrodystrophy||http://www.orpha.net/ORDO/Orphanet_90119
7055||3349||CS57598||http://www.ebi.ac.uk/efo/EFO_0000028
7056||3349||CS57601||http://www.ebi.ac.uk/efo/EFO_0000029
7057||2354||Miyoshi myopathy||http://www.orpha.net/ORDO/Orphanet_45448
7058||3349||CS57587||http://www.ebi.ac.uk/efo/EFO_0000024
7059||5700||Keratoderma hereditarium mutilans||http://www.orpha.net/ORDO/Orphanet_494
7060||3349||CS57591||http://www.ebi.ac.uk/efo/EFO_0000025
7062||5005||soil metagenome||http://purl.obolibrary.org/obo/NCBITaxon_410658
7061||5877||Familial keratoacanthoma||http://www.orpha.net/ORDO/Orphanet_493
7063||3349||CS57595||http://www.ebi.ac.uk/efo/EFO_0000026
7065||12401||Transgrediens et progrediens palmoplantar keratoderma||http://www.orpha.net/ORDO/Orphanet_495
7064||3349||CS57596||http://www.ebi.ac.uk/efo/EFO_0000027
7066||3349||CS57580||http://www.ebi.ac.uk/efo/EFO_0000020
7068||325||Keratosis pilaris atrophicans||http://www.orpha.net/ORDO/Orphanet_498
7067||772||hepatic stellate cell||http://purl.obolibrary.org/obo/CL_0000632
7069||3349||CS57581||http://www.ebi.ac.uk/efo/EFO_0000021
7070||3349||CS57583||http://www.ebi.ac.uk/efo/EFO_0000022
7071||3349||CS57586||http://www.ebi.ac.uk/efo/EFO_0000023
7072||14537||basal cell||http://purl.obolibrary.org/obo/CL_0000646
7073||7589||multinucleated giant cell||http://purl.obolibrary.org/obo/CL_0000647
7074||7001||Syndromic hypothyroidism||http://www.orpha.net/ORDO/Orphanet_177107
7075||3349||CS57560||http://www.ebi.ac.uk/efo/EFO_0000015
7076||5777||Kniest dysplasia||http://www.orpha.net/ORDO/Orphanet_485
7077||3349||CS57563||http://www.ebi.ac.uk/efo/EFO_0000016
7078||15365||Congenital high-molecular-weight kininogen deficiency||http://www.orpha.net/ORDO/Orphanet_483
7079||3349||CS57551||http://www.ebi.ac.uk/efo/EFO_0000013
7080||3349||CS57556||http://www.ebi.ac.uk/efo/EFO_0000014
7082||3349||CS57572||http://www.ebi.ac.uk/efo/EFO_0000019
7081||1390||Kennedy disease||http://www.orpha.net/ORDO/Orphanet_481
7083||1211||Kearns-Sayre syndrome||http://www.orpha.net/ORDO/Orphanet_480
7084||3349||CS57569||http://www.ebi.ac.uk/efo/EFO_0000017
7085||3349||CS57570||http://www.ebi.ac.uk/efo/EFO_0000018
7086||10577||Disorder of multiple glycosylation||http://www.orpha.net/ORDO/Orphanet_309526
7087||3349||CS57548||http://www.ebi.ac.uk/efo/EFO_0000011
7089||3349||CS57549||http://www.ebi.ac.uk/efo/EFO_0000012
7088||742||Urachal cyst||http://www.orpha.net/ORDO/Orphanet_488
7090||2454||Krabbe disease||http://www.orpha.net/ORDO/Orphanet_487
7092||12539||Autosomal dominant severe congenital neutropenia||http://www.orpha.net/ORDO/Orphanet_486
7091||3349||CS57544||http://www.ebi.ac.uk/efo/EFO_0000010
7093||2683||Lissencephaly due to TUBA1A mutation||http://www.orpha.net/ORDO/Orphanet_171680
7094||9898||Parkinsonian-pyramidal syndrome||http://www.orpha.net/ORDO/Orphanet_171695
7095||10980||Proximal 16p11.2 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_261197
7096||5462||15q14 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_261190
7097||3349||CS57511||http://www.ebi.ac.uk/efo/EFO_0000002
7098||3349||CS57512||http://www.ebi.ac.uk/efo/EFO_0000003
7100||3349||CS57515||http://www.ebi.ac.uk/efo/EFO_0000004
7099||7319||Jeune syndrome||http://www.orpha.net/ORDO/Orphanet_474
7101||3349||CS57520||http://www.ebi.ac.uk/efo/EFO_0000005
7102||3349||CS57521||http://www.ebi.ac.uk/efo/EFO_0000006
7103||3349||CS57537||http://www.ebi.ac.uk/efo/EFO_0000007
7104||3349||CS57541||http://www.ebi.ac.uk/efo/EFO_0000008
7105||6305||Lysinuric protein intolerance||http://www.orpha.net/ORDO/Orphanet_470
7106||3349||CS57543||http://www.ebi.ac.uk/efo/EFO_0000009
7107||11881||Metabolic myopathy due to lactate transporter defect||http://www.orpha.net/ORDO/Orphanet_171690
7108||1721||Joubert syndrome||http://www.orpha.net/ORDO/Orphanet_475
7109||1022||Hypophthalmichthys molitrix||http://purl.obolibrary.org/obo/NCBITaxon_13095
7110||7486||Kallmann syndrome||http://www.orpha.net/ORDO/Orphanet_478
7112||306||KID syndrome||http://www.orpha.net/ORDO/Orphanet_477
7111||0||experimental factor||http://www.ebi.ac.uk/efo/EFO_0000001
7113||583||Autosomal recessive spastic paraplegia type 35||http://www.orpha.net/ORDO/Orphanet_171629
7114||759||Pseudohypoparathyroidism||http://www.orpha.net/ORDO/Orphanet_97593
7115||1826||Lotus uliginosus||http://purl.obolibrary.org/obo/NCBITaxon_181288
7116||13470||Autosomal recessive spastic paraplegia type 32||http://www.orpha.net/ORDO/Orphanet_171622
7117||11456||Partial duplication of chromosome 16||http://www.orpha.net/ORDO/Orphanet_262672
7118||11556||Fatal familial insomnia||http://www.orpha.net/ORDO/Orphanet_466
7119||11456||Partial duplication of chromosome 17||http://www.orpha.net/ORDO/Orphanet_262677
7120||4142||Non-acquired combined pituitary hormone deficiency||http://www.orpha.net/ORDO/Orphanet_467
7121||306||Incontinentia pigmenti||http://www.orpha.net/ORDO/Orphanet_464
7122||15365||Congenital plasminogen activator inhibitor type 1 deficiency||http://www.orpha.net/ORDO/Orphanet_465
7123||266||Hereditary fructose intolerance||http://www.orpha.net/ORDO/Orphanet_469
7124||9622||Recessive X-linked ichthyosis||http://www.orpha.net/ORDO/Orphanet_461
7125||8142||Trisomy 8p||http://www.orpha.net/ORDO/Orphanet_264450
7126||990||Hermansky-Pudlak syndrome type 8||http://www.orpha.net/ORDO/Orphanet_231537
7127||10994||calcitriol||http://purl.obolibrary.org/obo/CHEBI_17823
7128||15570||Superficial epidermolytic ichthyosis||http://www.orpha.net/ORDO/Orphanet_455
7129||10907||Harlequin ichthyosis||http://www.orpha.net/ORDO/Orphanet_457
7130||990||Hermansky-Pudlak syndrome type 7||http://www.orpha.net/ORDO/Orphanet_231531
7131||1419||X-linked lissencephaly with abnormal genitalia||http://www.orpha.net/ORDO/Orphanet_452
7132||5292||biosynthetic process||http://purl.obolibrary.org/obo/GO_0009058
7133||10994||gentamicin||http://purl.obolibrary.org/obo/CHEBI_17833
7135||11456||Partial trisomy of chromosome 20||http://www.orpha.net/ORDO/Orphanet_262692
7134||4139||Charcot-Marie-Tooth disease - deafness - intellectual disability||http://www.orpha.net/ORDO/Orphanet_90103
7136||10275||Generalized dominant dystrophic epidermolysis bullosa||http://www.orpha.net/ORDO/Orphanet_231568
7137||15365||Hemophilia||http://www.orpha.net/ORDO/Orphanet_448
7138||266||Neonatal hemochromatosis||http://www.orpha.net/ORDO/Orphanet_446
7140||4278||Paroxysmal nocturnal hemoglobinuria||http://www.orpha.net/ORDO/Orphanet_447
7139||7086||Defect in conserved oligomeric Golgi complex||http://www.orpha.net/ORDO/Orphanet_309568
7141||321||Marie Unna hereditary hypotrichosis||http://www.orpha.net/ORDO/Orphanet_444
7142||1314||Congenital hypothyroidism||http://www.orpha.net/ORDO/Orphanet_442
7143||6290||Developmental delay due to methylmalonate semialdehyde dehydrogenase deficiency||http://www.orpha.net/ORDO/Orphanet_289307
7146||10994||prochlorperazine||http://purl.obolibrary.org/obo/CHEBI_8435
7144||1022||Dendroctonus ponderosae||http://purl.obolibrary.org/obo/NCBITaxon_77166
7145||5536||Partial duplication of the short arm of chromosome 2||http://www.orpha.net/ORDO/Orphanet_262698
7147||10745||Familial hypospadias||http://www.orpha.net/ORDO/Orphanet_440
7148||770||WEHI-231 cell||http://purl.obolibrary.org/obo/BTO_0001093
7149||8193||scopolamine||http://purl.obolibrary.org/obo/CHEBI_16794
7150||7591||basophilic myelocyte||http://purl.obolibrary.org/obo/CL_0000614
7151||14510||basophil progenitor cell||http://purl.obolibrary.org/obo/CL_0000613
7152||11456||Partial trisomy/tetrasomy of chromosome 18||http://www.orpha.net/ORDO/Orphanet_262682
7153||7648||eosinophilic myelocyte||http://purl.obolibrary.org/obo/CL_0000612
7154||14510||eosinophil progenitor cell||http://purl.obolibrary.org/obo/CL_0000611
7155||9288||GABAergic neuron||http://purl.obolibrary.org/obo/CL_0000617
7156||10278||Late-onset localized junctional epidermolysis bullosa - intellectual disability||http://www.orpha.net/ORDO/Orphanet_231556
7157||306||Ito hypomelanosis||http://www.orpha.net/ORDO/Orphanet_435
7158||5287||Hypophosphatasia||http://www.orpha.net/ORDO/Orphanet_436
7160||1619||Primary failure of tooth eruption||http://www.orpha.net/ORDO/Orphanet_412206
7159||4810||Hypophosphatemic rickets||http://www.orpha.net/ORDO/Orphanet_437
7161||11456||Partial duplication of chromosome 19||http://www.orpha.net/ORDO/Orphanet_262687
7163||772||plant cell||http://purl.obolibrary.org/obo/CL_0000610
7162||7486||Normosmic congenital hypogonadotropic hypogonadism||http://www.orpha.net/ORDO/Orphanet_432
7164||1319||lysine||http://purl.obolibrary.org/obo/CHEBI_25094
7165||1826||Nuphar advena||http://purl.obolibrary.org/obo/NCBITaxon_77108
7166||6768||Severe combined immunodeficiency due to complete RAG1/2 deficiency||http://www.orpha.net/ORDO/Orphanet_331206
7167||10300||Distal 7q11.23 microduplication syndrome||http://www.orpha.net/ORDO/Orphanet_261102
7169||2672||abdominal cavity||http://purl.obolibrary.org/obo/UBERON_0003684
7168||1826||Populus tremula||http://purl.obolibrary.org/obo/NCBITaxon_113636
7170||990||Hermansky-Pudlak syndrome with pulmonary fibrosis||http://www.orpha.net/ORDO/Orphanet_231500
7172||3753||Congenital and infantile nephrotic syndrome||http://www.orpha.net/ORDO/Orphanet_97556
7171||8805||Mucopolysaccharidosis type 6, slowly progressing||http://www.orpha.net/ORDO/Orphanet_276223
7173||6187||Sporadic idiopathic steroid-resistant nephrotic syndrome with collapsing glomerulopathy||http://www.orpha.net/ORDO/Orphanet_97555
7174||6596||triglyceride||http://purl.obolibrary.org/obo/CHEBI_17855
7175||8386||Other immunodeficiency syndrome due to defects in adaptive immunity||http://www.orpha.net/ORDO/Orphanet_331217
7176||2672||sacrum||http://purl.obolibrary.org/obo/UBERON_0003690
7177||770||GM14581||http://purl.obolibrary.org/obo/CLO_0031585
7178||770||GM14568||http://purl.obolibrary.org/obo/CLO_0031580
7179||770||GM14569||http://purl.obolibrary.org/obo/CLO_0031581
7180||7319||Ivemark syndrome||http://www.orpha.net/ORDO/Orphanet_97548
7181||10676||Machado-Joseph disease type 1||http://www.orpha.net/ORDO/Orphanet_276238
7182||10994||2,4-dichlorophenol||http://purl.obolibrary.org/obo/CHEBI_16738
7183||4173||creatinine||http://purl.obolibrary.org/obo/CHEBI_16737
7184||1591||Non-syndromic male infertility due to sperm motility disorder||http://www.orpha.net/ORDO/Orphanet_276234
7185||10994||cinnamaldehyde||http://purl.obolibrary.org/obo/CHEBI_16731
7186||770||184B5 cell||http://purl.obolibrary.org/obo/BTO_0002180
7187||5502||Pasteurella multocida||http://purl.obolibrary.org/obo/NCBITaxon_747
7188||11867||middle lateral line neuromast||http://purl.obolibrary.org/obo/UBERON_2000939
7189||6684||Xeroderma pigmentosum complementation group A||http://www.orpha.net/ORDO/Orphanet_276249
7190||10652||obsolete_B-precursor acute lymphoblastic leukemia||http://www.ebi.ac.uk/efo/EFO_0000093
7191||122||B-cell acute lymphoblastic leukemia||http://www.ebi.ac.uk/efo/EFO_0000094
7193||1508||chronic lymphocytic leukemia||http://www.ebi.ac.uk/efo/EFO_0000095
7192||6323||Glycerol kinase deficiency||http://www.orpha.net/ORDO/Orphanet_308993
7195||2672||hindlimb muscle||http://purl.obolibrary.org/obo/UBERON_0003663
7194||1682||neoplasm of mature B-cells||http://www.ebi.ac.uk/efo/EFO_0000096
7196||10652||obsolete_B-lymphocyte||http://www.ebi.ac.uk/efo/EFO_0000097
7197||3980||BY4741||http://www.ebi.ac.uk/efo/EFO_0000098
7198||10652||obsolete_BY4741||http://www.ebi.ac.uk/efo/EFO_0000099
7199||10994||clomipramine||http://purl.obolibrary.org/obo/CHEBI_47780
7200||6309||Disorder of glyoxylate metabolism||http://www.orpha.net/ORDO/Orphanet_308998
7201||10994||orotic acid||http://purl.obolibrary.org/obo/CHEBI_16742
7202||10676||Machado-Joseph disease type 2||http://www.orpha.net/ORDO/Orphanet_276241
7203||10676||Machado-Joseph disease type 3||http://www.orpha.net/ORDO/Orphanet_276244
7204||5466||14q11.2 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_261120
7205||6865||Autosomal recessive hyper-IgE syndrome due to TYK2 deficiency||http://www.orpha.net/ORDO/Orphanet_331226
7206||7175||Hyper-IgE syndrome||http://www.orpha.net/ORDO/Orphanet_331223
7207||7175||Immunodeficiency due to absence of thymus||http://www.orpha.net/ORDO/Orphanet_331220
7209||2670||petiole||http://purl.obolibrary.org/obo/PO_0020038
7208||10215||HDL cholesterol||http://purl.obolibrary.org/obo/CHEBI_47775
7211||3349||CS57743||http://www.ebi.ac.uk/efo/EFO_0000084
7210||770||HMEpC cell||http://purl.obolibrary.org/obo/BTO_0002178
7213||3349||CS57750||http://www.ebi.ac.uk/efo/EFO_0000085
7212||770||184A1N4 cell||http://purl.obolibrary.org/obo/BTO_0002179
7215||3349||CS57740||http://www.ebi.ac.uk/efo/EFO_0000082
7214||5502||Haemophilus ducreyi||http://purl.obolibrary.org/obo/NCBITaxon_730
7216||3349||CS57742||http://www.ebi.ac.uk/efo/EFO_0000083
7218||3349||CS57753||http://www.ebi.ac.uk/efo/EFO_0000088
7217||2672||mouth floor||http://purl.obolibrary.org/obo/UBERON_0003679
7220||3349||CS57758||http://www.ebi.ac.uk/efo/EFO_0000089
7219||5502||Histophilus somni||http://purl.obolibrary.org/obo/NCBITaxon_731
7221||3349||CS57751||http://www.ebi.ac.uk/efo/EFO_0000086
7222||3349||CS57752||http://www.ebi.ac.uk/efo/EFO_0000087
7223||6684||Xeroderma pigmentosum complementation group C||http://www.orpha.net/ORDO/Orphanet_276255
7225||5540||Partial duplication of the short arm of chromosome 1||http://www.orpha.net/ORDO/Orphanet_264431
7224||10923||Monosomy 9p||http://www.orpha.net/ORDO/Orphanet_261112
7226||1582||Xeroderma pigmentosum complementation group B||http://www.orpha.net/ORDO/Orphanet_276252
7227||1582||Xeroderma pigmentosum complementation group D||http://www.orpha.net/ORDO/Orphanet_276258
7228||10652||obsolete_Arbisopsis thaliana||http://www.ebi.ac.uk/efo/EFO_0000091
7231||3349||CS57769||http://www.ebi.ac.uk/efo/EFO_0000090
7230||2672||peritrophic membrane||http://purl.obolibrary.org/obo/BTO_0001038
7229||990||Hermansky-Pudlak syndrome without pulmonary fibrosis||http://www.orpha.net/ORDO/Orphanet_231512
7232||7234||Selective IgM deficiency||http://www.orpha.net/ORDO/Orphanet_331235
7233||8190||hydrochloric acid||http://purl.obolibrary.org/obo/CHEBI_17883
7234||260||Immunodeficiency with isotype or light chain deficiencies with normal number of B-cells||http://www.orpha.net/ORDO/Orphanet_331232
7236||3349||CS57727||http://www.ebi.ac.uk/efo/EFO_0000076
7235||8826||J774.2 cell||http://purl.obolibrary.org/obo/BTO_0001030
7237||3349||CS57722||http://www.ebi.ac.uk/efo/EFO_0000075
7238||3349||CS57732||http://www.ebi.ac.uk/efo/EFO_0000078
7239||3349||CS57731||http://www.ebi.ac.uk/efo/EFO_0000077
7240||3349||CS57716||http://www.ebi.ac.uk/efo/EFO_0000072
7241||3349||CS57715||http://www.ebi.ac.uk/efo/EFO_0000071
7242||3349||CS57719||http://www.ebi.ac.uk/efo/EFO_0000074
7243||3349||CS57717||http://www.ebi.ac.uk/efo/EFO_0000073
7244||770||prostate cancer cell line||http://purl.obolibrary.org/obo/BTO_0001033
7245||3790||Immunodeficiency syndrome with hypopigmentation||http://www.orpha.net/ORDO/Orphanet_331249
7246||1902||Polymicrogyria||http://www.orpha.net/ORDO/Orphanet_35981
7247||3349||CS57733||http://www.ebi.ac.uk/efo/EFO_0000079
7248||260||Other immunodeficiency syndrome with predominantly antibody defects||http://www.orpha.net/ORDO/Orphanet_331244
7249||11457||Mosaic trisomy 8||http://www.orpha.net/ORDO/Orphanet_96061
7250||11457||Mosaic trisomy 10||http://www.orpha.net/ORDO/Orphanet_96063
7251||7992||Arnold-Chiari malformation type I||http://www.orpha.net/ORDO/Orphanet_268882
7252||11457||Mosaic trisomy 5||http://www.orpha.net/ORDO/Orphanet_96060
7253||7225||Distal trisomy 1p36||http://www.orpha.net/ORDO/Orphanet_96069
7254||3349||CS57735||http://www.ebi.ac.uk/efo/EFO_0000080
7255||3349||CS57737||http://www.ebi.ac.uk/efo/EFO_0000081
7256||260||Immunodeficiency with severe reduction in serum IgG and IgA with normal/elevated IgM and normal number of B-cells||http://www.orpha.net/ORDO/Orphanet_331240
7257||5466||14q12 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_261144
7258||11457||Mosaic trisomy 22||http://www.orpha.net/ORDO/Orphanet_96068
7259||1022||Strelkovimermis||http://purl.obolibrary.org/obo/NCBITaxon_382539
7260||1210||Infantile convulsions and choreoathetosis||http://www.orpha.net/ORDO/Orphanet_31709
7261||3349||CS57706||http://www.ebi.ac.uk/efo/EFO_0000067
7262||3349||CS57705||http://www.ebi.ac.uk/efo/EFO_0000066
7263||3349||CS57704||http://www.ebi.ac.uk/efo/EFO_0000065
7264||3349||CS57701||http://www.ebi.ac.uk/efo/EFO_0000064
7266||3349||CS57699||http://www.ebi.ac.uk/efo/EFO_0000063
7265||263||Mandibuloacral dysplasia with type A lipodystrophy||http://www.orpha.net/ORDO/Orphanet_90153
7267||3349||CS57692||http://www.ebi.ac.uk/efo/EFO_0000062
7268||263||Mandibuloacral dysplasia with type B lipodystrophy||http://www.orpha.net/ORDO/Orphanet_90154
7269||3349||CS57691||http://www.ebi.ac.uk/efo/EFO_0000061
7270||3349||CS57677||http://www.ebi.ac.uk/efo/EFO_0000060
7271||3349||CS57710||http://www.ebi.ac.uk/efo/EFO_0000069
7272||3349||CS57709||http://www.ebi.ac.uk/efo/EFO_0000068
7273||1022||Danaus plexippus||http://purl.obolibrary.org/obo/NCBITaxon_13037
7274||3349||CS57714||http://www.ebi.ac.uk/efo/EFO_0000070
7275||11457||Mosaic trisomy 4||http://www.orpha.net/ORDO/Orphanet_96059
7276||11456||Tetrasomy 21||http://www.orpha.net/ORDO/Orphanet_96055
7277||3349||CS57644||http://www.ebi.ac.uk/efo/EFO_0000050
7278||5502||Orientia tsutsugamushi||http://purl.obolibrary.org/obo/NCBITaxon_784
7279||14072||Non-hereditary late-onset primary lymphedema||http://www.orpha.net/ORDO/Orphanet_90185
7281||14072||Meige disease||http://www.orpha.net/ORDO/Orphanet_90186
7282||3349||CS57648||http://www.ebi.ac.uk/efo/EFO_0000052
7280||5502||Rickettsia prowazekii||http://purl.obolibrary.org/obo/NCBITaxon_782
7284||3349||CS57646||http://www.ebi.ac.uk/efo/EFO_0000051
7283||5502||Rickettsia rickettsii||http://purl.obolibrary.org/obo/NCBITaxon_783
7285||3349||CS57658||http://www.ebi.ac.uk/efo/EFO_0000054
7286||3349||CS57655||http://www.ebi.ac.uk/efo/EFO_0000053
7287||3349||CS57663||http://www.ebi.ac.uk/efo/EFO_0000056
7288||3349||CS57660||http://www.ebi.ac.uk/efo/EFO_0000055
7289||3349||CS57666||http://www.ebi.ac.uk/efo/EFO_0000058
7290||3349||CS57664||http://www.ebi.ac.uk/efo/EFO_0000057
7291||3349||CS57671||http://www.ebi.ac.uk/efo/EFO_0000059
7292||5502||Rickettsia conorii||http://purl.obolibrary.org/obo/NCBITaxon_781
7293||3349||CS57625||http://www.ebi.ac.uk/efo/EFO_0000041
7294||3349||CS57624||http://www.ebi.ac.uk/efo/EFO_0000040
7295||3349||CS57629||http://www.ebi.ac.uk/efo/EFO_0000045
7296||3349||CS57628||http://www.ebi.ac.uk/efo/EFO_0000044
7298||3349||CS57627||http://www.ebi.ac.uk/efo/EFO_0000043
7297||5502||Coxiella burnetii||http://purl.obolibrary.org/obo/NCBITaxon_777
7299||3349||CS57626||http://www.ebi.ac.uk/efo/EFO_0000042
7300||3349||CS57641||http://www.ebi.ac.uk/efo/EFO_0000049
7301||3349||CS57637||http://www.ebi.ac.uk/efo/EFO_0000048
7302||3349||CS57631||http://www.ebi.ac.uk/efo/EFO_0000047
7303||3349||CS57630||http://www.ebi.ac.uk/efo/EFO_0000046
7304||8203||Distal trisomy 3p||http://www.orpha.net/ORDO/Orphanet_96071
7305||7145||Distal trisomy 2p||http://www.orpha.net/ORDO/Orphanet_96070
7306||8127||Distal trisomy 7p||http://www.orpha.net/ORDO/Orphanet_96074
7307||8231||4p16.3 microduplication syndrome||http://www.orpha.net/ORDO/Orphanet_96072
7308||7757||16p13.3 microduplication syndrome||http://www.orpha.net/ORDO/Orphanet_96078
7309||7809||Beckwith-Wiedemann syndrome due to 11p15 microduplication||http://www.orpha.net/ORDO/Orphanet_96076
7310||10994||benzene||http://purl.obolibrary.org/obo/CHEBI_16716
7311||770||AG04655||http://purl.obolibrary.org/obo/CLO_0034915
7312||8805||Mucopolysaccharidosis type 6, rapidly progressing||http://www.orpha.net/ORDO/Orphanet_276212
7313||9856||Spinocerebellar ataxia type 36||http://www.orpha.net/ORDO/Orphanet_276198
7314||14970||hemoglobin measurement||http://www.ebi.ac.uk/efo/EFO_0004509
7316||770||GM14501||http://purl.obolibrary.org/obo/CLO_0031504
7315||7334||Isolated focal cortical dysplasia type Ia||http://www.orpha.net/ORDO/Orphanet_268973
7317||9856||Spinocerebellar ataxia type 35||http://www.orpha.net/ORDO/Orphanet_276193
7318||770||GM14503||http://purl.obolibrary.org/obo/CLO_0031509
7319||4723||Syndromic renal or urinary tract malformation||http://www.orpha.net/ORDO/Orphanet_93547
7320||4033||radiation induced mutation||http://www.ebi.ac.uk/efo/EFO_0004500
7321||14970||telomere length||http://www.ebi.ac.uk/efo/EFO_0004505
7322||14970||monocyte early outgrowth colony forming unit||http://www.ebi.ac.uk/efo/EFO_0004506
7323||4727||X-linked congenital disorder of glycosylation with intellectual disability as a major feature||http://www.orpha.net/ORDO/Orphanet_371054
7325||14970||D dimer measurement||http://www.ebi.ac.uk/efo/EFO_0004507
7324||1022||Montastraea faveolata||http://purl.obolibrary.org/obo/NCBITaxon_48498
7326||14970||spine bone size||http://www.ebi.ac.uk/efo/EFO_0004508
7327||14970||HOMA-IR||http://www.ebi.ac.uk/efo/EFO_0004501
7328||14970||adiponectin measurement||http://www.ebi.ac.uk/efo/EFO_0004502
7330||14970||hematological measurement||http://www.ebi.ac.uk/efo/EFO_0004503
7329||10994||N-acylethanolamine||http://purl.obolibrary.org/obo/CHEBI_52640
7331||1022||Nucella lapillus||http://purl.obolibrary.org/obo/NCBITaxon_51631
7332||14970||serum hepcidin measurement||http://www.ebi.ac.uk/efo/EFO_0004504
7333||15522||Congenital disorder of glycosylation with neurological involvement||http://www.orpha.net/ORDO/Orphanet_371047
7334||183||Isolated focal cortical dysplasia type I||http://www.orpha.net/ORDO/Orphanet_268961
7335||9856||Spinocerebellar ataxia type 32||http://www.orpha.net/ORDO/Orphanet_276183
7336||14970||HPV seropositivity||http://www.ebi.ac.uk/efo/EFO_0004510
7337||7350||femoral neck bone geometry||http://www.ebi.ac.uk/efo/EFO_0004511
7339||843||Rapid-onset dystonia-parkinsonism||http://www.orpha.net/ORDO/Orphanet_71517
7338||5502||Bartonella quintana||http://purl.obolibrary.org/obo/NCBITaxon_803
7340||4830||Basement membrane disease||http://www.orpha.net/ORDO/Orphanet_93550
7341||14970||serum creatinine measurement||http://www.ebi.ac.uk/efo/EFO_0004518
7342||14970||soluble P-selectin measurement||http://www.ebi.ac.uk/efo/EFO_0004519
7343||14970||bone fracture related measurement||http://www.ebi.ac.uk/efo/EFO_0004516
7344||14970||arterial stiffness measurement||http://www.ebi.ac.uk/efo/EFO_0004517
7346||14970||bone quantitative ultrasound measurement||http://www.ebi.ac.uk/efo/EFO_0004514
7345||914||Benign paroxysmal torticollis of infancy||http://www.orpha.net/ORDO/Orphanet_71518
7347||8579||muscle mass measurement||http://www.ebi.ac.uk/efo/EFO_0004515
7348||14970||bone measurement||http://www.ebi.ac.uk/efo/EFO_0004512
7349||7577||Primary qualitative or quantitative defects of alpha-dystroglycan||http://www.orpha.net/ORDO/Orphanet_371040
7350||8579||bone geometry||http://www.ebi.ac.uk/efo/EFO_0004513
7351||770||GM14478||http://purl.obolibrary.org/obo/CLO_0031529
7352||6325||Hypermethioninemia encephalopathy due to adenosine kinase deficiency||http://www.orpha.net/ORDO/Orphanet_289290
7353||4629||Rare disease with thoracic aortic aneurysm and aortic dissection||http://www.orpha.net/ORDO/Orphanet_285014
7354||183||Isolated focal cortical dysplasia type II||http://www.orpha.net/ORDO/Orphanet_268994
7355||5667||Familial renal amyloidosis due to lysozyme variant||http://www.orpha.net/ORDO/Orphanet_93561
7356||5667||Familial renal amyloidosis due to fibrinogen A alpha-chain variant||http://www.orpha.net/ORDO/Orphanet_93562
7357||5667||Familial renal amyloidosis due to Apolipoprotein AI variant||http://www.orpha.net/ORDO/Orphanet_93560
7358||7333||Congenital disorder of glycosylation with epilepsy as a major feature||http://www.orpha.net/ORDO/Orphanet_371071
7359||8194||Dianzani autoimmune lymphoproliferative disease||http://www.orpha.net/ORDO/Orphanet_275523
7360||1826||Aristolochia fimbriata||http://purl.obolibrary.org/obo/NCBITaxon_158543
7361||7334||Isolated focal cortical dysplasia type Ib||http://www.orpha.net/ORDO/Orphanet_268980
7362||7334||Isolated focal cortical dysplasia type Ic||http://www.orpha.net/ORDO/Orphanet_268987
7363||770||GM14506||http://purl.obolibrary.org/obo/CLO_0031519
7364||770||GM14507||http://purl.obolibrary.org/obo/CLO_0031517
7365||770||GM14504||http://purl.obolibrary.org/obo/CLO_0031516
7366||6028||Atypical hemolytic-uremic syndrome with MCP/CD46 anomaly||http://www.orpha.net/ORDO/Orphanet_93576
7367||6028||Atypical hemolytic-uremic syndrome with H factor anomaly||http://www.orpha.net/ORDO/Orphanet_93579
7368||6028||Atypical hemolytic-uremic syndrome with B factor anomaly||http://www.orpha.net/ORDO/Orphanet_93578
7369||770||GM14502||http://purl.obolibrary.org/obo/CLO_0031510
7370||6028||Atypical hemolytic-uremic syndrome with C3 anomaly||http://www.orpha.net/ORDO/Orphanet_93575
7371||11465||Dense deposit disease||http://www.orpha.net/ORDO/Orphanet_93571
7372||4728||Non-X-linked congenital disorder of glycosylation with intellectual disability as a major feature||http://www.orpha.net/ORDO/Orphanet_371064
7373||4454||magnesium||http://purl.obolibrary.org/obo/CHEBI_25107
7375||5025||Fusarium anthophilum||http://purl.obolibrary.org/obo/NCBITaxon_48485
7374||5486||Autoimmune lymphoproliferative syndrome with recurrent viral infections||http://www.orpha.net/ORDO/Orphanet_275517
7376||9345||Late-onset nephronophthisis||http://www.orpha.net/ORDO/Orphanet_93589
7377||11809||Familial cystic renal disease||http://www.orpha.net/ORDO/Orphanet_93587
7378||2897||Multiple endocrine neoplasia type 4||http://www.orpha.net/ORDO/Orphanet_276152
7379||5502||Streptomyces griseus subsp. griseus NBRC 13350||http://purl.obolibrary.org/obo/NCBITaxon_455632
7380||5956||L1 syndrome||http://www.orpha.net/ORDO/Orphanet_275543
7381||2545||ILSXISS28/TejJ||http://www.ebi.ac.uk/efo/EFO_0003018
7382||2545||ILSXISS46/TejJ||http://www.ebi.ac.uk/efo/EFO_0003019
7383||1986||collecting duct carcinoma||http://www.ebi.ac.uk/efo/EFO_0003016
7384||2229||transitional cell carcinoma of kidney||http://www.ebi.ac.uk/efo/EFO_0003017
7385||2162||breast fibrocystic disease||http://www.ebi.ac.uk/efo/EFO_0003014
7387||3068||aggressive behavior||http://www.ebi.ac.uk/efo/EFO_0003015
7388||5502||Porphyromonas gingivalis||http://purl.obolibrary.org/obo/NCBITaxon_837
7386||6028||Atypical hemolytic-uremic syndrome with anti-factor H antibodies||http://www.orpha.net/ORDO/Orphanet_93581
7389||2545||ILSXISS123/TejJ||http://www.ebi.ac.uk/efo/EFO_0003012
7390||6028||Atypical hemolytic-uremic syndrome with I factor anomaly||http://www.orpha.net/ORDO/Orphanet_93580
7391||13587||Mus musculus subspecies||http://www.ebi.ac.uk/efo/EFO_0003013
7392||2545||ILSXISS117/TejJ||http://www.ebi.ac.uk/efo/EFO_0003010
7393||2545||ILSXISS122/TejJ||http://www.ebi.ac.uk/efo/EFO_0003011
7394||4823||Congenital thrombotic thrombocytopenic purpura due to ADAMTS-13 deficiency||http://www.orpha.net/ORDO/Orphanet_93583
7395||8102||Primary hyperoxaluria type 1||http://www.orpha.net/ORDO/Orphanet_93598
7396||8102||Primary hyperoxaluria type 2||http://www.orpha.net/ORDO/Orphanet_93599
7397||770||GM14479||http://purl.obolibrary.org/obo/CLO_0031535
7398||114||acute myeloblastic leukemia without maturation||http://www.ebi.ac.uk/efo/EFO_0003027
7399||114||acute myeloblastic leukemia with maturation||http://www.ebi.ac.uk/efo/EFO_0003028
7400||1732||Myostatin-related muscle hypertrophy||http://www.orpha.net/ORDO/Orphanet_275534
7401||114||acute basophilic leukemia||http://www.ebi.ac.uk/efo/EFO_0003029
7403||10994||interferon beta||http://www.ebi.ac.uk/efo/EFO_0003023
7402||9345||Infantile nephronophthisis||http://www.orpha.net/ORDO/Orphanet_93591
7405||10994||interferon gamma||http://www.ebi.ac.uk/efo/EFO_0003024
7404||5984||Midline cerebral malformation||http://www.orpha.net/ORDO/Orphanet_268926
7408||13496||Synechococcus phage S-PM2||http://purl.obolibrary.org/obo/NCBITaxon_238854
7407||11809||Nephropathy secondary to a storage or other metabolic disease||http://www.orpha.net/ORDO/Orphanet_93593
7406||114||acute megakaryoblastic leukaemia||http://www.ebi.ac.uk/efo/EFO_0003025
7410||114||minimally differentiated acute myeloblastic leukemia||http://www.ebi.ac.uk/efo/EFO_0003026
7409||9345||Juvenile nephronophthisis||http://www.orpha.net/ORDO/Orphanet_93592
7411||770||GM14480||http://purl.obolibrary.org/obo/CLO_0031534
7414||2545||ILSXISS60/TejJ||http://www.ebi.ac.uk/efo/EFO_0003020
7413||266||Alpha-1-antichymotrypsin deficiency||http://www.orpha.net/ORDO/Orphanet_93594
7412||770||GM14481||http://purl.obolibrary.org/obo/CLO_0031533
7415||10994||interferon alpha||http://www.ebi.ac.uk/efo/EFO_0003021
7417||10994||interferon alpha 2a||http://www.ebi.ac.uk/efo/EFO_0003022
7416||770||GM14477||http://purl.obolibrary.org/obo/CLO_0031531
7418||1902||Cerebral cortical dysplasia||http://www.orpha.net/ORDO/Orphanet_268950
7419||5295||regulation of gene expression||http://purl.obolibrary.org/obo/GO_0010468
7420||5502||Bacteroides thetaiotaomicron||http://purl.obolibrary.org/obo/NCBITaxon_818
7421||5502||Bacteroides||http://purl.obolibrary.org/obo/NCBITaxon_816
7422||5502||Bacteroides fragilis||http://purl.obolibrary.org/obo/NCBITaxon_817
7423||5502||Chlamydia trachomatis||http://purl.obolibrary.org/obo/NCBITaxon_813
7424||7246||Unilateral polymicrogyria||http://www.orpha.net/ORDO/Orphanet_268943
7425||2897||Multiple endocrine neoplasia||http://www.orpha.net/ORDO/Orphanet_276161
7426||7246||Bilateral polymicrogyria||http://www.orpha.net/ORDO/Orphanet_268940
7427||2545||ILSXISS107/TejJ||http://www.ebi.ac.uk/efo/EFO_0003005
7428||2545||ILSXISS110/TejJ||http://www.ebi.ac.uk/efo/EFO_0003006
7430||2545||ILSXISS112/TejJ||http://www.ebi.ac.uk/efo/EFO_0003007
7429||5502||Bacteroides vulgatus||http://purl.obolibrary.org/obo/NCBITaxon_821
7431||2545||ILSXISS114/TejJ||http://www.ebi.ac.uk/efo/EFO_0003008
7432||2545||ILSXISS115/TejJ||http://www.ebi.ac.uk/efo/EFO_0003009
7433||2545||ILSXISS97/TejJ||http://www.ebi.ac.uk/efo/EFO_0003000
7434||2545||ILSXISS98/TejJ||http://www.ebi.ac.uk/efo/EFO_0003001
7435||7424||Unilateral focal polymicrogyria||http://www.orpha.net/ORDO/Orphanet_268947
7436||2545||ILSXISS99/TejJ||http://www.ebi.ac.uk/efo/EFO_0003002
7437||2545||ILSXISS100/TejJ||http://www.ebi.ac.uk/efo/EFO_0003003
7438||2545||ILSXISS103/TejJ||http://www.ebi.ac.uk/efo/EFO_0003004
7439||14970||lymphocyte count||http://www.ebi.ac.uk/efo/EFO_0004587
7440||10652||obsolete_gamma glutamyl transpeptidase measurement||http://www.ebi.ac.uk/efo/EFO_0004588
7441||14970||naphthyl-keratin adduct measurement||http://www.ebi.ac.uk/efo/EFO_0004585
7442||14970||complete blood cell count||http://www.ebi.ac.uk/efo/EFO_0004586
7443||10652||obsolete_alanine transaminase measurement||http://www.ebi.ac.uk/efo/EFO_0004583
7444||14970||mean platelet volume||http://www.ebi.ac.uk/efo/EFO_0004584
7445||14970||interleukin 18 measurement||http://www.ebi.ac.uk/efo/EFO_0004581
7447||5502||Staphylococcus aureus subsp. aureus USA300||http://purl.obolibrary.org/obo/NCBITaxon_367830
7446||9271||Congenital primary megaureter, obstructed form||http://www.orpha.net/ORDO/Orphanet_238646
7449||14970||liver enzyme measurement||http://www.ebi.ac.uk/efo/EFO_0004582
7448||11456||Partial duplication of chromosome 6||http://www.orpha.net/ORDO/Orphanet_262628
7450||2672||basibranchial bone||http://purl.obolibrary.org/obo/UBERON_0004740
7451||13689||cleithrum||http://purl.obolibrary.org/obo/UBERON_0004741
7452||9271||Primary megaureter, adult-onset form||http://www.orpha.net/ORDO/Orphanet_238642
7453||13689||dentary||http://purl.obolibrary.org/obo/UBERON_0004742
7454||4727||Oculocerebrorenal syndrome||http://www.orpha.net/ORDO/Orphanet_534
7455||1433||Miller-Dieker syndrome||http://www.orpha.net/ORDO/Orphanet_531
7456||8700||brachial circumference||http://www.ebi.ac.uk/efo/EFO_0004589
7457||5317||Lipoid proteinosis||http://www.orpha.net/ORDO/Orphanet_530
7458||10732||Lymphangioleiomyomatosis||http://www.orpha.net/ORDO/Orphanet_538
7460||33||childhood onset asthma||http://www.ebi.ac.uk/efo/EFO_0004591
7459||7463||purine nucleoside monophosphate biosynthetic process||http://purl.obolibrary.org/obo/GO_0009127
7461||10652||obsolete_aspirin induced asthma||http://www.ebi.ac.uk/efo/EFO_0004590
7462||5927||Amish infantile epilepsy syndrome||http://www.orpha.net/ORDO/Orphanet_171714
7463||7464||purine nucleoside monophosphate metabolic process||http://purl.obolibrary.org/obo/GO_0009126
7464||2288||nucleoside monophosphate metabolic process||http://purl.obolibrary.org/obo/GO_0009123
7466||2482||nucleoside monophosphate biosynthetic process||http://purl.obolibrary.org/obo/GO_0009124
7465||5306||Cutis laxa-Marfanoid syndrome||http://www.orpha.net/ORDO/Orphanet_171719
7467||1391||diabetes mellitus type 2 associated cataract||http://www.ebi.ac.uk/efo/EFO_0004596
7468||14583||variant Creutzfeld Jacob disease||http://www.ebi.ac.uk/efo/EFO_0004597
7469||3790||Familial hemophagocytic lymphohistiocytosis||http://www.orpha.net/ORDO/Orphanet_540
7470||1790||acute graft vs. host disease||http://www.ebi.ac.uk/efo/EFO_0004599
7471||10652||obsolete_thyroid stimulating hormone measurement||http://www.ebi.ac.uk/efo/EFO_0004592
7472||1398||gestational diabetes||http://www.ebi.ac.uk/efo/EFO_0004593
7473||9394||childhood eosinophilic esophagitis||http://www.ebi.ac.uk/efo/EFO_0004594
7475||5295||HIV mother to child transmission||http://www.ebi.ac.uk/efo/EFO_0004595
7474||9271||Congenital primary megaureter, nonrefluxing and unobstructed form||http://www.orpha.net/ORDO/Orphanet_238654
7476||11456||Partial duplication of chromosome 8||http://www.orpha.net/ORDO/Orphanet_262638
7477||9271||Congenital primary megaureter, refluxing form||http://www.orpha.net/ORDO/Orphanet_238650
7478||11456||Partial duplication of chromosome 7||http://www.orpha.net/ORDO/Orphanet_262633
7479||7481||ribonucleoside metabolic process||http://purl.obolibrary.org/obo/GO_0009119
7480||4139||Microcephaly - polymicrogyria - corpus callosum agenesis||http://www.orpha.net/ORDO/Orphanet_171703
7481||504||nucleoside metabolic process||http://purl.obolibrary.org/obo/GO_0009116
7482||2288||nucleotide metabolic process||http://purl.obolibrary.org/obo/GO_0009117
7483||4028||Short stature-delayed bone age due to thyroid hormone metabolism deficiency||http://www.orpha.net/ORDO/Orphanet_171706
7484||1603||Male infertility due to globozoospermia||http://www.orpha.net/ORDO/Orphanet_171709
7486||1568||Isolated congenital hypogonadotropic hypogonadism||http://www.orpha.net/ORDO/Orphanet_238666
7485||203||African||http://www.ebi.ac.uk/efo/EFO_0004561
7487||1761||cryptorchidism||http://www.ebi.ac.uk/efo/EFO_0004562
7488||14970||serum IgG measurement||http://www.ebi.ac.uk/efo/EFO_0004565
7490||1228||purine ribonucleotide biosynthetic process||http://purl.obolibrary.org/obo/GO_0009152
7489||5295||body weight gain||http://www.ebi.ac.uk/efo/EFO_0004566
7491||3980||Sigma 1278b||http://www.ebi.ac.uk/efo/EFO_0004563
7492||14165||pericardial fat||http://www.ebi.ac.uk/efo/EFO_0004564
7493||1227||purine ribonucleotide metabolic process||http://purl.obolibrary.org/obo/GO_0009150
7495||14970||brain serotonin transporter measurement||http://www.ebi.ac.uk/efo/EFO_0004569
7494||6290||Maple syrup urine disease||http://www.orpha.net/ORDO/Orphanet_511
7496||11385||Lesch-Nyhan syndrome||http://www.orpha.net/ORDO/Orphanet_510
7497||11456||Partial trisomy/tetrasomy of chromosome 9||http://www.orpha.net/ORDO/Orphanet_262643
7498||7489||anti-psychotic drug related weight gain||http://www.ebi.ac.uk/efo/EFO_0004567
7499||14970||serum non-albumin protein measurement||http://www.ebi.ac.uk/efo/EFO_0004568
7500||11456||Partial duplication of chromosome 10||http://www.orpha.net/ORDO/Orphanet_262648
7501||2454||Metachromatic leukodystrophy||http://www.orpha.net/ORDO/Orphanet_512
7502||7503||purine nucleoside triphosphate biosynthetic process||http://purl.obolibrary.org/obo/GO_0009145
7503||7512||purine nucleoside triphosphate metabolic process||http://purl.obolibrary.org/obo/GO_0009144
7504||14970||bilirubin measurement||http://www.ebi.ac.uk/efo/EFO_0004570
7505||14970||butyrylcholinesterase measurement||http://www.ebi.ac.uk/efo/EFO_0004571
7506||14970||C4BP measurement||http://www.ebi.ac.uk/efo/EFO_0004572
7507||14970||chemerin measurement||http://www.ebi.ac.uk/efo/EFO_0004573
7508||14970||total cholesterol measurement||http://www.ebi.ac.uk/efo/EFO_0004574
7509||14970||e-selectin measurement||http://www.ebi.ac.uk/efo/EFO_0004575
7510||14970||fetal hemoglobin measurement||http://www.ebi.ac.uk/efo/EFO_0004576
7511||2482||nucleoside triphosphate biosynthetic process||http://purl.obolibrary.org/obo/GO_0009142
7512||2288||nucleoside triphosphate metabolic process||http://purl.obolibrary.org/obo/GO_0009141
7513||5079||infant head circumference||http://www.ebi.ac.uk/efo/EFO_0004577
7514||14970||homocysteine measurement||http://www.ebi.ac.uk/efo/EFO_0004578
7517||14970||serum IgE measurement||http://www.ebi.ac.uk/efo/EFO_0004579
7515||11456||Partial duplication of chromosome 11||http://www.orpha.net/ORDO/Orphanet_262653
7516||6989||Isolated thyrotropin-releasing hormone deficiency||http://www.orpha.net/ORDO/Orphanet_238670
7518||11456||Partial trisomy/tetrasomy of the short arm of chromosome 12||http://www.orpha.net/ORDO/Orphanet_262658
7519||4803||Li-Fraumeni syndrome||http://www.orpha.net/ORDO/Orphanet_524
7521||2713||Hereditary leiomyomatosis and renal cell cancer||http://www.orpha.net/ORDO/Orphanet_523
7520||10994||angiotensin II||http://purl.obolibrary.org/obo/CHEBI_48432
7522||10740||Liddle syndrome||http://www.orpha.net/ORDO/Orphanet_526
7523||1393||Berardinelli-Seip congenital lipodystrophy||http://www.orpha.net/ORDO/Orphanet_528
7524||5868||Roch-Leri mesosomatous lipomatosis||http://www.orpha.net/ORDO/Orphanet_529
7525||5877||White sponge nevus||http://www.orpha.net/ORDO/Orphanet_171723
7526||618||pharyngula stage||http://purl.obolibrary.org/obo/UBERON_0004707
7527||9613||interleukin 18 (Homo sapiens)||http://www.ebi.ac.uk/efo/EFO_0004580
7528||9382||primordial germ cell||http://purl.obolibrary.org/obo/CL_0000670
7529||1014||planned process||http://www.ebi.ac.uk/efo/EFO_0004542
7530||14970||A1C measurement||http://www.ebi.ac.uk/efo/EFO_0004541
7531||1391||chronic fatigue syndrome||http://www.ebi.ac.uk/efo/EFO_0004540
7532||1826||Noccaea caerulescens||http://purl.obolibrary.org/obo/NCBITaxon_107243
7533||772||glutamatergic neuron||http://purl.obolibrary.org/obo/CL_0000679
7534||7860||Lafora disease||http://www.orpha.net/ORDO/Orphanet_501
7535||2252||Langer-Giedion syndrome||http://www.orpha.net/ORDO/Orphanet_502
7536||5300||Autosomal dominant Larsen syndrome||http://www.orpha.net/ORDO/Orphanet_503
7537||14970||population measurement||http://www.ebi.ac.uk/efo/EFO_0004557
7538||14970||antibody measurement||http://www.ebi.ac.uk/efo/EFO_0004556
7540||1022||Schmidtea mediterranea||http://purl.obolibrary.org/obo/NCBITaxon_79327
7539||10256||sodium chloride regimen||http://purl.obolibrary.org/obo/EO_0007048
7541||5317||LEOPARD syndrome||http://www.orpha.net/ORDO/Orphanet_500
7542||14970||glycoprotein measurement||http://www.ebi.ac.uk/efo/EFO_0004555
7543||10994||olmesartan||http://purl.obolibrary.org/obo/CHEBI_48416
7544||14970||genomic measurement||http://www.ebi.ac.uk/efo/EFO_0004554
7545||8191||scopolamine methobromide||http://purl.obolibrary.org/obo/CHEBI_61276
7546||10547||Beckwith-Wiedemann syndrome due to NSD1 mutation||http://www.orpha.net/ORDO/Orphanet_238613
7548||14970||amygdala reactivity measurement||http://www.ebi.ac.uk/efo/EFO_0004550
7547||5502||Salmonella enterica subsp. enterica serovar Abortusovis||http://purl.obolibrary.org/obo/NCBITaxon_53961
7549||772||pericyte||http://purl.obolibrary.org/obo/CL_0000669
7550||8793||Congenital muscular dystrophy with hyperlaxity||http://www.orpha.net/ORDO/Orphanet_371007
7551||288||Leigh syndrome||http://www.orpha.net/ORDO/Orphanet_506
7553||321||Graham Little-Piccardi-Lassueur syndrome||http://www.orpha.net/ORDO/Orphanet_505
7552||1022||Oncorhynchus gorbuscha||http://purl.obolibrary.org/obo/NCBITaxon_8017
7555||322||Leprechaunism||http://www.orpha.net/ORDO/Orphanet_508
7554||1022||Osmerus mordax||http://purl.obolibrary.org/obo/NCBITaxon_8014
7556||8574||mean corpuscular volume||http://www.ebi.ac.uk/efo/EFO_0004526
7558||10197||Obesity due to melanocortin 4 receptor deficiency||http://www.orpha.net/ORDO/Orphanet_71529
7557||10652||obsolete_bitter taste sensitivity||http://www.ebi.ac.uk/efo/EFO_0004525
7559||10652||obsolete_hemoglobin E disease||http://www.ebi.ac.uk/efo/EFO_0004523
7560||1022||Oncorhynchus kisutch||http://purl.obolibrary.org/obo/NCBITaxon_8019
7561||14970||lipid measurement||http://www.ebi.ac.uk/efo/EFO_0004529
7562||8574||mean corpuscular hemoglobin concentration||http://www.ebi.ac.uk/efo/EFO_0004528
7563||8574||mean corpuscular hemoglobin||http://www.ebi.ac.uk/efo/EFO_0004527
7565||14970||adhesion molecule measurement||http://www.ebi.ac.uk/efo/EFO_0004522
7564||10197||Obesity due to pro-opiomelanocortin deficiency||http://www.orpha.net/ORDO/Orphanet_71526
7566||8047||adhesion factor||http://www.ebi.ac.uk/efo/EFO_0004521
7567||14970||ICAM-1 measurement||http://www.ebi.ac.uk/efo/EFO_0004520
7568||1307||Obesity due to prohormone convertase I deficiency||http://www.orpha.net/ORDO/Orphanet_71528
7569||3454||glycoprotein biosynthetic process||http://purl.obolibrary.org/obo/GO_0009101
7570||1022||Oncorhynchus mykiss||http://purl.obolibrary.org/obo/NCBITaxon_8022
7571||1022||Oncorhynchus nerka||http://purl.obolibrary.org/obo/NCBITaxon_8023
7572||14970||serum albumin measurement||http://www.ebi.ac.uk/efo/EFO_0004535
7573||14970||creatine kinase measurement||http://www.ebi.ac.uk/efo/EFO_0004534
7574||13891||neonatal systemic lupus erthematosus||http://www.ebi.ac.uk/efo/EFO_0004537
7575||14970||total blood protein measurement||http://www.ebi.ac.uk/efo/EFO_0004536
7576||10652||obsolete_bronchopulmonary dysplasia||http://www.ebi.ac.uk/efo/EFO_0004538
7577||2395||Qualitative or quantitative defects of alpha-dystroglycan||http://www.orpha.net/ORDO/Orphanet_371024
7578||14970||urate measurement||http://www.ebi.ac.uk/efo/EFO_0004531
7579||14970||triglyceride measurement||http://www.ebi.ac.uk/efo/EFO_0004530
7580||14970||alkaline phosphatase measurement||http://www.ebi.ac.uk/efo/EFO_0004533
7581||14970||serum gamma-glutamyl transferase measurement||http://www.ebi.ac.uk/efo/EFO_0004532
7582||1022||Salmo salar||http://purl.obolibrary.org/obo/NCBITaxon_8030
7583||1022||Salvelinus fontinalis||http://purl.obolibrary.org/obo/NCBITaxon_8038
7584||4139||Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation||http://www.orpha.net/ORDO/Orphanet_289266
7585||1022||Salvelinus alpinus||http://purl.obolibrary.org/obo/NCBITaxon_8036
7586||1022||Salmo trutta||http://purl.obolibrary.org/obo/NCBITaxon_8032
7587||1826||Pyrus hybrid cultivar||http://purl.obolibrary.org/obo/NCBITaxon_239770
7588||772||erythroblast||http://purl.obolibrary.org/obo/CL_0000765
7589||7731||myeloid leukocyte||http://purl.obolibrary.org/obo/CL_0000766
7590||14578||basophil||http://purl.obolibrary.org/obo/CL_0000767
7591||7590||immature basophil||http://purl.obolibrary.org/obo/CL_0000768
7592||7591||basophilic metamyelocyte||http://purl.obolibrary.org/obo/CL_0000769
7593||1414||Autosomal dominant limb-girdle muscular dystrophy type 1E||http://www.orpha.net/ORDO/Orphanet_34517
7595||1415||Autosomal recessive limb-girdle muscular dystrophy type 2I||http://www.orpha.net/ORDO/Orphanet_34515
7594||8903||Congenital multicore myopathy with external ophthalmoplegia||http://www.orpha.net/ORDO/Orphanet_98905
7596||3804||Congenital myopathy with excess of thin filaments||http://www.orpha.net/ORDO/Orphanet_98904
7597||1414||Autosomal dominant limb-girdle muscular dystrophy type 1D||http://www.orpha.net/ORDO/Orphanet_34516
7598||9742||Dorfman-Chanarin disease||http://www.orpha.net/ORDO/Orphanet_98907
7599||266||Glycogen storage disease due to liver glycogen phosphorylase deficiency||http://www.orpha.net/ORDO/Orphanet_369
7600||1415||Autosomal recessive limb-girdle muscular dystrophy type 2G||http://www.orpha.net/ORDO/Orphanet_34514
7601||3349||CS57824||http://www.ebi.ac.uk/efo/EFO_0000132
7603||6572||Glycogen storage disease due to muscle glycogen phosphorylase deficiency||http://www.orpha.net/ORDO/Orphanet_368
7602||7611||nucleated thrombocyte||http://purl.obolibrary.org/obo/CL_0000762
7604||3349||CS57825||http://www.ebi.ac.uk/efo/EFO_0000133
7605||266||Glycogen storage disease due to glycogen branching enzyme deficiency||http://www.orpha.net/ORDO/Orphanet_367
7607||4261||Glycogen storage disease due to glycogen debranching enzyme deficiency||http://www.orpha.net/ORDO/Orphanet_366
7608||3349||CS57822||http://www.ebi.ac.uk/efo/EFO_0000130
7606||7611||erythroid lineage cell||http://purl.obolibrary.org/obo/CL_0000764
7610||4261||Glycogen storage disease due to acid maltase deficiency||http://www.orpha.net/ORDO/Orphanet_365
7609||3606||Amish nemaline myopathy||http://www.orpha.net/ORDO/Orphanet_98902
7612||3349||CS57823||http://www.ebi.ac.uk/efo/EFO_0000131
7611||772||myeloid cell||http://purl.obolibrary.org/obo/CL_0000763
7614||3349||CS57828||http://www.ebi.ac.uk/efo/EFO_0000136
7613||266||Glycogen storage disease due to glucose-6-phosphatase deficiency||http://www.orpha.net/ORDO/Orphanet_364
7615||3349||CS57834||http://www.ebi.ac.uk/efo/EFO_0000137
7616||3349||CS57826||http://www.ebi.ac.uk/efo/EFO_0000134
7618||3349||CS57827||http://www.ebi.ac.uk/efo/EFO_0000135
7619||212||Familial glucocorticoid deficiency||http://www.orpha.net/ORDO/Orphanet_361
7617||9696||Congenital fibrosis of extraocular muscles||http://www.orpha.net/ORDO/Orphanet_45358
7620||3766||Desminopathy||http://www.orpha.net/ORDO/Orphanet_98909
7621||10387||Neutral lipid storage myopathy||http://www.orpha.net/ORDO/Orphanet_98908
7622||3349||CS57835||http://www.ebi.ac.uk/efo/EFO_0000138
7623||3349||CS57836||http://www.ebi.ac.uk/efo/EFO_0000139
7624||14588||mononuclear osteoclast||http://purl.obolibrary.org/obo/CL_0000778
7625||14588||multinuclear osteoclast||http://purl.obolibrary.org/obo/CL_0000779
7626||7637||immature neutrophil||http://purl.obolibrary.org/obo/CL_0000776
7627||772||mesangial phagocyte||http://purl.obolibrary.org/obo/CL_0000777
7628||9102||Autosomal dominant primary hypomagnesemia with hypocalciuria||http://www.orpha.net/ORDO/Orphanet_34528
7630||14578||eosinophil||http://purl.obolibrary.org/obo/CL_0000771
7629||2415||Hereditary glaucoma||http://www.orpha.net/ORDO/Orphanet_359
7631||4810||Gitelman syndrome||http://www.orpha.net/ORDO/Orphanet_358
7632||7591||band form basophil||http://purl.obolibrary.org/obo/CL_0000770
7634||4655||fresh specimen||http://purl.obolibrary.org/obo/OBI_0000971
7633||4810||Familial primary hypomagnesemia||http://www.orpha.net/ORDO/Orphanet_34526
7635||10994||prazosin||http://purl.obolibrary.org/obo/CHEBI_8364
7636||9134||Familial primary hypomagnesemia with normocalciuria and normocalcemia||http://www.orpha.net/ORDO/Orphanet_34527
7637||14578||neutrophil||http://purl.obolibrary.org/obo/CL_0000775
7639||2300||Congenital muscular dystrophy with integrin alpha-7 deficiency||http://www.orpha.net/ORDO/Orphanet_34520
7638||5158||Gaucher disease||http://www.orpha.net/ORDO/Orphanet_355
7641||12358||Distal myopathy with early respiratory muscle involvement||http://www.orpha.net/ORDO/Orphanet_34521
7640||3349||CS57790||http://www.ebi.ac.uk/efo/EFO_0000120
7642||4986||GM1 gangliosidosis||http://www.orpha.net/ORDO/Orphanet_354
7643||7648||band form eosinophil||http://purl.obolibrary.org/obo/CL_0000774
7644||3349||CS57801||http://www.ebi.ac.uk/efo/EFO_0000121
7645||7648||eosinophilic metamyelocyte||http://purl.obolibrary.org/obo/CL_0000773
7646||11556||Gerstmann-Straussler-Scheinker syndrome||http://www.orpha.net/ORDO/Orphanet_356
7647||3349||CS57803||http://www.ebi.ac.uk/efo/EFO_0000122
7648||7630||immature eosinophil||http://purl.obolibrary.org/obo/CL_0000772
7649||3349||CS57807||http://www.ebi.ac.uk/efo/EFO_0000123
7650||6595||Galactosialidosis||http://www.orpha.net/ORDO/Orphanet_351
7651||3349||CS57810||http://www.ebi.ac.uk/efo/EFO_0000124
7652||3349||CS57811||http://www.ebi.ac.uk/efo/EFO_0000125
7653||1415||Autosomal recessive limb-girdle muscular dystrophy type 2C||http://www.orpha.net/ORDO/Orphanet_353
7655||3349||CS57812||http://www.ebi.ac.uk/efo/EFO_0000126
7654||266||Galactosemia||http://www.orpha.net/ORDO/Orphanet_352
7656||3349||CS57813||http://www.ebi.ac.uk/efo/EFO_0000127
7657||3349||CS57816||http://www.ebi.ac.uk/efo/EFO_0000128
7658||3349||CS57820||http://www.ebi.ac.uk/efo/EFO_0000129
7659||10994||ecdysone||http://purl.obolibrary.org/obo/CHEBI_16688
7660||15191||cardiac myocyte||http://purl.obolibrary.org/obo/CL_0000746
7661||3349||CS57875||http://www.ebi.ac.uk/efo/EFO_0000154
7662||2415||Corneal dystrophy||http://www.orpha.net/ORDO/Orphanet_34533
7663||3349||CS57876||http://www.ebi.ac.uk/efo/EFO_0000155
7664||3349||CS57873||http://www.ebi.ac.uk/efo/EFO_0000152
7665||1826||Ribes nigrum||http://purl.obolibrary.org/obo/NCBITaxon_78511
7666||6771||Hirschsprung disease||http://www.orpha.net/ORDO/Orphanet_388
7667||3349||CS57874||http://www.ebi.ac.uk/efo/EFO_0000153
7668||3349||CS57870||http://www.ebi.ac.uk/efo/EFO_0000150
7669||3349||CS57871||http://www.ebi.ac.uk/efo/EFO_0000151
7670||4728||Guanidinoacetate methyltransferase deficiency||http://www.orpha.net/ORDO/Orphanet_382
7671||1831||Griscelli disease||http://www.orpha.net/ORDO/Orphanet_381
7672||13770||Greig cephalopolysyndactyly syndrome||http://www.orpha.net/ORDO/Orphanet_380
7673||3349||CS57886||http://www.ebi.ac.uk/efo/EFO_0000158
7674||3349||CS57890||http://www.ebi.ac.uk/efo/EFO_0000159
7675||4706||Neurodegeneration with brain iron accumulation||http://www.orpha.net/ORDO/Orphanet_385
7676||12318||Palmoplantar keratoderma-sclerodactyly syndrome||http://www.orpha.net/ORDO/Orphanet_384
7677||3349||CS57883||http://www.ebi.ac.uk/efo/EFO_0000156
7679||3349||CS57884||http://www.ebi.ac.uk/efo/EFO_0000157
7678||5239||X-linked mixed deafness with perilymphatic gusher||http://www.orpha.net/ORDO/Orphanet_383
7680||10374||Trisomy 17p||http://www.orpha.net/ORDO/Orphanet_261290
7681||10804||20p12.3 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_261295
7684||3349||CS57842||http://www.ebi.ac.uk/efo/EFO_0000141
7683||4803||Gorlin syndrome||http://www.orpha.net/ORDO/Orphanet_377
7682||9302||Isolated growth hormone deficiency type III||http://www.orpha.net/ORDO/Orphanet_231692
7686||3349||CS57843||http://www.ebi.ac.uk/efo/EFO_0000142
7685||5300||Gordon syndrome||http://www.orpha.net/ORDO/Orphanet_376
7688||3349||CS57847||http://www.ebi.ac.uk/efo/EFO_0000143
7687||5191||Chronic granulomatous disease||http://www.orpha.net/ORDO/Orphanet_379
7689||3349||CS57848||http://www.ebi.ac.uk/efo/EFO_0000144
7690||3349||CS57840||http://www.ebi.ac.uk/efo/EFO_0000140
7691||4655||paraffin specimen||http://purl.obolibrary.org/obo/OBI_0000950
7692||3349||CS57867||http://www.ebi.ac.uk/efo/EFO_0000149
7693||6572||Glycogen storage disease due to muscle phosphofructokinase deficiency||http://www.orpha.net/ORDO/Orphanet_371
7694||6572||Glycogen storage disease due to phosphorylase kinase deficiency||http://www.orpha.net/ORDO/Orphanet_370
7696||3349||CS57850||http://www.ebi.ac.uk/efo/EFO_0000145
7695||2252||Simpson-Golabi-Behmel syndrome||http://www.orpha.net/ORDO/Orphanet_373
7697||3349||CS57854||http://www.ebi.ac.uk/efo/EFO_0000146
7698||3349||CS57858||http://www.ebi.ac.uk/efo/EFO_0000147
7699||3349||CS57859||http://www.ebi.ac.uk/efo/EFO_0000148
7700||4775||Goldenhar syndrome||http://www.orpha.net/ORDO/Orphanet_374
7701||6899||Von Hippel anomaly||http://www.orpha.net/ORDO/Orphanet_98941
7702||10439||Coloboma of eye lens||http://www.orpha.net/ORDO/Orphanet_98943
7704||14537||somatic stem cell||http://purl.obolibrary.org/obo/CL_0000723
7703||10439||Coloboma of choroid and retina||http://www.orpha.net/ORDO/Orphanet_98942
7705||15365||Congenital factor XI deficiency||http://www.orpha.net/ORDO/Orphanet_329
7707||11065||mole per liter||http://www.ebi.ac.uk/efo/EFO_0004381
7706||266||Glycogen storage disease due to liver phosphorylase kinase deficiency||http://www.orpha.net/ORDO/Orphanet_264580
7708||11067||nanogram per liter||http://www.ebi.ac.uk/efo/EFO_0004382
7709||1694||Familial thrombocytosis||http://www.orpha.net/ORDO/Orphanet_71493
7710||11507||milli-International Unit per milliliter||http://www.ebi.ac.uk/efo/EFO_0004379
7712||11067||microgram per day||http://www.ebi.ac.uk/efo/EFO_0004378
7711||5048||Apparent mineralocorticoid excess||http://www.orpha.net/ORDO/Orphanet_320
7713||11067||milligram per deciliter||http://www.ebi.ac.uk/efo/EFO_0004374
7715||11067||milligram per square meter||http://www.ebi.ac.uk/efo/EFO_0004373
7714||3744||extracellular matrix||http://purl.obolibrary.org/obo/GO_0031012
7717||11258||Congenital symblepharon||http://www.orpha.net/ORDO/Orphanet_98948
7716||421||Congenital factor VII deficiency||http://www.orpha.net/ORDO/Orphanet_327
7718||11258||Complete cryptophthalmia||http://www.orpha.net/ORDO/Orphanet_98949
7719||421||Congenital factor X deficiency||http://www.orpha.net/ORDO/Orphanet_328
7720||421||Congenital factor II deficiency||http://www.orpha.net/ORDO/Orphanet_325
7721||15365||Congenital factor V deficiency||http://www.orpha.net/ORDO/Orphanet_326
7722||10439||Coloboma of iris||http://www.orpha.net/ORDO/Orphanet_98944
7723||2454||Fabry disease||http://www.orpha.net/ORDO/Orphanet_324
7724||9680||Coloboma of macula||http://www.orpha.net/ORDO/Orphanet_98945
7725||4014||Multiple osteochondromas||http://www.orpha.net/ORDO/Orphanet_321
7726||9953||Coloboma of eyelid||http://www.orpha.net/ORDO/Orphanet_98946
7727||742||Exstrophy-epispadias complex||http://www.orpha.net/ORDO/Orphanet_322
7728||10439||Coloboma of optic papilla||http://www.orpha.net/ORDO/Orphanet_98947
7729||4655||frozen specimen||http://purl.obolibrary.org/obo/OBI_0000922
7730||4981||labeled specimen||http://purl.obolibrary.org/obo/OBI_0000924
7731||772||leukocyte||http://purl.obolibrary.org/obo/CL_0000738
7732||9302||Isolated growth hormone deficiency type II||http://www.orpha.net/ORDO/Orphanet_231679
7733||11067||microgram per square centimeter||http://www.ebi.ac.uk/efo/EFO_0004370
7734||11067||gram per kilogram per day||http://www.ebi.ac.uk/efo/EFO_0004371
7735||7736||social desirability||http://www.ebi.ac.uk/efo/EFO_0004366
7736||5838||personality trait||http://www.ebi.ac.uk/efo/EFO_0004365
7737||11507||Number of molecules||http://www.ebi.ac.uk/efo/EFO_0004368
7738||4430||induces sterile inflammation||http://www.ebi.ac.uk/efo/EFO_0004367
7739||7943||Primary hypertrophic osteoarthropathy||http://www.orpha.net/ORDO/Orphanet_248095
7740||5295||psychomotor performance||http://www.ebi.ac.uk/efo/EFO_0004362
7741||11618||neurobehavioral manifestations||http://www.ebi.ac.uk/efo/EFO_0004364
7742||8698||information processing speed||http://www.ebi.ac.uk/efo/EFO_0004363
7743||5882||Erythroderma desquamativum||http://www.orpha.net/ORDO/Orphanet_314
7744||5985||Erythrokeratoderma  en cocardes ||http://www.orpha.net/ORDO/Orphanet_315
7745||4601||Progressive symmetric erythrokeratodermia||http://www.orpha.net/ORDO/Orphanet_316
7747||798||Colobomatous microphthalmia||http://www.orpha.net/ORDO/Orphanet_98938
7746||4601||Erythrokeratodermia variabilis||http://www.orpha.net/ORDO/Orphanet_317
7750||5502||Butyrivibrio proteoclasticus B316||http://purl.obolibrary.org/obo/NCBITaxon_515622
7749||8699||Hyperphenylalaninemia||http://www.orpha.net/ORDO/Orphanet_238583
7748||10652||obsolete_microgram per milliliter||http://www.ebi.ac.uk/efo/EFO_0004369
7752||15570||Epidermolytic ichthyosis||http://www.orpha.net/ORDO/Orphanet_312
7751||9302||Isolated growth hormone deficiency type IB||http://www.orpha.net/ORDO/Orphanet_231671
7753||6497||Huntington disease-like 2||http://www.orpha.net/ORDO/Orphanet_98934
7754||9743||Lamellar ichthyosis||http://www.orpha.net/ORDO/Orphanet_313
7755||1826||Zea mays subsp. mays||http://purl.obolibrary.org/obo/NCBITaxon_381124
7756||9288||dopaminergic neuron||http://purl.obolibrary.org/obo/CL_0000700
7757||7117||Partial duplication of the short arm of chromosome 16||http://www.orpha.net/ORDO/Orphanet_262794
7758||6930||Spinal muscular atrophy with respiratory distress type 1||http://www.orpha.net/ORDO/Orphanet_98920
7759||14725||Theiler stage 5||http://www.ebi.ac.uk/efo/EFO_0004397
7760||3349||CS57789||http://www.ebi.ac.uk/efo/EFO_0000119
7761||14725||Theiler stage 4||http://www.ebi.ac.uk/efo/EFO_0004396
7763||3349||CS57785||http://www.ebi.ac.uk/efo/EFO_0000118
7762||8365||Familial clubfoot due to 17q23.1q23.2 microduplication||http://www.orpha.net/ORDO/Orphanet_238578
7764||14725||Theiler stage 3||http://www.ebi.ac.uk/efo/EFO_0004395
7765||3349||CS57783||http://www.ebi.ac.uk/efo/EFO_0000117
7766||14725||Theiler stage 2||http://www.ebi.ac.uk/efo/EFO_0004394
7767||3349||CS57779||http://www.ebi.ac.uk/efo/EFO_0000116
7768||3349||CS57778||http://www.ebi.ac.uk/efo/EFO_0000115
7769||3349||CS57777||http://www.ebi.ac.uk/efo/EFO_0000114
7770||3229||Familial Mediterranean fever||http://www.orpha.net/ORDO/Orphanet_342
7772||14725||Theiler stage 7||http://www.ebi.ac.uk/efo/EFO_0004399
7771||3349||CS57776||http://www.ebi.ac.uk/efo/EFO_0000113
7774||14725||Theiler stage 6||http://www.ebi.ac.uk/efo/EFO_0004398
7773||3349||CS57771||http://www.ebi.ac.uk/efo/EFO_0000112
7775||3349||CS57770||http://www.ebi.ac.uk/efo/EFO_0000111
7776||10652||obsolete_spinal cord||http://www.ebi.ac.uk/efo/EFO_0000110
7777||3229||Hyperimmunoglobulinemia D with periodic fever||http://www.orpha.net/ORDO/Orphanet_343
7778||4267||Fucosidosis||http://www.orpha.net/ORDO/Orphanet_349
7779||3019||Frasier syndrome||http://www.orpha.net/ORDO/Orphanet_347
7780||9302||Isolated growth hormone deficiency type IA||http://www.orpha.net/ORDO/Orphanet_231662
7781||6321||Fructose-1,6-bisphosphatase deficiency||http://www.orpha.net/ORDO/Orphanet_348
7782||3768||Alpha-crystallinopathy||http://www.orpha.net/ORDO/Orphanet_98910
7783||8937||cumulus cell||http://purl.obolibrary.org/obo/CL_0000711
7785||2552||mouse postnatal||http://www.ebi.ac.uk/efo/EFO_0004390
7784||10652||obsolete_CNS brain striatum MMHCC||http://www.ebi.ac.uk/efo/EFO_0000109
7786||7785||Theiler stage 27||http://www.ebi.ac.uk/efo/EFO_0004391
7787||14725||Theiler stage 1||http://www.ebi.ac.uk/efo/EFO_0004393
7789||11067||weight percent by volume||http://www.ebi.ac.uk/efo/EFO_0004384
7788||10652||obsolete_CNS brain hippocampus MMHCC||http://www.ebi.ac.uk/efo/EFO_0000106
7791||13999||Autosomal recessive early-onset inflammatory bowel disease||http://www.orpha.net/ORDO/Orphanet_238569
7792||11067||nanogram per microliter||http://www.ebi.ac.uk/efo/EFO_0004383
7790||10652||obsolete_CNS brain cerebellum MMHCC||http://www.ebi.ac.uk/efo/EFO_0000105
7795||15368||progesterone receptor binding||http://purl.obolibrary.org/obo/GO_0033142
7793||11067||total particulate matter per liter||http://www.ebi.ac.uk/efo/EFO_0004386
7796||10994||castasterone||http://purl.obolibrary.org/obo/CHEBI_23051
7794||10652||obsolete_olfactory lobe||http://www.ebi.ac.uk/efo/EFO_0000108
7798||11067||picogram per milliliter||http://www.ebi.ac.uk/efo/EFO_0004385
7797||10652||obsolete_hypothalamus||http://www.ebi.ac.uk/efo/EFO_0000107
7799||11067||picomole per 10 6 cells||http://www.ebi.ac.uk/efo/EFO_0004388
7800||10652||obsolete_B lymphocyte_7800||http://www.ebi.ac.uk/efo/EFO_0000102
7801||11506||inch||http://www.ebi.ac.uk/efo/EFO_0004387
7802||15365||Congenital factor XII deficiency||http://www.orpha.net/ORDO/Orphanet_330
7803||15365||Congenital factor XIII deficiency||http://www.orpha.net/ORDO/Orphanet_331
7804||770||UCH-1||http://www.ebi.ac.uk/efo/EFO_0004389
7805||10652||obsolete_Becker s muscular dystrophy||http://www.ebi.ac.uk/efo/EFO_0000103
7806||10994||5-fluorouracil||http://purl.obolibrary.org/obo/CHEBI_46345
7810||4261||Glycogen storage disease due to LAMP-2 deficiency||http://www.orpha.net/ORDO/Orphanet_34587
7808||6294||Congenital intrinsic factor deficiency||http://www.orpha.net/ORDO/Orphanet_332
7809||7515||Partial duplication of the short arm of chromosome 11||http://www.orpha.net/ORDO/Orphanet_262785
7811||8916||Postsynaptic congenital myasthenic syndromes||http://www.orpha.net/ORDO/Orphanet_98913
7807||10994||cathasterone||http://purl.obolibrary.org/obo/CHEBI_23057
7812||5868||Farber lipogranulomatosis||http://www.orpha.net/ORDO/Orphanet_333
7813||8916||Presynaptic congenital myasthenic syndromes||http://www.orpha.net/ORDO/Orphanet_98914
7816||3980||BY5251||http://www.ebi.ac.uk/efo/EFO_0000100
7814||2730||Distal myotilinopathy||http://www.orpha.net/ORDO/Orphanet_98911
7815||15||Familial atrial fibrillation||http://www.orpha.net/ORDO/Orphanet_334
7817||15365||Congenital fibrinogen deficiency||http://www.orpha.net/ORDO/Orphanet_335
7818||3741||Late-onset distal myopathy, Markesbery-Griggs type||http://www.orpha.net/ORDO/Orphanet_98912
7819||1235||Fibrodysplasia ossificans progressiva||http://www.orpha.net/ORDO/Orphanet_337
7820||5877||Familial multiple fibrofolliculoma||http://www.orpha.net/ORDO/Orphanet_338
7821||8916||Synaptic congenital myasthenic syndromes||http://www.orpha.net/ORDO/Orphanet_98915
7822||770||ND02579||http://purl.obolibrary.org/obo/CLO_0014404
7823||5504||Primary dystonia, DYT21 type||http://www.orpha.net/ORDO/Orphanet_306734
7824||5502||Shigella sonnei||http://purl.obolibrary.org/obo/NCBITaxon_624
7825||5502||Shigella flexneri||http://purl.obolibrary.org/obo/NCBITaxon_623
7826||9753||Abnormality of gastrointestinal vasculature||http://purl.obolibrary.org/obo/HP_0004296
7827||1826||Hordeum vulgare subsp. spontaneum||http://purl.obolibrary.org/obo/NCBITaxon_77009
7828||3866||Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome||http://www.orpha.net/ORDO/Orphanet_37042
7829||238||Immunodeficiency by defective expression of HLA class 1||http://www.orpha.net/ORDO/Orphanet_34592
7830||5502||Agrobacterium larrymoorei||http://purl.obolibrary.org/obo/NCBITaxon_160699
7831||7757||16p13.11 microduplication syndrome||http://www.orpha.net/ORDO/Orphanet_261243
7832||770||GM17249||http://purl.obolibrary.org/obo/CLO_0014409
7833||770||GM17248||http://purl.obolibrary.org/obo/CLO_0014408
7834||770||GM17245||http://purl.obolibrary.org/obo/CLO_0014415
7835||770||GM17246||http://purl.obolibrary.org/obo/CLO_0014416
7836||770||GM17247||http://purl.obolibrary.org/obo/CLO_0014417
7838||770||GM17241||http://purl.obolibrary.org/obo/CLO_0014411
7837||5502||Salmonella enterica subsp. enterica serovar Heidelberg||http://purl.obolibrary.org/obo/NCBITaxon_611
7839||770||GM17242||http://purl.obolibrary.org/obo/CLO_0014412
7841||770||GM17243||http://purl.obolibrary.org/obo/CLO_0014413
7840||10980||16p13.11 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_261236
7842||770||GM17244||http://purl.obolibrary.org/obo/CLO_0014414
7843||770||GM17240||http://purl.obolibrary.org/obo/CLO_0014410
7845||5502||Leptospira interrogans serovar Lai str. 56601||http://purl.obolibrary.org/obo/NCBITaxon_189518
7844||9649||ceramide||http://purl.obolibrary.org/obo/CHEBI_17761
7846||5048||Corticosteroid-binding globulin deficiency||http://www.orpha.net/ORDO/Orphanet_199247
7847||7849||Non progressive epilepsy and/or ataxia with myoclonus as a major feature||http://www.orpha.net/ORDO/Orphanet_306759
7848||10677||14q11.2 microduplication syndrome||http://www.orpha.net/ORDO/Orphanet_261229
7849||9919||Epilepsy and/or ataxia with myoclonus as major feature||http://www.orpha.net/ORDO/Orphanet_306756
7850||10732||Pulmonary capillary hemangiomatosis||http://www.orpha.net/ORDO/Orphanet_199241
7851||13496||Choristoneura fumiferana MNPV||http://purl.obolibrary.org/obo/NCBITaxon_208973
7852||9905||Primary myoclonus||http://www.orpha.net/ORDO/Orphanet_306750
7853||10994||allyl alcohol||http://purl.obolibrary.org/obo/CHEBI_16605
7854||4701||Distal 16p11.2 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_261222
7855||10994||trichloroethylene||http://purl.obolibrary.org/obo/CHEBI_16602
7856||5502||Yersinia pseudotuberculosis||http://purl.obolibrary.org/obo/NCBITaxon_633
7857||5502||Yersinia pestis||http://purl.obolibrary.org/obo/NCBITaxon_632
7858||4732||Rare paroxysmal movement disorder||http://www.orpha.net/ORDO/Orphanet_306768
7859||5502||Yersinia enterocolitica||http://purl.obolibrary.org/obo/NCBITaxon_630
7861||5502||Pseudomonas aeruginosa PAO1||http://purl.obolibrary.org/obo/NCBITaxon_208964
7860||7849||Progressive epilepsy and/or ataxia with myoclonus as a major feature||http://www.orpha.net/ORDO/Orphanet_306762
7862||4732||Motor stereotypies||http://www.orpha.net/ORDO/Orphanet_306765
7863||5502||Pseudomonas aeruginosa UCBPP-PA14||http://purl.obolibrary.org/obo/NCBITaxon_208963
7864||10994||N,N-dimethylformamide||http://purl.obolibrary.org/obo/CHEBI_17741
7865||10994||diethylhexyl phthalate||http://purl.obolibrary.org/obo/CHEBI_17747
7866||1022||Emiliania huxleyi CCMP1516||http://purl.obolibrary.org/obo/NCBITaxon_280463
7867||10980||16p11.2p12.2 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_261211
7868||14235||Goto-Kakizaki||http://www.ebi.ac.uk/efo/EFO_0000179
7869||1006||gastric carcinoma||http://www.ebi.ac.uk/efo/EFO_0000178
7870||1022||Paxillus involutus||http://purl.obolibrary.org/obo/NCBITaxon_71150
7871||5502||Vibrio alginolyticus||http://purl.obolibrary.org/obo/NCBITaxon_663
7872||2656||DEL cells||http://www.ebi.ac.uk/efo/EFO_0000170
7873||10652||obsolete_Ewing family tumor||http://www.ebi.ac.uk/efo/EFO_0000173
7874||10994||carbohydrate||http://purl.obolibrary.org/obo/CHEBI_23008
7875||10652||obsolete_Daudi Burkitt s lymphoma cell line||http://www.ebi.ac.uk/efo/EFO_0000172
7876||3980||FUM1||http://www.ebi.ac.uk/efo/EFO_0000175
7877||2002||Ewing sarcoma||http://www.ebi.ac.uk/efo/EFO_0000174
7878||14235||Fischer 344||http://www.ebi.ac.uk/efo/EFO_0000176
7879||5502||Vibrio cholerae||http://purl.obolibrary.org/obo/NCBITaxon_666
7880||2712||HIV-1 infection||http://www.ebi.ac.uk/efo/EFO_0000180
7881||10994||methanol||http://purl.obolibrary.org/obo/CHEBI_17790
7882||10652||obsolete_chronic lymphocytic leukemia||http://www.ebi.ac.uk/efo/EFO_0000169
7885||1826||Leymus triticoides||http://purl.obolibrary.org/obo/NCBITaxon_86021
7883||5287||Classical homocystinuria||http://www.orpha.net/ORDO/Orphanet_394
7884||10652||obsolete_CTL sensitivity||http://www.ebi.ac.uk/efo/EFO_0000168
7887||3349||CS8581||http://www.ebi.ac.uk/efo/EFO_0000167
7886||2454||Homocystinuria due to methylene tetrahydrofolate reductase deficiency||http://www.orpha.net/ORDO/Orphanet_395
7888||15||Holt-Oram syndrome||http://www.orpha.net/ORDO/Orphanet_392
7889||5409||46,XX testicular disorder of sex development||http://www.orpha.net/ORDO/Orphanet_393
7890||3349||CS57904||http://www.ebi.ac.uk/efo/EFO_0000162
7891||3349||CS57901||http://www.ebi.ac.uk/efo/EFO_0000161
7892||3349||CS57896||http://www.ebi.ac.uk/efo/EFO_0000160
7893||5868||Familial multiple lipomatosis||http://www.orpha.net/ORDO/Orphanet_199276
7894||3349||CS57924||http://www.ebi.ac.uk/efo/EFO_0000166
7895||5483||17q23.1q23.2 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_261279
7897||3349||CS57923||http://www.ebi.ac.uk/efo/EFO_0000165
7896||5868||Familial angiolipomatosis||http://www.orpha.net/ORDO/Orphanet_199279
7898||3349||CS57908||http://www.ebi.ac.uk/efo/EFO_0000164
7901||13496||Lake Victoria marburgvirus - Angola2005||http://purl.obolibrary.org/obo/NCBITaxon_378830
7900||3349||CS57905||http://www.ebi.ac.uk/efo/EFO_0000163
7899||7918||Huntington disease||http://www.orpha.net/ORDO/Orphanet_399
7902||9899||Frontotemporal neurodegeneration with movement disorder||http://www.orpha.net/ORDO/Orphanet_306708
7903||10641||17q12 microduplication syndrome||http://www.orpha.net/ORDO/Orphanet_261272
7904||1826||Leymus cinereus||http://purl.obolibrary.org/obo/NCBITaxon_86020
7905||9918||Harlequin syndrome||http://www.orpha.net/ORDO/Orphanet_199282
7906||970||mucinous carcinoma||http://www.ebi.ac.uk/efo/EFO_0000197
7908||1006||metastatic prostate cancer||http://www.ebi.ac.uk/efo/EFO_0000196
7907||5928||Chilblain lupus||http://www.orpha.net/ORDO/Orphanet_90280
7910||2860||oral squamous cell carcinoma||http://www.ebi.ac.uk/efo/EFO_0000199
7909||1826||Eucalyptus grandis||http://purl.obolibrary.org/obo/NCBITaxon_71139
7911||15424||myelodysplastic syndrome||http://www.ebi.ac.uk/efo/EFO_0000198
7912||10652||obsolete_MMHCC part||http://www.ebi.ac.uk/efo/EFO_0000193
7913||10652||obsolete_MELAS syndrome||http://www.ebi.ac.uk/efo/EFO_0000192
7914||1485||metabolic syndrome||http://www.ebi.ac.uk/efo/EFO_0000195
7915||8656||Hereditary hypercarotenemia and vitamin A deficiency||http://www.orpha.net/ORDO/Orphanet_199285
7916||10652||obsolete_malignant peripheral nerve sheath tumor class||http://www.ebi.ac.uk/efo/EFO_0000194
7917||5483||17q12 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_261265
7918||4732||Neurodegenerative disease with chorea||http://www.orpha.net/ORDO/Orphanet_306719
7919||12737||Cervicothoracic spina bifida cystica||http://www.orpha.net/ORDO/Orphanet_268766
7920||12737||Cervical spina bifida cystica||http://www.orpha.net/ORDO/Orphanet_268762
7921||10652||obsolete_liver heptocellular carcinoma||http://www.ebi.ac.uk/efo/EFO_0000189
7922||10997||Distal 17p13.3 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_261257
7923||10652||obsolete_liver carcinoma||http://www.ebi.ac.uk/efo/EFO_0000188
7924||772||Kaposi s sarcoma cell||http://www.ebi.ac.uk/efo/EFO_0000187
7925||970||invasive ductal carcinoma||http://www.ebi.ac.uk/efo/EFO_0000186
7926||10652||obsolete_infiltrating lobular carcinoma||http://www.ebi.ac.uk/efo/EFO_0000185
7928||4142||Congenital isolated ACTH deficiency||http://www.orpha.net/ORDO/Orphanet_199296
7929||5502||Vibrio vulnificus||http://purl.obolibrary.org/obo/NCBITaxon_672
7927||10652||obsolete_infiltrating ductal carcinoma||http://www.ebi.ac.uk/efo/EFO_0000184
7930||1497||Hodgkins lymphoma||http://www.ebi.ac.uk/efo/EFO_0000183
7931||1006||hepatocellular carcinoma||http://www.ebi.ac.uk/efo/EFO_0000182
7932||2860||head and neck squamous cell carcinoma||http://www.ebi.ac.uk/efo/EFO_0000181
7933||10652||obsolete_lymphoblastic leukemia MOLT-4||http://www.ebi.ac.uk/efo/EFO_0000190
7934||12737||Upper thoracic spina bifida cystica||http://www.orpha.net/ORDO/Orphanet_268770
7935||1497||MALT lymphoma||http://www.ebi.ac.uk/efo/EFO_0000191
7936||5472||16q24.3 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_261250
7937||5502||Vibrio parahaemolyticus||http://purl.obolibrary.org/obo/NCBITaxon_670
7938||7944||Episodic ataxia type 5||http://www.orpha.net/ORDO/Orphanet_211067
7939||1186||Primary osteolysis||http://www.orpha.net/ORDO/Orphanet_93449
7940||4734||Lysosomal storage disease with skeletal involvement||http://www.orpha.net/ORDO/Orphanet_93448
7941||1186||Primary bone dysplasia with defective bone mineralization||http://www.orpha.net/ORDO/Orphanet_93447
7942||1186||Primary bone dysplasia with decreased bone density||http://www.orpha.net/ORDO/Orphanet_93446
7943||1186||Primary bone dysplasia with increased bone density||http://www.orpha.net/ORDO/Orphanet_93444
7944||4692||Hereditary episodic ataxia||http://www.orpha.net/ORDO/Orphanet_211062
7945||6573||metabolite role||http://purl.obolibrary.org/obo/CHEBI_25212
7946||1186||Chondrodysplasia punctata||http://www.orpha.net/ORDO/Orphanet_93442
7947||7943||Neonatal osteosclerotic dysplasia||http://www.orpha.net/ORDO/Orphanet_93443
7948||1186||Slender bone dysplasia||http://www.orpha.net/ORDO/Orphanet_93440
7950||770||GM17225||http://purl.obolibrary.org/obo/CLO_0014371
7949||1186||Primary bone dysplasia with multiple joint dislocations||http://www.orpha.net/ORDO/Orphanet_93441
7951||770||GM17221||http://purl.obolibrary.org/obo/CLO_0014377
7952||770||GM17220||http://purl.obolibrary.org/obo/CLO_0014375
7953||6246||Syndrome with synostosis or other joint formation defect||http://www.orpha.net/ORDO/Orphanet_93459
7954||7992||Neurenteric cyst||http://www.orpha.net/ORDO/Orphanet_268865
7955||6231||Patellar dysostosis||http://www.orpha.net/ORDO/Orphanet_93455
7956||6249||Non-syndromic polydactyly, syndactyly and/or hyperphalangy||http://www.orpha.net/ORDO/Orphanet_93458
7957||6249||Non-syndromic limb reduction defect||http://www.orpha.net/ORDO/Orphanet_93457
7958||7992||Primary tethered chord syndrome||http://www.orpha.net/ORDO/Orphanet_268861
7959||770||GM17223||http://purl.obolibrary.org/obo/CLO_0014367
7960||770||GM17224||http://purl.obolibrary.org/obo/CLO_0014369
7961||1186||Cleidocranial dysplasia and isolated cranial ossification defect||http://www.orpha.net/ORDO/Orphanet_93451
7962||6231||Dysostosis with predominant craniofacial involvement||http://www.orpha.net/ORDO/Orphanet_93453
7964||770||GM17229||http://purl.obolibrary.org/obo/CLO_0014362
7963||6231||Dysostosis with predominant vertebral and costal involvement||http://www.orpha.net/ORDO/Orphanet_93454
7967||770||GM17222||http://purl.obolibrary.org/obo/CLO_0014366
7966||1186||Primary bone dysplasia with disorganized development of skeletal components||http://www.orpha.net/ORDO/Orphanet_93450
7965||7992||Isolated amyelia||http://www.orpha.net/ORDO/Orphanet_268868
7968||3573||Filamin-related bone disorder||http://www.orpha.net/ORDO/Orphanet_93425
7969||3573||Perlecan-related bone disorder||http://www.orpha.net/ORDO/Orphanet_93424
7970||3573||Sulfation-related bone disorder||http://www.orpha.net/ORDO/Orphanet_93423
7971||3573||Type 11 collagen-related bone disorder||http://www.orpha.net/ORDO/Orphanet_93422
7972||1186||Multiple epiphyseal dysplasia and pseudoachondroplasia||http://www.orpha.net/ORDO/Orphanet_93429
7973||1186||Short rib dysplasia||http://www.orpha.net/ORDO/Orphanet_93426
7974||1022||Python regius||http://purl.obolibrary.org/obo/NCBITaxon_51751
7975||7022||Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, simple virilizing form||http://www.orpha.net/ORDO/Orphanet_315311
7976||770||GM17256||http://purl.obolibrary.org/obo/CLO_0014396
7977||770||GM17250||http://purl.obolibrary.org/obo/CLO_0014397
7979||3573||FGFR3-related chondrodysplasia||http://www.orpha.net/ORDO/Orphanet_93420
7978||770||GM17258||http://purl.obolibrary.org/obo/CLO_0014394
7981||3573||Type 2 collagen-related bone disorder||http://www.orpha.net/ORDO/Orphanet_93421
7980||770||GM17255||http://purl.obolibrary.org/obo/CLO_0014395
7982||770||GM17252||http://purl.obolibrary.org/obo/CLO_0014392
7983||770||GM17257||http://purl.obolibrary.org/obo/CLO_0014393
7984||1186||Spondylodysplastic dysplasia||http://www.orpha.net/ORDO/Orphanet_93434
7985||770||GM17251||http://purl.obolibrary.org/obo/CLO_0014391
7986||1186||Acromelic dysplasia||http://www.orpha.net/ORDO/Orphanet_93436
7988||770||GM14521||http://purl.obolibrary.org/obo/CLO_0031612
7987||770||GM17254||http://purl.obolibrary.org/obo/CLO_0014390
7989||1186||Mesomelic and rhizo-mesomelic dysplasia||http://www.orpha.net/ORDO/Orphanet_93438
7990||1186||Acromesomelic dysplasia||http://www.orpha.net/ORDO/Orphanet_93437
7993||10994||chloramphenicol||http://purl.obolibrary.org/obo/CHEBI_17698
7991||1186||Bent bone dysplasia||http://www.orpha.net/ORDO/Orphanet_93439
7992||6464||Malformation of the neurenteric canal, spinal cord and column||http://www.orpha.net/ORDO/Orphanet_268843
7994||7022||Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, salt wasting form||http://www.orpha.net/ORDO/Orphanet_315306
7995||5502||Burkholderia multivorans||http://purl.obolibrary.org/obo/NCBITaxon_87883
7996||770||GM17253||http://purl.obolibrary.org/obo/CLO_0014389
7997||5025||Lachancea||http://purl.obolibrary.org/obo/NCBITaxon_300275
7998||770||GM17259||http://purl.obolibrary.org/obo/CLO_0014388
7999||770||GM14508||http://purl.obolibrary.org/obo/CLO_0031610
8000||770||GM14520||http://purl.obolibrary.org/obo/CLO_0031611
8001||1186||Multiple metaphyseal dysplasia||http://www.orpha.net/ORDO/Orphanet_93430
8002||5508||Lipoma associated with neurospinal dysraphism||http://www.orpha.net/ORDO/Orphanet_268832
8003||8002||Lipomyelomeningocele||http://www.orpha.net/ORDO/Orphanet_268835
8004||770||GM17238||http://purl.obolibrary.org/obo/CLO_0014332
8005||5502||Escherichia coli str. K-12 substr. MG1655||http://purl.obolibrary.org/obo/NCBITaxon_511145
8007||770||GM17237||http://purl.obolibrary.org/obo/CLO_0014330
8006||8002||Leptomyelolipoma||http://www.orpha.net/ORDO/Orphanet_268838
8008||770||GM17236||http://purl.obolibrary.org/obo/CLO_0014336
8009||770||GM17235||http://purl.obolibrary.org/obo/CLO_0014334
8010||770||GM17233||http://purl.obolibrary.org/obo/CLO_0014338
8011||14124||Occipital encephalocele||http://www.orpha.net/ORDO/Orphanet_268823
8012||8027||Cranial meningocele||http://www.orpha.net/ORDO/Orphanet_268820
8014||5877||Hemihyperplasia-multiple lipomatosis syndrome||http://www.orpha.net/ORDO/Orphanet_276280
8013||9853||Spinocerebellar ataxia type 30||http://www.orpha.net/ORDO/Orphanet_211017
8015||14124||Basal encephalocele||http://www.orpha.net/ORDO/Orphanet_268829
8016||1022||Anemonia viridis||http://purl.obolibrary.org/obo/NCBITaxon_51769
8017||14124||Parietal encephalocele||http://www.orpha.net/ORDO/Orphanet_268826
8018||7757||16p11.2p12.2 microduplication syndrome||http://www.orpha.net/ORDO/Orphanet_261204
8019||770||GM17239||http://purl.obolibrary.org/obo/CLO_0014327
8020||770||GM14584||http://purl.obolibrary.org/obo/CLO_0031668
8021||8559||Posterior meningocele||http://www.orpha.net/ORDO/Orphanet_268810
8022||5502||Actinobacillus pleuropneumoniae||http://purl.obolibrary.org/obo/NCBITaxon_715
8023||8559||Myelocystocele||http://www.orpha.net/ORDO/Orphanet_268813
8024||4786||Overgrowth syndrome||http://www.orpha.net/ORDO/Orphanet_93460
8025||5502||Aggregatibacter actinomycetemcomitans||http://purl.obolibrary.org/obo/NCBITaxon_714
8026||1186||Lethal chondrodysplasia||http://www.orpha.net/ORDO/Orphanet_93465
8027||5508||Cephalocele||http://www.orpha.net/ORDO/Orphanet_268817
8028||770||GM14582||http://purl.obolibrary.org/obo/CLO_0031666
8029||770||GM14583||http://purl.obolibrary.org/obo/CLO_0031665
8030||770||GM17228||http://purl.obolibrary.org/obo/CLO_0014359
8031||770||GM17227||http://purl.obolibrary.org/obo/CLO_0014358
8032||770||GM17226||http://purl.obolibrary.org/obo/CLO_0014356
8033||1582||Xeroderma pigmentosum complementation group F||http://www.orpha.net/ORDO/Orphanet_276264
8034||1582||Xeroderma pigmentosum complementation group G||http://www.orpha.net/ORDO/Orphanet_276267
8035||9869||Autosomal dominant proximal spinal muscular atrophy||http://www.orpha.net/ORDO/Orphanet_211037
8036||6684||Xeroderma pigmentosum complementation group E||http://www.orpha.net/ORDO/Orphanet_276261
8037||770||GM17231||http://purl.obolibrary.org/obo/CLO_0014341
8038||770||GM17232||http://purl.obolibrary.org/obo/CLO_0014344
8039||5502||Haemophilus influenzae||http://purl.obolibrary.org/obo/NCBITaxon_727
8040||8861||Scheie syndrome||http://www.orpha.net/ORDO/Orphanet_93474
8041||4267||Hurler syndrome||http://www.orpha.net/ORDO/Orphanet_93473
8043||4267||Hurler-Scheie syndrome||http://www.orpha.net/ORDO/Orphanet_93476
8042||770||GM17234||http://purl.obolibrary.org/obo/CLO_0014340
8044||770||GM17230||http://purl.obolibrary.org/obo/CLO_0014347
8045||9664||Axenfeld anomaly||http://www.orpha.net/ORDO/Orphanet_98978
8046||11066||Juvenile glaucoma||http://www.orpha.net/ORDO/Orphanet_98977
8047||1125||biological macromolecule||http://www.ebi.ac.uk/efo/EFO_0004446
8048||2984||Chandler syndrome||http://www.orpha.net/ORDO/Orphanet_98979
8049||6573||peer review quality control role||http://www.ebi.ac.uk/efo/EFO_0004447
8050||7497||Partial trisomy of the short arm of chromosome 9||http://www.orpha.net/ORDO/Orphanet_262767
8051||13881||AB SOLiD 5500||http://www.ebi.ac.uk/efo/EFO_0004440
8052||13881||AB SOLiD 4hq System||http://www.ebi.ac.uk/efo/EFO_0004441
8053||15538||environmental history||http://www.ebi.ac.uk/efo/EFO_0004444
8054||4571||cohort||http://www.ebi.ac.uk/efo/EFO_0004445
8055||13881||AB SOLiD System 2.0||http://www.ebi.ac.uk/efo/EFO_0004442
8056||4296||material supplier||http://www.ebi.ac.uk/efo/EFO_0004443
8057||13501||Autosomal dominant spastic paraplegia type 38||http://www.orpha.net/ORDO/Orphanet_171617
8059||13471||Autosomal dominant spastic paraplegia type 37||http://www.orpha.net/ORDO/Orphanet_171612
8058||9624||Fleck corneal dystrophy||http://www.orpha.net/ORDO/Orphanet_98970
8061||5502||Lactococcus lactis subsp. hordniae||http://purl.obolibrary.org/obo/NCBITaxon_203404
8060||9624||Posterior amorphous corneal dystrophy||http://www.orpha.net/ORDO/Orphanet_98971
8062||9621||Central cloudy dystrophy of Francois||http://www.orpha.net/ORDO/Orphanet_98972
8063||9621||Posterior polymorphous corneal dystrophy||http://www.orpha.net/ORDO/Orphanet_98973
8064||9621||Fuchs endothelial corneal dystrophy||http://www.orpha.net/ORDO/Orphanet_98974
8065||9621||Congenital hereditary endothelial dystrophy type I||http://www.orpha.net/ORDO/Orphanet_98975
8066||11066||Congenital glaucoma||http://www.orpha.net/ORDO/Orphanet_98976
8067||6573||carcinogen role||http://www.ebi.ac.uk/efo/EFO_0004457
8068||14970||C-reactive protein measurement||http://www.ebi.ac.uk/efo/EFO_0004458
8070||14970||ferritin measurement||http://www.ebi.ac.uk/efo/EFO_0004459
8069||5977||Cerulean cataract||http://www.orpha.net/ORDO/Orphanet_98989
8072||15396||Anterior polar cataract||http://www.orpha.net/ORDO/Orphanet_98988
8071||7500||Partial duplication of the short arm of chromosome 10||http://www.orpha.net/ORDO/Orphanet_262776
8073||451||Familial hyperaldosteronism type I||http://www.orpha.net/ORDO/Orphanet_403
8074||5037||Familial hypocalciuric hypercalcemia||http://www.orpha.net/ORDO/Orphanet_405
8075||451||Familial hyperaldosteronism type II||http://www.orpha.net/ORDO/Orphanet_404
8076||10994||cyclosporin A||http://purl.obolibrary.org/obo/CHEBI_4031
8077||8147||Chuvash erythrocytosis||http://www.orpha.net/ORDO/Orphanet_238557
8078||10652||obsolete_Arabidopsis Growth Stage 6.30||http://www.ebi.ac.uk/efo/EFO_0004451
8079||10652||obsolete_Arabidopsis Growth Stage 6.50||http://www.ebi.ac.uk/efo/EFO_0004452
8080||10652||obsolete_Arabidopsis Growth Stage 8.00||http://www.ebi.ac.uk/efo/EFO_0004453
8081||10652||obsolete_Arabidopsis Growth Stage 9.70||http://www.ebi.ac.uk/efo/EFO_0004454
8082||13883||cot filtration||http://www.ebi.ac.uk/efo/EFO_0004455
8083||10994||roxindole||http://purl.obolibrary.org/obo/CHEBI_48558
8084||10994||cyfluthrin||http://purl.obolibrary.org/obo/CHEBI_4034
8085||799||reduce cholesterol levels||http://www.ebi.ac.uk/efo/EFO_0004456
8087||1613||Parkes Weber syndrome||http://www.orpha.net/ORDO/Orphanet_90307
8086||567||X-linked spastic paraplegia type 34||http://www.orpha.net/ORDO/Orphanet_171607
8088||1613||Klippel-Tr naunay syndrome||http://www.orpha.net/ORDO/Orphanet_90308
8089||10032||Ehlers-Danlos syndrome type 1||http://www.orpha.net/ORDO/Orphanet_90309
8090||15396||Congenital cataract, Volkmann type||http://www.orpha.net/ORDO/Orphanet_98983
8091||6285||Glycine encephalopathy||http://www.orpha.net/ORDO/Orphanet_407
8092||2984||Cogan-Reese syndrome||http://www.orpha.net/ORDO/Orphanet_98980
8093||7192||Isolated glycerol kinase deficiency||http://www.orpha.net/ORDO/Orphanet_408
8094||2984||Essential iris atrophy||http://www.orpha.net/ORDO/Orphanet_98981
8095||325||Acanthosis nigricans - Insulin resistance - muscle cramps - acral enlargement||http://www.orpha.net/ORDO/Orphanet_90301
8096||325||Hyperkeratosis lenticularis perstans||http://www.orpha.net/ORDO/Orphanet_409
8097||15396||Coppock-like cataract||http://www.orpha.net/ORDO/Orphanet_98986
8098||15396||Cataract, Hutterite type||http://www.orpha.net/ORDO/Orphanet_98987
8099||15396||Pulverulent cataract||http://www.orpha.net/ORDO/Orphanet_98984
8100||15396||Cataract with Y-shaped suture opacities||http://www.orpha.net/ORDO/Orphanet_98985
8101||799||dopaminergic antagonist||http://purl.obolibrary.org/obo/CHEBI_48561
8102||7200||Primary hyperoxaluria||http://www.orpha.net/ORDO/Orphanet_416
8103||6302||Hyperornithinemia-hyperammonemia-homocitrullinuria||http://www.orpha.net/ORDO/Orphanet_415
8104||9623||Subepithelial mucinous corneal dystrophy||http://www.orpha.net/ORDO/Orphanet_98959
8105||2454||Gyrate atrophy of choroid and retina||http://www.orpha.net/ORDO/Orphanet_414
8106||1733||Hyperlipoproteinemia type 4||http://www.orpha.net/ORDO/Orphanet_413
8107||10994||cyclophosphamide hydrate||http://purl.obolibrary.org/obo/CHEBI_4026
8109||6587||Hyperlipoproteinemia type 3||http://www.orpha.net/ORDO/Orphanet_412
8108||9623||Microcystic corneal dystrophy||http://www.orpha.net/ORDO/Orphanet_98956
8110||1733||Hyperlipoproteinemia type 1||http://www.orpha.net/ORDO/Orphanet_411
8111||8193||cyclophosphamide||http://purl.obolibrary.org/obo/CHEBI_4027
8112||9623||Lisch epithelial corneal dystrophy||http://www.orpha.net/ORDO/Orphanet_98955
8114||14970||glucose measurement||http://www.ebi.ac.uk/efo/EFO_0004468
8113||9623||Honey-droplet corneal dystrophy||http://www.orpha.net/ORDO/Orphanet_98958
8116||14970||HOMA-B||http://www.ebi.ac.uk/efo/EFO_0004469
8115||9623||Gelatinous drop-like corneal dystrophy||http://www.orpha.net/ORDO/Orphanet_98957
8117||14970||fasting blood insulin measurement||http://www.ebi.ac.uk/efo/EFO_0004466
8118||14970||insulin measurement||http://www.ebi.ac.uk/efo/EFO_0004467
8119||14970||brain measurement||http://www.ebi.ac.uk/efo/EFO_0004464
8120||14970||fasting blood glucose measurement||http://www.ebi.ac.uk/efo/EFO_0004465
8121||13496||Zaire ebolavirus - Gabon (1994-1997)||http://purl.obolibrary.org/obo/NCBITaxon_128947
8122||14970||PR interval||http://www.ebi.ac.uk/efo/EFO_0004462
8123||8184||Atypical hypotonia - cystinuria syndrome||http://www.orpha.net/ORDO/Orphanet_238523
8124||14970||angiotensin converting enzyme activity measurement||http://www.ebi.ac.uk/efo/EFO_0004463
8125||14970||soluble transferrin receptor measurement||http://www.ebi.ac.uk/efo/EFO_0004460
8128||14970||iron biomarker measurement||http://www.ebi.ac.uk/efo/EFO_0004461
8127||7478||Partial duplication of the short arm of chromosome 7||http://www.orpha.net/ORDO/Orphanet_262749
8126||10366||abnormal renal physiology||http://purl.obolibrary.org/obo/HP_0012211
8129||13496||Sudan ebolavirus||http://purl.obolibrary.org/obo/NCBITaxon_186540
8130||5502||Roseburia inulinivorans||http://purl.obolibrary.org/obo/NCBITaxon_360807
8131||15601||Inverse Marcus-Gunn phenomenon||http://www.orpha.net/ORDO/Orphanet_98951
8132||7448||Partial duplication of the short arm of chromosome 6||http://www.orpha.net/ORDO/Orphanet_262740
8133||9623||Meesmann corneal dystrophy||http://www.orpha.net/ORDO/Orphanet_98954
8134||14179||Hyperprolinemia type 1||http://www.orpha.net/ORDO/Orphanet_419
8135||756||Neonatal severe primary hyperparathyroidism||http://www.orpha.net/ORDO/Orphanet_417
8137||11258||Partial cryptophthalmia||http://www.orpha.net/ORDO/Orphanet_98950
8136||212||Congenital adrenal hyperplasia||http://www.orpha.net/ORDO/Orphanet_418
8138||13572||Apolipoprotein A-I deficiency||http://www.orpha.net/ORDO/Orphanet_425
8139||10994||phenylbutazone||http://purl.obolibrary.org/obo/CHEBI_48574
8140||1313||Familial hyperthyroidism due to mutations in TSH receptor||http://www.orpha.net/ORDO/Orphanet_424
8141||5048||Familial hypoaldosteronism||http://www.orpha.net/ORDO/Orphanet_427
8142||7476||Partial duplication of the short arm of chromosome 8||http://www.orpha.net/ORDO/Orphanet_262758
8143||9624||Macular corneal dystrophy||http://www.orpha.net/ORDO/Orphanet_98969
8145||4087||Malignant hyperthermia||http://www.orpha.net/ORDO/Orphanet_423
8144||9624||Schnyder corneal dystrophy||http://www.orpha.net/ORDO/Orphanet_98967
8146||10732||Idiopathic and/or familial pulmonary arterial hypertension||http://www.orpha.net/ORDO/Orphanet_422
8148||14970||insulin sensitivity measurement||http://www.ebi.ac.uk/efo/EFO_0004471
8147||11946||Congenital secondary polycythemia||http://www.orpha.net/ORDO/Orphanet_238536
8149||5180||C57BL/6||http://www.ebi.ac.uk/efo/EFO_0004472
8150||9624||Lattice corneal dystrophy type I||http://www.orpha.net/ORDO/Orphanet_98964
8151||9624||Granular corneal dystrophy type I||http://www.orpha.net/ORDO/Orphanet_98962
8152||9624||Granular corneal dystrophy type II||http://www.orpha.net/ORDO/Orphanet_98963
8154||1249||Autosomal dominant hypocalcemia||http://www.orpha.net/ORDO/Orphanet_428
8155||9623||Thiel-Behnke corneal dystrophy||http://www.orpha.net/ORDO/Orphanet_98960
8153||10745||Familial vesicoureteral reflux||http://www.orpha.net/ORDO/Orphanet_289365
8156||1232||Hypochondroplasia||http://www.orpha.net/ORDO/Orphanet_429
8157||9623||Reis-B cklers corneal dystrophy||http://www.orpha.net/ORDO/Orphanet_98961
8158||770||GM14535||http://purl.obolibrary.org/obo/CLO_0031600
8159||8191||methyl methanesulfonate||http://purl.obolibrary.org/obo/CHEBI_25255
8160||14725||Theiler stage 9||http://www.ebi.ac.uk/efo/EFO_0004401
8161||14725||Theiler stage 8||http://www.ebi.ac.uk/efo/EFO_0004400
8162||3790||Autosomal recessive lymphoproliferative disease||http://www.orpha.net/ORDO/Orphanet_238505
8163||14725||Theiler stage 14||http://www.ebi.ac.uk/efo/EFO_0004405
8164||14725||Theiler stage 13||http://www.ebi.ac.uk/efo/EFO_0004404
8165||14725||Theiler stage 12||http://www.ebi.ac.uk/efo/EFO_0004403
8166||14725||Theiler stage 10||http://www.ebi.ac.uk/efo/EFO_0004402
8168||14725||Theiler stage 19||http://www.ebi.ac.uk/efo/EFO_0004409
8167||6862||Partial trisomy/tetrasomy of the short arm of chromosome 5||http://www.orpha.net/ORDO/Orphanet_262725
8169||14725||Theiler stage 18||http://www.ebi.ac.uk/efo/EFO_0004408
8170||14725||Theiler stage 16||http://www.ebi.ac.uk/efo/EFO_0004407
8171||14725||Theiler stage 15||http://www.ebi.ac.uk/efo/EFO_0004406
8172||3745||Early-onset myopathy with fatal cardiomyopathy||http://www.orpha.net/ORDO/Orphanet_289377
8173||13770||Brachydactyly-syndactyly, Zhao type||http://www.orpha.net/ORDO/Orphanet_93409
8174||770||GM14509||http://purl.obolibrary.org/obo/CLO_0031609
8175||770||GM14533||http://purl.obolibrary.org/obo/CLO_0031607
8176||10567||Syndactyly type 3||http://www.orpha.net/ORDO/Orphanet_93404
8177||10567||Syndactyly type 4||http://www.orpha.net/ORDO/Orphanet_93405
8178||10567||Syndactyly type 5||http://www.orpha.net/ORDO/Orphanet_93406
8179||770||GM14532||http://purl.obolibrary.org/obo/CLO_0031606
8180||1338||Congenital sialidosis type 2||http://www.orpha.net/ORDO/Orphanet_93400
8182||770||GM14536||http://purl.obolibrary.org/obo/CLO_0031601
8181||10567||Syndactyly type 1||http://www.orpha.net/ORDO/Orphanet_93402
8183||10567||Syndactyly type 2||http://www.orpha.net/ORDO/Orphanet_93403
8185||14725||Theiler stage 20||http://www.ebi.ac.uk/efo/EFO_0004410
8184||4810||Hypotonia - cystinuria type 1||http://www.orpha.net/ORDO/Orphanet_238517
8186||14725||Theiler stage 25||http://www.ebi.ac.uk/efo/EFO_0004412
8187||14725||Theiler stage 23||http://www.ebi.ac.uk/efo/EFO_0004411
8188||11178||joule per square meter||http://www.ebi.ac.uk/efo/EFO_0004414
8189||11067||microliter per liter||http://www.ebi.ac.uk/efo/EFO_0004413
8190||10994||acid||http://www.ebi.ac.uk/efo/EFO_0004416
8191||10994||ionic salt||http://www.ebi.ac.uk/efo/EFO_0004415
8192||11199||unit of flow rate||http://www.ebi.ac.uk/efo/EFO_0004418
8193||10994||amide||http://www.ebi.ac.uk/efo/EFO_0004417
8194||4803||Lymphoproliferative syndrome||http://www.orpha.net/ORDO/Orphanet_238510
8195||8192||milligram per day||http://www.ebi.ac.uk/efo/EFO_0004419
8196||13496||Reston ebolavirus||http://purl.obolibrary.org/obo/NCBITaxon_186539
8197||13496||Zaire ebolavirus||http://purl.obolibrary.org/obo/NCBITaxon_186538
8198||12353||Myosclerosis||http://www.orpha.net/ORDO/Orphanet_289380
8199||1125||exon||http://www.ebi.ac.uk/efo/EFO_0004423
8200||1125||exome||http://www.ebi.ac.uk/efo/EFO_0004422
8201||1125||transcriptome||http://www.ebi.ac.uk/efo/EFO_0004421
8202||1125||genome||http://www.ebi.ac.uk/efo/EFO_0004420
8203||6853||Partial duplication of the short arm of chromosome 3||http://www.orpha.net/ORDO/Orphanet_262707
8204||8246||immature alpha-beta T cell||http://purl.obolibrary.org/obo/CL_0000790
8205||8246||mature alpha-beta T cell||http://purl.obolibrary.org/obo/CL_0000791
8206||5838||inbred||http://www.ebi.ac.uk/efo/EFO_0004429
8207||7036||CD4-positive, CD25-positive, alpha-beta regulatory T cell||http://purl.obolibrary.org/obo/CL_0000792
8209||4263||FAIRE-seq||http://www.ebi.ac.uk/efo/EFO_0004428
8208||7036||CD4-positive, alpha-beta intraepithelial T cell||http://purl.obolibrary.org/obo/CL_0000793
8211||11178||joule per square centimeter||http://www.ebi.ac.uk/efo/EFO_0004427
8210||7037||CD8-positive, alpha-beta cytotoxic T cell||http://purl.obolibrary.org/obo/CL_0000794
8212||5838||karyotype||http://www.ebi.ac.uk/efo/EFO_0004426
8213||7037||CD8-positive, alpha-beta regulatory T cell||http://purl.obolibrary.org/obo/CL_0000795
8214||2813||initial time point||http://www.ebi.ac.uk/efo/EFO_0004425
8215||8216||CD8-alpha-beta-positive, alpha-beta intraepithelial T cell||http://purl.obolibrary.org/obo/CL_0000796
8216||8205||alpha-beta intraepithelial T cell||http://purl.obolibrary.org/obo/CL_0000797
8217||9803||family relationship||http://www.ebi.ac.uk/efo/EFO_0004424
8218||8219||immature gamma-delta T cell||http://purl.obolibrary.org/obo/CL_0000799
8220||15396||Zonular cataract||http://www.orpha.net/ORDO/Orphanet_98995
8219||14549||gamma-delta T cell||http://purl.obolibrary.org/obo/CL_0000798
8221||15396||Partial congenital cataract||http://www.orpha.net/ORDO/Orphanet_98992
8222||15396||Nuclear cataract||http://www.orpha.net/ORDO/Orphanet_98991
8223||15396||Total congenital cataract||http://www.orpha.net/ORDO/Orphanet_98994
8224||15396||Posterior polar cataract||http://www.orpha.net/ORDO/Orphanet_98993
8225||15396||Coralliform cataract||http://www.orpha.net/ORDO/Orphanet_98990
8226||13881||454 GS FLX sequencer||http://www.ebi.ac.uk/efo/EFO_0004432
8228||13881||454 GS sequencer||http://www.ebi.ac.uk/efo/EFO_0004431
8227||8906||Hereditary myopathy with lactic acidosis due to ISCU deficiency||http://www.orpha.net/ORDO/Orphanet_43115
8229||13881||454 GS Junior sequencer||http://www.ebi.ac.uk/efo/EFO_0004434
8230||13881||454 GS FLX Titanium sequencer||http://www.ebi.ac.uk/efo/EFO_0004433
8231||6861||Partial duplication of the short arm of chromosome 4||http://www.orpha.net/ORDO/Orphanet_262716
8232||5838||outbred||http://www.ebi.ac.uk/efo/EFO_0004430
8233||4655||agar stab specimen||http://purl.obolibrary.org/obo/OBI_0000981
8234||7624||mononuclear odontoclast||http://purl.obolibrary.org/obo/CL_0000781
8235||13881||AB SOLiD System 3.0||http://www.ebi.ac.uk/efo/EFO_0004439
8236||10580||myeloid dendritic cell||http://purl.obolibrary.org/obo/CL_0000782
8237||9378||multinuclear odontoclast||http://purl.obolibrary.org/obo/CL_0000780
8238||13881||AB SOLiD 5500xl||http://www.ebi.ac.uk/efo/EFO_0004436
8239||12772||mature B cell||http://purl.obolibrary.org/obo/CL_0000785
8240||13881||AB SOLiD System||http://www.ebi.ac.uk/efo/EFO_0004435
8241||10537||plasma cell||http://purl.obolibrary.org/obo/CL_0000786
8242||13881||AB SOLiD 4 System||http://www.ebi.ac.uk/efo/EFO_0004438
8243||13881||AB SOLiD PI System||http://www.ebi.ac.uk/efo/EFO_0004437
8245||4027||prednisolone||http://purl.obolibrary.org/obo/CHEBI_8378
8244||8621||plasmacytoid dendritic cell||http://purl.obolibrary.org/obo/CL_0000784
8246||14549||alpha-beta T cell||http://purl.obolibrary.org/obo/CL_0000789
8247||8239||naive B cell||http://purl.obolibrary.org/obo/CL_0000788
8248||8239||memory B cell||http://purl.obolibrary.org/obo/CL_0000787
8249||1826||Citrus sunki||http://purl.obolibrary.org/obo/NCBITaxon_237574
8250||10994||dibenzazepines||http://purl.obolibrary.org/obo/CHEBI_47804
8251||10994||sulforaphane||http://purl.obolibrary.org/obo/CHEBI_47807
8252||770||GM17272||http://purl.obolibrary.org/obo/CLO_0013214
8253||770||GM17270||http://purl.obolibrary.org/obo/CLO_0013212
8254||770||GM17271||http://purl.obolibrary.org/obo/CLO_0013213
8255||843||Infantile dystonia-parkinsonism||http://www.orpha.net/ORDO/Orphanet_238455
8256||2866||Stevens-Johnson syndrome||http://www.ebi.ac.uk/efo/EFO_0004276
8257||7675||Kufor-Rakeb syndrome||http://www.orpha.net/ORDO/Orphanet_306674
8258||10652||obsolete_sick sinus syndrome||http://www.ebi.ac.uk/efo/EFO_0004275
8259||15526||gout||http://www.ebi.ac.uk/efo/EFO_0004274
8261||15526||scoliosis||http://www.ebi.ac.uk/efo/EFO_0004273
8260||7086||SLC35A1-CDG||http://www.orpha.net/ORDO/Orphanet_238459
8262||770||GM17279||http://purl.obolibrary.org/obo/CLO_0013210
8263||11562||suntan||http://www.ebi.ac.uk/efo/EFO_0004279
8264||8292||sudden cardiac arrest||http://www.ebi.ac.uk/efo/EFO_0004278
8265||11614||brain infarction||http://www.ebi.ac.uk/efo/EFO_0004277
8266||1638||thoracic aortic aneurysm||http://www.ebi.ac.uk/efo/EFO_0004282
8267||15416||goiter||http://www.ebi.ac.uk/efo/EFO_0004283
8268||2165||movement disorder||http://www.ebi.ac.uk/efo/EFO_0004280
8269||10969||testicular neoplasm||http://www.ebi.ac.uk/efo/EFO_0004281
8270||3536||Spondyloepimetaphyseal dysplasia, aggrecan type||http://www.orpha.net/ORDO/Orphanet_171866
8271||10411||Cockayne syndrome type 2||http://www.orpha.net/ORDO/Orphanet_90322
8274||13471||Autosomal dominant spastic paraplegia type 42||http://www.orpha.net/ORDO/Orphanet_171863
8272||10411||Cockayne syndrome type 1||http://www.orpha.net/ORDO/Orphanet_90321
8273||10994||carbon dioxide||http://purl.obolibrary.org/obo/CHEBI_16526
8275||9134||Isolated autosomal dominant hypomagnesemia, Glaudemans type||http://www.orpha.net/ORDO/Orphanet_199326
8276||2354||Congenital myopathy, Paradas type||http://www.orpha.net/ORDO/Orphanet_199329
8277||4903||trans-zeatin||http://purl.obolibrary.org/obo/CHEBI_16522
8278||10994||D-serine||http://purl.obolibrary.org/obo/CHEBI_16523
8281||4139||Intellectual disability - cataracts - kyphosis||http://www.orpha.net/ORDO/Orphanet_171860
8280||5466||14q22q23 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_264200
8279||10411||Cockayne syndrome type 3||http://www.orpha.net/ORDO/Orphanet_90324
8282||1211||Pearson syndrome||http://www.orpha.net/ORDO/Orphanet_699
8283||1174||Endocrine-cerebro-osteodysplasia syndrome||http://www.orpha.net/ORDO/Orphanet_199332
8284||1150||partial epilepsy||http://www.ebi.ac.uk/efo/EFO_0004263
8285||2102||panic disorder||http://www.ebi.ac.uk/efo/EFO_0004262
8286||10979||peripheral arterial disease||http://www.ebi.ac.uk/efo/EFO_0004265
8289||10994||caspofungin||http://purl.obolibrary.org/obo/CHEBI_474180
8288||1015||vascular disease||http://www.ebi.ac.uk/efo/EFO_0004264
8287||10661||15q11q13 microduplication syndrome||http://www.orpha.net/ORDO/Orphanet_238446
8290||14915||biliary liver cirrhosis||http://www.ebi.ac.uk/efo/EFO_0004267
8291||15416||primary ovarian insufficiency||http://www.ebi.ac.uk/efo/EFO_0004266
8292||11549||cardiac arrhythmia||http://www.ebi.ac.uk/efo/EFO_0004269
8293||1403||sclerosing cholangitis||http://www.ebi.ac.uk/efo/EFO_0004268
8294||10032||Ehlers-Danlos syndrome type 2||http://www.orpha.net/ORDO/Orphanet_90318
8295||6610||Hunter-McAlpine craniosynostosis||http://www.orpha.net/ORDO/Orphanet_97340
8296||2165||restless legs syndrome||http://www.ebi.ac.uk/efo/EFO_0004270
8297||3074||retinal vein||http://www.ebi.ac.uk/efo/EFO_0004271
8298||1391||anemia||http://www.ebi.ac.uk/efo/EFO_0004272
8299||15185||Familial dementia, British type||http://www.orpha.net/ORDO/Orphanet_97345
8300||8714||Generalized pseudohypoaldosteronism type 1||http://www.orpha.net/ORDO/Orphanet_171876
8301||15185||Familial dementia, Danish type||http://www.orpha.net/ORDO/Orphanet_97346
8302||8714||Renal pseudohypoaldosteronism type 1||http://www.orpha.net/ORDO/Orphanet_171871
8303||1732||Rare genetic deafness||http://www.orpha.net/ORDO/Orphanet_96210
8304||288||Pancreatic insufficiency - anemia - hyperostosis||http://www.orpha.net/ORDO/Orphanet_199337
8305||5918||Blau syndrome||http://www.orpha.net/ORDO/Orphanet_90340
8306||266||Familial hypercholanemia||http://www.orpha.net/ORDO/Orphanet_238475
8307||1022||Piriformospora indica||http://purl.obolibrary.org/obo/NCBITaxon_65672
8308||2414||Normocalcemic tumoral calcinosis||http://www.orpha.net/ORDO/Orphanet_306658
8309||4087||Paramyotonia congenita of Von Eulenburg||http://www.orpha.net/ORDO/Orphanet_684
8311||4706||Hereditary spastic paraplegia||http://www.orpha.net/ORDO/Orphanet_685
8310||8323||osteonecrosis||http://www.ebi.ac.uk/efo/EFO_0004259
8313||4087||Hyperkalemic periodic paralysis||http://www.orpha.net/ORDO/Orphanet_682
8312||2672||optic nerve||http://www.ebi.ac.uk/efo/EFO_0004258
8314||2102||neurotic disorder||http://www.ebi.ac.uk/efo/EFO_0004257
8315||4706||Progressive supranuclear palsy||http://www.orpha.net/ORDO/Orphanet_683
8316||10990||neuromyelitis optica||http://www.ebi.ac.uk/efo/EFO_0004256
8318||4087||Hypokalemic periodic paralysis||http://www.orpha.net/ORDO/Orphanet_681
8317||8970||nephrotic syndrome||http://www.ebi.ac.uk/efo/EFO_0004255
8319||8970||membranous glomerulonephritis||http://www.ebi.ac.uk/efo/EFO_0004254
8320||8970||nephrolithiasis||http://www.ebi.ac.uk/efo/EFO_0004253
8321||2162||nasopharyngeal neoplasm||http://www.ebi.ac.uk/efo/EFO_0004252
8322||2162||myeloproliferative disorder||http://www.ebi.ac.uk/efo/EFO_0004251
8323||15526||bone disease||http://www.ebi.ac.uk/efo/EFO_0004260
8324||8323||osteitis deformans||http://www.ebi.ac.uk/efo/EFO_0004261
8325||8791||Myopathy with hexagonally cross-linked tubular arrays||http://www.orpha.net/ORDO/Orphanet_171889
8326||6432||Combined oxidative phosphorylation defect type 7||http://www.orpha.net/ORDO/Orphanet_254930
8327||7353||Autosomal recessive cutis laxa type 1||http://www.orpha.net/ORDO/Orphanet_90349
8328||10138||Autosomal dominant cutis laxa||http://www.orpha.net/ORDO/Orphanet_90348
8329||3617||Cap myopathy||http://www.orpha.net/ORDO/Orphanet_171881
8331||6684||Xeroderma pigmentosum variant||http://www.orpha.net/ORDO/Orphanet_90342
8330||8791||Cylindrical spirals myopathy||http://www.orpha.net/ORDO/Orphanet_171886
8333||3019||Tetragametic chimerism||http://www.orpha.net/ORDO/Orphanet_199310
8332||306||Papillon-Lef vre syndrome||http://www.orpha.net/ORDO/Orphanet_678
8334||9898||Hemiparkinsonism-hemiatrophy syndrome||http://www.orpha.net/ORDO/Orphanet_306669
8335||5939||Malignant atrophic papulosis||http://www.orpha.net/ORDO/Orphanet_679
8336||770||GM17277||http://purl.obolibrary.org/obo/CLO_0013208
8337||2700||meningococcal infection||http://www.ebi.ac.uk/efo/EFO_0004249
8338||1784||male infertility||http://www.ebi.ac.uk/efo/EFO_0004248
8339||770||GM17275||http://purl.obolibrary.org/obo/CLO_0013202
8340||6904||Accessory pancreas||http://www.orpha.net/ORDO/Orphanet_674
8341||6904||Annular pancreas||http://www.orpha.net/ORDO/Orphanet_675
8343||770||GM17278||http://purl.obolibrary.org/obo/CLO_0013204
8342||5055||Hereditary chronic pancreatitis||http://www.orpha.net/ORDO/Orphanet_676
8344||10652||obsolete_iris||http://www.ebi.ac.uk/efo/EFO_0004245
8346||11231||interstitial lung disease||http://www.ebi.ac.uk/efo/EFO_0004244
8345||2414||Familial tumoral calcinosis||http://www.orpha.net/ORDO/Orphanet_306661
8347||6432||Combined oxidative phosphorylation defect type 2||http://www.orpha.net/ORDO/Orphanet_254920
8348||2102||mood disorder||http://www.ebi.ac.uk/efo/EFO_0004247
8350||4122||Pallister-Hall syndrome||http://www.orpha.net/ORDO/Orphanet_672
8349||1790||mucocutaneous lymph node syndrome||http://www.ebi.ac.uk/efo/EFO_0004246
8352||6432||Combined oxidative phosphorylation defect type 4||http://www.orpha.net/ORDO/Orphanet_254925
8351||10652||obsolete_Hirschsprung disease||http://www.ebi.ac.uk/efo/EFO_0004241
8353||6589||heroin dependence||http://www.ebi.ac.uk/efo/EFO_0004240
8354||2162||carcinoid tumor||http://www.ebi.ac.uk/efo/EFO_0004243
8355||2102||obsessive-compulsive disorder||http://www.ebi.ac.uk/efo/EFO_0004242
8356||306||Hypohidrotic ectodermal dysplasia||http://www.orpha.net/ORDO/Orphanet_238468
8357||10652||obsolete_Moyamoya disease||http://www.ebi.ac.uk/efo/EFO_0004250
8358||9779||Unilateral renal hypoplasia||http://www.orpha.net/ORDO/Orphanet_97361
8360||590||Rosselli-Gulienetti syndrome||http://www.orpha.net/ORDO/Orphanet_90339
8359||9779||Bilateral renal hypoplasia||http://www.orpha.net/ORDO/Orphanet_97362
8361||4785||Robinow syndrome||http://www.orpha.net/ORDO/Orphanet_97360
8362||2252||15q13.3 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_199318
8363||3305||Unilateral multicystic dysplastic kidney||http://www.orpha.net/ORDO/Orphanet_97363
8364||3305||Bilateral multicystic dysplastic kidney||http://www.orpha.net/ORDO/Orphanet_97364
8365||6246||Familial clubfoot with or without associated lower limb anomalies||http://www.orpha.net/ORDO/Orphanet_199315
8366||742||Renal tubular dysgenesis of genetic origin||http://www.orpha.net/ORDO/Orphanet_97369
8367||13999||Primary intestinal lymphangiectasia||http://www.orpha.net/ORDO/Orphanet_90362
8368||10399||Rhizomelic chondrodysplasia punctata type 1||http://www.orpha.net/ORDO/Orphanet_309789
8369||10994||pimozide||http://purl.obolibrary.org/obo/CHEBI_8212
8370||1022||Sparus aurata||http://purl.obolibrary.org/obo/NCBITaxon_8175
8371||321||Hypotrichosis simplex of the scalp||http://www.orpha.net/ORDO/Orphanet_90368
8372||1022||Orchesella cincta||http://purl.obolibrary.org/obo/NCBITaxon_48709
8373||10994||pioglitazone||http://purl.obolibrary.org/obo/CHEBI_8228
8374||10399||Rhizomelic chondrodysplasia punctata type 2||http://www.orpha.net/ORDO/Orphanet_309796
8375||7942||Autosomal recessive cutis laxa type 2||http://www.orpha.net/ORDO/Orphanet_90350
8377||5502||Pseudomonas fluorescens Pf0-1||http://purl.obolibrary.org/obo/NCBITaxon_205922
8376||10503||Brittle cornea syndrome||http://www.orpha.net/ORDO/Orphanet_90354
8378||5502||Ehrlichia chaffeensis str. Arkansas||http://purl.obolibrary.org/obo/NCBITaxon_205920
8379||1022||Lateolabrax japonicus||http://purl.obolibrary.org/obo/NCBITaxon_8164
8380||8191||lithium chloride||http://purl.obolibrary.org/obo/CHEBI_48607
8381||5502||Clostridium perfringens str. 13||http://purl.obolibrary.org/obo/NCBITaxon_195102
8382||2842||life expectancy||http://www.ebi.ac.uk/efo/EFO_0004299
8383||14970||clinical laboratory measurement||http://www.ebi.ac.uk/efo/EFO_0004297
8384||14970||cardiovascular measurement||http://www.ebi.ac.uk/efo/EFO_0004298
8385||14435||ventricular function, left||http://www.ebi.ac.uk/efo/EFO_0004295
8386||201||Primary immunodeficiency due to a defect in adaptive immunity||http://www.orpha.net/ORDO/Orphanet_179006
8387||14435||thyroid function||http://www.ebi.ac.uk/efo/EFO_0004296
8388||10721||Hyperbiliverdinemia||http://www.orpha.net/ORDO/Orphanet_276405
8389||4931||X small rings||http://www.orpha.net/ORDO/Orphanet_96201
8390||1022||Maylandia||http://purl.obolibrary.org/obo/NCBITaxon_143623
8391||10994||20-hydroxyecdysone||http://purl.obolibrary.org/obo/CHEBI_16587
8392||2162||colonic neoplasm||http://www.ebi.ac.uk/efo/EFO_0004288
8393||1508||lymphoid leukemia||http://www.ebi.ac.uk/efo/EFO_0004289
8394||2162||upper aerodigestive tract neoplasm||http://www.ebi.ac.uk/efo/EFO_0004284
8395||14308||adenohypophyseal placode||http://purl.obolibrary.org/obo/UBERON_0009122
8396||11618||albuminuria||http://www.ebi.ac.uk/efo/EFO_0004285
8397||8288||venous thromboembolism||http://www.ebi.ac.uk/efo/EFO_0004286
8398||13689||gill filament||http://purl.obolibrary.org/obo/UBERON_0009120
8399||8292||ventricular fibrillation||http://www.ebi.ac.uk/efo/EFO_0004287
8400||7086||Defect in V-ATPase||http://www.orpha.net/ORDO/Orphanet_309778
8401||772||diploid cell||http://purl.obolibrary.org/obo/CL_0000415
8402||5962||10q22.3q23.3 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_276413
8403||7529||vaccination||http://www.ebi.ac.uk/efo/EFO_0004292
8404||1783||braces||http://www.ebi.ac.uk/efo/EFO_0004291
8405||14435||atrial function, left||http://www.ebi.ac.uk/efo/EFO_0004294
8406||1766||recombination||http://www.ebi.ac.uk/efo/EFO_0004293
8407||11618||sneezing||http://www.ebi.ac.uk/efo/EFO_0004290
8408||8190||Hexadecanoic acid||http://purl.obolibrary.org/obo/CHEBI_15756
8409||10768||10q22.3q23.3 microduplication syndrome||http://www.orpha.net/ORDO/Orphanet_276422
8410||10994||dichloromethane||http://purl.obolibrary.org/obo/CHEBI_15767
8411||8035||Lower motor neuron syndrome with late-adult onset||http://www.orpha.net/ORDO/Orphanet_276435
8412||2322||Premature aging appearance-developmental delay-cardiac arrhythmia syndrome||http://www.orpha.net/ORDO/Orphanet_276432
8413||6341||Anonychia - onychodystrophy||http://www.orpha.net/ORDO/Orphanet_90390
8414||1393||Short fifth metacarpals - insulin resistance||http://www.orpha.net/ORDO/Orphanet_66518
8415||7605||Glycogen storage disease due to glycogen branching enzyme deficiency, adult neuromuscular form||http://www.orpha.net/ORDO/Orphanet_308712
8416||1826||Cardamine sp. SIM-2007||http://purl.obolibrary.org/obo/NCBITaxon_487795
8417||9718||Morning glory syndrome||http://www.orpha.net/ORDO/Orphanet_35737
8418||10886||leptin||http://www.ebi.ac.uk/efo/EFO_0003199
8419||1826||Picea engelmannii x Picea glauca||http://purl.obolibrary.org/obo/NCBITaxon_373101
8420||4472||48,XXXY syndrome||http://www.orpha.net/ORDO/Orphanet_96263
8421||4472||49,XXXXY syndrome||http://www.orpha.net/ORDO/Orphanet_96264
8422||8715||Leydig cell hypoplasia due to complete LH resistance||http://www.orpha.net/ORDO/Orphanet_96265
8423||8715||Leydig cell hypoplasia due to partial LH resistance||http://www.orpha.net/ORDO/Orphanet_96266
8424||11538||organ development||http://purl.obolibrary.org/obo/GO_0048513
8425||10886||ocimene||http://www.ebi.ac.uk/efo/EFO_0003191
8426||7966||Genochondromatosis type 2||http://www.orpha.net/ORDO/Orphanet_93398
8427||1338||Juvenile sialidosis type 2||http://www.orpha.net/ORDO/Orphanet_93399
8428||2021||Brachydactyly type A2||http://www.orpha.net/ORDO/Orphanet_93396
8429||2021||Brachydactyly type A7||http://www.orpha.net/ORDO/Orphanet_93397
8430||2021||Brachydactyly type A4||http://www.orpha.net/ORDO/Orphanet_93394
8431||2021||Ballard syndrome||http://www.orpha.net/ORDO/Orphanet_93395
8432||10246||Trisomy 1q||http://www.orpha.net/ORDO/Orphanet_261344
8433||10765||2p15p16.1 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_261349
8434||5524||Distal 22q11.2 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_261330
8435||2021||Brachydactyly type A5||http://www.orpha.net/ORDO/Orphanet_93389
8436||10886||thrombin||http://www.ebi.ac.uk/efo/EFO_0003183
8437||2021||Brachydactyly type E||http://www.orpha.net/ORDO/Orphanet_93387
8438||2021||Brachydactyly type A1||http://www.orpha.net/ORDO/Orphanet_93388
8439||2021||Brachydactyly type A6||http://www.orpha.net/ORDO/Orphanet_93382
8440||2021||Brachydactyly type B||http://www.orpha.net/ORDO/Orphanet_93383
8441||2021||Brachydactyly type C||http://www.orpha.net/ORDO/Orphanet_93384
8442||4840||Distal 22q11.2 microduplication syndrome||http://www.orpha.net/ORDO/Orphanet_261337
8443||762||Thiamine-responsive encephalopathy||http://www.orpha.net/ORDO/Orphanet_199348
8444||8791||Congenital myopathy with cores||http://www.orpha.net/ORDO/Orphanet_172976
8446||5502||uncultured sulfate-reducing bacterium||http://purl.obolibrary.org/obo/NCBITaxon_153939
8445||10886||pleiotrophin||http://www.ebi.ac.uk/efo/EFO_0003172
8447||203||Hispanic||http://www.ebi.ac.uk/efo/EFO_0003169
8448||10994||staurosporine||http://purl.obolibrary.org/obo/CHEBI_15738
8449||203||Hawaiian||http://www.ebi.ac.uk/efo/EFO_0003168
8450||203||Pima Indian||http://www.ebi.ac.uk/efo/EFO_0003167
8451||203||Latino||http://www.ebi.ac.uk/efo/EFO_0003166
8452||8465||Korean||http://www.ebi.ac.uk/efo/EFO_0003165
8453||8465||Japanese||http://www.ebi.ac.uk/efo/EFO_0003164
8454||203||Irish||http://www.ebi.ac.uk/efo/EFO_0003163
8455||203||Iranian||http://www.ebi.ac.uk/efo/EFO_0003162
8456||4692||EAST syndrome||http://www.orpha.net/ORDO/Orphanet_199343
8457||8904||Muscular dystrophy, Selcen type||http://www.orpha.net/ORDO/Orphanet_199340
8458||7380||X-linked complicated spastic paraplegia type 1||http://www.orpha.net/ORDO/Orphanet_306617
8459||8465||Filipino||http://www.ebi.ac.uk/efo/EFO_0003160
8460||8464||Han Chinese||http://www.ebi.ac.uk/efo/EFO_0003161
8461||203||Caucasian||http://www.ebi.ac.uk/efo/EFO_0003156
8462||203||British||http://www.ebi.ac.uk/efo/EFO_0003155
8463||203||Eastern Indian||http://www.ebi.ac.uk/efo/EFO_0003158
8464||203||Chinese||http://www.ebi.ac.uk/efo/EFO_0003157
8465||203||Asian||http://www.ebi.ac.uk/efo/EFO_0003152
8466||203||American||http://www.ebi.ac.uk/efo/EFO_0003151
8467||203||Asian/Pacific Islander||http://www.ebi.ac.uk/efo/EFO_0003154
8468||203||Asian Indian||http://www.ebi.ac.uk/efo/EFO_0003153
8469||843||Adult-onset dystonia-parkinsonism||http://www.orpha.net/ORDO/Orphanet_199351
8470||4705||CARASIL||http://www.orpha.net/ORDO/Orphanet_199354
8471||203||European-American||http://www.ebi.ac.uk/efo/EFO_0003159
8472||6288||Gamma-glutamylcysteine synthetase deficiency||http://www.orpha.net/ORDO/Orphanet_33574
8474||10994||warfarin||http://purl.obolibrary.org/obo/CHEBI_10033
8473||2403||Laing early-onset distal myopathy||http://www.orpha.net/ORDO/Orphanet_59135
8475||6288||5-oxoprolinase deficiency||http://www.orpha.net/ORDO/Orphanet_33572
8476||6288||Gamma-glutamyl transpeptidase deficiency||http://www.orpha.net/ORDO/Orphanet_33573
8477||10143||Anauxetic dysplasia||http://www.orpha.net/ORDO/Orphanet_93347
8478||10994||cis-ketoconazole||http://purl.obolibrary.org/obo/CHEBI_47519
8479||7981||Spondyloepimetaphyseal dysplasia congenita, Strudwick type||http://www.orpha.net/ORDO/Orphanet_93346
8480||10143||X-linked spondyloepimetaphyseal dysplasia||http://www.orpha.net/ORDO/Orphanet_93349
8481||4803||Familial multinodular goiter||http://www.orpha.net/ORDO/Orphanet_276399
8482||5602||Paternal 20q13.2q13.3 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_261304
8483||7605||Glycogen storage disease due to glycogen branching enzyme deficiency, childhood neuromuscular form||http://www.orpha.net/ORDO/Orphanet_308698
8484||10886||neuromedin U||http://www.ebi.ac.uk/efo/EFO_0003266
8485||10143||Spondyloepimetaphyseal dysplasia, Irapa type||http://www.orpha.net/ORDO/Orphanet_93351
8486||10143||Spondyloepimetaphyseal dysplasia, Shohat type||http://www.orpha.net/ORDO/Orphanet_93352
8487||10143||Spondyloepimetaphyseal dysplasia, Missouri type||http://www.orpha.net/ORDO/Orphanet_93356
8488||10143||SPONASTRIME dysplasia||http://www.orpha.net/ORDO/Orphanet_93357
8489||10143||Spondyloepimetaphyseal dysplasia - short limb - abnormal calcification||http://www.orpha.net/ORDO/Orphanet_93358
8490||10886||tumor necrosis factor-alpha||http://www.ebi.ac.uk/efo/EFO_0003271
8491||4014||Spondyloepimetaphyseal dysplasia with joint laxity||http://www.orpha.net/ORDO/Orphanet_93359
8492||3974||thrombopoietin||http://www.ebi.ac.uk/efo/EFO_0003236
8494||10994||chitin octamer||http://www.ebi.ac.uk/efo/EFO_0003237
8493||5602||20q13.33 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_261311
8497||1022||Heliconius erato petiverana||http://purl.obolibrary.org/obo/NCBITaxon_64531
8495||7135||Trisomy 20p||http://www.orpha.net/ORDO/Orphanet_261318
8496||7605||Glycogen storage disease due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form||http://www.orpha.net/ORDO/Orphanet_308684
8498||5025||Arthroderma benhamiae||http://purl.obolibrary.org/obo/NCBITaxon_63400
8499||5025||Arthroderma otae||http://purl.obolibrary.org/obo/NCBITaxon_63405
8500||12235||CINCA syndrome with NLRP3 mutations||http://www.orpha.net/ORDO/Orphanet_93365
8501||5025||Arthroderma gypseum||http://purl.obolibrary.org/obo/NCBITaxon_63402
8502||10886||follicle stimulating hormone||http://www.ebi.ac.uk/efo/EFO_0003234
8503||10143||Spondyloepimetaphyseal dysplasia with multiple dislocations||http://www.orpha.net/ORDO/Orphanet_93360
8504||3974||erythropoietin||http://www.ebi.ac.uk/efo/EFO_0003233
8505||12235||CINCA syndrome without NLRP3 mutations||http://www.orpha.net/ORDO/Orphanet_93367
8506||5037||Disorders of vitamin D metabolism||http://www.orpha.net/ORDO/Orphanet_289098
8507||1826||Amborella trichopoda||http://purl.obolibrary.org/obo/NCBITaxon_13333
8508||4259||response to lithium ion||http://purl.obolibrary.org/obo/GO_0010226
8509||5623||21q22.11q22.12 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_261323
8510||5025||Trichophyton megninii||http://purl.obolibrary.org/obo/NCBITaxon_63416
8511||10886||flagellin||http://www.ebi.ac.uk/efo/EFO_0003241
8512||5025||Trichophyton verrucosum||http://purl.obolibrary.org/obo/NCBITaxon_63417
8513||8074||Familial hypocalciuric hypercalcemia type 1||http://www.orpha.net/ORDO/Orphanet_93372
8514||3854||Pyrococcus furiosus DSM 3638||http://purl.obolibrary.org/obo/NCBITaxon_186497
8515||10994||dexamethasone||http://purl.obolibrary.org/obo/CHEBI_41879
8516||9681||Sorsby s fundus dystrophy||http://www.orpha.net/ORDO/Orphanet_59181
8517||3540||Autosomal dominant brachyolmia||http://www.orpha.net/ORDO/Orphanet_93304
8518||7970||Brachyolmia type 1, Toledo type||http://www.orpha.net/ORDO/Orphanet_93303
8519||13318||Brachyolmia, Maroteaux type||http://www.orpha.net/ORDO/Orphanet_93302
8520||13318||Brachyolmia type 1, Hobaek type||http://www.orpha.net/ORDO/Orphanet_93301
8521||10141||Multiple epiphyseal dysplasia type 1||http://www.orpha.net/ORDO/Orphanet_93308
8522||7970||Multiple epiphyseal dysplasia type 4||http://www.orpha.net/ORDO/Orphanet_93307
8524||10994||methylmercury||http://purl.obolibrary.org/obo/CHEBI_49747
8523||5502||Streptococcus pneumoniae D39||http://purl.obolibrary.org/obo/NCBITaxon_373153
8525||10141||Multiple epiphyseal dysplasia type 5||http://www.orpha.net/ORDO/Orphanet_93311
8526||4706||Pelizaeus-Merzbacher disease||http://www.orpha.net/ORDO/Orphanet_702
8527||321||Alopecia universalis||http://www.orpha.net/ORDO/Orphanet_701
8528||321||Alopecia totalis||http://www.orpha.net/ORDO/Orphanet_700
8529||2252||Peters plus syndrome||http://www.orpha.net/ORDO/Orphanet_709
8530||6897||Peters anomaly||http://www.orpha.net/ORDO/Orphanet_708
8531||5700||Pendred syndrome||http://www.orpha.net/ORDO/Orphanet_705
8532||7981||Spondylometaphyseal dysplasia,  corner fracture  type||http://www.orpha.net/ORDO/Orphanet_93315
8533||3540||Spondylometaphyseal dysplasia, Kozlowski type||http://www.orpha.net/ORDO/Orphanet_93314
8534||7984||Spondylometaphyseal dysplasia, Sedaghatian type||http://www.orpha.net/ORDO/Orphanet_93317
8535||7981||Spondylometaphyseal dysplasia, Schmidt type||http://www.orpha.net/ORDO/Orphanet_93316
8536||6030||Radial hemimelia||http://www.orpha.net/ORDO/Orphanet_93321
8537||6030||Tibial hemimelia||http://www.orpha.net/ORDO/Orphanet_93322
8538||1022||Corallus||http://purl.obolibrary.org/obo/NCBITaxon_51859
8539||6030||Ulnar hemimelia||http://www.orpha.net/ORDO/Orphanet_93320
8540||12737||Lumbosacral spina bifida cystica||http://www.orpha.net/ORDO/Orphanet_268758
8541||770||AG04351||http://purl.obolibrary.org/obo/CLO_0034796
8542||3314||Autosomal recessive omodysplasia||http://www.orpha.net/ORDO/Orphanet_93329
8543||3314||Autosomal dominant omodysplasia||http://www.orpha.net/ORDO/Orphanet_93328
8544||1570||Autosomal dominant Kenny-Caffey syndrome||http://www.orpha.net/ORDO/Orphanet_93325
8546||12737||Thoracolumbosacral spina bifida cystica||http://www.orpha.net/ORDO/Orphanet_268752
8545||1570||Autosomal recessive Kenny-Caffey syndrome||http://www.orpha.net/ORDO/Orphanet_93324
8547||6030||Fibular hemimelia||http://www.orpha.net/ORDO/Orphanet_93323
8548||770||GM17274||http://purl.obolibrary.org/obo/CLO_0013193
8549||6244||Pelviscapular dysplasia||http://www.orpha.net/ORDO/Orphanet_93333
8550||770||AG04147||http://purl.obolibrary.org/obo/CLO_0034780
8551||9613||oncostatin M||http://www.ebi.ac.uk/efo/EFO_0003200
8552||770||GM17276||http://purl.obolibrary.org/obo/CLO_0013199
8553||12737||Total spina bifida cystica||http://www.orpha.net/ORDO/Orphanet_268748
8554||770||GM17273||http://purl.obolibrary.org/obo/CLO_0013197
8555||457||growth chamber study||http://purl.obolibrary.org/obo/EO_0007269
8556||1391||Biliary atresia||http://www.orpha.net/ORDO/Orphanet_30391
8557||13825||Polydactyly of a biphalangeal thumb||http://www.orpha.net/ORDO/Orphanet_93339
8558||13825||Polysyndactyly||http://www.orpha.net/ORDO/Orphanet_93338
8559||6197||Spina bifida cystica||http://www.orpha.net/ORDO/Orphanet_268744
8560||13727||Postaxial polydactyly type B||http://www.orpha.net/ORDO/Orphanet_93335
8561||13727||Postaxial polydactyly type A||http://www.orpha.net/ORDO/Orphanet_93334
8562||13825||Polydactyly of an index finger||http://www.orpha.net/ORDO/Orphanet_93337
8563||13825||Polydactyly of a triphalangeal thumb||http://www.orpha.net/ORDO/Orphanet_93336
8564||5541||Upper thoracic spina bifida aperta||http://www.orpha.net/ORDO/Orphanet_268740
8565||1306||Prader-Willi syndrome||http://www.orpha.net/ORDO/Orphanet_739
8566||378||Porphyria||http://www.orpha.net/ORDO/Orphanet_738
8567||1564||Porokeratosis plantaris palmaris et disseminata||http://www.orpha.net/ORDO/Orphanet_737
8568||11887||Alpha delta granule deficiency||http://www.orpha.net/ORDO/Orphanet_734
8569||5939||Porokeratosis of Mibelli||http://www.orpha.net/ORDO/Orphanet_735
8570||7330||platelet count||http://www.ebi.ac.uk/efo/EFO_0004309
8571||7330||leukocyte count||http://www.ebi.ac.uk/efo/EFO_0004308
8573||3833||Familial adenomatous polyposis||http://www.orpha.net/ORDO/Orphanet_733
8572||8114||glucose tolerance test||http://www.ebi.ac.uk/efo/EFO_0004307
8574||7330||erythrocyte indices||http://www.ebi.ac.uk/efo/EFO_0004306
8576||7377||Autosomal recessive polycystic kidney disease||http://www.orpha.net/ORDO/Orphanet_731
8575||8574||erythrocyte count||http://www.ebi.ac.uk/efo/EFO_0004305
8577||7330||blood sedimentation||http://www.ebi.ac.uk/efo/EFO_0004304
8578||14970||vital signs||http://www.ebi.ac.uk/efo/EFO_0004303
8579||14970||anthropometry||http://www.ebi.ac.uk/efo/EFO_0004302
8580||14970||blood viscosity||http://www.ebi.ac.uk/efo/EFO_0004301
8581||2842||longevity||http://www.ebi.ac.uk/efo/EFO_0004300
8582||770||GM17260||http://purl.obolibrary.org/obo/CLO_0013182
8583||770||GM17261||http://purl.obolibrary.org/obo/CLO_0013183
8584||10994||naphthalene||http://purl.obolibrary.org/obo/CHEBI_16482
8585||770||GM17266||http://purl.obolibrary.org/obo/CLO_0013181
8586||4994||Mendelian susceptibility to mycobacterial diseases||http://www.orpha.net/ORDO/Orphanet_748
8587||15365||Congenital prekallikrein deficiency||http://www.orpha.net/ORDO/Orphanet_749
8589||3068||smoking cessation||http://www.ebi.ac.uk/efo/EFO_0004319
8588||4572||Hereditary thrombophilia due to congenital protein S deficiency||http://www.orpha.net/ORDO/Orphanet_743
8591||3068||smoking behavior||http://www.ebi.ac.uk/efo/EFO_0004318
8590||616||Proteus syndrome||http://www.orpha.net/ORDO/Orphanet_744
8592||4572||Hereditary thrombophilia due to congenital protein C deficiency||http://www.orpha.net/ORDO/Orphanet_745
8593||2454||Mitochondrial trifunctional protein deficiency||http://www.orpha.net/ORDO/Orphanet_746
8594||3068||drinking behavior||http://www.ebi.ac.uk/efo/EFO_0004315
8595||770||GM17267||http://purl.obolibrary.org/obo/CLO_0013179
8597||14970||forced expiratory volume||http://www.ebi.ac.uk/efo/EFO_0004314
8596||382||Hutchinson-Gilford progeria syndrome||http://www.orpha.net/ORDO/Orphanet_740
8598||3068||extraversion||http://www.ebi.ac.uk/efo/EFO_0004317
8599||3068||exploratory behavior||http://www.ebi.ac.uk/efo/EFO_0004316
8600||378||Prolidase deficiency||http://www.orpha.net/ORDO/Orphanet_742
8601||772||coelomocyte||http://purl.obolibrary.org/obo/CL_0000421
8602||14970||heart function measurement||http://www.ebi.ac.uk/efo/EFO_0004311
8604||770||GM17269||http://purl.obolibrary.org/obo/CLO_0013176
8603||7330||partial thromboplastin time||http://www.ebi.ac.uk/efo/EFO_0004310
8605||14970||maximal midexpiratory flow rate||http://www.ebi.ac.uk/efo/EFO_0004313
8606||770||GM17268||http://purl.obolibrary.org/obo/CLO_0013177
8607||14970||vital capacity||http://www.ebi.ac.uk/efo/EFO_0004312
8608||770||GM17262||http://purl.obolibrary.org/obo/CLO_0013173
8609||1022||Platichthys flesus||http://purl.obolibrary.org/obo/NCBITaxon_8260
8610||1022||Hippoglossus hippoglossus||http://purl.obolibrary.org/obo/NCBITaxon_8267
8611||1833||Phenylketonuria||http://www.orpha.net/ORDO/Orphanet_716
8612||7694||Glycogen storage disease due to muscle phosphorylase kinase deficiency||http://www.orpha.net/ORDO/Orphanet_715
8613||12343||Hemolytic anemia due to diphosphoglycerate mutase deficiency||http://www.orpha.net/ORDO/Orphanet_714
8614||6899||Isolated Pierre Robin syndrome||http://www.orpha.net/ORDO/Orphanet_718
8615||8652||Disorder of manganese transport||http://www.orpha.net/ORDO/Orphanet_309851
8616||10580||Langerhans cell||http://purl.obolibrary.org/obo/CL_0000453
8617||770||GM17264||http://purl.obolibrary.org/obo/CLO_0013168
8618||770||GM17263||http://purl.obolibrary.org/obo/CLO_0013169
8619||9760||Hemolytic anemia due to glucophosphate isomerase deficiency||http://www.orpha.net/ORDO/Orphanet_712
8620||4727||Glycogen storage disease due to phosphoglycerate kinase 1 deficiency||http://www.orpha.net/ORDO/Orphanet_713
8622||6695||Pfeiffer syndrome||http://www.orpha.net/ORDO/Orphanet_710
8621||7731||dendritic cell||http://purl.obolibrary.org/obo/CL_0000451
8623||266||Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome||http://www.orpha.net/ORDO/Orphanet_309854
8624||6572||Glycogen storage disease due to phosphoglucomutase deficiency||http://www.orpha.net/ORDO/Orphanet_711
8625||770||GM17265||http://purl.obolibrary.org/obo/CLO_0013163
8626||8071||Trisomy 10p||http://www.orpha.net/ORDO/Orphanet_171929
8627||10994||alpha-methyl-L-dopa||http://purl.obolibrary.org/obo/CHEBI_61058
8628||14435||molecular function||http://purl.obolibrary.org/obo/GO_0003674
8629||4706||Alpers syndrome||http://www.orpha.net/ORDO/Orphanet_726
8630||10860||Continuous spikes and waves during sleep||http://www.orpha.net/ORDO/Orphanet_725
8631||10994||nicotine||http://purl.obolibrary.org/obo/CHEBI_18723
8632||15129||brown fat cell||http://purl.obolibrary.org/obo/CL_0000449
8633||11433||parathyroid||http://purl.obolibrary.org/obo/CL_0000446
8634||772||follicular dendritic cell||http://purl.obolibrary.org/obo/CL_0000442
8635||323||Pili bifurcati||http://www.orpha.net/ORDO/Orphanet_720
8637||11888||Gray platelet syndrome||http://www.orpha.net/ORDO/Orphanet_721
8636||8652||Disorder of iron metabolism and transport||http://www.orpha.net/ORDO/Orphanet_309842
8638||6054||Hypoplasminogenemia||http://www.orpha.net/ORDO/Orphanet_722
8639||8652||Disorder of zinc metabolism||http://www.orpha.net/ORDO/Orphanet_309845
8640||10994||tacrolimus hydrate||http://purl.obolibrary.org/obo/CHEBI_61057
8641||8652||Disorder of magnesium transport||http://www.orpha.net/ORDO/Orphanet_309848
8642||5502||Burkholderia ambifaria||http://purl.obolibrary.org/obo/NCBITaxon_152480
8643||14970||corneal topography||http://www.ebi.ac.uk/efo/EFO_0004345
8644||14970||neuroimaging measurement||http://www.ebi.ac.uk/efo/EFO_0004346
8645||8700||waist-hip ratio||http://www.ebi.ac.uk/efo/EFO_0004343
8646||8652||Disorder of copper metabolism||http://www.orpha.net/ORDO/Orphanet_309839
8647||8730||birth weight||http://www.ebi.ac.uk/efo/EFO_0004344
8648||8700||body fat distribution||http://www.ebi.ac.uk/efo/EFO_0004341
8651||770||GM17290||http://purl.obolibrary.org/obo/CLO_0013140
8650||8700||waist circumference||http://www.ebi.ac.uk/efo/EFO_0004342
8649||8910||Isolated cytochrome C oxidase deficiency||http://www.orpha.net/ORDO/Orphanet_254905
8653||4987||Renal tubulopathy - encephalopathy - liver failure||http://www.orpha.net/ORDO/Orphanet_254902
8652||8679||Disorder of mineral absorption and transport||http://www.orpha.net/ORDO/Orphanet_309836
8655||12335||X-linked myopathy with excessive autophagy||http://www.orpha.net/ORDO/Orphanet_25980
8654||8700||body mass index||http://www.ebi.ac.uk/efo/EFO_0004340
8657||561||Rett syndrome||http://www.orpha.net/ORDO/Orphanet_778
8656||8681||Disorder of other vitamins and cofactors metabolism and transport||http://www.orpha.net/ORDO/Orphanet_309833
8659||1826||Spartina maritima||http://purl.obolibrary.org/obo/NCBITaxon_49786
8658||1299||X-linked non-syndromic intellectual disability||http://www.orpha.net/ORDO/Orphanet_777
8660||2252||X-linked intellectual disability with marfanoid habitus||http://www.orpha.net/ORDO/Orphanet_776
8661||1826||Spartina anglica||http://purl.obolibrary.org/obo/NCBITaxon_49785
8662||11899||X-linked intellectual disability, Martinez type||http://www.orpha.net/ORDO/Orphanet_775
8663||6301||Disorder of catecholamine synthesis||http://www.orpha.net/ORDO/Orphanet_309830
8664||5317||Hereditary hemorrhagic telangiectasia||http://www.orpha.net/ORDO/Orphanet_774
8665||3068||addictive behaviour||http://www.ebi.ac.uk/efo/EFO_0004347
8666||2454||Refsum disease||http://www.orpha.net/ORDO/Orphanet_773
8668||772||follicle cell||http://purl.obolibrary.org/obo/CL_0000477
8669||5287||Infantile Refsum disease||http://www.orpha.net/ORDO/Orphanet_772
8667||7330||hematocrit||http://www.ebi.ac.uk/efo/EFO_0004348
8670||1826||Capsella rubella||http://purl.obolibrary.org/obo/NCBITaxon_81985
8671||5295||circadian rhythm||http://www.ebi.ac.uk/efo/EFO_0004354
8672||10652||obsolete_sensation||http://www.ebi.ac.uk/efo/EFO_0004355
8674||4122||Axenfeld-Rieger syndrome||http://www.orpha.net/ORDO/Orphanet_782
8673||10652||obsolete_taste||http://www.ebi.ac.uk/efo/EFO_0004356
8675||14970||electroencephalogram measurement||http://www.ebi.ac.uk/efo/EFO_0004357
8676||12543||reasoning||http://www.ebi.ac.uk/efo/EFO_0004350
8677||8910||Isolated ATP synthase deficiency||http://www.orpha.net/ORDO/Orphanet_254913
8679||15571||Disorder of metabolite absorption and transport||http://www.orpha.net/ORDO/Orphanet_309824
8678||8709||resting heart rate||http://www.ebi.ac.uk/efo/EFO_0004351
8680||15538||mortality||http://www.ebi.ac.uk/efo/EFO_0004352
8681||8679||Disorder of vitamin and non-protein cofactor absorption and transport ||http://www.orpha.net/ORDO/Orphanet_309827
8682||770||GM17292||http://purl.obolibrary.org/obo/CLO_0013136
8683||8675||event-related brain oscillation||http://www.ebi.ac.uk/efo/EFO_0004358
8684||2021||Rubinstein-Taybi syndrome||http://www.orpha.net/ORDO/Orphanet_783
8686||770||GM17291||http://purl.obolibrary.org/obo/CLO_0013135
8685||1125||telomere||http://www.ebi.ac.uk/efo/EFO_0004359
8687||770||GM17294||http://purl.obolibrary.org/obo/CLO_0013138
8688||1191||Glucocorticoid resistance||http://www.orpha.net/ORDO/Orphanet_786
8689||770||GM17293||http://purl.obolibrary.org/obo/CLO_0013137
8690||2681||Pseudoxanthoma elasticum||http://www.orpha.net/ORDO/Orphanet_758
8691||1022||Gillichthys mirabilis||http://purl.obolibrary.org/obo/NCBITaxon_8222
8692||3352||Arabidopsis halleri||http://purl.obolibrary.org/obo/NCBITaxon_81970
8693||8697||Disorder of bilirubin metabolism and excretion||http://www.orpha.net/ORDO/Orphanet_309816
8694||3068||suicidal ideation||http://www.ebi.ac.uk/efo/EFO_0004320
8696||7036||CD4-positive helper T cell||http://purl.obolibrary.org/obo/CL_0000492
8695||8193||tetraethylenepentamine||http://purl.obolibrary.org/obo/CHEBI_49798
8697||15571||Disorder of porphyrin and haem metabolism||http://www.orpha.net/ORDO/Orphanet_309813
8698||5295||mental process||http://www.ebi.ac.uk/efo/EFO_0004323
8699||6301||Disorder of pterin metabolism||http://www.orpha.net/ORDO/Orphanet_309819
8700||8579||body weights and measures||http://www.ebi.ac.uk/efo/EFO_0004324
8701||3068||suicide, attempted||http://www.ebi.ac.uk/efo/EFO_0004321
8704||770||GM17295||http://purl.obolibrary.org/obo/CLO_0013127
8703||1390||46,XY disorder of sex development due to 5-alpha-reductase 2 deficiency||http://www.orpha.net/ORDO/Orphanet_753
8702||8602||electrocardiography||http://www.ebi.ac.uk/efo/EFO_0004327
8706||1390||46,XY disorder of sex development due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency||http://www.orpha.net/ORDO/Orphanet_752
8705||8602||exercise test||http://www.ebi.ac.uk/efo/EFO_0004328
8707||10860||Benign occipital epilepsy||http://www.orpha.net/ORDO/Orphanet_25968
8708||8578||blood pressure||http://www.ebi.ac.uk/efo/EFO_0004325
8712||770||GM17296||http://purl.obolibrary.org/obo/CLO_0013124
8711||772||stromal cell||http://purl.obolibrary.org/obo/CL_0000499
8710||7972||Pseudoachondroplasia||http://www.orpha.net/ORDO/Orphanet_750
8709||8578||heart rate||http://www.ebi.ac.uk/efo/EFO_0004326
8713||10740||Pseudohypoaldosteronism type 2||http://www.orpha.net/ORDO/Orphanet_757
8714||4810||Pseudohypoaldosteronism type 1||http://www.orpha.net/ORDO/Orphanet_756
8716||15494||Disorder of peroxisomal alpha-, beta- and omega-oxidation||http://www.orpha.net/ORDO/Orphanet_309810
8715||1390||Leydig cell hypoplasia||http://www.orpha.net/ORDO/Orphanet_755
8717||8594||alcohol drinking||http://www.ebi.ac.uk/efo/EFO_0004329
8718||1390||Androgen insensitivity syndrome||http://www.orpha.net/ORDO/Orphanet_754
8719||322||Rabson-Mendenhall syndrome||http://www.orpha.net/ORDO/Orphanet_769
8720||1022||Thunnus thynnus||http://purl.obolibrary.org/obo/NCBITaxon_8237
8721||10399||Rhizomelic chondrodysplasia punctata type 3||http://www.orpha.net/ORDO/Orphanet_309803
8722||8594||coffee consumption||http://www.ebi.ac.uk/efo/EFO_0004330
8723||10652||obsolete_tooth eruption||http://www.ebi.ac.uk/efo/EFO_0004331
8724||8698||episodic memory||http://www.ebi.ac.uk/efo/EFO_0004333
8726||12543||intuition||http://www.ebi.ac.uk/efo/EFO_0004334
8725||238||Purine nucleoside phosphorylase deficiency||http://www.orpha.net/ORDO/Orphanet_760
8727||8698||memory, short-term||http://www.ebi.ac.uk/efo/EFO_0004335
8728||12543||speech perception||http://www.ebi.ac.uk/efo/EFO_0004336
8729||12543||intelligence||http://www.ebi.ac.uk/efo/EFO_0004337
8730||8700||body weight||http://www.ebi.ac.uk/efo/EFO_0004338
8732||3560||Pycnodysostosis||http://www.orpha.net/ORDO/Orphanet_763
8731||8700||body height||http://www.ebi.ac.uk/efo/EFO_0004339
8734||14599||mucosal type mast cell||http://purl.obolibrary.org/obo/CL_0000485
8733||12343||Hemolytic anemia due to red cell pyruvate kinase deficiency||http://www.orpha.net/ORDO/Orphanet_766
8735||14599||connective tissue type mast cell||http://purl.obolibrary.org/obo/CL_0000484
8736||4727||Pyruvate dehydrogenase deficiency||http://www.orpha.net/ORDO/Orphanet_765
8737||15||Familial long QT syndrome||http://www.orpha.net/ORDO/Orphanet_768
8738||8024||Marshall-Smith syndrome||http://www.orpha.net/ORDO/Orphanet_561
8739||10652||obsolete_epidermolytic hyperkeratosis||http://www.ebi.ac.uk/efo/EFO_0004137
8740||5912||McCune-Albright syndrome||http://www.orpha.net/ORDO/Orphanet_562
8741||10652||obsolete_basal cell nevus syndrome||http://www.ebi.ac.uk/efo/EFO_0004136
8742||9901||Congenital hereditary facial paralysis with variable hearing loss||http://www.orpha.net/ORDO/Orphanet_306530
8743||10652||obsolete_Machado-Joseph disease||http://www.ebi.ac.uk/efo/EFO_0004135
8744||14970||tumor size||http://www.ebi.ac.uk/efo/EFO_0004134
8745||306||Marshall syndrome||http://www.orpha.net/ORDO/Orphanet_560
8746||10652||obsolete_angioedemas, hereditary||http://www.ebi.ac.uk/efo/EFO_0004133
8747||10652||obsolete_aniridia||http://www.ebi.ac.uk/efo/EFO_0004132
8748||10652||obsolete_Angelman syndrome||http://www.ebi.ac.uk/efo/EFO_0004131
8749||10652||obsolete_Diamond-Blackfan anemia||http://www.ebi.ac.uk/efo/EFO_0004130
8750||1210||Familial or sporadic hemiplegic migraine||http://www.orpha.net/ORDO/Orphanet_569
8751||1211||22q11.2 deletion syndrome||http://www.orpha.net/ORDO/Orphanet_567
8752||6897||Microphthalmia, Lenz type||http://www.orpha.net/ORDO/Orphanet_568
8753||8780||Ataxia neuropathy spectrum||http://www.orpha.net/ORDO/Orphanet_254818
8754||10852||Distal monosomy 19p13.3||http://www.orpha.net/ORDO/Orphanet_96129
8755||330||Menkes disease||http://www.orpha.net/ORDO/Orphanet_565
8756||5880||Hereditary acrokeratotic poikiloderma of Kindler-Weary||http://www.orpha.net/ORDO/Orphanet_306539
8757||6897||Congenital microcoria||http://www.orpha.net/ORDO/Orphanet_566
8758||10652||obsolete_Caffey disease||http://www.ebi.ac.uk/efo/EFO_0004139
8759||4715||Meckel syndrome||http://www.orpha.net/ORDO/Orphanet_564
8760||5116||bundle branch block||http://www.ebi.ac.uk/efo/EFO_0004138
8761||11473||Monosomy 22||http://www.orpha.net/ORDO/Orphanet_96123
8762||3854||Thermoplasma acidophilum DSM 1728||http://purl.obolibrary.org/obo/NCBITaxon_273075
8763||10300||7q11.23 microduplication syndrome||http://www.orpha.net/ORDO/Orphanet_96121
8764||10910||Distal monosomy 7p||http://www.orpha.net/ORDO/Orphanet_96126
8765||2252||Distal monosomy 6p||http://www.orpha.net/ORDO/Orphanet_96125
8766||10652||obsolete_campomelic dysplasia||http://www.ebi.ac.uk/efo/EFO_0004140
8767||2866||Darier s disease||http://www.ebi.ac.uk/efo/EFO_0004124
8768||15526||acrocephalosyndactylia||http://www.ebi.ac.uk/efo/EFO_0004123
8769||12161||Adie syndrome||http://www.ebi.ac.uk/efo/EFO_0004126
8770||4266||MELAS||http://www.orpha.net/ORDO/Orphanet_550
8772||4266||MERRF||http://www.orpha.net/ORDO/Orphanet_551
8771||1732||growth hormone-secreting pituitary adenoma||http://www.ebi.ac.uk/efo/EFO_0004125
8774||13883||ArrayExpress experiment type||http://www.ebi.ac.uk/efo/EFO_0004120
8773||307||Hypotrichosis-deafness syndrome||http://www.orpha.net/ORDO/Orphanet_330029
8776||2672||chordamesoderm||http://purl.obolibrary.org/obo/UBERON_0004880
8775||6420||Mitochondrial DNA depletion syndrome, encephalomyopathic form||http://www.orpha.net/ORDO/Orphanet_254803
8777||10652||obsolete_neurofibromatosis type II||http://www.ebi.ac.uk/efo/EFO_0004122
8778||4775||Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome||http://www.orpha.net/ORDO/Orphanet_306542
8779||10652||obsolete_achondroplasia||http://www.ebi.ac.uk/efo/EFO_0004121
8781||9862||Isolated anorectal malformation||http://www.orpha.net/ORDO/Orphanet_557
8780||10132||Multiple mitochondrial DNA deletion syndrome||http://www.orpha.net/ORDO/Orphanet_254807
8783||2603||Marfan syndrome||http://www.orpha.net/ORDO/Orphanet_558
8782||5959||Porencephaly-microcephaly-bilateral congenital cataract syndrome||http://www.orpha.net/ORDO/Orphanet_306547
8784||2462||Marinesco-Sj gren syndrome||http://www.orpha.net/ORDO/Orphanet_559
8787||12331||Autosomal recessive sideroblastic anemia||http://www.orpha.net/ORDO/Orphanet_260305
8785||5055||MODY||http://www.orpha.net/ORDO/Orphanet_552
8786||8970||nephritis, hereditary||http://www.ebi.ac.uk/efo/EFO_0004128
8788||15416||hyperthyroxinemia||http://www.ebi.ac.uk/efo/EFO_0004127
8789||9236||familial amyloid neuropathy||http://www.ebi.ac.uk/efo/EFO_0004129
8790||2390||Rigid spine syndrome||http://www.orpha.net/ORDO/Orphanet_97244
8791||12348||Congenital myopathy||http://www.orpha.net/ORDO/Orphanet_97245
8793||11864||Congenital muscular dystrophy||http://www.orpha.net/ORDO/Orphanet_97242
8792||10783||Non-distal trisomy 9q||http://www.orpha.net/ORDO/Orphanet_96112
8794||9681||Pontocerebellar hypoplasia type 3||http://www.orpha.net/ORDO/Orphanet_97249
8795||8191||butyrate||http://purl.obolibrary.org/obo/CHEBI_17968
8796||8791||Zebra body myopathy||http://www.orpha.net/ORDO/Orphanet_97240
8797||15583||FASTQ format||http://www.ebi.ac.uk/efo/EFO_0004155
8799||15583||Sequence Read Format (SRF)||http://www.ebi.ac.uk/efo/EFO_0004154
8798||380||Mucopolysaccharidosis type 2||http://www.orpha.net/ORDO/Orphanet_580
8801||15483||Unspecified mitochondrial disorder||http://www.orpha.net/ORDO/Orphanet_254837
8800||10652||obsolete_cleidocranial dysplasia||http://www.ebi.ac.uk/efo/EFO_0004153
8802||2165||chorea||http://www.ebi.ac.uk/efo/EFO_0004152
8803||4427||protein modification process||http://purl.obolibrary.org/obo/GO_0036211
8806||15583||SOLiD native csfasta format||http://www.ebi.ac.uk/efo/EFO_0004159
8807||5486||FADD-related immunodeficiency||http://www.orpha.net/ORDO/Orphanet_306550
8805||6597||Mucopolysaccharidosis type 6||http://www.orpha.net/ORDO/Orphanet_583
8804||10994||cefazolin||http://purl.obolibrary.org/obo/CHEBI_474053
8808||13297||random RNA-Seq across whole transcriptome||http://www.ebi.ac.uk/efo/EFO_0004158
8809||6597||Mucopolysaccharidosis type 7||http://www.orpha.net/ORDO/Orphanet_584
8810||8843||Mitochondrial protein import disorder||http://www.orpha.net/ORDO/Orphanet_254834
8812||15583||BAM format||http://www.ebi.ac.uk/efo/EFO_0004157
8811||6597||Mucopolysaccharidosis type 3||http://www.orpha.net/ORDO/Orphanet_581
8813||15583||Standard Flowgram Format (SFF)||http://www.ebi.ac.uk/efo/EFO_0004156
8814||6597||Mucopolysaccharidosis type 4||http://www.orpha.net/ORDO/Orphanet_582
8815||5877||Muir-Torre syndrome||http://www.orpha.net/ORDO/Orphanet_587
8816||1843||Muscle-eye-brain disease||http://www.orpha.net/ORDO/Orphanet_588
8817||5287||Multiple sulfatase deficiency||http://www.orpha.net/ORDO/Orphanet_585
8818||10732||Cystic fibrosis||http://www.orpha.net/ORDO/Orphanet_586
8819||760||Primary microcephaly-epilepsy-permanent neonatal diabetes syndrome||http://www.orpha.net/ORDO/Orphanet_306558
8821||10994||puromycin||http://purl.obolibrary.org/obo/CHEBI_17939
8820||4840||Distal trisomy 22q||http://www.orpha.net/ORDO/Orphanet_96109
8822||8791||Reducing body myopathy||http://www.orpha.net/ORDO/Orphanet_97239
8823||10657||Distal trisomy 16q||http://www.orpha.net/ORDO/Orphanet_96106
8824||10689||Distal trisomy 20q||http://www.orpha.net/ORDO/Orphanet_96107
8825||10752||Distal trisomy 13q||http://www.orpha.net/ORDO/Orphanet_96105
8826||770||J-774 cell||http://purl.obolibrary.org/obo/BTO_0002279
8827||10761||Distal trisomy 11q||http://www.orpha.net/ORDO/Orphanet_96103
8829||2344||Rippling muscle disease||http://www.orpha.net/ORDO/Orphanet_97238
8828||10768||Distal trisomy 10q||http://www.orpha.net/ORDO/Orphanet_96102
8830||9636||Ligneous conjunctivitis||http://www.orpha.net/ORDO/Orphanet_97231
8831||10783||Distal trisomy 9q||http://www.orpha.net/ORDO/Orphanet_96101
8832||8791||Fingerprint body myopathy||http://www.orpha.net/ORDO/Orphanet_97232
8833||10291||Distal trisomy 8q||http://www.orpha.net/ORDO/Orphanet_96100
8834||6572||Glycogen storage disease due to phosphoglycerate mutase deficiency||http://www.orpha.net/ORDO/Orphanet_97234
8835||8843||Mitochondrial substrate carrier disorder||http://www.orpha.net/ORDO/Orphanet_254830
8836||13301||finishing sequencing assay||http://www.ebi.ac.uk/efo/EFO_0004161
8837||1022||Oryzias latipes||http://purl.obolibrary.org/obo/NCBITaxon_8090
8838||4263||CTS (Concatenated Tag Sequencing)||http://www.ebi.ac.uk/efo/EFO_0004162
8839||13297||whole chromosome random sequencing||http://www.ebi.ac.uk/efo/EFO_0004160
8840||2162||colorectal neoplasm||http://www.ebi.ac.uk/efo/EFO_0004142
8841||10652||obsolete_perineum||http://www.ebi.ac.uk/efo/EFO_0004141
8842||1485||acatalasia||http://www.ebi.ac.uk/efo/EFO_0004144
8843||15483||Mitochondrial membrane transport disorder||http://www.orpha.net/ORDO/Orphanet_254827
8844||2165||carpal tunnel syndrome||http://www.ebi.ac.uk/efo/EFO_0004143
8846||288||Mitochondrial oxidative phosphorylation disorder with no known mechanism||http://www.orpha.net/ORDO/Orphanet_254822
8845||4775||Moebius syndrome||http://www.orpha.net/ORDO/Orphanet_570
8847||10652||obsolete_central core myopathy||http://www.ebi.ac.uk/efo/EFO_0004146
8848||2546||myopathy||http://www.ebi.ac.uk/efo/EFO_0004145
8850||238||Immunodeficiency by defective expression of HLA class 2||http://www.orpha.net/ORDO/Orphanet_572
8849||5977||Autosomal dominant childhood-onset cortical cataract||http://www.orpha.net/ORDO/Orphanet_306561
8851||10652||obsolete_Charcot-Marie-Tooth disease||http://www.ebi.ac.uk/efo/EFO_0004148
8852||323||Monilethrix||http://www.orpha.net/ORDO/Orphanet_573
8854||6432||Severe X-linked mitochondrial encephalomyopathy||http://www.orpha.net/ORDO/Orphanet_238329
8853||10652||obsolete_Sotos syndrome||http://www.ebi.ac.uk/efo/EFO_0004147
8855||11473||Monosomy 21||http://www.orpha.net/ORDO/Orphanet_574
8856||2165||neuropathy||http://www.ebi.ac.uk/efo/EFO_0004149
8857||41||Muckle-Wells syndrome||http://www.orpha.net/ORDO/Orphanet_575
8858||6588||Mucolipidosis type 2||http://www.orpha.net/ORDO/Orphanet_576
8859||6588||Mucolipidosis type 3||http://www.orpha.net/ORDO/Orphanet_577
8860||9681||Mucolipidosis type 4||http://www.orpha.net/ORDO/Orphanet_578
8861||6597||Mucopolysaccharidosis type 1||http://www.orpha.net/ORDO/Orphanet_579
8862||770||macrophage cell line||http://purl.obolibrary.org/obo/BTO_0002278
8863||5700||Riboflavin transporter deficiency||http://www.orpha.net/ORDO/Orphanet_97229
8864||10994||lipopolysaccharide||http://purl.obolibrary.org/obo/CHEBI_16412
8865||8190||indole-3-acetic acid||http://purl.obolibrary.org/obo/CHEBI_16411
8866||1022||Poecilia reticulata||http://purl.obolibrary.org/obo/NCBITaxon_8081
8867||1022||Xiphophorus||http://purl.obolibrary.org/obo/NCBITaxon_8082
8868||10652||obsolete_cherubism||http://www.ebi.ac.uk/efo/EFO_0004150
8869||10652||obsolete_Alagille syndrome||http://www.ebi.ac.uk/efo/EFO_0004151
8870||10682||Familial hyperinsulinism||http://www.orpha.net/ORDO/Orphanet_276525
8871||772||prokaryotic cell||http://purl.obolibrary.org/obo/CL_0000520
8872||772||fungal cell||http://purl.obolibrary.org/obo/CL_0000521
8873||13276||Lethal infantile mitochondrial myopathy||http://www.orpha.net/ORDO/Orphanet_254857
8874||13883||reduced representation preparation||http://www.ebi.ac.uk/efo/EFO_0004178
8875||13276||Pure mitochondrial myopathy||http://www.orpha.net/ORDO/Orphanet_254854
8876||13883||restriction digest||http://www.ebi.ac.uk/efo/EFO_0004179
8877||13883||ChIP||http://www.ebi.ac.uk/efo/EFO_0004176
8878||1826||Cuscuta pentagona||http://purl.obolibrary.org/obo/NCBITaxon_112407
8879||8940||Micrococcal Nuclease digestion||http://www.ebi.ac.uk/efo/EFO_0004177
8880||11842||Sodium channelopathy-related small fiber neuropathy||http://www.orpha.net/ORDO/Orphanet_306577
8881||8918||cot filtration for theoretical single copy genomic DNA||http://www.ebi.ac.uk/efo/EFO_0004174
8882||13883||Methylation Spanning Linker Library (MSLL) processing||http://www.ebi.ac.uk/efo/EFO_0004175
8884||4335||nucleic acid library construction protocol||http://www.ebi.ac.uk/efo/EFO_0004184
8883||2201||Familial papillary thyroid carcinoma with renal papillary neoplasia||http://www.orpha.net/ORDO/Orphanet_97290
8885||13883||size fractionation||http://www.ebi.ac.uk/efo/EFO_0004183
8886||13883||Rapid Amplification of cDNA Ends||http://www.ebi.ac.uk/efo/EFO_0004182
8887||13883||cap analysis gene expression||http://www.ebi.ac.uk/efo/EFO_0004181
8888||13883||DNA selection through 5-methylcytidine antibody||http://www.ebi.ac.uk/efo/EFO_0004180
8889||204||Immunodeficiency due to MASP-2 deficiency||http://www.orpha.net/ORDO/Orphanet_331187
8890||13249||Maternally-inherited mitochondrial dystonia||http://www.orpha.net/ORDO/Orphanet_254851
8891||288||Congenital cataract - progressive muscular hypotonia - hearing loss - developmental delay||http://www.orpha.net/ORDO/Orphanet_330054
8893||3694||17beta-estradiol||http://purl.obolibrary.org/obo/CHEBI_16469
8892||2252||Bohring-Opitz syndrome||http://www.orpha.net/ORDO/Orphanet_97297
8896||193||Constitutional neutropenia with extra-haematopoietic manifestations||http://www.orpha.net/ORDO/Orphanet_331184
8894||772||syncytiotrophoblast cell||http://purl.obolibrary.org/obo/CL_0000525
8895||8846||Lethal encephalopathy due to mitochondrial and peroxisomal fission defect||http://www.orpha.net/ORDO/Orphanet_330050
8897||14126||culture supernatant||http://purl.obolibrary.org/obo/BTO_0002217
8898||1022||Fundulus heteroclitus||http://purl.obolibrary.org/obo/NCBITaxon_8078
8899||10994||asymmetric dimethylarginine||http://purl.obolibrary.org/obo/CHEBI_17929
8900||8444||Central core disease||http://www.orpha.net/ORDO/Orphanet_597
8901||1848||X-linked centronuclear myopathy||http://www.orpha.net/ORDO/Orphanet_596
8902||12322||Distal myopathy||http://www.orpha.net/ORDO/Orphanet_599
8903||2390||Multiminicore myopathy||http://www.orpha.net/ORDO/Orphanet_598
8905||13883||RAPD||http://www.ebi.ac.uk/efo/EFO_0004167
8904||12348||Myofibrillar myopathy||http://www.orpha.net/ORDO/Orphanet_593
8906||4987||Exercise intolerance with lactic acidosis||http://www.orpha.net/ORDO/Orphanet_254843
8907||13883||hypomethylated partial restriction digest||http://www.ebi.ac.uk/efo/EFO_0004168
8908||13883||methyl filtration||http://www.ebi.ac.uk/efo/EFO_0004169
8909||8791||Centronuclear myopathy||http://www.orpha.net/ORDO/Orphanet_595
8910||21||Isolated oxidative phosphorylation complex disorder||http://www.orpha.net/ORDO/Orphanet_254846
8911||15583||SOLiD native qual format||http://www.ebi.ac.uk/efo/EFO_0004163
8912||3310||Autosomal dominant Opitz G/BBB syndrome||http://www.orpha.net/ORDO/Orphanet_306588
8913||15583||Illumina native qseq format||http://www.ebi.ac.uk/efo/EFO_0004164
8914||15583||Illumina native scarf format||http://www.ebi.ac.uk/efo/EFO_0004165
8915||15583||Illumina native fastq format||http://www.ebi.ac.uk/efo/EFO_0004166
8916||9751||Congenital myasthenic syndrome||http://www.orpha.net/ORDO/Orphanet_590
8917||8918||cot filtration for single or low copy genomic DNA||http://www.ebi.ac.uk/efo/EFO_0004171
8918||4335||nucleic acid sequencing protocol||http://www.ebi.ac.uk/efo/EFO_0004170
8919||8918||cot filtration for highly repetitive genomic DNA||http://www.ebi.ac.uk/efo/EFO_0004173
8920||8918||cot filtration for moderately repetitive genomic DNA||http://www.ebi.ac.uk/efo/EFO_0004172
8921||194||Other immunodeficiency syndromes due to defects in innate immunity||http://www.orpha.net/ORDO/Orphanet_331193
8922||2897||Carney-Stratakis syndrome||http://www.orpha.net/ORDO/Orphanet_97286
8923||10994||alpha-D-glucose||http://purl.obolibrary.org/obo/CHEBI_17925
8924||204||Immunodeficiency due to ficolin3 deficiency||http://www.orpha.net/ORDO/Orphanet_331190
8925||306||Curly hair-acral keratoderma-caries syndrome||http://www.orpha.net/ORDO/Orphanet_307766
8926||3310||X-linked Opitz G/BBB syndrome||http://www.orpha.net/ORDO/Orphanet_306597
8927||2162||skin neoplasm||http://www.ebi.ac.uk/efo/EFO_0004198
8928||8927||dysplastic nevus||http://www.ebi.ac.uk/efo/EFO_0004199
8929||2714||viral human hepatitis infection||http://www.ebi.ac.uk/efo/EFO_0004196
8930||8929||hepatitis B infection||http://www.ebi.ac.uk/efo/EFO_0004197
8931||12151||trichomoniasis||http://purl.obolibrary.org/obo/DOID_1947
8932||6264||Mitochondrial DNA depletion syndrome, myopathic form||http://www.orpha.net/ORDO/Orphanet_254875
8933||5611||Hemoglobin Lepore - beta-thalassemia||http://www.orpha.net/ORDO/Orphanet_330032
8934||6420||Mitochondrial DNA depletion syndrome, hepatocerebral form||http://www.orpha.net/ORDO/Orphanet_254871
8935||5295||disease course||http://purl.obolibrary.org/obo/OGMS_0000063
8936||1319||alanine||http://purl.obolibrary.org/obo/CHEBI_16449
8937||772||granulosa cell||http://purl.obolibrary.org/obo/CL_0000501
8938||12318||Autosomal dominant diffuse mutilating palmoplantar keratoderma||http://www.orpha.net/ORDO/Orphanet_307773
8939||13883||enrichment of methylated DNA||http://www.ebi.ac.uk/efo/EFO_0004185
8940||13883||Deoxyribonuclease digestion||http://www.ebi.ac.uk/efo/EFO_0004186
8941||13883||cDNA library construction||http://www.ebi.ac.uk/efo/EFO_0004187
8942||13883||hybrid selection of targets||http://www.ebi.ac.uk/efo/EFO_0004188
8943||13883||DNA shearing||http://www.ebi.ac.uk/efo/EFO_0004189
8944||10994||phenytoin||http://purl.obolibrary.org/obo/CHEBI_8107
8946||13276||Mitochondrial myopathy with reversible cytochrome C oxidase deficiency||http://www.orpha.net/ORDO/Orphanet_254864
8945||1732||androgenetic alopecia||http://www.ebi.ac.uk/efo/EFO_0004191
8948||12539||Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency||http://www.orpha.net/ORDO/Orphanet_331176
8947||1750||open-angle glaucoma||http://www.ebi.ac.uk/efo/EFO_0004190
8949||1006||basal cell carcinoma||http://www.ebi.ac.uk/efo/EFO_0004193
8950||2866||alopecia areata||http://www.ebi.ac.uk/efo/EFO_0004192
8951||10215||LDL cholesterol||http://www.ebi.ac.uk/efo/EFO_0004195
8952||8970||IGA glomerulonephritis||http://www.ebi.ac.uk/efo/EFO_0004194
8953||1022||Gadus morhua||http://purl.obolibrary.org/obo/NCBITaxon_8049
8954||15191||smooth muscle myoblast||http://purl.obolibrary.org/obo/CL_0000514
8955||14504||skeletal muscle myoblast||http://purl.obolibrary.org/obo/CL_0000515
8956||9293||Autosomal dominant methemoglobinemia||http://www.orpha.net/ORDO/Orphanet_330041
8957||2252||Cerebro-oculo-nasal syndrome||http://www.orpha.net/ORDO/Orphanet_66625
8958||12531||non-alcoholic fatty liver disease||http://www.ebi.ac.uk/efo/EFO_0003095
8959||766||ganglioglioma||http://www.ebi.ac.uk/efo/EFO_0003094
8961||1006||adrenocortical carcinoma||http://www.ebi.ac.uk/efo/EFO_0003093
8960||8780||Autosomal dominant progressive external ophthalmoplegia||http://www.orpha.net/ORDO/Orphanet_254892
8962||10652||obsolete_neurofibromatosis||http://www.ebi.ac.uk/efo/EFO_0003092
8963||10652||obsolete_spinocerebellar ataxia type 17||http://www.ebi.ac.uk/efo/EFO_0003091
8964||10652||obsolete_spinocerebellar ataxia type 7||http://www.ebi.ac.uk/efo/EFO_0003090
8965||6543||Deafness - encephaloneuropathy - obesity - valvulopathy||http://www.orpha.net/ORDO/Orphanet_254898
8966||10652||obsolete_spinocerebellar ataxia type 1||http://www.ebi.ac.uk/efo/EFO_0003089
8967||15312||atrial myocardium||http://www.ebi.ac.uk/efo/EFO_0003087
8968||15312||ventricular myocardium||http://www.ebi.ac.uk/efo/EFO_0003088
8969||1505||dedifferentiated liposarcoma||http://www.ebi.ac.uk/efo/EFO_0003085
8970||1391||kidney disease||http://www.ebi.ac.uk/efo/EFO_0003086
8971||1022||Myzus persicae||http://purl.obolibrary.org/obo/NCBITaxon_13164
8972||1307||Obesity due to congenital leptin deficiency||http://www.orpha.net/ORDO/Orphanet_66628
8974||2252||Goldberg-Shprintzen megacolon syndrome||http://www.orpha.net/ORDO/Orphanet_66629
8973||5025||Microsporum ferrugineum||http://purl.obolibrary.org/obo/NCBITaxon_77205
8975||5502||Rickettsia prowazekii Rp22||http://purl.obolibrary.org/obo/NCBITaxon_449216
8976||11347||Autosomal dominant hyperinsulinism due to SUR1 deficiency||http://www.orpha.net/ORDO/Orphanet_276575
8978||11333||Paternal uniparental disomy of chromosome 7||http://www.orpha.net/ORDO/Orphanet_96192
8977||770||COLO205||http://www.ebi.ac.uk/efo/EFO_0003082
8979||8753||Spinocerebellar ataxia with epilepsy||http://www.orpha.net/ORDO/Orphanet_254881
8980||11333||Paternal uniparental disomy of chromosome 6||http://www.orpha.net/ORDO/Orphanet_96191
8981||770||SK-MEL-28||http://www.ebi.ac.uk/efo/EFO_0003081
8983||11333||Paternal uniparental disomy of chromosome 5||http://www.orpha.net/ORDO/Orphanet_96190
8982||1505||round cell liposarcoma||http://www.ebi.ac.uk/efo/EFO_0003084
8984||1505||pleomorphic liposarcoma||http://www.ebi.ac.uk/efo/EFO_0003083
8985||11333||Paternal uniparental disomy of chromosome 21||http://www.orpha.net/ORDO/Orphanet_96195
8986||8780||Autosomal recessive progressive external ophthalmoplegia||http://www.orpha.net/ORDO/Orphanet_254886
8987||11333||Paternal uniparental disomy of chromosome 20||http://www.orpha.net/ORDO/Orphanet_96194
8988||10547||Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome 11||http://www.orpha.net/ORDO/Orphanet_96193
8989||10652||obsolete_yolk sac||http://www.ebi.ac.uk/efo/EFO_0003078
8990||10652||obsolete_X-linked agammaglobulinemia||http://www.ebi.ac.uk/efo/EFO_0003079
8991||770||ES cell line||http://www.ebi.ac.uk/efo/EFO_0003074
8992||1485||xanthoma||http://www.ebi.ac.uk/efo/EFO_0003075
8993||14614||thyrocyte||http://www.ebi.ac.uk/efo/EFO_0003076
8994||3069||trabecular meshwork||http://www.ebi.ac.uk/efo/EFO_0003077
8995||6294||Gr sbeck-Imerslund disease||http://www.orpha.net/ORDO/Orphanet_35858
8996||10159||Peripheral precocious puberty||http://www.orpha.net/ORDO/Orphanet_178040
8997||10286||Disease with diffuse palmoplantar keratoderma as a major feature||http://www.orpha.net/ORDO/Orphanet_307711
8998||1022||Melopsittacus undulatus||http://purl.obolibrary.org/obo/NCBITaxon_13146
8999||11331||Maternal uniparental disomy of chromosome 21||http://www.orpha.net/ORDO/Orphanet_96187
9000||11331||Maternal uniparental disomy of chromosome 20||http://www.orpha.net/ORDO/Orphanet_96186
9001||11331||Maternal uniparental disomy of chromosome 22||http://www.orpha.net/ORDO/Orphanet_96188
9002||11331||Maternal uniparental disomy of chromosome 9||http://www.orpha.net/ORDO/Orphanet_96183
9003||6202||Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7||http://www.orpha.net/ORDO/Orphanet_96182
9004||10633||Maternal uniparental disomy of chromosome 16||http://www.orpha.net/ORDO/Orphanet_96185
9005||11331||Maternal uniparental disomy of chromosome 14||http://www.orpha.net/ORDO/Orphanet_96184
9006||11331||Maternal uniparental disomy of chromosome 6||http://www.orpha.net/ORDO/Orphanet_96181
9007||11331||Maternal uniparental disomy of chromosome 4||http://www.orpha.net/ORDO/Orphanet_96180
9008||11347||Hyperinsulinism due to UCP2 deficiency||http://www.orpha.net/ORDO/Orphanet_276556
9009||10994||phenol||http://purl.obolibrary.org/obo/CHEBI_15882
9010||4951||Dilated cardiomyopathy with ataxia||http://www.orpha.net/ORDO/Orphanet_66634
9012||11331||Maternal uniparental disomy of chromosome 2||http://www.orpha.net/ORDO/Orphanet_96179
9011||5700||Sensorineural hearing loss - early graying - essential tremor||http://www.orpha.net/ORDO/Orphanet_66633
9013||2405||Ring chromosome 16||http://www.orpha.net/ORDO/Orphanet_96178
9014||2252||Kleefstra syndrome||http://www.orpha.net/ORDO/Orphanet_261494
9015||4139||CEDNIK syndrome||http://www.orpha.net/ORDO/Orphanet_66631
9016||2405||Ring chromosome 15||http://www.orpha.net/ORDO/Orphanet_96177
9018||2405||Ring chromosome 13||http://www.orpha.net/ORDO/Orphanet_96176
9017||6231||Congenital pseudoarthrosis of clavicle||http://www.orpha.net/ORDO/Orphanet_66630
9019||2405||Ring chromosome 11||http://www.orpha.net/ORDO/Orphanet_96175
9020||2405||Ring chromosome 9||http://www.orpha.net/ORDO/Orphanet_96173
9021||2405||Ring chromosome 3||http://www.orpha.net/ORDO/Orphanet_96172
9022||2405||Ring chromosome 2||http://www.orpha.net/ORDO/Orphanet_96171
9023||4928||Emanuel syndrome||http://www.orpha.net/ORDO/Orphanet_96170
9024||2165||Pick disease||http://www.ebi.ac.uk/efo/EFO_0003096
9025||2700||empyema||http://www.ebi.ac.uk/efo/EFO_0003097
9026||10652||obsolete_meningioma||http://www.ebi.ac.uk/efo/EFO_0003098
9028||15416||Cushing syndrome||http://www.ebi.ac.uk/efo/EFO_0003099
9027||4259||response to ximelagatran||http://purl.obolibrary.org/obo/GO_0036288
9029||7120||Non-acquired combined pituitary hormone deficiencies without extra-pituitary malformations||http://www.orpha.net/ORDO/Orphanet_178025
9030||13516||response to iloperidone||http://purl.obolibrary.org/obo/GO_0036287
9031||6302||Hyperinsulinism-hyperammonemia syndrome||http://www.orpha.net/ORDO/Orphanet_35878
9032||7963||Diaphanospondylodysostosis||http://www.orpha.net/ORDO/Orphanet_66637
9033||12136||large cell lung carcinoma||http://www.ebi.ac.uk/efo/EFO_0003050
9034||2672||calf||http://www.ebi.ac.uk/efo/EFO_0003051
9035||10659||Non-distal monosomy 12q||http://www.orpha.net/ORDO/Orphanet_96160
9036||10994||sucrose||http://purl.obolibrary.org/obo/CHEBI_17992
9037||5502||Helicobacter pylori P12||http://purl.obolibrary.org/obo/NCBITaxon_570508
9038||5602||Non-distal monosomy 20q||http://www.orpha.net/ORDO/Orphanet_96164
9040||4928||Recombinant 8 syndrome||http://www.orpha.net/ORDO/Orphanet_96167
9039||5209||Xq27.3q28 duplication syndrome||http://www.orpha.net/ORDO/Orphanet_261483
9041||1022||Geospiza scandens||http://purl.obolibrary.org/obo/NCBITaxon_48886
9042||5457||Monosomy 13q34||http://www.orpha.net/ORDO/Orphanet_96168
9044||2252||Koolen-De Vries syndrome||http://www.orpha.net/ORDO/Orphanet_96169
9043||1022||Geospiza magnirostris||http://purl.obolibrary.org/obo/NCBITaxon_48885
9045||4259||response to statin||http://purl.obolibrary.org/obo/GO_0036273
9046||12747||response to lapatinib||http://purl.obolibrary.org/obo/GO_0036274
9047||1022||Geospiza conirostris||http://purl.obolibrary.org/obo/NCBITaxon_48882
9050||12741||response to 5  fluorouracil||http://purl.obolibrary.org/obo/GO_0036275
9049||4272||Alpha-thalassemia - myelodysplastic syndrome||http://www.orpha.net/ORDO/Orphanet_231401
9048||1022||Geospiza fortis||http://purl.obolibrary.org/obo/NCBITaxon_48883
9051||4259||response to antidepressant||http://purl.obolibrary.org/obo/GO_0036276
9052||4259||response to diruetic||http://purl.obolibrary.org/obo/GO_0036270
9053||4259||response to methylphenidate||http://purl.obolibrary.org/obo/GO_0036271
9054||12747||response to gemcitabine||http://purl.obolibrary.org/obo/GO_0036272
9055||10652||obsolete_ilium||http://www.ebi.ac.uk/efo/EFO_0003049
9056||770||HES2||http://www.ebi.ac.uk/efo/EFO_0003048
9058||6728||Achondrogenesis type 2||http://www.orpha.net/ORDO/Orphanet_93296
9057||8929||hepatitis C infection||http://www.ebi.ac.uk/efo/EFO_0003047
9060||5295||heart transplant rejection||http://www.ebi.ac.uk/efo/EFO_0003046
9059||6244||Okihiro syndrome||http://www.orpha.net/ORDO/Orphanet_93293
9061||770||H9||http://www.ebi.ac.uk/efo/EFO_0003045
9063||4259||response to anticonvulsant||http://purl.obolibrary.org/obo/GO_0036277
9062||770||NCI-H460||http://www.ebi.ac.uk/efo/EFO_0003044
9064||6728||Achondrogenesis type 1A||http://www.orpha.net/ORDO/Orphanet_93299
9065||770||NCI-H1299||http://www.ebi.ac.uk/efo/EFO_0003043
9067||770||H1-hESC||http://www.ebi.ac.uk/efo/EFO_0003042
9066||6728||Hypochondrogenesis||http://www.orpha.net/ORDO/Orphanet_93297
9069||2672||esophageal epithelium||http://www.ebi.ac.uk/efo/EFO_0003041
9068||6728||Achondrogenesis type 1B||http://www.orpha.net/ORDO/Orphanet_93298
9070||770||embryonic cell line||http://www.ebi.ac.uk/efo/EFO_0003040
9071||5602||Distal monosomy 20q||http://www.orpha.net/ORDO/Orphanet_96152
9072||10994||2-deoxy-D-glucose||http://purl.obolibrary.org/obo/CHEBI_15866
9073||5466||Distal monosomy 14q||http://www.orpha.net/ORDO/Orphanet_96150
9074||13448||floor plate of midbrain||http://purl.obolibrary.org/obo/UBERON_0003307
9075||10994||allopurinol||http://purl.obolibrary.org/obo/CHEBI_40279
9077||5502||Fusobacterium nucleatum||http://purl.obolibrary.org/obo/NCBITaxon_851
9076||7340||Congenital nephrotic syndrome-interstitial lung disease-epidermolysis bullosa syndrome||http://www.orpha.net/ORDO/Orphanet_306504
9078||770||EAhy 926 cell||http://www.ebi.ac.uk/efo/EFO_0003039
9079||4887||Monosomy Xp21||http://www.orpha.net/ORDO/Orphanet_261476
9081||7172||LAMB2-related infantile-onset nephrotic syndrome||http://www.orpha.net/ORDO/Orphanet_306507
9080||10652||obsolete_colon mucosa||http://www.ebi.ac.uk/efo/EFO_0003038
9083||2866||cellulitis||http://www.ebi.ac.uk/efo/EFO_0003035
9082||7970||Spondyloepimetaphyseal dysplasia, Pakistani type||http://www.orpha.net/ORDO/Orphanet_93282
9084||3536||Spondyloepiphyseal dysplasia, Kimberley type||http://www.orpha.net/ORDO/Orphanet_93283
9085||770||CMK||http://www.ebi.ac.uk/efo/EFO_0003037
9086||10143||Spondyloepiphyseal dysplasia tarda||http://www.orpha.net/ORDO/Orphanet_93284
9087||772||clear cell||http://www.ebi.ac.uk/efo/EFO_0003036
9088||2700||abscess||http://www.ebi.ac.uk/efo/EFO_0003030
9089||2700||bacteriemia||http://www.ebi.ac.uk/efo/EFO_0003033
9090||15426||anaplastic large cell lymphoma||http://www.ebi.ac.uk/efo/EFO_0003032
9091||11347||Autosomal dominant hyperinsulinism due to Kir6.2 deficiency||http://www.orpha.net/ORDO/Orphanet_276580
9092||770||SK-N-SH||http://www.ebi.ac.uk/efo/EFO_0003072
9093||15414||asymptomatic myeloma||http://www.ebi.ac.uk/efo/EFO_0003073
9094||3432||buttock||http://www.ebi.ac.uk/efo/EFO_0003070
9095||7981||Mild spondyloepiphyseal dysplasia due to COL2A1 mutation with early-onset osteoarthritis||http://www.orpha.net/ORDO/Orphanet_93279
9096||10652||obsolete_sacrum||http://www.ebi.ac.uk/efo/EFO_0003071
9097||6022||Kleefstra syndrome due to 9q34 microdeletion||http://www.orpha.net/ORDO/Orphanet_96147
9098||5962||Distal monosomy 10q||http://www.orpha.net/ORDO/Orphanet_96148
9099||10659||Distal monosomy 12q||http://www.orpha.net/ORDO/Orphanet_96149
9100||9342||Diazoxide-resistant hyperinsulinism||http://www.orpha.net/ORDO/Orphanet_276585
9101||6079||Distal monosomy 4q||http://www.orpha.net/ORDO/Orphanet_96145
9102||7633||Familial primary hypomagnesemia with hypocalcuria||http://www.orpha.net/ORDO/Orphanet_306519
9103||11892||Short rib-polydactyly syndrome, Saldino-Noonan type||http://www.orpha.net/ORDO/Orphanet_93270
9104||7633||Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis||http://www.orpha.net/ORDO/Orphanet_306516
9105||5502||Desulfovibrio vulgaris str. Hildenborough||http://purl.obolibrary.org/obo/NCBITaxon_882
9106||5502||Desulfovibrio vulgaris||http://purl.obolibrary.org/obo/NCBITaxon_881
9109||221||rib||http://www.ebi.ac.uk/efo/EFO_0003066
9108||583||Autosomal recessive spastic paraplegia type 48||http://www.orpha.net/ORDO/Orphanet_306511
9107||10225||Monostotic fibrous dysplasia||http://www.orpha.net/ORDO/Orphanet_93277
9110||14759||foot||http://www.ebi.ac.uk/efo/EFO_0003065
9111||770||primary cell line||http://www.ebi.ac.uk/efo/EFO_0003064
9113||2676||polymyositis||http://www.ebi.ac.uk/efo/EFO_0003063
9112||10225||Polyostotic fibrous dysplasia||http://www.orpha.net/ORDO/Orphanet_93276
9115||3002||Thanatophoric dysplasia type 2||http://www.orpha.net/ORDO/Orphanet_93274
9114||10652||obsolete_elbow||http://www.ebi.ac.uk/efo/EFO_0003069
9117||10633||Short rib-polydactyly syndrome, Verma-Naumoff type||http://www.orpha.net/ORDO/Orphanet_93271
9116||10652||obsolete_shoulder||http://www.ebi.ac.uk/efo/EFO_0003068
9118||4319||latissimus dorsi||http://www.ebi.ac.uk/efo/EFO_0003067
9119||11892||Short rib-polydactyly syndrome, Majewski type||http://www.orpha.net/ORDO/Orphanet_93269
9121||12136||non-small cell lung carcinoma||http://www.ebi.ac.uk/efo/EFO_0003060
9120||11892||Short rib-polydactyly syndrome, Beemer-Langer type||http://www.orpha.net/ORDO/Orphanet_93268
9122||8190||arachidonic acid||http://purl.obolibrary.org/obo/CHEBI_15843
9123||770||OVCAR3||http://www.ebi.ac.uk/efo/EFO_0003061
9124||14771||peroneal nerve||http://www.ebi.ac.uk/efo/EFO_0003062
9125||10994||oligogalacturonide||http://purl.obolibrary.org/obo/CHEBI_62533
9126||1826||Geranium dissectum||http://purl.obolibrary.org/obo/NCBITaxon_326028
9127||6751||Diazoxide-resistant focal hyperinsulinism due to SUR1 deficiency||http://www.orpha.net/ORDO/Orphanet_276598
9128||10910||Non-distal monosomy 7p||http://www.orpha.net/ORDO/Orphanet_96136
9129||3854||Methanobrevibacter smithii ATCC 35061||http://purl.obolibrary.org/obo/NCBITaxon_420247
9130||5502||Dichelobacter nodosus||http://purl.obolibrary.org/obo/NCBITaxon_870
9131||9901||Isolated hereditary congenital facial paralysis||http://www.orpha.net/ORDO/Orphanet_306527
9132||14898||forearm||http://www.ebi.ac.uk/efo/EFO_0003053
9133||10652||obsolete_fibula||http://www.ebi.ac.uk/efo/EFO_0003052
9135||770||LP1||http://www.ebi.ac.uk/efo/EFO_0003055
9134||7633||Familial primary hypomagnesemia with normocalcuria||http://www.orpha.net/ORDO/Orphanet_306522
9136||6610||Cloverleaf skull - multiple congenital anomalies||http://www.orpha.net/ORDO/Orphanet_93267
9137||10652||obsolete_tibia||http://www.ebi.ac.uk/efo/EFO_0003054
9138||8622||Pfeiffer syndrome type 3||http://www.orpha.net/ORDO/Orphanet_93260
9139||10652||obsolete_mediastinum||http://www.ebi.ac.uk/efo/EFO_0003057
9140||770||M14||http://www.ebi.ac.uk/efo/EFO_0003056
9141||6610||Crouzon syndrome - acanthosis nigricans||http://www.orpha.net/ORDO/Orphanet_93262
9142||10652||obsolete_NCIH460||http://www.ebi.ac.uk/efo/EFO_0003058
9144||1761||villitis||http://www.ebi.ac.uk/efo/EFO_0003110
9143||5502||Lactobacillus parabuchneri||http://purl.obolibrary.org/obo/NCBITaxon_152331
9145||10994||bezafibrate||http://purl.obolibrary.org/obo/CHEBI_47612
9146||10652||obsolete_polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy||http://www.ebi.ac.uk/efo/EFO_0003113
9147||13666||pauciarticular juvenile rheumatoid arthritis||http://www.ebi.ac.uk/efo/EFO_0003114
9148||10652||obsolete_neuronal ceroid lipofuscinosis||http://www.ebi.ac.uk/efo/EFO_0003111
9149||10652||obsolete_late infantile neuronal ceroid lipofuscinosis||http://www.ebi.ac.uk/efo/EFO_0003112
9151||3643||Skin ulcer||http://purl.obolibrary.org/obo/HP_0200042
9150||770||NCI-H1334||http://www.ebi.ac.uk/efo/EFO_0003117
9152||770||NCI-H157||http://www.ebi.ac.uk/efo/EFO_0003118
9153||770||EBC-1||http://www.ebi.ac.uk/efo/EFO_0003115
9154||770||NCI-H125||http://www.ebi.ac.uk/efo/EFO_0003116
9155||1826||Eucalyptus nitens||http://purl.obolibrary.org/obo/NCBITaxon_87674
9156||770||NCI-H1648||http://www.ebi.ac.uk/efo/EFO_0003119
9157||5502||Anaplasma phagocytophilum||http://purl.obolibrary.org/obo/NCBITaxon_948
9158||3114||Fragile X-associated tremor/ataxia syndrome||http://www.orpha.net/ORDO/Orphanet_93256
9159||770||NCI-H2279||http://www.ebi.ac.uk/efo/EFO_0003120
9160||770||NCI-H2882||http://www.ebi.ac.uk/efo/EFO_0003121
9161||770||NCI-H2287||http://www.ebi.ac.uk/efo/EFO_0003122
9162||770||NCI-H3255||http://www.ebi.ac.uk/efo/EFO_0003123
9163||770||NCI-H520||http://www.ebi.ac.uk/efo/EFO_0003124
9164||770||NCI-H820||http://www.ebi.ac.uk/efo/EFO_0003125
9165||770||HCC1171||http://www.ebi.ac.uk/efo/EFO_0003126
9166||770||HCC1159||http://www.ebi.ac.uk/efo/EFO_0003127
9167||770||HCC1359||http://www.ebi.ac.uk/efo/EFO_0003128
9168||770||HCC15||http://www.ebi.ac.uk/efo/EFO_0003129
9169||11538||system development||http://purl.obolibrary.org/obo/GO_0048731
9170||8622||Pfeiffer syndrome type 1||http://www.orpha.net/ORDO/Orphanet_93258
9171||8622||Pfeiffer syndrome type 2||http://www.orpha.net/ORDO/Orphanet_93259
9172||770||HCC515||http://www.ebi.ac.uk/efo/EFO_0003135
9174||770||HCC78||http://www.ebi.ac.uk/efo/EFO_0003136
9173||10994||ciprofloxacin||http://purl.obolibrary.org/obo/CHEBI_100241
9175||770||HCC44||http://www.ebi.ac.uk/efo/EFO_0003133
9176||5502||Wolbachia pipientis||http://purl.obolibrary.org/obo/NCBITaxon_955
9177||770||HCC461||http://www.ebi.ac.uk/efo/EFO_0003134
9178||770||HCC366||http://www.ebi.ac.uk/efo/EFO_0003131
9179||770||HCC4006||http://www.ebi.ac.uk/efo/EFO_0003132
9180||6187||Sporadic idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation||http://www.orpha.net/ORDO/Orphanet_93222
9182||5502||Bdellovibrio bacteriovorus||http://purl.obolibrary.org/obo/NCBITaxon_959
9181||6187||Sporadic idiopathic steroid-resistant nephrotic syndrome with minimal changes||http://www.orpha.net/ORDO/Orphanet_93221
9183||770||HCC193||http://www.ebi.ac.uk/efo/EFO_0003130
9184||6187||Sporadic idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis||http://www.orpha.net/ORDO/Orphanet_93220
9185||1022||Litomosoides sigmodontis||http://purl.obolibrary.org/obo/NCBITaxon_42156
9186||10994||norfloxacin||http://purl.obolibrary.org/obo/CHEBI_100246
9187||770||HCjE||http://www.ebi.ac.uk/efo/EFO_0003139
9188||770||HCC827||http://www.ebi.ac.uk/efo/EFO_0003137
9189||770||HCC95||http://www.ebi.ac.uk/efo/EFO_0003138
9190||1015||heart failure||http://www.ebi.ac.uk/efo/EFO_0003144
9191||9190||high output heart failure||http://www.ebi.ac.uk/efo/EFO_0003145
9192||9190||symptomatic heart failure||http://www.ebi.ac.uk/efo/EFO_0003146
9193||9192||mild heart failure||http://www.ebi.ac.uk/efo/EFO_0003147
9194||770||LC2/AD||http://www.ebi.ac.uk/efo/EFO_0003140
9195||770||LK-2||http://www.ebi.ac.uk/efo/EFO_0003141
9196||770||Lu130||http://www.ebi.ac.uk/efo/EFO_0003142
9197||4738||CLIP-seq||http://www.ebi.ac.uk/efo/EFO_0003143
9198||9192||moderate heart failure||http://www.ebi.ac.uk/efo/EFO_0003148
9199||9190||advanced heart failure||http://www.ebi.ac.uk/efo/EFO_0003149
9200||15365||Combined deficiency of factor V and factor VIII||http://www.orpha.net/ORDO/Orphanet_35909
9201||203||African American||http://www.ebi.ac.uk/efo/EFO_0003150
9202||2670||root cortex||http://purl.obolibrary.org/obo/PO_0000258
9204||770||GM17286||http://purl.obolibrary.org/obo/CLO_0013086
9203||1022||Pomacentrus moluccensis||http://purl.obolibrary.org/obo/NCBITaxon_80956
9205||770||GM17285||http://purl.obolibrary.org/obo/CLO_0013090
9206||770||GM17284||http://purl.obolibrary.org/obo/CLO_0013092
9207||7159||Autosomal recessive hypophosphatemic rickets||http://www.orpha.net/ORDO/Orphanet_289176
9208||33||aspirin induced asthma||http://purl.obolibrary.org/obo/HP_0012042
9209||770||GM17289||http://purl.obolibrary.org/obo/CLO_0013077
9210||6187||Sporadic idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis||http://www.orpha.net/ORDO/Orphanet_93218
9211||9344||Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis||http://www.orpha.net/ORDO/Orphanet_93217
9212||9344||Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation||http://www.orpha.net/ORDO/Orphanet_93214
9213||770||GM17287||http://purl.obolibrary.org/obo/CLO_0013082
9214||9344||Familial idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis||http://www.orpha.net/ORDO/Orphanet_93213
9215||9344||Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes||http://www.orpha.net/ORDO/Orphanet_93216
9216||770||GM17288||http://purl.obolibrary.org/obo/CLO_0013080
9217||1022||Folsomia candida||http://purl.obolibrary.org/obo/NCBITaxon_158441
9218||5502||Nitrosomonas europaea||http://purl.obolibrary.org/obo/NCBITaxon_915
9219||4928||8p inverted duplication/deletion syndrome||http://www.orpha.net/ORDO/Orphanet_96092
9220||10266||Distal trisomy 2q||http://www.orpha.net/ORDO/Orphanet_96094
9221||10257||3q26 microduplication syndrome||http://www.orpha.net/ORDO/Orphanet_96095
9222||10284||Distal trisomy 4q||http://www.orpha.net/ORDO/Orphanet_96096
9223||10287||Distal trisomy 5q||http://www.orpha.net/ORDO/Orphanet_96097
9224||10276||Distal trisomy 6q||http://www.orpha.net/ORDO/Orphanet_96098
9225||2656||adductor mandibulae||http://purl.obolibrary.org/obo/UBERON_0011683
9226||10652||obsolete_alopecia||http://www.ebi.ac.uk/efo/EFO_0003109
9227||11618||essential tremor||http://www.ebi.ac.uk/efo/EFO_0003108
9228||10886||myoglobin||http://purl.obolibrary.org/obo/CHEBI_7044
9229||1732||spina bifida||http://www.ebi.ac.uk/efo/EFO_0003105
9230||5502||Buchnera sp.||http://purl.obolibrary.org/obo/NCBITaxon_64684
9231||109||adrenocortical adenoma||http://www.ebi.ac.uk/efo/EFO_0003104
9232||10652||obsolete_spinal muscular atrophy with respiratory distress||http://www.ebi.ac.uk/efo/EFO_0003107
9234||5343||pneumonia||http://www.ebi.ac.uk/efo/EFO_0003106
9233||5502||Acidithiobacillus ferrooxidans||http://purl.obolibrary.org/obo/NCBITaxon_920
9235||1763||testicular seminoma||http://www.ebi.ac.uk/efo/EFO_0003101
9236||8856||peripheral neuropathy||http://www.ebi.ac.uk/efo/EFO_0003100
9237||2700||urinary tract infection||http://www.ebi.ac.uk/efo/EFO_0003103
9238||2700||osteomyelitis||http://www.ebi.ac.uk/efo/EFO_0003102
9239||770||GM17281||http://purl.obolibrary.org/obo/CLO_0013097
9240||770||GM17280||http://purl.obolibrary.org/obo/CLO_0013096
9241||770||GM17283||http://purl.obolibrary.org/obo/CLO_0013095
9242||770||GM17282||http://purl.obolibrary.org/obo/CLO_0013094
9243||772||border follicle cell||http://purl.obolibrary.org/obo/CL_0000579
9244||10994||diethylstilbestrol||http://purl.obolibrary.org/obo/CHEBI_41922
9245||770||GM15036||http://purl.obolibrary.org/obo/CLO_0030311
9246||9292||Beta-thalassemia - X-linked thrombocytopenia||http://www.orpha.net/ORDO/Orphanet_231393
9248||2672||cervix epithelium||http://purl.obolibrary.org/obo/UBERON_0004801
9247||772||monocyte||http://purl.obolibrary.org/obo/CL_0000576
9249||4454||lead||http://purl.obolibrary.org/obo/CHEBI_25016
9250||8791||Nemaline myopathy||http://www.orpha.net/ORDO/Orphanet_607
9251||1767||Proximal myotonic myopathy||http://www.orpha.net/ORDO/Orphanet_606
9252||3745||Tibial muscular dystrophy||http://www.orpha.net/ORDO/Orphanet_609
9253||1022||Haplochromis burtoni||http://purl.obolibrary.org/obo/NCBITaxon_8153
9255||770||GM15038||http://purl.obolibrary.org/obo/CLO_0030309
9254||1022||Astatotilapia||http://purl.obolibrary.org/obo/NCBITaxon_8152
9257||10994||cis-aconitate(3-)||http://purl.obolibrary.org/obo/CHEBI_16383
9256||770||GM15029||http://purl.obolibrary.org/obo/CLO_0030305
9258||5967||PTEN hamartoma tumor syndrome||http://www.orpha.net/ORDO/Orphanet_306498
9259||10090||neutrophilic promyelocyte||http://purl.obolibrary.org/obo/CL_0000564
9260||12358||Distal myopathy with vocal cord weakness||http://www.orpha.net/ORDO/Orphanet_600
9261||12770||nucleate erythrocyte||http://purl.obolibrary.org/obo/CL_0000562
9262||1918||Distal myopathy, Nonaka type||http://www.orpha.net/ORDO/Orphanet_602
9264||12358||Distal myopathy, Welander type||http://www.orpha.net/ORDO/Orphanet_603
9263||7626||band form neutrophil||http://purl.obolibrary.org/obo/CL_0000560
9265||871||granulocyte monocyte progenitor cell||http://purl.obolibrary.org/obo/CL_0000557
9266||7611||megakaryocyte||http://purl.obolibrary.org/obo/CL_0000556
9267||14514||promonocyte||http://purl.obolibrary.org/obo/CL_0000559
9268||772||reticulocyte||http://purl.obolibrary.org/obo/CL_0000558
9270||5877||Familial melanoma||http://www.orpha.net/ORDO/Orphanet_618
9269||9320||Hypocalcemic vitamin D-dependent rickets||http://www.orpha.net/ORDO/Orphanet_289157
9271||742||Congenital primary megaureter||http://www.orpha.net/ORDO/Orphanet_617
9272||5974||Familial atrial myxoma||http://www.orpha.net/ORDO/Orphanet_615
9273||4087||Thomsen and Becker disease||http://www.orpha.net/ORDO/Orphanet_614
9274||7588||polychromatophilic erythroblast||http://purl.obolibrary.org/obo/CL_0000550
9275||4087||Potassium-aggravated myotonia||http://www.orpha.net/ORDO/Orphanet_612
9276||7588||orthochromatic erythroblast||http://purl.obolibrary.org/obo/CL_0000552
9278||2313||Bethlem myopathy||http://www.orpha.net/ORDO/Orphanet_610
9277||10085||megakaryocyte progenitor cell||http://purl.obolibrary.org/obo/CL_0000553
9279||772||proerythroblast||http://purl.obolibrary.org/obo/CL_0000547
9280||8696||T-helper 2 cell||http://purl.obolibrary.org/obo/CL_0000546
9281||8696||T-helper 1 cell||http://purl.obolibrary.org/obo/CL_0000545
9282||4834||Nance-Horan syndrome||http://www.orpha.net/ORDO/Orphanet_627
9283||5877||Large congenital melanocytic nevus||http://www.orpha.net/ORDO/Orphanet_626
9284||9302||Short stature due to growth hormone qualitative anomaly||http://www.orpha.net/ORDO/Orphanet_629
9285||1232||Diastrophic dwarfism||http://www.orpha.net/ORDO/Orphanet_628
9286||7588||basophilic erythroblast||http://purl.obolibrary.org/obo/CL_0000549
9287||6294||Homocystinuria without methylmalonic aciduria||http://www.orpha.net/ORDO/Orphanet_622
9288||772||neuron||http://purl.obolibrary.org/obo/CL_0000540
9289||5928||Familial multiple nevi flammei||http://www.orpha.net/ORDO/Orphanet_624
9290||1022||Oreochromis niloticus||http://purl.obolibrary.org/obo/NCBITaxon_8128
9291||6771||Common mesentery||http://www.orpha.net/ORDO/Orphanet_620
9293||15574||Hereditary methemoglobinemia||http://www.orpha.net/ORDO/Orphanet_621
9292||4490||Beta-thalassemia with other manifestations||http://www.orpha.net/ORDO/Orphanet_231386
9294||7731||lymphocyte||http://purl.obolibrary.org/obo/CL_0000542
9295||4803||Neurofibromatosis type 2||http://www.orpha.net/ORDO/Orphanet_637
9296||5912||Neurofibromatosis-Noonan syndrome||http://www.orpha.net/ORDO/Orphanet_638
9297||4139||MEDNIK syndrome||http://www.orpha.net/ORDO/Orphanet_171851
9298||204||Immunodeficiency with factor H anomaly||http://www.orpha.net/ORDO/Orphanet_200421
9300||13881||454 GS 20 sequencer||http://www.ebi.ac.uk/efo/EFO_0004206
9299||4255||Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia||http://www.orpha.net/ORDO/Orphanet_632
9301||12551||pathological myopia||http://www.ebi.ac.uk/efo/EFO_0004207
9302||4142||Non-acquired isolated growth hormone deficiency||http://www.orpha.net/ORDO/Orphanet_631
9303||13881||Illumina HiSeq 1000||http://www.ebi.ac.uk/efo/EFO_0004204
9304||13881||Illumina MiSeq||http://www.ebi.ac.uk/efo/EFO_0004205
9305||616||Neurofibromatosis type 1||http://www.orpha.net/ORDO/Orphanet_636
9306||2866||Vitiligo||http://www.ebi.ac.uk/efo/EFO_0004208
9307||9743||Netherton syndrome||http://www.orpha.net/ORDO/Orphanet_634
9308||1309||Laron syndrome||http://www.orpha.net/ORDO/Orphanet_633
9309||10652||obsolete_Hypospadias||http://www.ebi.ac.uk/efo/EFO_0004209
9310||2034||Illumina Genome Analyzer IIx||http://www.ebi.ac.uk/efo/EFO_0004202
9311||13881||Illumina HiSeq 2000||http://www.ebi.ac.uk/efo/EFO_0004203
9312||2034||Illumina Genome Analyzer||http://www.ebi.ac.uk/efo/EFO_0004200
9313||2034||Illumina Genome Analyzer II||http://www.ebi.ac.uk/efo/EFO_0004201
9314||5025||Saccharomyces pastorianus Weihenstephan 34/70||http://purl.obolibrary.org/obo/NCBITaxon_520522
9315||10994||bortezomib||http://purl.obolibrary.org/obo/CHEBI_52717
9316||2447||Polyneuropathy - hearing loss - ataxia - retinitis pigmentosa - cataract||http://www.orpha.net/ORDO/Orphanet_171848
9317||1767||Noonan syndrome||http://www.orpha.net/ORDO/Orphanet_648
9318||5700||Norrie disease||http://www.orpha.net/ORDO/Orphanet_649
9319||2415||Blindness-scoliosis-arachnodactyly syndrome||http://www.orpha.net/ORDO/Orphanet_171844
9320||8506||Hypocalcemic rickets||http://www.orpha.net/ORDO/Orphanet_289103
9321||5024||anorexia nervosa||http://www.ebi.ac.uk/efo/EFO_0004215
9323||2102||conduct disorder||http://www.ebi.ac.uk/efo/EFO_0004216
9322||6910||Hereditary neuropathy with liability to pressure palsies||http://www.orpha.net/ORDO/Orphanet_640
9325||11842||Giant axonal neuropathy||http://www.orpha.net/ORDO/Orphanet_643
9324||10652||obsolete_Biliary atresia||http://www.ebi.ac.uk/efo/EFO_0004217
9326||11030||marijuana dependence||http://www.ebi.ac.uk/efo/EFO_0004218
9327||6900||Hereditary sensory and autonomic neuropathy type 4||http://www.orpha.net/ORDO/Orphanet_642
9328||10056||CD8-Positive T-Lymphocytes||http://www.ebi.ac.uk/efo/EFO_0004219
9329||5025||Trichoderma atroviride||http://purl.obolibrary.org/obo/NCBITaxon_63577
9330||9740||NARP syndrome||http://www.orpha.net/ORDO/Orphanet_644
9331||5475||Nijmegen breakage syndrome||http://www.orpha.net/ORDO/Orphanet_647
9332||4706||Niemann-Pick disease type C||http://www.orpha.net/ORDO/Orphanet_646
9333||10906||gallstones||http://www.ebi.ac.uk/efo/EFO_0004210
9334||1485||Hypertriglyceridemia||http://www.ebi.ac.uk/efo/EFO_0004211
9335||2866||Keloid||http://www.ebi.ac.uk/efo/EFO_0004212
9336||12161||Otosclerosis||http://www.ebi.ac.uk/efo/EFO_0004213
9337||1638||Abdominal Aortic Aneurysm||http://www.ebi.ac.uk/efo/EFO_0004214
9338||1619||Amelogenesis imperfecta and gingival hyperplasia syndrome||http://www.orpha.net/ORDO/Orphanet_171836
9339||770||GM15072||http://purl.obolibrary.org/obo/CLO_0030337
9340||6610||Craniosynostosis - hydrocephalus - Arnold-Chiari malformation type I - radioulnar synostosis||http://www.orpha.net/ORDO/Orphanet_171839
9341||8938||Mutilating palmoplantar keratoderma with periorificial keratotic plaques||http://www.orpha.net/ORDO/Orphanet_659
9342||8024||Congenital isolated hyperinsulinism||http://www.orpha.net/ORDO/Orphanet_657
9343||12770||enucleate erythrocyte||http://purl.obolibrary.org/obo/CL_0000595
9344||3753||Familial idiopathic steroid-resistant nephrotic syndrome||http://www.orpha.net/ORDO/Orphanet_656
9345||7377||Nephronophthisis||http://www.orpha.net/ORDO/Orphanet_655
9346||14915||drug-induced liver injury||http://www.ebi.ac.uk/efo/EFO_0004228
9347||1022||Spermophilus lateralis||http://purl.obolibrary.org/obo/NCBITaxon_76772
9348||4812||Nephroblastoma||http://www.orpha.net/ORDO/Orphanet_654
9349||11021||Dupuytren Contracture||http://www.ebi.ac.uk/efo/EFO_0004229
9350||4803||Multiple endocrine neoplasia type 2||http://www.orpha.net/ORDO/Orphanet_653
9353||14583||Creutzfeldt Jacob Disease||http://www.ebi.ac.uk/efo/EFO_0004226
9351||772||conidium||http://purl.obolibrary.org/obo/CL_0000599
9352||1276||Multiple endocrine neoplasia type 1||http://www.orpha.net/ORDO/Orphanet_652
9355||6232||Dengue Hemorrhagic Fever||http://www.ebi.ac.uk/efo/EFO_0004227
9354||9288||pyramidal cell||http://purl.obolibrary.org/obo/CL_0000598
9356||1675||Coronary Restenosis||http://www.ebi.ac.uk/efo/EFO_0004224
9357||7407||LCAT deficiency||http://www.orpha.net/ORDO/Orphanet_650
9358||1675||Coronary Vasospasm||http://www.ebi.ac.uk/efo/EFO_0004225
9359||12594||Astigmatism||http://www.ebi.ac.uk/efo/EFO_0004222
9360||10652||obsolete_Keratoconus||http://www.ebi.ac.uk/efo/EFO_0004223
9361||9057||Chronic Hepatitis C infection||http://www.ebi.ac.uk/efo/EFO_0004220
9362||10994||zardaverine||http://purl.obolibrary.org/obo/CHEBI_46548
9363||10652||obsolete_External ear||http://www.ebi.ac.uk/efo/EFO_0004221
9364||770||GM15056||http://purl.obolibrary.org/obo/CLO_0030328
9365||2832||6q16 deletion syndrome||http://www.orpha.net/ORDO/Orphanet_171829
9366||3854||Sulfolobus solfataricus P2||http://purl.obolibrary.org/obo/NCBITaxon_273057
9368||3560||Autosomal recessive malignant osteopetrosis||http://www.orpha.net/ORDO/Orphanet_667
9369||1711||aorta endothelium||http://purl.obolibrary.org/obo/UBERON_0004851
9367||204||Immunodeficiency with factor I anomaly||http://www.orpha.net/ORDO/Orphanet_200418
9370||9976||hyomandibular cartilage||http://purl.obolibrary.org/obo/UBERON_0011607
9372||7942||Osteogenesis imperfecta||http://www.orpha.net/ORDO/Orphanet_666
9371||10187||alveolar macrophage||http://purl.obolibrary.org/obo/CL_0000583
9374||1226||Otopalatodigital syndrome||http://www.orpha.net/ORDO/Orphanet_669
9373||7626||neutrophilic metamyelocyte||http://purl.obolibrary.org/obo/CL_0000582
9376||8190||linoleic acids||http://purl.obolibrary.org/obo/CHEBI_25048
9375||10187||peritoneal macrophage||http://purl.obolibrary.org/obo/CL_0000581
9378||14588||odontoclast||http://purl.obolibrary.org/obo/CL_0000588
9379||5103||Graves disease||http://www.ebi.ac.uk/efo/EFO_0004237
9377||9696||Maternally-inherited progressive external ophthalmoplegia||http://www.orpha.net/ORDO/Orphanet_663
9380||12161||hearing loss||http://www.ebi.ac.uk/efo/EFO_0004238
9383||2021||Albright hereditary osteodystrophy||http://www.orpha.net/ORDO/Orphanet_665
9382||772||germ cell||http://purl.obolibrary.org/obo/CL_0000586
9381||8930||chronic hepatitis B infection||http://www.ebi.ac.uk/efo/EFO_0004239
9384||4727||Ornithine transcarbamylase deficiency||http://www.orpha.net/ORDO/Orphanet_664
9385||11618||leukopenia||http://www.ebi.ac.uk/efo/EFO_0004233
9386||1761||erectile dysfunction||http://www.ebi.ac.uk/efo/EFO_0004234
9388||12497||exfoliation syndrome||http://www.ebi.ac.uk/efo/EFO_0004235
9387||9918||Ondine syndrome||http://www.orpha.net/ORDO/Orphanet_661
9389||8970||focal segmental glomerulosclerosis||http://www.ebi.ac.uk/efo/EFO_0004236
9390||770||GM15061||http://purl.obolibrary.org/obo/CLO_0030324
9391||7626||neutrophilic myelocyte||http://purl.obolibrary.org/obo/CL_0000580
9392||10943||endometrial neoplasm||http://www.ebi.ac.uk/efo/EFO_0004230
9393||10652||obsolete_brachial artery||http://www.ebi.ac.uk/efo/EFO_0004231
9394||1403||eosinophilic esophagitis||http://www.ebi.ac.uk/efo/EFO_0004232
9395||10561||Blepharophimosis - epicanthus inversus - ptosis due to polyA expansion||http://www.orpha.net/ORDO/Orphanet_261579
9396||10561||Blepharophimosis - epicanthus inversus - ptosis due to a point mutation||http://www.orpha.net/ORDO/Orphanet_261572
9397||1022||Laccaria bicolor S238N-H82||http://purl.obolibrary.org/obo/NCBITaxon_486041
9398||14124||Nasal encephalocele||http://www.orpha.net/ORDO/Orphanet_141118
9399||2509||Proximal spinal muscular atrophy type 4||http://www.orpha.net/ORDO/Orphanet_83420
9400||6097||Familial adenomatous polyposis due to 5q22.2 microdeletion||http://www.orpha.net/ORDO/Orphanet_261584
9401||10994||biotin||http://purl.obolibrary.org/obo/CHEBI_15956
9402||12112||Congenital tracheal stenosis||http://www.orpha.net/ORDO/Orphanet_141127
9403||6572||Glycogen storage disease due to glycogen synthase deficiency||http://www.orpha.net/ORDO/Orphanet_308520
9404||9320||Hypocalcemic vitamin D-resistant rickets||http://www.orpha.net/ORDO/Orphanet_93160
9405||9558||Glomuvenous malformation||http://www.orpha.net/ORDO/Orphanet_83454
9406||9768||Bilateral renal dysplasia||http://www.orpha.net/ORDO/Orphanet_93173
9408||9410||Hemifacial microsomia||http://www.orpha.net/ORDO/Orphanet_141136
9407||9768||Unilateral renal dysplasia||http://www.orpha.net/ORDO/Orphanet_93172
9409||2396||Partial prune belly syndrome||http://www.orpha.net/ORDO/Orphanet_93178
9410||13661||Oculo-auriculo-vertebral spectrum||http://www.orpha.net/ORDO/Orphanet_141132
9411||10994||sn-glycerol 3-phosphate||http://purl.obolibrary.org/obo/CHEBI_15978
9412||8903||Antenatal multiminicore disease with arthrogryposis multiplex congenita||http://www.orpha.net/ORDO/Orphanet_178148
9413||843||Brain dopamine-serotonin vesicular transport disease||http://www.orpha.net/ORDO/Orphanet_352649
9414||8903||Moderate multiminicore disease with hand involvement||http://www.orpha.net/ORDO/Orphanet_178145
9415||5502||Pseudomonas syringae pv. phaseolicola||http://purl.obolibrary.org/obo/NCBITaxon_319
9416||6625||Autosomal recessive cerebellar ataxia with late-onset spasticity||http://www.orpha.net/ORDO/Orphanet_352641
9417||9862||Rectal duplication||http://www.orpha.net/ORDO/Orphanet_171220
9418||7939||Phalangeal microgeodic syndrome||http://www.orpha.net/ORDO/Orphanet_352636
9419||5502||Ralstonia pickettii||http://purl.obolibrary.org/obo/NCBITaxon_329
9420||2509||Proximal spinal muscular atrophy type 3||http://www.orpha.net/ORDO/Orphanet_83419
9421||2509||Proximal spinal muscular atrophy type 2||http://www.orpha.net/ORDO/Orphanet_83418
9422||1022||Peromyscus polionotus||http://purl.obolibrary.org/obo/NCBITaxon_42413
9423||5472||16q24.1 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_352629
9424||13202||JT709||http://www.ebi.ac.uk/efo/EFO_0004088
9425||13202||SS149||http://www.ebi.ac.uk/efo/EFO_0004089
9426||13202||DR1572||http://www.ebi.ac.uk/efo/EFO_0004086
9427||13202||GR1307||http://www.ebi.ac.uk/efo/EFO_0004087
9428||9444||processed array data file||http://www.ebi.ac.uk/efo/EFO_0004096
9429||15538||data file||http://www.ebi.ac.uk/efo/EFO_0004095
9430||14992||scanned image||http://www.ebi.ac.uk/efo/EFO_0004094
9431||13202||CB4858||http://www.ebi.ac.uk/efo/EFO_0004093
9432||13202||VC199||http://www.ebi.ac.uk/efo/EFO_0004092
9433||13202||TK22||http://www.ebi.ac.uk/efo/EFO_0004091
9434||13202||MQ887||http://www.ebi.ac.uk/efo/EFO_0004090
9435||5502||Pseudomonas mendocina||http://purl.obolibrary.org/obo/NCBITaxon_300
9436||5502||Ralstonia solanacearum||http://purl.obolibrary.org/obo/NCBITaxon_305
9437||770||GM17110||http://purl.obolibrary.org/obo/CLO_0014964
9438||1022||Lithognathus mormyrus||http://purl.obolibrary.org/obo/NCBITaxon_50591
9439||5502||Pseudomonas putida||http://purl.obolibrary.org/obo/NCBITaxon_303
9440||4951||McLeod neuroacanthocytosis syndrome||http://www.orpha.net/ORDO/Orphanet_59306
9441||2162||Gestational trophoblastic neoplasm||http://www.orpha.net/ORDO/Orphanet_59305
9442||10717||Ichthyosis - hypotrichosis - sclerosing cholangitis||http://www.orpha.net/ORDO/Orphanet_59303
9443||9444||MAGE-TAB array data matrix file||http://www.ebi.ac.uk/efo/EFO_0004097
9444||9429||array data file||http://www.ebi.ac.uk/efo/EFO_0004098
9445||9443||derived MAGE-TAB array data matrix file||http://www.ebi.ac.uk/efo/EFO_0004099
9446||13306||Symptomatic form of Coffin-Lowry syndrome in female carriers||http://www.orpha.net/ORDO/Orphanet_276630
9447||10994||hyaluronan||http://purl.obolibrary.org/obo/CHEBI_16336
9448||5663||Cobblestone lissencephaly without muscular or ocular involvement||http://www.orpha.net/ORDO/Orphanet_352682
9449||9517||EM435||http://www.ebi.ac.uk/efo/EFO_0004070
9450||1033||CEW1||http://www.ebi.ac.uk/efo/EFO_0004071
9453||13202||AA120||http://www.ebi.ac.uk/efo/EFO_0004072
9451||5295||pathological process||http://purl.obolibrary.org/obo/OBI_1110122
9452||5663||Congenital muscular alpha-dystroglycanopathy with brain and eye anomalies||http://www.orpha.net/ORDO/Orphanet_352687
9454||13202||CB66||http://www.ebi.ac.uk/efo/EFO_0004073
9456||13202||CB120||http://www.ebi.ac.uk/efo/EFO_0004074
9455||10994||17beta-hydroxy-5alpha-androstan-3-one||http://purl.obolibrary.org/obo/CHEBI_16330
9457||13199||HK104||http://www.ebi.ac.uk/efo/EFO_0004065
9458||10994||sodium selenite||http://purl.obolibrary.org/obo/CHEBI_48843
9459||770||GM00144||http://purl.obolibrary.org/obo/CLO_0025850
9460||13199||VT847||http://www.ebi.ac.uk/efo/EFO_0004064
9461||5357||SB146||http://www.ebi.ac.uk/efo/EFO_0004067
9462||315||EM464||http://www.ebi.ac.uk/efo/EFO_0004066
9463||12511||DF5018||http://www.ebi.ac.uk/efo/EFO_0004069
9464||11859||DF5033||http://www.ebi.ac.uk/efo/EFO_0004068
9465||770||GM17116||http://purl.obolibrary.org/obo/CLO_0014953
9466||770||GM17115||http://purl.obolibrary.org/obo/CLO_0014952
9468||770||GM17118||http://purl.obolibrary.org/obo/CLO_0014951
9467||5502||Agrobacterium||http://purl.obolibrary.org/obo/NCBITaxon_357
9469||770||GM17117||http://purl.obolibrary.org/obo/CLO_0014950
9470||5502||Agrobacterium tumefaciens||http://purl.obolibrary.org/obo/NCBITaxon_358
9471||770||GM17111||http://purl.obolibrary.org/obo/CLO_0014947
9472||770||GM17112||http://purl.obolibrary.org/obo/CLO_0014948
9473||13448||midbrain basal plate||http://purl.obolibrary.org/obo/UBERON_0010285
9474||13202||DR20||http://www.ebi.ac.uk/efo/EFO_0004080
9476||13202||DR26||http://www.ebi.ac.uk/efo/EFO_0004081
9475||7050||Autosomal dominant intermediate Charcot-Marie-Tooth disease type F||http://www.orpha.net/ORDO/Orphanet_352670
9477||5048||Primary pigmented nodular adrenocortical disease||http://www.orpha.net/ORDO/Orphanet_189439
9478||13202||DR1564||http://www.ebi.ac.uk/efo/EFO_0004084
9479||13202||DR1567||http://www.ebi.ac.uk/efo/EFO_0004085
9480||13202||DR40||http://www.ebi.ac.uk/efo/EFO_0004082
9481||2996||X-linked Charcot-Marie-Tooth disease type 6||http://www.orpha.net/ORDO/Orphanet_352675
9482||13202||DR47||http://www.ebi.ac.uk/efo/EFO_0004083
9483||13202||CB306||http://www.ebi.ac.uk/efo/EFO_0004078
9484||13202||CB205||http://www.ebi.ac.uk/efo/EFO_0004077
9485||13202||CB189||http://www.ebi.ac.uk/efo/EFO_0004076
9486||13202||CB155||http://www.ebi.ac.uk/efo/EFO_0004075
9487||13202||CB1370||http://www.ebi.ac.uk/efo/EFO_0004079
9488||770||GM17119||http://purl.obolibrary.org/obo/CLO_0014942
9489||770||GM17113||http://purl.obolibrary.org/obo/CLO_0014943
9490||770||GM17114||http://purl.obolibrary.org/obo/CLO_0014945
9491||5502||Thermus thermophilus HB8||http://purl.obolibrary.org/obo/NCBITaxon_300852
9492||8190||cholic acid||http://purl.obolibrary.org/obo/CHEBI_16359
9493||8781||Low anorectal malformation||http://www.orpha.net/ORDO/Orphanet_171215
9494||13202||CB678||http://www.ebi.ac.uk/efo/EFO_0004050
9495||4139||9q21 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_352665
9496||13202||CB4555||http://www.ebi.ac.uk/efo/EFO_0004051
9497||9623||Corneal intraepithelial dyskeratosis with palmoplantar hyperkeratosis and laryngeal dyskeratosis||http://www.orpha.net/ORDO/Orphanet_352662
9498||13202||CB4853||http://www.ebi.ac.uk/efo/EFO_0004052
9499||13202||CB184||http://www.ebi.ac.uk/efo/EFO_0004047
9500||13202||CB128||http://www.ebi.ac.uk/efo/EFO_0004046
9501||13202||CB491||http://www.ebi.ac.uk/efo/EFO_0004049
9502||13202||CB185||http://www.ebi.ac.uk/efo/EFO_0004048
9503||13202||AB2||http://www.ebi.ac.uk/efo/EFO_0004043
9504||13202||AB1||http://www.ebi.ac.uk/efo/EFO_0004042
9505||13202||CB88||http://www.ebi.ac.uk/efo/EFO_0004045
9506||5667||Familial renal amyloidosis due to Apolipoprotein AII variant||http://www.orpha.net/ORDO/Orphanet_238269
9507||13202||CB30||http://www.ebi.ac.uk/efo/EFO_0004044
9508||8190||3-nitropropionic acid||http://purl.obolibrary.org/obo/CHEBI_16348
9509||8781||High anorectal malformation||http://www.orpha.net/ORDO/Orphanet_171201
9510||5502||Xanthomonas campestris pv. campestris||http://purl.obolibrary.org/obo/NCBITaxon_340
9511||13202||NL2099||http://www.ebi.ac.uk/efo/EFO_0004062
9512||13199||AF16||http://www.ebi.ac.uk/efo/EFO_0004063
9513||13202||TR389||http://www.ebi.ac.uk/efo/EFO_0004060
9514||13202||TR403||http://www.ebi.ac.uk/efo/EFO_0004061
9515||4706||Early-onset progressive neurodegeneration - blindness - ataxia - spasticity||http://www.orpha.net/ORDO/Orphanet_352654
9516||8781||Intermediate anorectal malformation||http://www.orpha.net/ORDO/Orphanet_171208
9517||6299||Oscheius myriophila||http://purl.obolibrary.org/obo/NCBITaxon_281680
9518||13202||RC301||http://www.ebi.ac.uk/efo/EFO_0004059
9519||13202||MT3847||http://www.ebi.ac.uk/efo/EFO_0004058
9520||13202||CB4932||http://www.ebi.ac.uk/efo/EFO_0004057
9521||13202||CB4857||http://www.ebi.ac.uk/efo/EFO_0004056
9522||13202||CB4856||http://www.ebi.ac.uk/efo/EFO_0004055
9523||13202||CB4855||http://www.ebi.ac.uk/efo/EFO_0004054
9524||13202||CB4854||http://www.ebi.ac.uk/efo/EFO_0004053
9525||9623||Hereditary benign intraepithelial dyskeratosis||http://www.orpha.net/ORDO/Orphanet_352657
9526||10994||diclofenac||http://purl.obolibrary.org/obo/CHEBI_47381
9527||12431||Hemifacial hypertrophy||http://www.orpha.net/ORDO/Orphanet_141145
9528||5502||Salmonella enterica subsp. enterica serovar Enteritidis||http://purl.obolibrary.org/obo/NCBITaxon_149539
9529||1766||gene trap||http://www.ebi.ac.uk/efo/EFO_0004030
9530||13202||N2||http://www.ebi.ac.uk/efo/EFO_0004028
9531||13725||Drosophila simulans HW09||http://www.ebi.ac.uk/efo/EFO_0004029
9532||1766||transgenic||http://www.ebi.ac.uk/efo/EFO_0004020
9533||1766||transposition||http://www.ebi.ac.uk/efo/EFO_0004021
9534||9536||reciprocal translocation||http://www.ebi.ac.uk/efo/EFO_0004022
9535||9536||Roberstonian translocation||http://www.ebi.ac.uk/efo/EFO_0004023
9536||751||translocation||http://www.ebi.ac.uk/efo/EFO_0004024
9537||13202||AA86||http://www.ebi.ac.uk/efo/EFO_0004025
9538||13202||AA87||http://www.ebi.ac.uk/efo/EFO_0004026
9539||1249||Familial isolated hypoparathyroidism due to impaired PTH secretion||http://www.orpha.net/ORDO/Orphanet_189466
9540||13202||AA89||http://www.ebi.ac.uk/efo/EFO_0004027
9541||770||NPC||http://www.ebi.ac.uk/efo/EFO_0004041
9542||772||mouse embryonic fibroblast cell||http://www.ebi.ac.uk/efo/EFO_0004040
9543||12418||Isolated congenital hypoglossia/aglossia||http://www.orpha.net/ORDO/Orphanet_141152
9544||770||GM17107||http://purl.obolibrary.org/obo/CLO_0014903
9545||772||mouse neural progenitor cell||http://www.ebi.ac.uk/efo/EFO_0004039
9546||770||GM17104||http://purl.obolibrary.org/obo/CLO_0014900
9547||770||GM17105||http://purl.obolibrary.org/obo/CLO_0014901
9548||770||GM17106||http://purl.obolibrary.org/obo/CLO_0014902
9549||15538||experiment accession||http://www.ebi.ac.uk/efo/EFO_0004033
9550||15538||discretized differential expression||http://www.ebi.ac.uk/efo/EFO_0004034
9551||13725||Drosophila simulans NC48||http://www.ebi.ac.uk/efo/EFO_0004031
9552||13725||Drosophile simulans MD106||http://www.ebi.ac.uk/efo/EFO_0004032
9553||770||MEF cell line||http://www.ebi.ac.uk/efo/EFO_0004037
9554||772||mouse embryonic stem cell||http://www.ebi.ac.uk/efo/EFO_0004038
9555||13115||mating type F minus||http://www.ebi.ac.uk/efo/EFO_0004035
9556||13115||mating type h plus||http://www.ebi.ac.uk/efo/EFO_0004036
9557||3308||Glossopalatine ankylosis||http://www.orpha.net/ORDO/Orphanet_141163
9558||4705||Genetic neurovascular malformation||http://www.orpha.net/ORDO/Orphanet_371436
9559||11556||Genetic cerebrovascular dementia||http://www.orpha.net/ORDO/Orphanet_371439
9560||12322||Genetic periodic paralysis||http://www.orpha.net/ORDO/Orphanet_371433
9561||5502||Bradyrhizobium japonicum||http://purl.obolibrary.org/obo/NCBITaxon_375
9562||9569||mutant strain||http://www.ebi.ac.uk/efo/EFO_0004006
9563||9567||recombinant congenic strain||http://www.ebi.ac.uk/efo/EFO_0004007
9564||9569||recombinant inbred strain||http://www.ebi.ac.uk/efo/EFO_0004008
9565||9569||segregating inbred strain||http://www.ebi.ac.uk/efo/EFO_0004009
9566||9569||coisogenic strain||http://www.ebi.ac.uk/efo/EFO_0004002
9567||9569||congenic strain||http://www.ebi.ac.uk/efo/EFO_0004003
9568||9569||consomic strain||http://www.ebi.ac.uk/efo/EFO_0004004
9569||9570||inbred Mus musculus strain||http://www.ebi.ac.uk/efo/EFO_0004005
9570||13587||Mus musculus strain type||http://www.ebi.ac.uk/efo/EFO_0004000
9571||9570||closed colony random bred strain||http://www.ebi.ac.uk/efo/EFO_0004001
9572||7939||Multicentric osteolysis-nodulosis-arthropathy spectrum||http://www.orpha.net/ORDO/Orphanet_371428
9573||5502||Sinorhizobium meliloti||http://purl.obolibrary.org/obo/NCBITaxon_382
9574||5502||Rhizobium leguminosarum||http://purl.obolibrary.org/obo/NCBITaxon_384
9575||6751||Diazoxide-resistant focal hyperinsulinism due to Kir6.2 deficiency||http://www.orpha.net/ORDO/Orphanet_276603
9576||1766||targeted mutation||http://www.ebi.ac.uk/efo/EFO_0004019
9577||8870||Adult-onset non-insulinoma persistent hyperinsulinemic hypoglycemia||http://www.orpha.net/ORDO/Orphanet_276608
9578||1766||inversion||http://www.ebi.ac.uk/efo/EFO_0004017
9579||1766||spontaneous mutation||http://www.ebi.ac.uk/efo/EFO_0004018
9580||1766||duplication||http://www.ebi.ac.uk/efo/EFO_0004015
9581||1766||insertion||http://www.ebi.ac.uk/efo/EFO_0004016
9582||9536||balanced reciprocal translocation||http://www.ebi.ac.uk/efo/EFO_0004013
9583||1766||deletion||http://www.ebi.ac.uk/efo/EFO_0004014
9584||9567||major histocompatibility congenic strain||http://www.ebi.ac.uk/efo/EFO_0004011
9585||13115||mating type F||http://www.ebi.ac.uk/efo/EFO_0004012
9586||9569||wild-derived inbred strain||http://www.ebi.ac.uk/efo/EFO_0004010
9587||831||protein glycosylation in endoplasmic reticulum||http://purl.obolibrary.org/obo/GO_0033577
9588||9593||seq library source flag||http://www.ebi.ac.uk/efo/EFO_0004113
9589||9593||seq library strategy flag||http://www.ebi.ac.uk/efo/EFO_0004112
9590||9593||seq instrument model flag||http://www.ebi.ac.uk/efo/EFO_0004115
9591||9593||seq library selection flag||http://www.ebi.ac.uk/efo/EFO_0004114
9592||9593||seq file type flag||http://www.ebi.ac.uk/efo/EFO_0004111
9593||15538||validation flag||http://www.ebi.ac.uk/efo/EFO_0004110
9594||306||EEC syndrome and related syndrome||http://www.orpha.net/ORDO/Orphanet_98609
9595||9604||Anomaly of the secretory and excretory apparatus of the lacrimal system||http://www.orpha.net/ORDO/Orphanet_98608
9596||9593||Atlas experiment type flag||http://www.ebi.ac.uk/efo/EFO_0004117
9597||9604||Excretory apparatus of the lacrimal system anomaly||http://www.orpha.net/ORDO/Orphanet_98605
9598||9593||QC type flag||http://www.ebi.ac.uk/efo/EFO_0004116
9599||9597||Syndromic orbital border hypoplasia||http://www.orpha.net/ORDO/Orphanet_98606
9600||9593||AE experiment type flag||http://www.ebi.ac.uk/efo/EFO_0004119
9601||9604||Secretory apparatus of the lacrimal system anomaly||http://www.orpha.net/ORDO/Orphanet_98603
9602||9593||factor type flag||http://www.ebi.ac.uk/efo/EFO_0004118
9603||9601||Congenital alacrima||http://www.orpha.net/ORDO/Orphanet_98604
9604||4807||Rare lacrimal system disease||http://www.orpha.net/ORDO/Orphanet_98602
9605||9983||Eyebrow/eyelashes pigmentation anomaly||http://www.orpha.net/ORDO/Orphanet_98601
9606||9983||Eyebrow/eyelashes distichiasis||http://www.orpha.net/ORDO/Orphanet_98600
9607||11802||Rare syndrome with cardiac malformations||http://www.orpha.net/ORDO/Orphanet_156532
9608||4843||Genetic syndromic esophageal malformation||http://www.orpha.net/ORDO/Orphanet_371445
9609||9612||seq_library_source||http://www.ebi.ac.uk/efo/EFO_0004104
9610||15583||seq file type||http://www.ebi.ac.uk/efo/EFO_0004103
9611||4263||seq_library_strategy||http://www.ebi.ac.uk/efo/EFO_0004102
9612||15538||validation type||http://www.ebi.ac.uk/efo/EFO_0004101
9613||10886||interleukin||http://www.ebi.ac.uk/efo/EFO_0004100
9614||10994||phenobarbital||http://purl.obolibrary.org/obo/CHEBI_8069
9615||10652||obsolete_factor type||http://www.ebi.ac.uk/efo/EFO_0004109
9616||13883||Atlas experiment type||http://www.ebi.ac.uk/efo/EFO_0004108
9617||6573||Atlas Quality Control type||http://www.ebi.ac.uk/efo/EFO_0004107
9618||1783||seq instrument model||http://www.ebi.ac.uk/efo/EFO_0004106
9619||13883||seq_library_selection||http://www.ebi.ac.uk/efo/EFO_0004105
9620||1826||Sedum alfredii||http://purl.obolibrary.org/obo/NCBITaxon_439688
9621||7662||Posterior corneal dystrophy||http://www.orpha.net/ORDO/Orphanet_98627
9622||7662||Syndromic corneal dystrophy||http://www.orpha.net/ORDO/Orphanet_98628
9623||7662||Superficial corneal dystrophy||http://www.orpha.net/ORDO/Orphanet_98625
9624||7662||Stromal corneal dystrophy||http://www.orpha.net/ORDO/Orphanet_98626
9625||5081||Syndromic myopia||http://www.orpha.net/ORDO/Orphanet_98620
9626||11272||Syndromic keratoconus||http://www.orpha.net/ORDO/Orphanet_98623
9627||9628||Syndromic hyperopia||http://www.orpha.net/ORDO/Orphanet_98622
9628||5081||Rare hyperopia and astigmatism||http://www.orpha.net/ORDO/Orphanet_98621
9629||9635||Conjunctival lymphangiectasia||http://www.orpha.net/ORDO/Orphanet_98614
9630||9636||Pigmented conjunctival lesion||http://www.orpha.net/ORDO/Orphanet_98615
9631||9636||Conjunctival tumor||http://www.orpha.net/ORDO/Orphanet_98616
9632||9631||Bulbar conjunctival dermoid or conjunctival dermolipoma||http://www.orpha.net/ORDO/Orphanet_98617
9633||4263||Helicos sequencing||http://purl.obolibrary.org/obo/OBI_0000697
9634||5081||Rare isolated myopia||http://www.orpha.net/ORDO/Orphanet_98619
9635||9636||Conjunctival vascular anomaly||http://www.orpha.net/ORDO/Orphanet_98611
9636||4807||Rare conjunctival disease||http://www.orpha.net/ORDO/Orphanet_98610
9637||10994||phenylephrine||http://purl.obolibrary.org/obo/CHEBI_8093
9638||9635||Conjunctival telangiectasia||http://www.orpha.net/ORDO/Orphanet_98613
9639||5502||Brevibacterium aurantiacum||http://purl.obolibrary.org/obo/NCBITaxon_273384
9640||9635||Conjunctival hemangioma or hemolymphangioma||http://www.orpha.net/ORDO/Orphanet_98612
9641||9651||Dentocutaneous disease with cataract||http://www.orpha.net/ORDO/Orphanet_98649
9642||9651||Musculoskeletal disease with cataract||http://www.orpha.net/ORDO/Orphanet_98648
9643||9651||Cardiac disease with cataract||http://www.orpha.net/ORDO/Orphanet_98647
9644||5502||Escherichia coli BL21||http://purl.obolibrary.org/obo/NCBITaxon_511693
9645||8191||N-allyl-1-phenyl-2,3,4,5-tetrahydro-3-benzazepine-7,8-diol hydrobromide||http://purl.obolibrary.org/obo/CHEBI_63978
9646||10994||hydrogen peroxide||http://purl.obolibrary.org/obo/CHEBI_16240
9647||10994||quercetin||http://purl.obolibrary.org/obo/CHEBI_16243
9648||9651||Cerebral disease with cataract||http://www.orpha.net/ORDO/Orphanet_98645
9649||6596||phospholipid||http://purl.obolibrary.org/obo/CHEBI_16247
9650||9651||Renal disease with cataract||http://www.orpha.net/ORDO/Orphanet_98646
9651||9654||Systemic disease with cataract||http://www.orpha.net/ORDO/Orphanet_98643
9652||9651||Cataract associated with a metabolic disease||http://www.orpha.net/ORDO/Orphanet_98644
9653||8191||pergolide mesylate||http://purl.obolibrary.org/obo/CHEBI_8021
9654||9655||Syndromic cataract||http://www.orpha.net/ORDO/Orphanet_98641
9655||5084||Rare cataract||http://www.orpha.net/ORDO/Orphanet_98640
9657||5025||Arthroderma uncinatum||http://purl.obolibrary.org/obo/NCBITaxon_74035
9656||9667||Secondary glaucoma due to a proliferation and differentiation anomaly||http://www.orpha.net/ORDO/Orphanet_98637
9658||9663||Corneoiridogoniodysgenesis||http://www.orpha.net/ORDO/Orphanet_98636
9659||3044||perphenazine||http://purl.obolibrary.org/obo/CHEBI_8028
9660||2415||Rare disease with glaucoma as a major feature||http://www.orpha.net/ORDO/Orphanet_98638
9661||3866||Intestinal epithelial dysplasia||http://www.orpha.net/ORDO/Orphanet_92050
9662||4173||dibenzothiazepine||http://purl.obolibrary.org/obo/CHEBI_39268
9663||9667||Glaucoma associated with neural crest cell migration anomaly||http://www.orpha.net/ORDO/Orphanet_98632
9664||9663||Goniodysgenesis||http://www.orpha.net/ORDO/Orphanet_98633
9665||9663||Iridogoniodysgenesis||http://www.orpha.net/ORDO/Orphanet_98634
9666||9663||Corneogoniodysgenesis||http://www.orpha.net/ORDO/Orphanet_98635
9667||7629||Secondary dysgenetic glaucoma||http://www.orpha.net/ORDO/Orphanet_98631
9668||9679||Congenital vitreoretinal dysplasia||http://www.orpha.net/ORDO/Orphanet_98669
9669||799||muscarinic antagonist||http://purl.obolibrary.org/obo/CHEBI_48876
9670||799||cholinergic antagonist||http://purl.obolibrary.org/obo/CHEBI_48873
9671||8191||N-methyl-6-chloro-1-(3-methylphenyl)-2,3,4,5-tetrahydro-3-benzazepine-7,8-diol hydrobromide||http://purl.obolibrary.org/obo/CHEBI_63996
9673||10994||chitosan||http://purl.obolibrary.org/obo/CHEBI_16261
9672||770||GM14679||http://purl.obolibrary.org/obo/CLO_0031953
9674||13496||Ngari virus||http://purl.obolibrary.org/obo/NCBITaxon_273357
9675||9965||Genetic macular dystrophy||http://www.orpha.net/ORDO/Orphanet_98664
9676||9965||Syndromic retinitis pigmentosa||http://www.orpha.net/ORDO/Orphanet_98661
9677||9965||Unclassified familial retinal dystrophy||http://www.orpha.net/ORDO/Orphanet_98662
9678||9690||Disease predisposing to age-related macular degeneration||http://www.orpha.net/ORDO/Orphanet_98667
9679||9690||Vitreoretinopathy||http://www.orpha.net/ORDO/Orphanet_98668
9680||9675||Colobomatous and areolar dystrophy||http://www.orpha.net/ORDO/Orphanet_98665
9681||9675||Unclassified primitive or secondary maculopathy||http://www.orpha.net/ORDO/Orphanet_98666
9682||9690||Color-vision disease||http://www.orpha.net/ORDO/Orphanet_98658
9683||11868||differential expression analysis data transformation||http://purl.obolibrary.org/obo/OBI_0000650
9684||10994||benzothiadiazole||http://purl.obolibrary.org/obo/CHEBI_48864
9685||9651||Craniofacial anomaly with cataract||http://www.orpha.net/ORDO/Orphanet_98650
9686||5084||Lens size anomaly||http://www.orpha.net/ORDO/Orphanet_98652
9687||5084||Lens position anomaly||http://www.orpha.net/ORDO/Orphanet_98653
9688||5084||Lens shape anomaly||http://www.orpha.net/ORDO/Orphanet_98655
9689||10994||phenacetin||http://purl.obolibrary.org/obo/CHEBI_8050
9690||2415||Genetic vitreous-retinal disease||http://www.orpha.net/ORDO/Orphanet_98657
9691||5070||Oculomotor apraxia or related oculomotor disease||http://www.orpha.net/ORDO/Orphanet_98688
9692||9698||Supranuclear oculomotor palsy||http://www.orpha.net/ORDO/Orphanet_98687
9693||5070||Myopathy with eye involvement||http://www.orpha.net/ORDO/Orphanet_98689
9695||10994||sodium tungstate dihydrate||http://purl.obolibrary.org/obo/CHEBI_63939
9694||9696||Craniostenosis associated with a strabismus||http://www.orpha.net/ORDO/Orphanet_98684
9696||9704||Syndrome with a symptomatic strabismus||http://www.orpha.net/ORDO/Orphanet_98683
9697||13176||Congenital trochlear nerve palsy||http://www.orpha.net/ORDO/Orphanet_98686
9699||10994||cadmium dichloride hemipentahydrate||http://purl.obolibrary.org/obo/CHEBI_63938
9698||5070||Oculomotor palsy||http://www.orpha.net/ORDO/Orphanet_98685
9700||8191||cyclazosin hydrochloride||http://purl.obolibrary.org/obo/CHEBI_63935
9701||10994||Aroclor 1254||http://purl.obolibrary.org/obo/CHEBI_63933
9703||1022||Wyeomyia smithii||http://purl.obolibrary.org/obo/NCBITaxon_174621
9702||9704||Essential strabismus||http://www.orpha.net/ORDO/Orphanet_98682
9704||5070||Rare strabismus and restriction syndrome||http://www.orpha.net/ORDO/Orphanet_98681
9705||8191||bathocuproine disulfonic acid||http://purl.obolibrary.org/obo/CHEBI_63934
9706||306||Trichothiodystrophy||http://www.orpha.net/ORDO/Orphanet_33364
9707||4766||Parietal foramina||http://www.orpha.net/ORDO/Orphanet_60015
9708||4887||Atypical Norrie disease due to monosomy Xp11.3||http://www.orpha.net/ORDO/Orphanet_261501
9709||10531||X-linked recessive optic atrophy||http://www.orpha.net/ORDO/Orphanet_98678
9710||9713||Autosomal recessive syndromic optic atrophy||http://www.orpha.net/ORDO/Orphanet_98677
9712||10994||testosterone||http://purl.obolibrary.org/obo/CHEBI_17347
9711||9713||Autosomal recessive isolated optic atrophy||http://www.orpha.net/ORDO/Orphanet_98676
9714||10994||trimethyltin||http://purl.obolibrary.org/obo/CHEBI_63948
9713||10531||Autosomal recessive optic atrophy||http://www.orpha.net/ORDO/Orphanet_98675
9715||10994||2,3-bis(4-hydroxyphenyl)propionitrile||http://purl.obolibrary.org/obo/CHEBI_63949
9716||8846||Autosomal dominant optic atrophy, classic type||http://www.orpha.net/ORDO/Orphanet_98673
9717||10531||Autosomal dominant optic atrophy||http://www.orpha.net/ORDO/Orphanet_98672
9718||2415||Optic neuropathy||http://www.orpha.net/ORDO/Orphanet_98671
9721||5502||Candidatus Kuenenia stuttgartiensis||http://purl.obolibrary.org/obo/NCBITaxon_174633
9719||9679||Vitreoretinal degeneration||http://www.orpha.net/ORDO/Orphanet_98670
9720||10732||Pulmonary alveolar microlithiasis||http://www.orpha.net/ORDO/Orphanet_60025
9722||10994||sodium tungstate||http://purl.obolibrary.org/obo/CHEBI_63940
9723||10994||ferrozine monosodium salt||http://purl.obolibrary.org/obo/CHEBI_63942
9724||13496||Rocio virus||http://purl.obolibrary.org/obo/NCBITaxon_64315
9725||10994||nitrogen atom||http://purl.obolibrary.org/obo/CHEBI_25555
9726||4762||Intestinal malformation||http://www.orpha.net/ORDO/Orphanet_97945
9727||4762||Gastroduodenal malformation||http://www.orpha.net/ORDO/Orphanet_97944
9730||1022||Cimex lectularius||http://purl.obolibrary.org/obo/NCBITaxon_79782
9728||5025||Penicillium rugulosum||http://purl.obolibrary.org/obo/NCBITaxon_121627
9729||10994||celastrol||http://purl.obolibrary.org/obo/CHEBI_63959
9731||10994||ionomycin||http://purl.obolibrary.org/obo/CHEBI_63954
9732||8191||arsenic trichloride||http://purl.obolibrary.org/obo/CHEBI_63952
9734||8681||Disorder of thiamine metabolism and transport||http://www.orpha.net/ORDO/Orphanet_298644
9733||10994||2-acetylaminofluorene||http://purl.obolibrary.org/obo/CHEBI_17356
9735||10994||isoxaben||http://purl.obolibrary.org/obo/CHEBI_63956
9736||11323||Ring chromosome Y||http://www.orpha.net/ORDO/Orphanet_261529
9737||5185||Paternal uniparental disomy of chromosome X||http://www.orpha.net/ORDO/Orphanet_261524
9738||9739||Genetic keratinization disorder associated with ocular features||http://www.orpha.net/ORDO/Orphanet_98697
9739||2415||Genodermatosis with ocular features||http://www.orpha.net/ORDO/Orphanet_98696
9740||10693||Mitochondrial disease with eye involvement||http://www.orpha.net/ORDO/Orphanet_98695
9741||9748||Spinocerebellar degenerescence and spastic paraparesis with an oculomotor anomaly||http://www.orpha.net/ORDO/Orphanet_98694
9742||9738||Syndromic ichthyosis associated with ocular features||http://www.orpha.net/ORDO/Orphanet_98699
9743||9738||Ichthyosis associated with ocular features||http://www.orpha.net/ORDO/Orphanet_98698
9744||8191||N(6)-acetimidoyl-L-lysine dihydrochloride||http://purl.obolibrary.org/obo/CHEBI_63964
9745||8190||7-chlorokynurenic acid||http://purl.obolibrary.org/obo/CHEBI_63965
9746||2481||sporophyte development stage||http://purl.obolibrary.org/obo/PO_0028002
9747||9748||Spinocerebellar ataxia with oculomotor anomaly||http://www.orpha.net/ORDO/Orphanet_98693
9748||5070||Nervous system anomaly with eye involvement||http://www.orpha.net/ORDO/Orphanet_98692
9749||5070||Abnormal eye movements||http://www.orpha.net/ORDO/Orphanet_98691
9750||10994||quinoline||http://purl.obolibrary.org/obo/CHEBI_17362
9751||9693||Myasthenic syndrome with eye involvement||http://www.orpha.net/ORDO/Orphanet_98690
9752||5185||Maternal uniparental disomy of chromosome X||http://www.orpha.net/ORDO/Orphanet_261519
9753||1595||abnormality of the gastrointestinal tract||http://purl.obolibrary.org/obo/HP_0011024
9754||6768||Reticular dysgenesis||http://www.orpha.net/ORDO/Orphanet_33355
9755||6641||Generalized galactose epimerase deficiency||http://www.orpha.net/ORDO/Orphanet_308487
9756||196||renal system process||http://purl.obolibrary.org/obo/GO_0003014
9757||3753||Autosomal dominant intermediate Charcot-Marie-Tooth disease type E||http://www.orpha.net/ORDO/Orphanet_93114
9758||1391||pulmonary sarcoidosis||http://purl.obolibrary.org/obo/DOID_13406
9759||6897||Congenital primary aphakia||http://www.orpha.net/ORDO/Orphanet_83461
9760||6309||Disorder of glycolysis||http://www.orpha.net/ORDO/Orphanet_308459
9761||9765||Abnormal glucose homeostasis||http://purl.obolibrary.org/obo/HP_0011014
9762||9761||Abnormality of blood glucose concentration||http://purl.obolibrary.org/obo/HP_0011015
9763||742||Posterior urethral valve||http://www.orpha.net/ORDO/Orphanet_93110
9765||2063||abnormality of carbohydrate metabolism/homeostasis||http://purl.obolibrary.org/obo/HP_0011013
9764||5055||Renal cysts and diabetes syndrome||http://www.orpha.net/ORDO/Orphanet_93111
9766||12178||chronic||http://purl.obolibrary.org/obo/HP_0011010
9767||13036||age of onset||http://purl.obolibrary.org/obo/HP_0011007
9768||742||Renal dysplasia||http://www.orpha.net/ORDO/Orphanet_93108
9769||12178||acute||http://purl.obolibrary.org/obo/HP_0011009
9770||8193||polyamide||http://purl.obolibrary.org/obo/CHEBI_51953
9771||7207||Thymic aplasia||http://www.orpha.net/ORDO/Orphanet_83471
9773||6641||Erythrocyte galactose epimerase deficiency||http://www.orpha.net/ORDO/Orphanet_308473
9772||9710||CAMOS syndrome||http://www.orpha.net/ORDO/Orphanet_83472
9774||5959||Megalencephaly - polymicrogyria - postaxial polydactyly - hydrocephalus||http://www.orpha.net/ORDO/Orphanet_83473
9776||5864||Mowat-Wilson syndrome due to monosomy 2q22||http://www.orpha.net/ORDO/Orphanet_261537
9775||6309||Disorder of fructose metabolism||http://www.orpha.net/ORDO/Orphanet_308463
9777||6309||Disorder of galactose metabolism||http://www.orpha.net/ORDO/Orphanet_308467
9778||4874||49,XXXYY syndrome||http://www.orpha.net/ORDO/Orphanet_261534
9779||742||Renal hypoplasia||http://www.orpha.net/ORDO/Orphanet_93101
9780||508||methyl (-)-jasmonate||http://purl.obolibrary.org/obo/CHEBI_15929
9781||742||Unilateral renal agenesis||http://www.orpha.net/ORDO/Orphanet_93100
9782||2603||Loeys-Dietz syndrome||http://www.orpha.net/ORDO/Orphanet_60030
9783||10994||atrazine||http://purl.obolibrary.org/obo/CHEBI_15930
9784||10994||artesunate||http://purl.obolibrary.org/obo/CHEBI_63918
9785||10994||symphytine oxide||http://purl.obolibrary.org/obo/CHEBI_63917
9786||10994||iloprost||http://purl.obolibrary.org/obo/CHEBI_63916
9787||10994||3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluoro-1-decanol||http://purl.obolibrary.org/obo/CHEBI_63919
9789||10994||2-butoxyethanol||http://purl.obolibrary.org/obo/CHEBI_63921
9788||15||Congenital heart block||http://www.orpha.net/ORDO/Orphanet_60041
9790||5928||Megalencephaly-capillary malformation-polymicrogyria syndrome||http://www.orpha.net/ORDO/Orphanet_60040
9791||10994||nicotinic acid||http://purl.obolibrary.org/obo/CHEBI_15940
9792||8190||latanoprost free acid||http://purl.obolibrary.org/obo/CHEBI_63925
9793||10994||riddelliine||http://purl.obolibrary.org/obo/CHEBI_63924
9794||10994||cinidon ethyl||http://purl.obolibrary.org/obo/CHEBI_63927
9795||6305||Disorder of neutral amino acid transport||http://www.orpha.net/ORDO/Orphanet_308451
9796||8191||menadione sodium sulfonate||http://purl.obolibrary.org/obo/CHEBI_63928
9797||6008||Mowat-Wilson syndrome due to a ZEB2 point mutation||http://www.orpha.net/ORDO/Orphanet_261552
9798||4028||Peripheral resistance to thyroid hormones||http://www.orpha.net/ORDO/Orphanet_97927
9799||5025||Trichoderma reesei QM6a||http://purl.obolibrary.org/obo/NCBITaxon_431241
9800||6371||Aminoacylase deficiency||http://www.orpha.net/ORDO/Orphanet_308448
9801||5855||Blepharophimosis - epicanthus inversus - ptosis due to 3q23 microdeletion||http://www.orpha.net/ORDO/Orphanet_261559
9802||2457||Vitamin B12-responsive methylmalonic acidemia, type cblDv2||http://www.orpha.net/ORDO/Orphanet_308442
9803||5278||disposition||http://www.ifomis.org/bfo/1.1/snap#Disposition
9804||770||GM17102||http://purl.obolibrary.org/obo/CLO_0014896
9805||770||GM17103||http://purl.obolibrary.org/obo/CLO_0014898
9806||6825||CLN13 disease||http://www.orpha.net/ORDO/Orphanet_352709
9807||770||GM17108||http://purl.obolibrary.org/obo/CLO_0014889
9808||770||GM17109||http://purl.obolibrary.org/obo/CLO_0014887
9809||9812||Tessier number 4 facial cleft||http://www.orpha.net/ORDO/Orphanet_141258
9810||7605||Glycogen storage disease due to glycogen branching enzyme deficiency, non progressive hepatic form||http://www.orpha.net/ORDO/Orphanet_308638
9811||10994||furosemide||http://purl.obolibrary.org/obo/CHEBI_47426
9812||4832||Oblique facial cleft||http://www.orpha.net/ORDO/Orphanet_141253
9814||10994||allergenic agent||http://purl.obolibrary.org/obo/CHEBI_50904
9813||2672||amnioserosa||http://purl.obolibrary.org/obo/UBERON_0010302
9815||2447||Attenuated Ch diak-Higashi syndrome||http://www.orpha.net/ORDO/Orphanet_352723
9816||5795||Disorder of melanin metabolism||http://www.orpha.net/ORDO/Orphanet_352728
9817||7605||Glycogen storage disease due to glycogen branching enzyme deficiency, congenital neuromuscular form||http://www.orpha.net/ORDO/Orphanet_308670
9818||7605||Glycogen storage disease due to glycogen branching enzyme deficiency, fatal perinatal neuromuscular form||http://www.orpha.net/ORDO/Orphanet_308655
9819||799||antiemetic||http://purl.obolibrary.org/obo/CHEBI_50919
9820||8656||Progressive retinal dystrophy due to retinol transport defect||http://www.orpha.net/ORDO/Orphanet_352718
9821||4785||Facial dysmorphism - immunodeficiency - livedo - short stature||http://www.orpha.net/ORDO/Orphanet_352712
9822||12189||type II hypersensitivity||http://purl.obolibrary.org/obo/GO_0002445
9823||7610||Glycogen storage disease due to acid maltase deficiency, adult onset||http://www.orpha.net/ORDO/Orphanet_308604
9824||2430||Oculocutaneous albinism type 7||http://www.orpha.net/ORDO/Orphanet_352745
9825||10994||phytol||http://purl.obolibrary.org/obo/CHEBI_17327
9826||10732||Genetic interstitial lung disease||http://www.orpha.net/ORDO/Orphanet_264992
9827||1827||Ocular albinism with congenital sensorineural deafness||http://www.orpha.net/ORDO/Orphanet_352740
9828||5025||Magnaporthe grisea||http://purl.obolibrary.org/obo/NCBITaxon_148305
9829||9833||Temperature-sensitive oculocutaneous albinism type 1||http://www.orpha.net/ORDO/Orphanet_352737
9830||9833||Minimal pigment oculocutaneous albinism type 1||http://www.orpha.net/ORDO/Orphanet_352734
9831||1826||Rorippa amphibia||http://purl.obolibrary.org/obo/NCBITaxon_65951
9832||1826||Rorippa sylvestris||http://purl.obolibrary.org/obo/NCBITaxon_65952
9833||2430||Oculocutaneous albinism type 1||http://www.orpha.net/ORDO/Orphanet_352731
9834||7605||Glycogen storage disease due to glycogen branching enzyme deficiency, progressive hepatic form||http://www.orpha.net/ORDO/Orphanet_308621
9835||10994||morphine||http://purl.obolibrary.org/obo/CHEBI_17303
9836||5502||Synechococcus sp. CC9311||http://purl.obolibrary.org/obo/NCBITaxon_64471
9837||13689||palatoquadrate arch||http://purl.obolibrary.org/obo/UBERON_0011085
9838||9753||Functional abnormality of the gastrointestinal tract||http://purl.obolibrary.org/obo/HP_0012719
9839||10994||ethanol||http://purl.obolibrary.org/obo/CHEBI_16236
9840||9451||infect||http://purl.obolibrary.org/obo/OBI_1110021
9841||5502||Helicobacter pylori||http://purl.obolibrary.org/obo/NCBITaxon_210
9842||13689||dorsal fin musculature||http://purl.obolibrary.org/obo/UBERON_2000648
9843||10994||imipramine||http://purl.obolibrary.org/obo/CHEBI_47499
9844||8193||1,1 -azobis(N,N-dimethylformamide)||http://purl.obolibrary.org/obo/CHEBI_48958
9845||15364||Polyploidy||http://www.orpha.net/ORDO/Orphanet_96321
9846||11323||Isochromosome Y||http://www.orpha.net/ORDO/Orphanet_96325
9847||770||GM02767||http://purl.obolibrary.org/obo/CLO_0014806
9848||11462||Cough||http://purl.obolibrary.org/obo/HP_0012735
9849||6341||Anonychia congenita totalis||http://www.orpha.net/ORDO/Orphanet_94150
9850||5502||Brucella abortus||http://purl.obolibrary.org/obo/NCBITaxon_235
9851||3744||apoplast||http://purl.obolibrary.org/obo/GO_0048046
9852||5502||Francisella tularensis||http://purl.obolibrary.org/obo/NCBITaxon_263
9853||2490||Autosomal dominant cerebellar ataxia type 3||http://www.orpha.net/ORDO/Orphanet_94148
9854||2490||Autosomal dominant cerebellar ataxia type 4||http://www.orpha.net/ORDO/Orphanet_94149
9855||870||Spinocerebellar ataxia type 7||http://www.orpha.net/ORDO/Orphanet_94147
9856||2490||Autosomal dominant cerebellar ataxia type 1||http://www.orpha.net/ORDO/Orphanet_94145
9857||4832||Rare otorhinolaryngological malformation||http://www.orpha.net/ORDO/Orphanet_96333
9858||11333||Paternal uniparental disomy of chromosome 14||http://www.orpha.net/ORDO/Orphanet_96334
9859||9812||Tessier number 6 facial cleft||http://www.orpha.net/ORDO/Orphanet_141265
9860||9812||Tessier number 5 facial cleft||http://www.orpha.net/ORDO/Orphanet_141261
9861||4832||Lateral facial cleft||http://www.orpha.net/ORDO/Orphanet_141269
9862||4762||Anorectal malformation||http://www.orpha.net/ORDO/Orphanet_96346
9863||9861||Commissural facial cleft||http://www.orpha.net/ORDO/Orphanet_141276
9864||8753||Recessive mitochondrial ataxia syndrome||http://www.orpha.net/ORDO/Orphanet_94125
9865||11829||Spinocerebellar ataxia type 1 with axonal neuropathy||http://www.orpha.net/ORDO/Orphanet_94124
9866||11831||Cerebellar ataxia, Cayman type||http://www.orpha.net/ORDO/Orphanet_94122
9867||3072||segmental intercostal artery||http://purl.obolibrary.org/obo/UBERON_2000677
9868||5502||Pseudomonas aeruginosa||http://purl.obolibrary.org/obo/NCBITaxon_287
9869||5893||Genetic motor neuron disease||http://www.orpha.net/ORDO/Orphanet_98505
9870||5025||Trichophyton terrestre||http://purl.obolibrary.org/obo/NCBITaxon_81845
9871||5025||Arthroderma cajetani||http://purl.obolibrary.org/obo/NCBITaxon_81846
9872||5502||Pseudomonas fluorescens||http://purl.obolibrary.org/obo/NCBITaxon_294
9873||5502||Bifidobacterium animalis subsp. lactis||http://purl.obolibrary.org/obo/NCBITaxon_302911
9874||5502||Burkholderia cepacia||http://purl.obolibrary.org/obo/NCBITaxon_292
9875||9899||Huntington disease-like 3||http://www.orpha.net/ORDO/Orphanet_157946
9876||238||Combined immunodeficiency with skin granulomas||http://www.orpha.net/ORDO/Orphanet_157949
9877||5502||Staphylococcus aureus subsp. aureus MW2||http://purl.obolibrary.org/obo/NCBITaxon_196620
9878||7918||Huntington disease-like 1||http://www.orpha.net/ORDO/Orphanet_157941
9879||5502||Corynebacterium glutamicum ATCC 13032||http://purl.obolibrary.org/obo/NCBITaxon_196627
9880||13883||reverse transcription PCR||http://purl.obolibrary.org/obo/OBI_0000552
9881||321||ANE syndrome||http://www.orpha.net/ORDO/Orphanet_157954
9882||10994||dinitrophenol||http://purl.obolibrary.org/obo/CHEBI_39352
9883||5502||Acidithiobacillus ferrooxidans ATCC 23270||http://purl.obolibrary.org/obo/NCBITaxon_243159
9884||2441||Alagille syndrome due to 20p12 microdeletion||http://www.orpha.net/ORDO/Orphanet_261600
9885||11556||Metabolic disease with dementia||http://www.orpha.net/ORDO/Orphanet_98543
9886||9888||Late-onset ataxia with dementia||http://www.orpha.net/ORDO/Orphanet_98540
9887||5502||Dehalococcoides ethenogenes 195||http://purl.obolibrary.org/obo/NCBITaxon_243164
9888||15185||Ataxia with dementia||http://www.orpha.net/ORDO/Orphanet_98538
9889||4430||fungicide||http://purl.obolibrary.org/obo/CHEBI_24127
9890||9888||Early-onset ataxia with dementia||http://www.orpha.net/ORDO/Orphanet_98539
9891||2672||horizontal septum||http://purl.obolibrary.org/obo/UBERON_0003901
9892||2252||Hypotonia-speech impairment-severe cognitive delay syndrome||http://www.orpha.net/ORDO/Orphanet_371364
9893||13691||pancreas primordium||http://purl.obolibrary.org/obo/UBERON_0003921
9894||5981||Non-syndromic pontocerebellar hypoplasia||http://www.orpha.net/ORDO/Orphanet_98523
9895||4732||Rare genetic parkinsonian disorder||http://www.orpha.net/ORDO/Orphanet_307052
9896||10994||lufenuron||http://purl.obolibrary.org/obo/CHEBI_39384
9897||1022||Monosiga brevicollis||http://purl.obolibrary.org/obo/NCBITaxon_81824
9898||9895||Rare parkinsonian syndrome due to genetic neurodegenerative disease||http://www.orpha.net/ORDO/Orphanet_307055
9899||4732||Miscellaneous movement disorder due to genetic neurodegenerative disease||http://www.orpha.net/ORDO/Orphanet_307058
9900||2672||cartilage element of chondrocranium||http://purl.obolibrary.org/obo/UBERON_0003932
9901||5987||Cranial nerve and nuclear aplasia||http://www.orpha.net/ORDO/Orphanet_98518
9902||13448||pancreatic bud||http://purl.obolibrary.org/obo/UBERON_0003922
9903||4732||Rare genetic tremor disorder||http://www.orpha.net/ORDO/Orphanet_307061
9904||13496||Human respiratory syncytial virus B1||http://purl.obolibrary.org/obo/NCBITaxon_79692
9905||4732||Rare genetic myoclonus||http://www.orpha.net/ORDO/Orphanet_307064
9906||10994||glucose||http://purl.obolibrary.org/obo/CHEBI_17234
9907||1319||homocysteine||http://purl.obolibrary.org/obo/CHEBI_17230
9908||9944||Palpebral tumor||http://www.orpha.net/ORDO/Orphanet_98580
9909||9908||Precancerous lesion of palpebral epidermis||http://www.orpha.net/ORDO/Orphanet_98583
9910||9908||Palpebral sebaceous gland tumor||http://www.orpha.net/ORDO/Orphanet_98585
9911||9908||Malignant tumor of palpebral epidermis||http://www.orpha.net/ORDO/Orphanet_98584
9912||9913||Palpebral lentiginosis||http://www.orpha.net/ORDO/Orphanet_98587
9913||9908||Pigmented palpebral tumor||http://www.orpha.net/ORDO/Orphanet_98586
9914||13689||postoptic commissure||http://purl.obolibrary.org/obo/UBERON_0003936
9915||9913||Palpebral malignant melanoma||http://www.orpha.net/ORDO/Orphanet_98589
9916||9913||Palpebral nevus||http://www.orpha.net/ORDO/Orphanet_98588
9917||13689||mesenchyme pectoral fin||http://purl.obolibrary.org/obo/UBERON_0003934
9918||1732||Rare genetic neurological disorder||http://www.orpha.net/ORDO/Orphanet_71859
9919||9905||Rare genetic disease with myoclonus as a major feature||http://www.orpha.net/ORDO/Orphanet_307067
9920||9059||Okihiro syndrome due to a point mutation||http://www.orpha.net/ORDO/Orphanet_261647
9921||10143||Smith-McCort dysplasia||http://www.orpha.net/ORDO/Orphanet_178355
9922||10994||carbon monoxide||http://purl.obolibrary.org/obo/CHEBI_17245
9923||9940||host intracellular part||http://purl.obolibrary.org/obo/GO_0033646
9925||10994||mono(2-ethylhexyl) phthalate||http://purl.obolibrary.org/obo/CHEBI_17243
9924||9944||Canthal anomaly||http://www.orpha.net/ORDO/Orphanet_98572
9926||9946||Secondary ectropion||http://www.orpha.net/ORDO/Orphanet_98571
9927||10994||endothelin-1||http://purl.obolibrary.org/obo/CHEBI_153671
9928||9946||Congenital ectropion||http://www.orpha.net/ORDO/Orphanet_98570
9929||9924||Malposition of external canthus||http://www.orpha.net/ORDO/Orphanet_98576
9930||9924||Telecanthus||http://www.orpha.net/ORDO/Orphanet_98575
9931||9932||Syndromic epicanthus||http://www.orpha.net/ORDO/Orphanet_98574
9932||9924||Epicanthal fold||http://www.orpha.net/ORDO/Orphanet_98573
9933||9935||Congenital upper palpebral retraction||http://www.orpha.net/ORDO/Orphanet_98579
9934||9935||Ptosis||http://www.orpha.net/ORDO/Orphanet_98578
9935||9944||Kinetic eyelid anomaly||http://www.orpha.net/ORDO/Orphanet_98577
9936||1826||Pinus resinosa||http://purl.obolibrary.org/obo/NCBITaxon_54921
9937||13496||Human herpesvirus 8||http://purl.obolibrary.org/obo/NCBITaxon_37296
9938||12162||age-related nuclear cataract||http://purl.obolibrary.org/obo/HP_0011142
9939||5602||Okihiro syndrome due to 20q13 microdeletion||http://www.orpha.net/ORDO/Orphanet_261638
9940||6004||host cell part||http://purl.obolibrary.org/obo/GO_0033643
9941||10153||Syndromic microphthalmia type 5||http://www.orpha.net/ORDO/Orphanet_178364
9942||5880||UV-sensitive syndrome||http://www.orpha.net/ORDO/Orphanet_178338
9943||9944||Eyelid malformation||http://www.orpha.net/ORDO/Orphanet_98561
9944||4807||Rare palpebral disease||http://www.orpha.net/ORDO/Orphanet_98560
9945||1595||bile duct inflammation||http://purl.obolibrary.org/obo/MP_0003254
9946||9944||Eyelids malposition disorder||http://www.orpha.net/ORDO/Orphanet_98567
9947||9953||Syndromic palpebral coloboma||http://www.orpha.net/ORDO/Orphanet_98566
9948||9949||Secondary entropion||http://www.orpha.net/ORDO/Orphanet_98569
9949||9946||Congenital entropion||http://www.orpha.net/ORDO/Orphanet_98568
9950||9943||Microblepharon - ablephara||http://www.orpha.net/ORDO/Orphanet_98563
9951||9943||Cryptophthalmia||http://www.orpha.net/ORDO/Orphanet_98562
9952||9953||Syndromic ankyloblepharon||http://www.orpha.net/ORDO/Orphanet_98565
9953||9943||Eyelid border anomaly||http://www.orpha.net/ORDO/Orphanet_98564
9954||4624||Heinz body anemia||http://www.orpha.net/ORDO/Orphanet_178330
9955||9965|| land Islands eye disease||http://www.orpha.net/ORDO/Orphanet_178333
9956||2441||Alagille syndrome due to a NOTCH2 point mutation||http://www.orpha.net/ORDO/Orphanet_261629
9957||10994||myrcene||http://purl.obolibrary.org/obo/CHEBI_17221
9958||4750||Rare eye disease due to a differentiation anomaly||http://www.orpha.net/ORDO/Orphanet_98558
9959||2515||Syndromic aniridia||http://www.orpha.net/ORDO/Orphanet_98557
9960||9961||Anophthalmia - microphthalmia||http://www.orpha.net/ORDO/Orphanet_98555
9961||4750||Major induction processes eye anomaly||http://www.orpha.net/ORDO/Orphanet_98554
9962||5025||Paracoccidioides brasiliensis||http://purl.obolibrary.org/obo/NCBITaxon_121759
9963||10994||oligomycin||http://purl.obolibrary.org/obo/CHEBI_25675
9964||2441||Alagille syndrome due to a JAG1 point mutation||http://www.orpha.net/ORDO/Orphanet_261619
9965||9690||Retinal dystrophy||http://www.orpha.net/ORDO/Orphanet_71862
9966||10159||Aromatase excess syndrome||http://www.orpha.net/ORDO/Orphanet_178345
9967||10143||Ehlers-Danlos syndrome, spondylocheirodysplastic type||http://www.orpha.net/ORDO/Orphanet_157965
9968||9961||Oculoauricular syndrome, Schorderet type||http://www.orpha.net/ORDO/Orphanet_157962
9969||1022||Rhamphochromis sp.  chilingali ||http://purl.obolibrary.org/obo/NCBITaxon_454631
9970||2672||mature ovarian follicle||http://purl.obolibrary.org/obo/UBERON_0003982
9971||7610||Glycogen storage disease due to acid maltase deficiency, infantile onset||http://www.orpha.net/ORDO/Orphanet_308552
9972||8793||Congenital muscular dystrophy due to LMNA mutation||http://www.orpha.net/ORDO/Orphanet_157973
9973||5025||Candida dubliniensis||http://purl.obolibrary.org/obo/NCBITaxon_42374
9974||616||Neuroectodermal melanolysosomal disease||http://www.orpha.net/ORDO/Orphanet_33445
9975||7610||Glycogen storage disease due to acid maltase deficiency, juvenile onset||http://www.orpha.net/ORDO/Orphanet_308573
9976||2672||pharyngeal arch cartilage||http://purl.obolibrary.org/obo/UBERON_0011004
9977||9983||Eyebrow/eyelashes structural anomaly||http://www.orpha.net/ORDO/Orphanet_98599
9978||9983||Eyelashes hypertrophy||http://www.orpha.net/ORDO/Orphanet_98597
9979||9983||Congenital absence of the eyebrow/eyelashes||http://www.orpha.net/ORDO/Orphanet_98598
9980||9983||Eyebrow/eyelashes hypertrichosis||http://www.orpha.net/ORDO/Orphanet_98595
9981||9983||Eyebrow hypertrophy||http://www.orpha.net/ORDO/Orphanet_98596
9982||9908||Neurogenic palpebral tumor||http://www.orpha.net/ORDO/Orphanet_98593
9984||5912||Reticulate acropigmentation of Kitamura||http://www.orpha.net/ORDO/Orphanet_178307
9983||9944||Rare eyebrow/eyelashes anomaly||http://www.orpha.net/ORDO/Orphanet_98594
9985||9908||Mesenchymatous palpebral tumor||http://www.orpha.net/ORDO/Orphanet_98591
9986||9908||Palpebral tumor with a vascular malformation||http://www.orpha.net/ORDO/Orphanet_98592
9987||9908||Palpebral piliary tumor||http://www.orpha.net/ORDO/Orphanet_98590
9988||6011||8q22.1 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_178303
9989||9014||Kleefstra syndrome due to a point mutation||http://www.orpha.net/ORDO/Orphanet_261652
9990||1022||Xenopus laevis x Xenopus muelleri||http://purl.obolibrary.org/obo/NCBITaxon_481606
9991||5502||Erwinia chrysanthemi||http://purl.obolibrary.org/obo/NCBITaxon_556
9994||13724||Congenital vertical talus||http://www.orpha.net/ORDO/Orphanet_178382
9992||5025||Fusarium subglutinans||http://purl.obolibrary.org/obo/NCBITaxon_42677
9993||9997||Pectobacterium carotovorum subsp. carotovorum||http://purl.obolibrary.org/obo/NCBITaxon_555
9996||1247||Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency||http://www.orpha.net/ORDO/Orphanet_83639
9995||5502||Erwinia amylovora||http://purl.obolibrary.org/obo/NCBITaxon_552
9997||5502||Pectobacterium carotovorum||http://purl.obolibrary.org/obo/NCBITaxon_554
9998||3560||Osteopetrosis - hypogammaglobulinemia||http://www.orpha.net/ORDO/Orphanet_178389
9999||14145||Spectrin-associated autosomal recessive cerebellar ataxia||http://www.orpha.net/ORDO/Orphanet_352403
10000||6264||Mitochondrial neurogastrointestinal encephalomyopathy||http://www.orpha.net/ORDO/Orphanet_298
10001||4740||Enchondromatosis||http://www.orpha.net/ORDO/Orphanet_296
10002||10994||cortisol||http://purl.obolibrary.org/obo/CHEBI_17650
10003||10994||fluconazole||http://purl.obolibrary.org/obo/CHEBI_46081
10004||15177||Congenital malabsorptive diarrhea due to paucity of enteroendocrine cells||http://www.orpha.net/ORDO/Orphanet_83620
10005||5502||Escherichia fergusonii||http://purl.obolibrary.org/obo/NCBITaxon_564
10006||375||PELVIS syndrome||http://www.orpha.net/ORDO/Orphanet_83628
10007||5502||Escherichia coli||http://purl.obolibrary.org/obo/NCBITaxon_562
10008||4706||Leukoencephalopathy - metaphyseal chondrodysplasia||http://www.orpha.net/ORDO/Orphanet_83629
10009||6610||Osteosclerosis-developmental delay-craniosynostosis syndrome||http://www.orpha.net/ORDO/Orphanet_178377
10010||10994||uniconazole-P||http://purl.obolibrary.org/obo/CHEBI_38000
10011||1125||gene||http://purl.obolibrary.org/obo/SO_0000704
10012||7902||Corticobasal degeneration||http://www.orpha.net/ORDO/Orphanet_278
10013||6266||Severe combined immunodeficiency due to adenosine deaminase deficiency||http://www.orpha.net/ORDO/Orphanet_277
10014||6766||T-B  severe combined immunodeficiency due to gamma chain deficiency||http://www.orpha.net/ORDO/Orphanet_276
10015||6768||Severe combined immunodeficiency due to DCLRE1C deficiency||http://www.orpha.net/ORDO/Orphanet_275
10016||426||Bernard-Soulier syndrome||http://www.orpha.net/ORDO/Orphanet_274
10017||1767||Steinert myotonic dystrophy||http://www.orpha.net/ORDO/Orphanet_273
10018||1843||Congenital muscular dystrophy, Fukuyama type||http://www.orpha.net/ORDO/Orphanet_272
10019||9934||Oculopharyngeal muscular dystrophy||http://www.orpha.net/ORDO/Orphanet_270
10020||1022||Haliotis asinina||http://purl.obolibrary.org/obo/NCBITaxon_109174
10021||8636||Microcytic anemia with liver iron overload||http://www.orpha.net/ORDO/Orphanet_83642
10022||11899||X-linked recessive intellectual disability - macrocephaly - ciliary dysfunction||http://www.orpha.net/ORDO/Orphanet_83648
10023||5502||Zymomonas mobilis||http://purl.obolibrary.org/obo/NCBITaxon_542
10024||4122||Non-acquired combined pituitary hormone deficiency with spine abnormalities||http://www.orpha.net/ORDO/Orphanet_231720
10025||10994||2,4,6-trinitrotoluene||http://purl.obolibrary.org/obo/CHEBI_46053
10026||306||Ellis Van Creveld syndrome||http://www.orpha.net/ORDO/Orphanet_289
10027||12330||Hereditary elliptocytosis||http://www.orpha.net/ORDO/Orphanet_288
10028||5502||Citrobacter koseri||http://purl.obolibrary.org/obo/NCBITaxon_545
10029||10898||Ehlers-Danlos syndrome, hypermobility type||http://www.orpha.net/ORDO/Orphanet_285
10031||15365||Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation||http://www.orpha.net/ORDO/Orphanet_178396
10032||1596||Ehlers-Danlos syndrome, classic type||http://www.orpha.net/ORDO/Orphanet_287
10030||5502||Pantoea agglomerans||http://purl.obolibrary.org/obo/NCBITaxon_549
10033||7353||Ehlers-Danlos syndrome, vascular type||http://www.orpha.net/ORDO/Orphanet_286
10034||9696||Monosomy 5p||http://www.orpha.net/ORDO/Orphanet_281
10035||5700||Wolf-Hirschhorn syndrome||http://www.orpha.net/ORDO/Orphanet_280
10036||15214||Frontotemporal dementia||http://www.orpha.net/ORDO/Orphanet_282
10037||5502||Bordetella parapertussis||http://purl.obolibrary.org/obo/NCBITaxon_519
10038||10719||Transient infantile hypertriglyceridemia and hepatosteatosis||http://www.orpha.net/ORDO/Orphanet_300293
10039||5502||Bordetella bronchiseptica||http://purl.obolibrary.org/obo/NCBITaxon_518
10040||12331||Severe congenital hypochromic anemia with ringed sideroblasts||http://www.orpha.net/ORDO/Orphanet_300298
10042||5502||Ochrobactrum anthropi||http://purl.obolibrary.org/obo/NCBITaxon_529
10044||770||GM02783||http://purl.obolibrary.org/obo/CLO_0014788
10043||1022||Clonorchis sinensis||http://purl.obolibrary.org/obo/NCBITaxon_79923
10045||5502||Bordetella pertussis||http://purl.obolibrary.org/obo/NCBITaxon_520
10046||4775||Epibulbar lipodermoid - preauricular appendage - polythelia||http://www.orpha.net/ORDO/Orphanet_231742
10047||8204||CD4-positive, alpha-beta thymocyte||http://purl.obolibrary.org/obo/CL_0000810
10050||4264||Long chain acyl-CoA dehydrogenase deficiency||http://www.orpha.net/ORDO/Orphanet_99900
10049||2802||Congenital pulmonary alveolar proteinosis||http://www.orpha.net/ORDO/Orphanet_264675
10048||1302||Rare disorder with dystonia and other neurologic or systemic manifestation||http://www.orpha.net/ORDO/Orphanet_370106
10051||8204||CD8-positive, alpha-beta thymocyte||http://purl.obolibrary.org/obo/CL_0000811
10052||8205||mature NK T cell||http://purl.obolibrary.org/obo/CL_0000814
10053||772||memory T cell||http://purl.obolibrary.org/obo/CL_0000813
10055||3273||Primary dystonia, DYT17 type||http://www.orpha.net/ORDO/Orphanet_370103
10054||772||immature B cell||http://purl.obolibrary.org/obo/CL_0000816
10056||13367||regulatory T cell||http://purl.obolibrary.org/obo/CL_0000815
10057||12772||transitional stage B cell||http://purl.obolibrary.org/obo/CL_0000818
10058||12772||precursor B cell||http://purl.obolibrary.org/obo/CL_0000817
10059||8239||B-1 B cell||http://purl.obolibrary.org/obo/CL_0000819
10060||843||Ataxia-telangiectasia variant||http://www.orpha.net/ORDO/Orphanet_370109
10061||4264||Acyl-CoA dehydrogenase 9 deficiency||http://www.orpha.net/ORDO/Orphanet_99901
10062||7844||sphingomyelin||http://purl.obolibrary.org/obo/CHEBI_17636
10063||10064||gamma-delta intraepithelial T cell||http://purl.obolibrary.org/obo/CL_0000801
10064||8219||mature gamma-delta T cell||http://purl.obolibrary.org/obo/CL_0000800
10065||10206||immature single positive thymocyte||http://purl.obolibrary.org/obo/CL_0000805
10066||10063||CD4-negative CD8-negative gamma-delta intraepithelial T cell||http://purl.obolibrary.org/obo/CL_0000803
10067||10063||CD8-alpha alpha positive, gamma-delta intraepithelial T cell||http://purl.obolibrary.org/obo/CL_0000802
10068||8204||double-positive, alpha-beta thymocyte||http://purl.obolibrary.org/obo/CL_0000809
10069||10206||DN4 thymocyte||http://purl.obolibrary.org/obo/CL_0000808
10070||10206||DN3 thymocyte||http://purl.obolibrary.org/obo/CL_0000807
10071||10206||DN2 thymocyte||http://purl.obolibrary.org/obo/CL_0000806
10072||10994||nitrate||http://purl.obolibrary.org/obo/CHEBI_17632
10073||5306||Connective tissue disorder due to lysyl hydroxylase-3 deficiency||http://www.orpha.net/ORDO/Orphanet_300284
10074||5502||Xanthomonas oryzae pv. oryzae||http://purl.obolibrary.org/obo/NCBITaxon_64187
10075||6325||Cystathioninuria||http://www.orpha.net/ORDO/Orphanet_212
10076||10090||basophilic promyelocyte||http://purl.obolibrary.org/obo/CL_0000830
10077||899||Familial cylindromatosis||http://www.orpha.net/ORDO/Orphanet_211
10078||4810||Cystinuria||http://www.orpha.net/ORDO/Orphanet_214
10079||6575||Cystinosis||http://www.orpha.net/ORDO/Orphanet_213
10080||4706||Neuronal ceroid lipofuscinosis||http://www.orpha.net/ORDO/Orphanet_216
10081||9677||Congenital stationary night blindness||http://www.orpha.net/ORDO/Orphanet_215
10082||325||Darier disease||http://www.orpha.net/ORDO/Orphanet_218
10083||5964||Isolated Dandy-Walker malformation||http://www.orpha.net/ORDO/Orphanet_217
10084||11899||Digital anomalies - intellectual disability - short stature||http://www.orpha.net/ORDO/Orphanet_352487
10085||872||myeloid lineage restricted progenitor cell||http://purl.obolibrary.org/obo/CL_0000839
10087||772||hematopoietic multipotent progenitor cell||http://purl.obolibrary.org/obo/CL_0000837
10086||1415||Autosomal recessive limb-girdle muscular dystrophy type 2F||http://www.orpha.net/ORDO/Orphanet_219
10088||872||lymphoid lineage restricted progenitor cell||http://purl.obolibrary.org/obo/CL_0000838
10089||14510||myeloblast||http://purl.obolibrary.org/obo/CL_0000835
10090||14510||promyelocyte||http://purl.obolibrary.org/obo/CL_0000836
10091||10090||eosinophilic promyelocyte||http://purl.obolibrary.org/obo/CL_0000833
10092||14510||neutrophil progenitor cell||http://purl.obolibrary.org/obo/CL_0000834
10093||10085||mast cell progenitor||http://purl.obolibrary.org/obo/CL_0000831
10094||10089||eosinophilic myeloblast||http://purl.obolibrary.org/obo/CL_0000832
10095||5055||Maternally-inherited diabetes and deafness||http://www.orpha.net/ORDO/Orphanet_225
10096||5055||Neonatal diabetes mellitus||http://www.orpha.net/ORDO/Orphanet_224
10097||4810||Nephrogenic diabetes insipidus||http://www.orpha.net/ORDO/Orphanet_223
10099||5504||Primary dystonia, DYT6 type||http://www.orpha.net/ORDO/Orphanet_98806
10098||7353||Familial aortic dissection||http://www.orpha.net/ORDO/Orphanet_229
10100||3273||Primary dystonia, DYT4 type||http://www.orpha.net/ORDO/Orphanet_98805
10101||8699||Autosomal dominant dopa-responsive dystonia||http://www.orpha.net/ORDO/Orphanet_98808
10103||3273||Primary dystonia, DYT13 type||http://www.orpha.net/ORDO/Orphanet_98807
10102||7749||Dihydropteridine reductase deficiency||http://www.orpha.net/ORDO/Orphanet_226
10104||1415||Autosomal recessive limb-girdle muscular dystrophy due to ISPD deficiency||http://www.orpha.net/ORDO/Orphanet_352479
10105||12286||Paroxysmal kinesigenic dyskinesia||http://www.orpha.net/ORDO/Orphanet_98809
10106||3019||Denys-Drash syndrome||http://www.orpha.net/ORDO/Orphanet_220
10107||10085||thromboblast||http://purl.obolibrary.org/obo/CL_0000828
10108||10089||basophilic myeloblast||http://purl.obolibrary.org/obo/CL_0000829
10109||1022||Falco rusticolus||http://purl.obolibrary.org/obo/NCBITaxon_120794
10110||7035||mature natural killer cell||http://purl.obolibrary.org/obo/CL_0000824
10111||10088||pro-NK cell||http://purl.obolibrary.org/obo/CL_0000825
10112||10088||pro-B cell||http://purl.obolibrary.org/obo/CL_0000826
10113||10088||pro-T cell||http://purl.obolibrary.org/obo/CL_0000827
10114||10059||B-1a B cell||http://purl.obolibrary.org/obo/CL_0000820
10115||10059||B-1b B cell||http://purl.obolibrary.org/obo/CL_0000821
10116||8239||B-2 B cell||http://purl.obolibrary.org/obo/CL_0000822
10117||8780||Mitochondrial DNA deletion syndrome with progressive myopathy||http://www.orpha.net/ORDO/Orphanet_352470
10118||7035||immature natural killer cell||http://purl.obolibrary.org/obo/CL_0000823
10119||10272||Familial temporal epilepsy||http://www.orpha.net/ORDO/Orphanet_98819
10120||8707||Benign childhood occipital epilepsy, Gastaut type||http://www.orpha.net/ORDO/Orphanet_98816
10121||8707||Benign childhood occipital epilepsy, Panayiotopoulos type||http://www.orpha.net/ORDO/Orphanet_98815
10122||8356||Hypohidrotic ectodermal dysplasia with immunodeficiency||http://www.orpha.net/ORDO/Orphanet_98813
10123||12286||Paroxysmal non-kinesigenic dyskinesia||http://www.orpha.net/ORDO/Orphanet_98810
10124||12286||Paroxysmal exertion-induced dyskinesia||http://www.orpha.net/ORDO/Orphanet_98811
10125||6610||Crouzon disease||http://www.orpha.net/ORDO/Orphanet_207
10126||266||Crigler-Najjar syndrome||http://www.orpha.net/ORDO/Orphanet_205
10127||6476||response to vitamin||http://purl.obolibrary.org/obo/GO_0033273
10128||330||Crandall syndrome||http://www.orpha.net/ORDO/Orphanet_202
10130||5991||Cowden syndrome||http://www.orpha.net/ORDO/Orphanet_201
10129||10580||mature conventional dendritic cell||http://purl.obolibrary.org/obo/CL_0000841
10131||10580||immature conventional dendritic cell||http://purl.obolibrary.org/obo/CL_0000840
10132||288||Mitochondrial DNA maintenance syndrome||http://www.orpha.net/ORDO/Orphanet_352456
10133||7731||mononuclear cell||http://purl.obolibrary.org/obo/CL_0000842
10135||8239||follicular B cell||http://purl.obolibrary.org/obo/CL_0000843
10134||10272||Familial focal epilepsy with variable foci||http://www.orpha.net/ORDO/Orphanet_98820
10136||8239||germinal center B cell||http://purl.obolibrary.org/obo/CL_0000844
10137||8239||marginal zone B cell||http://purl.obolibrary.org/obo/CL_0000845
10138||2681||Cutis laxa||http://www.orpha.net/ORDO/Orphanet_209
10139||10132||Progressive external ophthalmoplegia - myopathy - emaciation||http://www.orpha.net/ORDO/Orphanet_352447
10140||7962||Frontonasal dysplasia||http://www.orpha.net/ORDO/Orphanet_250
10141||7972||Multiple epiphyseal dysplasia||http://www.orpha.net/ORDO/Orphanet_251
10142||10994||trichostatin A||http://purl.obolibrary.org/obo/CHEBI_46024
10143||1186||Spondyloepiphyseal dysplasia and spondyloepimetaphyseal dysplasia||http://www.orpha.net/ORDO/Orphanet_253
10144||1186||Spondylometaphyseal dysplasia||http://www.orpha.net/ORDO/Orphanet_254
10145||843||Dopa-responsive dystonia||http://www.orpha.net/ORDO/Orphanet_255
10146||10149||splenic metallophillic macrophage||http://purl.obolibrary.org/obo/CL_0000873
10147||5504||Early-onset generalized limb-onset dystonia||http://www.orpha.net/ORDO/Orphanet_256
10148||10149||splenic red pulp macrophage||http://purl.obolibrary.org/obo/CL_0000874
10150||1415||Epidermolysis bullosa simplex with muscular dystrophy||http://www.orpha.net/ORDO/Orphanet_257
10149||10188||splenic macrophage||http://purl.obolibrary.org/obo/CL_0000871
10151||2309||Congenital muscular dystrophy type 1A||http://www.orpha.net/ORDO/Orphanet_258
10153||9960||Syndromic microphthalmia||http://www.orpha.net/ORDO/Orphanet_202948
10152||10149||splenic marginal zone macrophage||http://purl.obolibrary.org/obo/CL_0000872
10154||10233||Peyer s patch macrophage||http://purl.obolibrary.org/obo/CL_0000870
10155||5502||Salmonella enterica subsp. enterica serovar Infantis||http://purl.obolibrary.org/obo/NCBITaxon_595
10156||5502||Salmonella enterica subsp. enterica serovar Muenchen||http://purl.obolibrary.org/obo/NCBITaxon_596
10157||5502||Salmonella enterica subsp. enterica serovar Gallinarum||http://purl.obolibrary.org/obo/NCBITaxon_594
10159||4194||Anomaly of puberty or/and menstrual cycle of genetic origin||http://www.orpha.net/ORDO/Orphanet_202940
10158||2404||Typical nemaline myopathy||http://www.orpha.net/ORDO/Orphanet_171436
10160||10163||meningeal macrophage||http://purl.obolibrary.org/obo/CL_0000879
10161||2404||Severe congenital nemaline myopathy||http://www.orpha.net/ORDO/Orphanet_171430
10162||5502||Salmonella||http://purl.obolibrary.org/obo/NCBITaxon_590
10163||10187||central nervous system macrophage||http://purl.obolibrary.org/obo/CL_0000878
10164||10165||splenic tingible body macrophage||http://purl.obolibrary.org/obo/CL_0000877
10165||10149||splenic white pulp macrophage||http://purl.obolibrary.org/obo/CL_0000876
10166||2404||Intermediate nemaline myopathy||http://www.orpha.net/ORDO/Orphanet_171433
10167||9247||non-classical monocyte||http://purl.obolibrary.org/obo/CL_0000875
10169||2404||Childhood-onset nemaline myopathy||http://www.orpha.net/ORDO/Orphanet_171439
10168||2012||somatic stem cell division||http://purl.obolibrary.org/obo/GO_0048103
10170||4957||Emery-Dreifuss muscular dystrophy||http://www.orpha.net/ORDO/Orphanet_261
10171||1414||Autosomal dominant limb-girdle muscular dystrophy type 1B||http://www.orpha.net/ORDO/Orphanet_264
10172||1414||Autosomal dominant limb-girdle muscular dystrophy type 1C||http://www.orpha.net/ORDO/Orphanet_265
10173||4957||Duchenne and Becker muscular dystrophy||http://www.orpha.net/ORDO/Orphanet_262
10174||12335||Limb-girdle muscular dystrophy||http://www.orpha.net/ORDO/Orphanet_263
10175||1415||Autosomal recessive limb-girdle muscular dystrophy type 2B||http://www.orpha.net/ORDO/Orphanet_268
10176||9247||classical monocyte||http://purl.obolibrary.org/obo/CL_0000860
10178||12771||elicited macrophage||http://purl.obolibrary.org/obo/CL_0000861
10177||12335||Facioscapulohumeral dystrophy||http://www.orpha.net/ORDO/Orphanet_269
10180||1414||Autosomal dominant limb-girdle muscular dystrophy type 1A||http://www.orpha.net/ORDO/Orphanet_266
10179||10178||suppressor macrophage||http://purl.obolibrary.org/obo/CL_0000862
10181||1415||Autosomal recessive limb-girdle muscular dystrophy type 2A||http://www.orpha.net/ORDO/Orphanet_267
10182||10178||inflammatory macrophage||http://purl.obolibrary.org/obo/CL_0000863
10183||1826||Populus yunnanensis||http://purl.obolibrary.org/obo/NCBITaxon_242124
10184||10232||tonsillar macrophage||http://purl.obolibrary.org/obo/CL_0000869
10185||10188||lymph node macrophage||http://purl.obolibrary.org/obo/CL_0000868
10186||10233||gastrointestinal tract (lamina propria) macrophage||http://purl.obolibrary.org/obo/CL_0000865
10187||12771||tissue-resident macrophage||http://purl.obolibrary.org/obo/CL_0000864
10188||10187||secondary lymphoid organ macrophage||http://purl.obolibrary.org/obo/CL_0000867
10189||10187||thymic macrophage||http://purl.obolibrary.org/obo/CL_0000866
10190||5025||Aspergillus oryzae RIB40||http://purl.obolibrary.org/obo/NCBITaxon_510516
10192||13587||Mus musculus musculus x M. m. domesticus||http://purl.obolibrary.org/obo/NCBITaxon_477815
10191||8663||Dopamine beta-hydroxylase deficiency||http://www.orpha.net/ORDO/Orphanet_230
10193||1306||Sickle cell anemia||http://www.orpha.net/ORDO/Orphanet_232
10194||12769||Macrostomia - preauricular tags - external ophthalmoplegia||http://www.orpha.net/ORDO/Orphanet_83619
10195||742||Duplication of urethra||http://www.orpha.net/ORDO/Orphanet_237
10196||6771||Digestive duplication||http://www.orpha.net/ORDO/Orphanet_238
10199||5502||Klebsiella pneumoniae||http://purl.obolibrary.org/obo/NCBITaxon_573
10198||10143||Dyggve-Melchior-Clausen disease||http://www.orpha.net/ORDO/Orphanet_239
10197||10876||Obesity due to congenital leptin resistance||http://www.orpha.net/ORDO/Orphanet_179490
10200||2252||Agammaglobulinemia - microcephaly - craniosynostosis - severe dermatitis||http://www.orpha.net/ORDO/Orphanet_83617
10201||10178||alternatively activated macrophage||http://purl.obolibrary.org/obo/CL_0000890
10203||7036||naive thymus-derived CD4-positive, alpha-beta T cell||http://purl.obolibrary.org/obo/CL_0000895
10202||9696||Duane retraction syndrome||http://www.orpha.net/ORDO/Orphanet_233
10205||266||Dubin-Johnson syndrome||http://www.orpha.net/ORDO/Orphanet_234
10204||7036||activated CD4-positive, alpha-beta T cell||http://purl.obolibrary.org/obo/CL_0000896
10208||306||Dubowitz syndrome||http://www.orpha.net/ORDO/Orphanet_235
10207||1307||Obesity due to leptin receptor gene deficiency||http://www.orpha.net/ORDO/Orphanet_179494
10206||9294||thymocyte||http://purl.obolibrary.org/obo/CL_0000893
10210||8050||Trisomy 9p||http://www.orpha.net/ORDO/Orphanet_236
10209||10113||DN1 thymic pro-T cell||http://purl.obolibrary.org/obo/CL_0000894
10211||8696||T-helper 17 cell||http://purl.obolibrary.org/obo/CL_0000899
10212||13367||naive T cell||http://purl.obolibrary.org/obo/CL_0000898
10213||7036||CD4-positive, alpha-beta memory T cell||http://purl.obolibrary.org/obo/CL_0000897
10214||4194||Hereditary site-specific ovarian cancer syndrome||http://www.orpha.net/ORDO/Orphanet_213524
10215||10915||cholesterol||http://purl.obolibrary.org/obo/CHEBI_16113
10216||4224||46,XY complete gonadal dysgenesis||http://www.orpha.net/ORDO/Orphanet_242
10218||4198||Familial ovarian cancer||http://www.orpha.net/ORDO/Orphanet_213517
10217||1528||46,XX gonadal dysgenesis||http://www.orpha.net/ORDO/Orphanet_243
10219||7989||L ri-Weill dyschondrosteosis||http://www.orpha.net/ORDO/Orphanet_240
10220||5912||Dyschromatosis universalis||http://www.orpha.net/ORDO/Orphanet_241
10221||1022||Epinephelus tauvina||http://purl.obolibrary.org/obo/NCBITaxon_203262
10222||5502||Proteus mirabilis||http://purl.obolibrary.org/obo/NCBITaxon_584
10223||8356||Autosomal recessive hypohidrotic ectodermal dysplasia||http://www.orpha.net/ORDO/Orphanet_248
10224||10163||choroid-plexus macrophage||http://purl.obolibrary.org/obo/CL_0000880
10225||7966||Fibrous dysplasia of bone||http://www.orpha.net/ORDO/Orphanet_249
10226||10163||perivascular macrophage||http://purl.obolibrary.org/obo/CL_0000881
10227||1171||Postaxial acrofacial dysostosis||http://www.orpha.net/ORDO/Orphanet_246
10228||10189||thymic medullary macrophage||http://purl.obolibrary.org/obo/CL_0000882
10230||11802||Arrhythmogenic right ventricular dysplasia||http://www.orpha.net/ORDO/Orphanet_247
10229||10189||thymic cortical macrophage||http://purl.obolibrary.org/obo/CL_0000883
10231||1591||Primary ciliary dyskinesia||http://www.orpha.net/ORDO/Orphanet_244
10232||10188||mucosa-associated lymphoid tissue macrophage||http://purl.obolibrary.org/obo/CL_0000884
10234||1171||Nager syndrome||http://www.orpha.net/ORDO/Orphanet_245
10233||10232||gut-associated lymphoid tissue macrophage||http://purl.obolibrary.org/obo/CL_0000885
10235||10185||lymph node subcapsular sinus macrophage||http://purl.obolibrary.org/obo/CL_0000887
10236||10232||nasal and broncial associated lymphoid tissue macrophage||http://purl.obolibrary.org/obo/CL_0000886
10237||7589||myeloid suppressor cell||http://purl.obolibrary.org/obo/CL_0000889
10239||2404||Adult-onset nemaline myopathy||http://www.orpha.net/ORDO/Orphanet_171442
10238||10185||lymph node tingible body macrophage||http://purl.obolibrary.org/obo/CL_0000888
10240||3756||Muscle filaminopathy||http://www.orpha.net/ORDO/Orphanet_171445
10241||7817||Familial afibrinogenemia||http://www.orpha.net/ORDO/Orphanet_98880
10242||1418||X-linked complex spastic paraplegia||http://www.orpha.net/ORDO/Orphanet_98888
10243||4697||Bleeding diathesis due to glycoprotein VI deficiency||http://www.orpha.net/ORDO/Orphanet_98885
10244||4697||Bleeding diathesis due to integrin alpha2-beta1 deficiency||http://www.orpha.net/ORDO/Orphanet_98886
10245||7817||Familial dysfibrinogenemia||http://www.orpha.net/ORDO/Orphanet_98881
10246||5540||Partial duplication of the long arm of chromosome 1||http://www.orpha.net/ORDO/Orphanet_262833
10247||7426||Bilateral perisylvian polymicrogyria||http://www.orpha.net/ORDO/Orphanet_98889
10248||2770||polyA RNA||http://purl.obolibrary.org/obo/OBI_0000869
10249||2477||Congenital dyserythropoietic anemia type III||http://www.orpha.net/ORDO/Orphanet_98870
10250||2477||Congenital dyserythropoietic anemia type II||http://www.orpha.net/ORDO/Orphanet_98873
10251||3750||mitochondrial respiratory-chain inhibitor||http://purl.obolibrary.org/obo/CHEBI_25355
10252||7137||Hemophilia B||http://www.orpha.net/ORDO/Orphanet_98879
10253||7137||Hemophilia A||http://www.orpha.net/ORDO/Orphanet_98878
10254||10994||mevalonate||http://purl.obolibrary.org/obo/CHEBI_25350
10255||10994||low-density lipoprotein||http://purl.obolibrary.org/obo/CHEBI_39026
10256||2822||plant treatment||http://purl.obolibrary.org/obo/EO_0001001
10257||6853||Partial duplication of the long arm of chromosome 3||http://www.orpha.net/ORDO/Orphanet_262851
10258||10286||Isolated diffuse palmoplantar keratoderma||http://www.orpha.net/ORDO/Orphanet_307148
10259||9709||Early-onset X-linked optic atrophy||http://www.orpha.net/ORDO/Orphanet_98890
10260||5972||Periventricular nodular heterotopia||http://www.orpha.net/ORDO/Orphanet_98892
10261||8793||Congenital muscular dystrophy type 1B||http://www.orpha.net/ORDO/Orphanet_98893
10262||2323||Becker muscular dystrophy||http://www.orpha.net/ORDO/Orphanet_98895
10263||2323||Duchenne muscular dystrophy||http://www.orpha.net/ORDO/Orphanet_98896
10264||8902||Oculopharyngodistal myopathy||http://www.orpha.net/ORDO/Orphanet_98897
10265||9649||phosphatidylethanolamine||http://purl.obolibrary.org/obo/CHEBI_16038
10266||5536||Partial duplication of the long arm of chromosome 2||http://www.orpha.net/ORDO/Orphanet_262842
10267||5502||Photorhabdus luminescens subsp. laumondii TTO1||http://purl.obolibrary.org/obo/NCBITaxon_243265
10268||7407||Congenital disorder of glycosylation with nephropathy as a major feature||http://www.orpha.net/ORDO/Orphanet_371207
10269||12824||Cold-induced sweating syndrome||http://www.orpha.net/ORDO/Orphanet_157820
10270||7860||Unverricht-Lundborg disease||http://www.orpha.net/ORDO/Orphanet_308
10271||7847||Juvenile myoclonic epilepsy||http://www.orpha.net/ORDO/Orphanet_307
10272||763||Familial partial epilepsy||http://www.orpha.net/ORDO/Orphanet_309
10273||770||ND00151||http://purl.obolibrary.org/obo/CLO_0030688
10274||5502||Desulfovibrio alaskensis G20||http://purl.obolibrary.org/obo/NCBITaxon_207559
10275||327||Dystrophic epidermolysis bullosa||http://www.orpha.net/ORDO/Orphanet_303
10277||327||Epidermolysis bullosa simplex||http://www.orpha.net/ORDO/Orphanet_304
10276||7448||Partial duplication of the long arm of chromosome 6||http://www.orpha.net/ORDO/Orphanet_262878
10278||327||Junctional epidermolysis bullosa||http://www.orpha.net/ORDO/Orphanet_305
10280||378||Congenital disorder of glycosylation with skin involvement||http://www.orpha.net/ORDO/Orphanet_371200
10279||763||Benign familial infantile epilepsy||http://www.orpha.net/ORDO/Orphanet_306
10281||6276||Bifunctional enzyme deficiency||http://www.orpha.net/ORDO/Orphanet_300
10282||5882||Epidermodysplasia verruciformis||http://www.orpha.net/ORDO/Orphanet_302
10283||5502||Burkholderia thailandensis||http://purl.obolibrary.org/obo/NCBITaxon_57975
10284||6861||Partial duplication of the long arm of chromosome 4||http://www.orpha.net/ORDO/Orphanet_262860
10286||592||Diffuse palmoplantar keratoderma||http://www.orpha.net/ORDO/Orphanet_307141
10285||5700||Congenital disorder of glycosylation with deafness as a major feature||http://www.orpha.net/ORDO/Orphanet_371212
10287||6862||Partial trisomy of the long arm of chromosome 5||http://www.orpha.net/ORDO/Orphanet_262869
10288||1022||Pleuronichthys verticalis||http://purl.obolibrary.org/obo/NCBITaxon_195635
10289||2401||X-linked Emery-Dreifuss muscular dystrophy||http://www.orpha.net/ORDO/Orphanet_98863
10290||2477||Congenital dyserythropoietic anemia type I||http://www.orpha.net/ORDO/Orphanet_98869
10291||7476||Partial duplication of the long arm of chromosome 8||http://www.orpha.net/ORDO/Orphanet_262896
10293||12329||Southeast Asian ovalocytosis||http://www.orpha.net/ORDO/Orphanet_98868
10292||6249||Congenital pseudoarthrosis of the limbs||http://www.orpha.net/ORDO/Orphanet_157808
10294||10567||Mesoaxial synostotic syndactyly with phalangeal reduction||http://www.orpha.net/ORDO/Orphanet_157801
10295||5287||Congenital disorder of glycosylation with developmental anomaly||http://www.orpha.net/ORDO/Orphanet_371235
10296||10170||Autosomal dominant Emery-Dreifuss muscular dystrophy||http://www.orpha.net/ORDO/Orphanet_98853
10297||10170||Autosomal recessive Emery-Dreifuss muscular dystrophy||http://www.orpha.net/ORDO/Orphanet_98855
10298||2354||Distal myopathy with anterior tibial onset||http://www.orpha.net/ORDO/Orphanet_178400
10299||12715||Charcot-Marie-Tooth disease type 2B1||http://www.orpha.net/ORDO/Orphanet_98856
10300||7478||Partial duplication of the long arm of chromosome 7||http://www.orpha.net/ORDO/Orphanet_262887
10301||2997||Autosomal dominant Charcot-Marie-Tooth disease type 2D||http://www.orpha.net/ORDO/Orphanet_99938
10302||2997||Autosomal dominant Charcot-Marie-Tooth disease type 2E||http://www.orpha.net/ORDO/Orphanet_99939
10303||2997||Autosomal dominant Charcot-Marie-Tooth disease type 2B||http://www.orpha.net/ORDO/Orphanet_99936
10304||5502||Salmonella enterica subsp. enterica serovar Thompson||http://purl.obolibrary.org/obo/NCBITaxon_600
10305||2997||Autosomal dominant Charcot-Marie-Tooth disease type 2C||http://www.orpha.net/ORDO/Orphanet_99937
10306||11472||Partial deletion of chromosome 5||http://www.orpha.net/ORDO/Orphanet_261786
10307||5502||Salmonella enterica subsp. enterica serovar Pullorum||http://purl.obolibrary.org/obo/NCBITaxon_605
10308||11472||Partial deletion of chromosome 4||http://www.orpha.net/ORDO/Orphanet_261781
10309||10143||Dyssegmental dysplasia, Rolland-Desbuquois type||http://www.orpha.net/ORDO/Orphanet_156731
10310||843||Combined cervical dystonia||http://www.orpha.net/ORDO/Orphanet_370114
10311||13448||liver primordium||http://purl.obolibrary.org/obo/UBERON_0003894
10312||11472||Partial deletion of chromosome 3||http://www.orpha.net/ORDO/Orphanet_261776
10313||2672||fallopian tube||http://purl.obolibrary.org/obo/UBERON_0003889
10314||11472||Partial deletion of chromosome 2||http://www.orpha.net/ORDO/Orphanet_261771
10315||11888||Medich giant platelet syndrome||http://www.orpha.net/ORDO/Orphanet_370127
10316||2999||Charcot-Marie-Tooth disease type 4B2||http://www.orpha.net/ORDO/Orphanet_99956
10318||13689||neural arch||http://purl.obolibrary.org/obo/UBERON_0003861
10317||11888||White platelet syndrome||http://www.orpha.net/ORDO/Orphanet_370131
10319||7675||Neuroferritinopathy||http://www.orpha.net/ORDO/Orphanet_157846
10320||799||antiatherogenic agent||http://purl.obolibrary.org/obo/CHEBI_50855
10321||5502||Myxococcus xanthus||http://purl.obolibrary.org/obo/NCBITaxon_34
10322||2672||pharyngeal arch derived gill||http://purl.obolibrary.org/obo/UBERON_0011150
10323||2999||Charcot-Marie-Tooth disease type 4E||http://www.orpha.net/ORDO/Orphanet_99951
10324||2999||Charcot-Marie-Tooth disease type 4D||http://www.orpha.net/ORDO/Orphanet_99950
10325||5502||Xylella fastidiosa 9a5c||http://purl.obolibrary.org/obo/NCBITaxon_160492
10326||2999||Charcot-Marie-Tooth disease type 4B1||http://www.orpha.net/ORDO/Orphanet_99955
10327||2999||Charcot-Marie-Tooth disease type 4H||http://www.orpha.net/ORDO/Orphanet_99954
10328||2999||Charcot-Marie-Tooth disease type 4G||http://www.orpha.net/ORDO/Orphanet_99953
10329||2999||Charcot-Marie-Tooth disease type 4F||http://www.orpha.net/ORDO/Orphanet_99952
10330||2997||Autosomal dominant Charcot-Marie-Tooth disease type 2L||http://www.orpha.net/ORDO/Orphanet_99945
10331||2997||Autosomal dominant Charcot-Marie-Tooth disease type 2A1||http://www.orpha.net/ORDO/Orphanet_99946
10332||2997||Autosomal dominant Charcot-Marie-Tooth disease type 2A2||http://www.orpha.net/ORDO/Orphanet_99947
10335||11472||Partial deletion of chromosome 7||http://www.orpha.net/ORDO/Orphanet_261796
10333||2999||Charcot-Marie-Tooth disease type 4A||http://www.orpha.net/ORDO/Orphanet_99948
10334||10143||Spondyloepimetaphyseal dysplasia, matrilin-3 type||http://www.orpha.net/ORDO/Orphanet_156728
10336||2999||Charcot-Marie-Tooth disease type 4C||http://www.orpha.net/ORDO/Orphanet_99949
10337||10994||doxycycline||http://purl.obolibrary.org/obo/CHEBI_50845
10338||10994||norflurazon||http://purl.obolibrary.org/obo/CHEBI_50842
10339||5502||Pseudomonas putida KT2440||http://purl.obolibrary.org/obo/NCBITaxon_160488
10340||5502||Listeria monocytogenes serotype 4b str. F2365||http://purl.obolibrary.org/obo/NCBITaxon_265669
10341||2997||Autosomal dominant Charcot-Marie-Tooth disease type 2F||http://www.orpha.net/ORDO/Orphanet_99940
10342||2997||Autosomal dominant Charcot-Marie-Tooth disease type 2I||http://www.orpha.net/ORDO/Orphanet_99942
10343||2997||Autosomal dominant Charcot-Marie-Tooth disease type 2G||http://www.orpha.net/ORDO/Orphanet_99941
10345||4254||Pantothenate kinase-associated neurodegeneration||http://www.orpha.net/ORDO/Orphanet_157850
10344||2997||Autosomal dominant Charcot-Marie-Tooth disease type 2K||http://www.orpha.net/ORDO/Orphanet_99944
10348||11472||Partial deletion of chromosome 6||http://www.orpha.net/ORDO/Orphanet_261791
10347||2997||Autosomal dominant Charcot-Marie-Tooth disease type 2J||http://www.orpha.net/ORDO/Orphanet_99943
10346||2672||silk gland||http://purl.obolibrary.org/obo/UBERON_0011146
10349||5502||Herminiimonas arsenicoxydans||http://purl.obolibrary.org/obo/NCBITaxon_204773
10350||10994||azinomycin B||http://purl.obolibrary.org/obo/CHEBI_50862
10351||3745||Hereditary proximal myopathy with early respiratory failure||http://www.orpha.net/ORDO/Orphanet_178464
10352||2454||Mitochondrial disease with peripheral neuropathy||http://www.orpha.net/ORDO/Orphanet_225703
10353||799||insulin-sensitizing drug||http://purl.obolibrary.org/obo/CHEBI_50864
10354||10994||3H-1,2-dithiole-3-thione||http://purl.obolibrary.org/obo/CHEBI_50866
10355||1299||Autosomal dominant non-syndromic intellectual disability||http://www.orpha.net/ORDO/Orphanet_178469
10356||10994||ciprofibrate||http://purl.obolibrary.org/obo/CHEBI_50867
10357||2672||telencephalon neural crest||http://purl.obolibrary.org/obo/UBERON_0003850
10358||2672||diencephalon neural crest||http://purl.obolibrary.org/obo/UBERON_0003851
10359||12335||X-linked myopathy with postural muscle atrophy||http://www.orpha.net/ORDO/Orphanet_178461
10360||5502||Rhodopirellula baltica||http://purl.obolibrary.org/obo/NCBITaxon_265606
10361||14856||mesencephalic neural crest||http://purl.obolibrary.org/obo/UBERON_0003849
10362||173||Benign recurrent intrahepatic cholestasis type 1||http://www.orpha.net/ORDO/Orphanet_99960
10363||173||Benign recurrent intrahepatic cholestasis type 2||http://www.orpha.net/ORDO/Orphanet_99961
10364||770||GM12264||http://purl.obolibrary.org/obo/CLO_0019004
10365||13883||nucleic acid hybridization||http://purl.obolibrary.org/obo/OBI_0302903
10366||2063||abnormality of the urinary system physiology||http://purl.obolibrary.org/obo/HP_0011277
10367||2252||Lethal multiple pterygium syndrome||http://www.orpha.net/ORDO/Orphanet_33108
10368||11472||Partial deletion of chromosome 1||http://www.orpha.net/ORDO/Orphanet_261766
10369||5502||Geobacter sulfurreducens PCA||http://purl.obolibrary.org/obo/NCBITaxon_243231
10370||7152||Partial trisomy/tetrasomy of the short arm of chromosome 18||http://www.orpha.net/ORDO/Orphanet_262812
10371||4238||Autosomal agammaglobulinemia||http://www.orpha.net/ORDO/Orphanet_33110
10372||10994||fludrocortisone||http://purl.obolibrary.org/obo/CHEBI_50885
10373||6400||Intermediate DEND syndrome||http://www.orpha.net/ORDO/Orphanet_99989
10374||7119||Partial duplication of the short arm of chromosome 17||http://www.orpha.net/ORDO/Orphanet_262803
10375||5502||Deinococcus radiodurans R1||http://purl.obolibrary.org/obo/NCBITaxon_243230
10376||1319||L-cysteine||http://purl.obolibrary.org/obo/CHEBI_17561
10377||5306||Marfanoid habitus - inguinal hernia - advanced bone age||http://www.orpha.net/ORDO/Orphanet_314041
10378||2323||Familial isolated dilated cardiomyopathy||http://www.orpha.net/ORDO/Orphanet_154
10379||1022||Lepeophtheirus salmonis||http://purl.obolibrary.org/obo/NCBITaxon_72036
10380||4264||Carnitine-acylcarnitine translocase deficiency||http://www.orpha.net/ORDO/Orphanet_159
10381||4959||Systemic primary carnitine deficiency||http://www.orpha.net/ORDO/Orphanet_158
10382||4996||Carnitine palmitoyltransferase II deficiency||http://www.orpha.net/ORDO/Orphanet_157
10383||4996||Carnitine palmitoyl transferase 1A deficiency||http://www.orpha.net/ORDO/Orphanet_156
10384||9654||Hereditary hyperferritinemia with congenital cataracts||http://www.orpha.net/ORDO/Orphanet_163
10385||11842||Charcot-Marie-Tooth disease||http://www.orpha.net/ORDO/Orphanet_166
10387||4191||Neutral lipid storage disease||http://www.orpha.net/ORDO/Orphanet_165
10386||4863||root stele||http://purl.obolibrary.org/obo/PO_0020124
10389||2252||7p22.1 microduplication syndrome||http://www.orpha.net/ORDO/Orphanet_314034
10388||6897||Cataract-glaucoma||http://www.orpha.net/ORDO/Orphanet_162
10391||321||Loose anagen syndrome||http://www.orpha.net/ORDO/Orphanet_168
10390||5502||Methylosinus trichosporium||http://purl.obolibrary.org/obo/NCBITaxon_426
10392||1831||Ch diak-Higashi syndrome||http://www.orpha.net/ORDO/Orphanet_167
10393||323||Ringed hair disease||http://www.orpha.net/ORDO/Orphanet_169
10394||15574||Hemoglobin D disease||http://www.orpha.net/ORDO/Orphanet_90039
10395||10732||Pulmonary venoocclusive disease||http://www.orpha.net/ORDO/Orphanet_31837
10396||9677||Choroideremia||http://www.orpha.net/ORDO/Orphanet_180
10397||5002||Progressive familial intrahepatic cholestasis||http://www.orpha.net/ORDO/Orphanet_172
10398||323||Woolly hair||http://www.orpha.net/ORDO/Orphanet_170
10399||7946||Rhizomelic chondrodysplasia punctata||http://www.orpha.net/ORDO/Orphanet_177
10400||7946||Non-rhizomelic chondrodysplasia punctata||http://www.orpha.net/ORDO/Orphanet_176
10401||306||Cartilage-hair hypoplasia||http://www.orpha.net/ORDO/Orphanet_175
10402||8001||Metaphyseal chondrodysplasia, Schmid type||http://www.orpha.net/ORDO/Orphanet_174
10403||5502||Acetobacter aceti||http://purl.obolibrary.org/obo/NCBITaxon_435
10404||1391||Birdshot chorioretinopathy||http://www.orpha.net/ORDO/Orphanet_179
10405||4740||Chordoma||http://www.orpha.net/ORDO/Orphanet_178
10406||12343||Non-spherocytic hemolytic anemia due to hexokinase deficiency||http://www.orpha.net/ORDO/Orphanet_90031
10407||12341||Hemolytic anemia due to glutathione reductase deficiency||http://www.orpha.net/ORDO/Orphanet_90030
10408||5843||Hereditary folate malabsorption||http://www.orpha.net/ORDO/Orphanet_90045
10409||5502||Rhodococcus aetherivorans||http://purl.obolibrary.org/obo/NCBITaxon_191292
10410||9656||Coats disease||http://www.orpha.net/ORDO/Orphanet_190
10411||382||Cockayne syndrome||http://www.orpha.net/ORDO/Orphanet_191
10412||8356||X-linked hypohidrotic ectodermal dysplasia||http://www.orpha.net/ORDO/Orphanet_181
10413||7966||Cherubism||http://www.orpha.net/ORDO/Orphanet_184
10414||6302||Citrullinemia||http://www.orpha.net/ORDO/Orphanet_187
10415||6432||Leukoencephalopathy - thalamus and brainstem anomalies - high lactate||http://www.orpha.net/ORDO/Orphanet_314051
10416||306||Hidrotic ectodermal dysplasia||http://www.orpha.net/ORDO/Orphanet_189
10417||5502||Legionella pneumophila||http://purl.obolibrary.org/obo/NCBITaxon_446
10419||15045||Primary familial polycythemia||http://www.orpha.net/ORDO/Orphanet_90042
10418||9900||neurocranial trabecula||http://purl.obolibrary.org/obo/UBERON_0005945
10420||12329||Familial pseudohyperkalemia||http://www.orpha.net/ORDO/Orphanet_90044
10421||10994||paracetamol||http://purl.obolibrary.org/obo/CHEBI_46195
10422||10110||cytotoxic CD56-dim natural killer cell||http://purl.obolibrary.org/obo/CL_0000939
10423||10110||CD56-bright cytokine secreting natural killer cell||http://purl.obolibrary.org/obo/CL_0000938
10424||1316||Orofaciodigital syndrome type 11||http://www.orpha.net/ORDO/Orphanet_141000
10425||10446||activated type II NK T cell||http://purl.obolibrary.org/obo/CL_0000931
10426||10447||CD4-negative, CD8-negative type I NK T cell secreting interleukin-4||http://purl.obolibrary.org/obo/CL_0000930
10427||10446||type II NK T cell secreting interleukin-4||http://purl.obolibrary.org/obo/CL_0000933
10428||5483||17q11 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_97685
10429||10446||type II NK T cell secreting interferon-gamma||http://purl.obolibrary.org/obo/CL_0000932
10430||8216||CD4-negative, CD8-negative, alpha-beta intraepithelial T cell||http://purl.obolibrary.org/obo/CL_0000935
10431||7036||CD4-positive, alpha-beta cytotoxic T cell||http://purl.obolibrary.org/obo/CL_0000934
10432||7035||pre-natural killer cell||http://purl.obolibrary.org/obo/CL_0000937
10433||10087||early lymphoid progenitor||http://purl.obolibrary.org/obo/CL_0000936
10434||10837||Sulfite oxidase deficiency due to molybdenum cofactor deficiency type C||http://www.orpha.net/ORDO/Orphanet_308400
10435||8646||Occipital horn syndrome||http://www.orpha.net/ORDO/Orphanet_198
10437||2252||Cornelia de Lange syndrome||http://www.orpha.net/ORDO/Orphanet_199
10436||5795||Disorder of beta and omega amino acid metabolism||http://www.orpha.net/ORDO/Orphanet_308407
10438||1316||Orofaciodigital syndrome type 9||http://www.orpha.net/ORDO/Orphanet_141007
10439||6897||Ocular coloboma||http://www.orpha.net/ORDO/Orphanet_194
10440||4928||Cat-eye syndrome||http://www.orpha.net/ORDO/Orphanet_195
10441||4701||Coffin-Lowry syndrome||http://www.orpha.net/ORDO/Orphanet_192
10442||2252||Cohen syndrome||http://www.orpha.net/ORDO/Orphanet_193
10443||10447||CD4-negative, CD8-negative type I NK T cell secreting interferon-gamma||http://purl.obolibrary.org/obo/CL_0000929
10444||10447||activated CD4-negative, CD8-negative type I NK T cell||http://purl.obolibrary.org/obo/CL_0000928
10445||10447||CD4-positive type I NK T cell secreting interleukin-4||http://purl.obolibrary.org/obo/CL_0000927
10446||10052||type II NK T cell||http://purl.obolibrary.org/obo/CL_0000922
10447||10052||type I NK T cell||http://purl.obolibrary.org/obo/CL_0000921
10448||8213||CD8-positive, CD28-negative, alpha-beta regulatory T cell||http://purl.obolibrary.org/obo/CL_0000920
10449||10447||CD4-positive type I NK T cell secreting interferon-gamma||http://purl.obolibrary.org/obo/CL_0000926
10450||10447||activated CD4-positive type I NK T cell||http://purl.obolibrary.org/obo/CL_0000925
10451||10447||CD4-negative, CD8-negative type I NK T cell||http://purl.obolibrary.org/obo/CL_0000924
10452||10447||CD4-positive type I NK T cell||http://purl.obolibrary.org/obo/CL_0000923
10453||1826||Andropogon gerardii||http://purl.obolibrary.org/obo/NCBITaxon_79824
10454||1022||Sebastes melanops||http://purl.obolibrary.org/obo/NCBITaxon_72085
10455||2672||nucleus of medial longitudinal fasciculus of medulla||http://purl.obolibrary.org/obo/UBERON_2000815
10456||10471||Tc1 cell||http://purl.obolibrary.org/obo/CL_0000917
10457||10064||dendritic epidermal T cell||http://purl.obolibrary.org/obo/CL_0000916
10458||8213||CD8-positive, CD25-positive, alpha-beta regulatory T cell||http://purl.obolibrary.org/obo/CL_0000919
10459||10471||Tc2 cell||http://purl.obolibrary.org/obo/CL_0000918
10460||10470||effector memory CD8-positive, alpha-beta T cell||http://purl.obolibrary.org/obo/CL_0000913
10461||10465||helper T cell||http://purl.obolibrary.org/obo/CL_0000912
10462||8216||CD8-alpha-alpha-positive, alpha-beta intraepithelial T cell||http://purl.obolibrary.org/obo/CL_0000915
10463||8204||immature NK T cell||http://purl.obolibrary.org/obo/CL_0000914
10465||13367||effector T cell||http://purl.obolibrary.org/obo/CL_0000911
10464||1022||Zoarces viviparus||http://purl.obolibrary.org/obo/NCBITaxon_48416
10466||10465||cytotoxic T cell||http://purl.obolibrary.org/obo/CL_0000910
10467||918||Methylmalonic acidemia due to methylmalonyl-CoA epimerase deficiency||http://www.orpha.net/ORDO/Orphanet_308425
10468||10898||Ehlers-Danlos syndrome, kyphoscoliotic and deafness type||http://www.orpha.net/ORDO/Orphanet_300179
10469||1595||Abdominal symptom||http://purl.obolibrary.org/obo/HP_0011458
10470||7037||CD8-positive, alpha-beta memory T cell||http://purl.obolibrary.org/obo/CL_0000909
10471||7037||CD8-positive, alpha-beta cytokine secreting effector T cell||http://purl.obolibrary.org/obo/CL_0000908
10472||10470||central memory CD8 positive, alpha-beta T cell||http://purl.obolibrary.org/obo/CL_0000907
10473||7037||activated CD8-positive, alpha-beta T cell||http://purl.obolibrary.org/obo/CL_0000906
10474||10213||effector memory CD4-positive, alpha-beta T cell||http://purl.obolibrary.org/obo/CL_0000905
10475||10213||central memory CD4-positive, alpha-beta T cell||http://purl.obolibrary.org/obo/CL_0000904
10477||11331||Maternal uniparental disomy of chromosome 13||http://www.orpha.net/ORDO/Orphanet_97678
10476||8207||natural T-regulatory cell||http://purl.obolibrary.org/obo/CL_0000903
10478||8207||induced T-regulatory cell||http://purl.obolibrary.org/obo/CL_0000902
10479||7036||Tr1 cell||http://purl.obolibrary.org/obo/CL_0000901
10480||7037||naive thymus-derived CD8-positive, alpha-beta T cell||http://purl.obolibrary.org/obo/CL_0000900
10481||2770||ncRNA||http://purl.obolibrary.org/obo/SO_0000655
10482||6290||Autism-epilepsy syndrome due to branched chain ketoacid dehydrogenase kinase deficiency||http://www.orpha.net/ORDO/Orphanet_308410
10483||5502||Methylobacterium extorquens||http://purl.obolibrary.org/obo/NCBITaxon_408
10484||10485||IgA memory B cell||http://purl.obolibrary.org/obo/CL_0000973
10485||8248||class switched memory B cell||http://purl.obolibrary.org/obo/CL_0000972
10486||10487||IgM memory B cell||http://purl.obolibrary.org/obo/CL_0000971
10487||8248||unswitched memory B cell||http://purl.obolibrary.org/obo/CL_0000970
10488||10491||IgA short lived plasma cell||http://purl.obolibrary.org/obo/CL_0000976
10489||10491||IgG short lived plasma cell||http://purl.obolibrary.org/obo/CL_0000977
10490||8241||long lived plasma cell||http://purl.obolibrary.org/obo/CL_0000974
10491||8241||short lived plasma cell||http://purl.obolibrary.org/obo/CL_0000975
10492||5502||Neisseria elongata||http://purl.obolibrary.org/obo/NCBITaxon_495
10493||10491||IgM short lived plasma cell||http://purl.obolibrary.org/obo/CL_0000978
10494||10485||IgG memory B cell||http://purl.obolibrary.org/obo/CL_0000979
10495||760||Focal epilepsy - intellectual disability - cerebro-cerebellar malformation||http://www.orpha.net/ORDO/Orphanet_352587
10496||762||Familial infantile myoclonic epilepsy||http://www.orpha.net/ORDO/Orphanet_352582
10497||5502||Photobacterium profundum||http://purl.obolibrary.org/obo/NCBITaxon_74109
10498||10510||Oculocutaneous or ocular albinism||http://www.orpha.net/ORDO/Orphanet_98706
10499||2415||Ectodermal malformation syndrome associated with ocular features||http://www.orpha.net/ORDO/Orphanet_98709
10500||10510||Pigmentation disorder with eye involvement, excluding albinism||http://www.orpha.net/ORDO/Orphanet_98708
10501||9739||Disease with potential neoplastic degeneration associated with ocular features||http://www.orpha.net/ORDO/Orphanet_98703
10502||10057||T3 B cell||http://purl.obolibrary.org/obo/CL_0000960
10503||2415||Connective tissue disease with eye involvement||http://www.orpha.net/ORDO/Orphanet_98702
10504||10135||Bm2 B cell||http://purl.obolibrary.org/obo/CL_0000962
10505||9739||Onycho-patellar syndrome with eye involvement||http://www.orpha.net/ORDO/Orphanet_98704
10506||10135||Bm1 B cell||http://purl.obolibrary.org/obo/CL_0000961
10507||10136||Bm3-delta B cell||http://purl.obolibrary.org/obo/CL_0000963
10508||10136||Bm2  B cell||http://purl.obolibrary.org/obo/CL_0000964
10510||9739||Pigmentation disorder with eye involvement||http://www.orpha.net/ORDO/Orphanet_98700
10509||10136||Bm3 B cell||http://purl.obolibrary.org/obo/CL_0000965
10511||9739||Phakomatosis with eye involvement||http://www.orpha.net/ORDO/Orphanet_98701
10512||10136||Bm4 B cell||http://purl.obolibrary.org/obo/CL_0000966
10513||8248||Bm5 B cell||http://purl.obolibrary.org/obo/CL_0000967
10514||8239||Be cell||http://purl.obolibrary.org/obo/CL_0000968
10515||8239||regulatory B cell||http://purl.obolibrary.org/obo/CL_0000969
10516||2252||Severe feeding difficulties - failure to thrive - microcephaly due to ASXL3 deficiency||http://www.orpha.net/ORDO/Orphanet_352577
10517||8191||fludarabine phosphate||http://purl.obolibrary.org/obo/CHEBI_63599
10518||10491||IgE short lived plasma cell||http://purl.obolibrary.org/obo/CL_0000951
10519||10607||IgE plasmablast||http://purl.obolibrary.org/obo/CL_0000950
10520||10057||T1 B cell||http://purl.obolibrary.org/obo/CL_0000958
10521||10057||T2 B cell||http://purl.obolibrary.org/obo/CL_0000959
10522||10058||pre-B-I cell||http://purl.obolibrary.org/obo/CL_0000956
10523||10525||large pre-B-II cell||http://purl.obolibrary.org/obo/CL_0000957
10524||10525||small pre-B-II cell||http://purl.obolibrary.org/obo/CL_0000954
10525||10058||pre-B-II cell||http://purl.obolibrary.org/obo/CL_0000955
10526||2063||cerebral degeneration||http://purl.obolibrary.org/obo/HP_0007313
10527||10523||preBCR-positive large pre-B-II cell||http://purl.obolibrary.org/obo/CL_0000952
10528||10523||preBCR-negative large pre-B-II cell||http://purl.obolibrary.org/obo/CL_0000953
10529||4931||Ataxia-telangiectasia||http://www.orpha.net/ORDO/Orphanet_100
10530||4266||Leber hereditary optic neuropathy||http://www.orpha.net/ORDO/Orphanet_104
10531||9718||Genetic optic atrophy||http://www.orpha.net/ORDO/Orphanet_103
10532||8205||mucosal invariant T cell||http://purl.obolibrary.org/obo/CL_0000940
10533||9854||Dentatorubral pallidoluysian atrophy||http://www.orpha.net/ORDO/Orphanet_101
10534||4775||BOR syndrome||http://www.orpha.net/ORDO/Orphanet_107
10535||742||Atresia of urethra||http://www.orpha.net/ORDO/Orphanet_105
10536||9294||lymphocyte of B lineage||http://purl.obolibrary.org/obo/CL_0000945
10537||10536||antibody secreting cell||http://purl.obolibrary.org/obo/CL_0000946
10538||2252||Bannayan-Riley-Ruvalcaba syndrome||http://www.orpha.net/ORDO/Orphanet_109
10539||10490||IgE plasma cell||http://purl.obolibrary.org/obo/CL_0000947
10540||10485||IgE memory B cell||http://purl.obolibrary.org/obo/CL_0000948
10541||10580||thymic conventional dendritic cell||http://purl.obolibrary.org/obo/CL_0000941
10542||8244||thymic plasmacytoid dendritic cell||http://purl.obolibrary.org/obo/CL_0000942
10543||10514||Be1 Cell||http://purl.obolibrary.org/obo/CL_0000943
10544||10514||Be2 cell||http://purl.obolibrary.org/obo/CL_0000944
10545||10607||IgD plasmablast||http://purl.obolibrary.org/obo/CL_0000949
10546||762||Progressive myoclonic epilepsy with dystonia||http://www.orpha.net/ORDO/Orphanet_352596
10547||4224||Beckwith-Wiedemann syndrome||http://www.orpha.net/ORDO/Orphanet_116
10548||2454||Beta-mannosidosis||http://www.orpha.net/ORDO/Orphanet_118
10549||1415||Autosomal recessive limb-girdle muscular dystrophy type 2E||http://www.orpha.net/ORDO/Orphanet_119
10550||4810||Bartter syndrome||http://www.orpha.net/ORDO/Orphanet_112
10551||5317||Bazex-Dupr -Christol syndrome||http://www.orpha.net/ORDO/Orphanet_113
10552||7949||Auriculoosteodysplasia||http://www.orpha.net/ORDO/Orphanet_114
10553||2603||Congenital contractural arachnodactyly||http://www.orpha.net/ORDO/Orphanet_115
10554||1306||Bardet-Biedl syndrome||http://www.orpha.net/ORDO/Orphanet_110
10555||4191||Barth syndrome||http://www.orpha.net/ORDO/Orphanet_111
10556||12769||Contractures-webbed neck-micrognathia-hypoplastic nipples syndrome||http://www.orpha.net/ORDO/Orphanet_314002
10557||4263||Illumina sequencing||http://purl.obolibrary.org/obo/OBI_0000724
10558||5502||Legionella longbeachae||http://purl.obolibrary.org/obo/NCBITaxon_450
10559||2252||Borjeson-Forssman-Lehmann syndrome||http://www.orpha.net/ORDO/Orphanet_127
10560||4785||Bloom syndrome||http://www.orpha.net/ORDO/Orphanet_125
10561||4931||Blepharophimosis - epicanthus inversus - ptosis||http://www.orpha.net/ORDO/Orphanet_126
10562||323||Bj rnstad syndrome||http://www.orpha.net/ORDO/Orphanet_123
10563||5300||Blackfan-Diamond anemia||http://www.orpha.net/ORDO/Orphanet_124
10564||2713||Birt-Hogg-Dub  syndrome||http://www.orpha.net/ORDO/Orphanet_122
10565||4139||Intellectual disability - obesity - brain malformations - facial dysmorphism||http://www.orpha.net/ORDO/Orphanet_352530
10566||6888||Primary erythermalgia||http://www.orpha.net/ORDO/Orphanet_90026
10567||7956||Syndactyly||http://www.orpha.net/ORDO/Orphanet_90025
10568||5700||Deafness with labyrinthine aplasia, microtia, and microdontia||http://www.orpha.net/ORDO/Orphanet_90024
10569||8896||Primary immunodeficiency syndrome due to p14 deficiency||http://www.orpha.net/ORDO/Orphanet_90023
10571||6306||Ketoacidosis due to beta-ketothiolase deficiency||http://www.orpha.net/ORDO/Orphanet_134
10570||10582||immature CD11c-negative plasmacytoid dendritic cell||http://purl.obolibrary.org/obo/CL_0000994
10573||15549||CACH syndrome||http://www.orpha.net/ORDO/Orphanet_135
10572||871||CD34-positive, CD38-positive common myeloid progenitor OR CD34-positive, CD38-positive common lymphoid progenitor||http://purl.obolibrary.org/obo/CL_0000995
10574||1826||Symplocarpus renifolius||http://purl.obolibrary.org/obo/NCBITaxon_477955
10576||4705||CADASIL||http://www.orpha.net/ORDO/Orphanet_136
10575||10614||immature CD11c-low plasmacytoid dendritic cell||http://purl.obolibrary.org/obo/CL_0000992
10577||15571||Congenital disorder of glycosylation||http://www.orpha.net/ORDO/Orphanet_137
10578||10614||mature CD11c-low plasmacytoid dendritic cell||http://purl.obolibrary.org/obo/CL_0000993
10579||1306||CHARGE syndrome||http://www.orpha.net/ORDO/Orphanet_138
10580||8621||conventional dendritic cell||http://purl.obolibrary.org/obo/CL_0000990
10581||5317||CHILD syndrome||http://www.orpha.net/ORDO/Orphanet_139
10583||7943||High bone mass osteogenesis imperfecta||http://www.orpha.net/ORDO/Orphanet_314029
10582||8244||CD11c-negative plasmacytoid dendritic cell||http://purl.obolibrary.org/obo/CL_0000991
10584||15||Brugada syndrome||http://www.orpha.net/ORDO/Orphanet_130
10585||6591||Butyrylcholinesterase deficiency||http://www.orpha.net/ORDO/Orphanet_132
10586||4266||Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency||http://www.orpha.net/ORDO/Orphanet_352563
10587||5502||Bifidobacterium breve UCC2003||http://purl.obolibrary.org/obo/NCBITaxon_326426
10588||5502||Lactobacillus helveticus CNRZ32||http://purl.obolibrary.org/obo/NCBITaxon_326425
10590||5502||Frankia alni ACN14a||http://purl.obolibrary.org/obo/NCBITaxon_326424
10589||5502||Acinetobacter baumannii||http://purl.obolibrary.org/obo/NCBITaxon_470
10591||13234||CD4-positive CD11b-positive dendritic cell||http://purl.obolibrary.org/obo/CL_0000999
10592||10580||CD8_alpha-negative CD11b-negative dendritic cell||http://purl.obolibrary.org/obo/CL_0000998
10593||10591||immature CD8_alpha-negative CD11b-positive dendritic cell||http://purl.obolibrary.org/obo/CL_0000997
10594||10582||mature CD11c-negative plasmacytoid dendritic cell||http://purl.obolibrary.org/obo/CL_0000996
10597||5502||Neisseria polysaccharea||http://purl.obolibrary.org/obo/NCBITaxon_489
10596||6302||Carbamoyl-phosphate synthase deficiency||http://www.orpha.net/ORDO/Orphanet_147
10595||8248||double negative memory B cell||http://purl.obolibrary.org/obo/CL_0000981
10599||378||Multiple carboxylase deficiency||http://www.orpha.net/ORDO/Orphanet_148
10598||10607||IgG plasmablast||http://purl.obolibrary.org/obo/CL_0000982
10601||970||Hereditary breast and ovarian cancer syndrome||http://www.orpha.net/ORDO/Orphanet_145
10600||10607||IgM plasmablast||http://purl.obolibrary.org/obo/CL_0000983
10602||10607||IgA plasmablast||http://purl.obolibrary.org/obo/CL_0000984
10603||5502||Neisseria gonorrhoeae||http://purl.obolibrary.org/obo/NCBITaxon_485
10604||5502||Neisseria lactamica||http://purl.obolibrary.org/obo/NCBITaxon_486
10605||5502||Neisseria meningitidis||http://purl.obolibrary.org/obo/NCBITaxon_487
10606||5502||Neisseria mucosa||http://purl.obolibrary.org/obo/NCBITaxon_488
10607||8239||plasmablast||http://purl.obolibrary.org/obo/CL_0000980
10608||3019||Campomelic dysplasia||http://www.orpha.net/ORDO/Orphanet_140
10609||10994||abamectin||http://purl.obolibrary.org/obo/CHEBI_39214
10610||4803||Hereditary nonpolyposis colon cancer||http://www.orpha.net/ORDO/Orphanet_144
10611||4706||Canavan disease||http://www.orpha.net/ORDO/Orphanet_141
10612||5502||Bacillus anthracis str. Sterne||http://purl.obolibrary.org/obo/NCBITaxon_260799
10613||5502||Neisseria||http://purl.obolibrary.org/obo/NCBITaxon_482
10614||8244||CD11c-low plasmacytoid dendritic cell||http://purl.obolibrary.org/obo/CL_0000989
10615||5502||Clostridium thermocellum ATCC 27405||http://purl.obolibrary.org/obo/NCBITaxon_203119
10616||5502||Neisseria flavescens||http://purl.obolibrary.org/obo/NCBITaxon_484
10617||5502||Neisseria cinerea||http://purl.obolibrary.org/obo/NCBITaxon_483
10618||9625||X-linked cone dysfunction syndrome with myopia||http://www.orpha.net/ORDO/Orphanet_90001
10619||10490||IgM plasma cell||http://purl.obolibrary.org/obo/CL_0000986
10620||10490||IgG plasma cell||http://purl.obolibrary.org/obo/CL_0000985
10622||772||hematopoietic cell||http://purl.obolibrary.org/obo/CL_0000988
10621||5502||Moraxella catarrhalis||http://purl.obolibrary.org/obo/NCBITaxon_480
10623||10490||IgA plasma cell||http://purl.obolibrary.org/obo/CL_0000987
10624||10272||Autosomal dominant nocturnal frontal lobe epilepsy||http://www.orpha.net/ORDO/Orphanet_98784
10625||10994||topotecan||http://purl.obolibrary.org/obo/CHEBI_63632
10626||2430||Oculocutaneous albinism type 5||http://www.orpha.net/ORDO/Orphanet_370091
10627||10994||topiramate||http://purl.obolibrary.org/obo/CHEBI_63631
10628||11472||Partial deletion of chromosome 19||http://www.orpha.net/ORDO/Orphanet_261841
10629||1826||Nicotiana attenuata||http://purl.obolibrary.org/obo/NCBITaxon_49451
10630||7152||Partial trisomy of the long arm of chromosome 18||http://www.orpha.net/ORDO/Orphanet_262977
10631||11472||Partial deletion of chromosome 20||http://www.orpha.net/ORDO/Orphanet_261846
10632||2430||Oculocutaneous albinism type 6||http://www.orpha.net/ORDO/Orphanet_370097
10633||9862||Syndromic anorectal malformation||http://www.orpha.net/ORDO/Orphanet_117573
10634||6064||pyrethroid ester insecticide||http://purl.obolibrary.org/obo/CHEBI_39116
10635||9856||Spinocerebellar ataxia type 18||http://www.orpha.net/ORDO/Orphanet_98771
10636||9856||Spinocerebellar ataxia type 19/22||http://www.orpha.net/ORDO/Orphanet_98772
10637||266||Congenital disorder of glycosylation with hepatic involvement||http://www.orpha.net/ORDO/Orphanet_371157
10638||9856||Spinocerebellar ataxia type 21||http://www.orpha.net/ORDO/Orphanet_98773
10639||11472||Partial deletion of chromosome 18||http://www.orpha.net/ORDO/Orphanet_261836
10640||11472||Partial deletion of chromosome 17||http://www.orpha.net/ORDO/Orphanet_261831
10641||7119||Partial duplication of the long arm of chromosome 17||http://www.orpha.net/ORDO/Orphanet_262968
10642||4942||Pan troglodytes troglodytes||http://purl.obolibrary.org/obo/NCBITaxon_37011
10643||2003||Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR1 deficiency||http://www.orpha.net/ORDO/Orphanet_99898
10644||9853||Spinocerebellar ataxia type 5||http://www.orpha.net/ORDO/Orphanet_98766
10645||9853||Spinocerebellar ataxia type 11||http://www.orpha.net/ORDO/Orphanet_98767
10646||9856||Spinocerebellar ataxia type 27||http://www.orpha.net/ORDO/Orphanet_98764
10647||9856||Spinocerebellar ataxia type 4||http://www.orpha.net/ORDO/Orphanet_98765
10648||9856||Spinocerebellar ataxia type 12||http://www.orpha.net/ORDO/Orphanet_98762
10649||9856||Spinocerebellar ataxia type 14||http://www.orpha.net/ORDO/Orphanet_98763
10650||9856||Spinocerebellar ataxia type 8||http://www.orpha.net/ORDO/Orphanet_98760
10651||4139||Proximal 16p11.2 microduplication syndrome||http://www.orpha.net/ORDO/Orphanet_370079
10652||0||obsolete class||http://www.geneontology.org/formats/oboInOwl#ObsoleteClass
10653||9854||Spinocerebellar ataxia type 10||http://www.orpha.net/ORDO/Orphanet_98761
10654||3750||aromatase inhibitor||http://purl.obolibrary.org/obo/CHEBI_50790
10655||6573||estrogen receptor antagonist role||http://purl.obolibrary.org/obo/CHEBI_50792
10656||4173||nevirapine||http://purl.obolibrary.org/obo/CHEBI_63613
10657||7117||Partial trisomy of the long arm of chromosome 16||http://www.orpha.net/ORDO/Orphanet_262959
10658||11472||Partial deletion of chromosome 16||http://www.orpha.net/ORDO/Orphanet_261826
10659||11372||Partial deletion of the long arm of chromosome 12||http://www.orpha.net/ORDO/Orphanet_261821
10660||5502||Salmonella bongori||http://purl.obolibrary.org/obo/NCBITaxon_54736
10661||11456||Partial duplication of the long arm of chromosome 15||http://www.orpha.net/ORDO/Orphanet_262950
10662||9856||Spinocerebellar ataxia type 15/16||http://www.orpha.net/ORDO/Orphanet_98769
10663||9856||Spinocerebellar ataxia type 13||http://www.orpha.net/ORDO/Orphanet_98768
10664||8565||Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15||http://www.orpha.net/ORDO/Orphanet_98754
10666||4981||material sample||http://purl.obolibrary.org/obo/OBI_0000747
10665||9856||Spinocerebellar ataxia type 1||http://www.orpha.net/ORDO/Orphanet_98755
10667||9856||Spinocerebellar ataxia type 2||http://www.orpha.net/ORDO/Orphanet_98756
10668||10096||Transient neonatal diabetes mellitus||http://www.orpha.net/ORDO/Orphanet_99886
10669||10096||Permanent neonatal diabetes mellitus||http://www.orpha.net/ORDO/Orphanet_99885
10670||1276||Hyperparathyroidism-jaw tumor syndrome||http://www.orpha.net/ORDO/Orphanet_99880
10671||11472||Partial deletion of chromosome 11||http://www.orpha.net/ORDO/Orphanet_261816
10672||11472||Partial deletion of chromosome 10||http://www.orpha.net/ORDO/Orphanet_261811
10673||10719||Acute infantile liver failure-multisystemic involvement syndrome||http://www.orpha.net/ORDO/Orphanet_370088
10674||15538||independent variable specification||http://purl.obolibrary.org/obo/OBI_0000750
10675||9853||Spinocerebellar ataxia type 6||http://www.orpha.net/ORDO/Orphanet_98758
10677||11456||Partial duplication of the long arm of chromosome 14||http://www.orpha.net/ORDO/Orphanet_262941
10676||9856||Spinocerebellar ataxia type 3||http://www.orpha.net/ORDO/Orphanet_98757
10678||9856||Spinocerebellar ataxia type 17||http://www.orpha.net/ORDO/Orphanet_98759
10679||6476||behavioral response to water deprivation||http://purl.obolibrary.org/obo/GO_0042630
10680||8791||Congenital lethal myopathy, Compton-North type||http://www.orpha.net/ORDO/Orphanet_210163
10681||2252||Autism spectrum disorder due to AUTS2 deficiency||http://www.orpha.net/ORDO/Orphanet_352490
10682||1732||Rare genetic endocrine disease||http://www.orpha.net/ORDO/Orphanet_156638
10683||11472||Partial deletion of chromosome 8||http://www.orpha.net/ORDO/Orphanet_261801
10684||11472||Partial deletion of chromosome 9||http://www.orpha.net/ORDO/Orphanet_261806
10685||4224||Noonan syndrome and Noonan-related syndrome||http://www.orpha.net/ORDO/Orphanet_98733
10686||5025||Neosartorya fennelliae||http://purl.obolibrary.org/obo/NCBITaxon_41048
10688||15538||controlled variable specification||http://purl.obolibrary.org/obo/OBI_0000785
10687||799||antispasmodic||http://purl.obolibrary.org/obo/CHEBI_53784
10689||7135||Partial trisomy of the long arm of chromosome 20||http://www.orpha.net/ORDO/Orphanet_262995
10690||10994||(E)-clothianidin||http://purl.obolibrary.org/obo/CHEBI_39177
10691||9918||Brain calcification, Rajab type||http://www.orpha.net/ORDO/Orphanet_178506
10692||9898||Perry syndrome||http://www.orpha.net/ORDO/Orphanet_178509
10693||2415||Metabolic disease associated with ocular features||http://www.orpha.net/ORDO/Orphanet_98710
10694||4717||Genetic vascular anomaly||http://www.orpha.net/ORDO/Orphanet_211240
10695||10693||Metabolic disease with cataract||http://www.orpha.net/ORDO/Orphanet_98712
10696||10693||Metabolic disease with corneal opacity||http://www.orpha.net/ORDO/Orphanet_98711
10697||10573||Late infantile CACH syndrome||http://www.orpha.net/ORDO/Orphanet_157716
10698||10573||Congenital or early infantile CACH syndrome||http://www.orpha.net/ORDO/Orphanet_157713
10699||10573||Juvenile or adult CACH syndrome||http://www.orpha.net/ORDO/Orphanet_157719
10700||10693||Metabolic disease with pigmentary retinitis||http://www.orpha.net/ORDO/Orphanet_98713
10701||7161||Partial duplication of the long arm of chromosome 19||http://www.orpha.net/ORDO/Orphanet_262986
10702||10693||Metabolic disease with macular cherry-red spot||http://www.orpha.net/ORDO/Orphanet_98714
10703||6315||Urocanic aciduria||http://www.orpha.net/ORDO/Orphanet_210128
10704||799||nutraceutical||http://purl.obolibrary.org/obo/CHEBI_50733
10705||799||antimalarial||http://purl.obolibrary.org/obo/CHEBI_38068
10706||799||estrogen receptor modulator||http://purl.obolibrary.org/obo/CHEBI_50739
10707||2252||Intellectual disability-facial dysmorphism-hand anomalies syndrome||http://www.orpha.net/ORDO/Orphanet_370010
10708||10143||Spondyloepimetaphyseal dysplasia, Isidor type||http://www.orpha.net/ORDO/Orphanet_370015
10709||6989||Resistance to thyrotropin-releasing hormone syndrome||http://www.orpha.net/ORDO/Orphanet_99832
10710||10144||Spondylometaphyseal dysplasia, Czarny-Ratajczak type||http://www.orpha.net/ORDO/Orphanet_370019
10711||6980||ATP metabolic process||http://purl.obolibrary.org/obo/GO_0046034
10713||799||anti-arrhythmia drug||http://purl.obolibrary.org/obo/CHEBI_38070
10712||9826||Congenital alveolar capillary dysplasia||http://www.orpha.net/ORDO/Orphanet_210122
10714||1826||Senecio chrysanthemifolius||http://purl.obolibrary.org/obo/NCBITaxon_121541
10715||1826||Senecio aethnensis||http://purl.obolibrary.org/obo/NCBITaxon_121540
10716||4692||Spastic ataxia||http://www.orpha.net/ORDO/Orphanet_316226
10717||10721||Genetic biliary tract disease||http://www.orpha.net/ORDO/Orphanet_156607
10718||4139||Ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome||http://www.orpha.net/ORDO/Orphanet_370022
10719||10721||Genetic parenchymatous liver disease||http://www.orpha.net/ORDO/Orphanet_156604
10720||1022||Isochrysis galbana||http://purl.obolibrary.org/obo/NCBITaxon_37099
10721||1732||Rare genetic hepatic disease||http://www.orpha.net/ORDO/Orphanet_156601
10722||307||Leukonychia totalis - acanthosis-nigricans-like lesions - abnormal hair||http://www.orpha.net/ORDO/Orphanet_210133
10723||10716||Autosomal dominant spastic ataxia||http://www.orpha.net/ORDO/Orphanet_316235
10724||1313||Familial gestational hyperthyroidism||http://www.orpha.net/ORDO/Orphanet_99819
10725||10610||Non-polyposis Turcot syndrome||http://www.orpha.net/ORDO/Orphanet_99817
10726||8573||Turcot syndrome with polyposis||http://www.orpha.net/ORDO/Orphanet_99818
10727||1732||Rare genetic urogenital disease||http://www.orpha.net/ORDO/Orphanet_156619
10728||238||LIG4 syndrome||http://www.orpha.net/ORDO/Orphanet_99812
10729||2391||Neuronal intestinal pseudoobstruction||http://www.orpha.net/ORDO/Orphanet_99811
10730||2302||Familial porencephaly||http://www.orpha.net/ORDO/Orphanet_99810
10731||9918||Inherited congenital spastic tetraplegia||http://www.orpha.net/ORDO/Orphanet_210141
10732||1732||Rare genetic respiratory disease||http://www.orpha.net/ORDO/Orphanet_156610
10733||4715||Lethal polymalformative syndrome, Boissel type||http://www.orpha.net/ORDO/Orphanet_210144
10734||11372||Partial deletion of the short arm of chromosome 12||http://www.orpha.net/ORDO/Orphanet_316244
10735||10716||Autosomal recessive spastic ataxia||http://www.orpha.net/ORDO/Orphanet_316240
10736||4834||Oculootodental syndrome||http://www.orpha.net/ORDO/Orphanet_99806
10737||613||PEHO-like syndrome||http://www.orpha.net/ORDO/Orphanet_99807
10738||760||Hemimegalencephaly||http://www.orpha.net/ORDO/Orphanet_99802
10739||6770||Haddad syndrome||http://www.orpha.net/ORDO/Orphanet_99803
10740||11809||Genetic hypertension||http://www.orpha.net/ORDO/Orphanet_156629
10742||1826||Senecio vulgaris subsp. vulgaris||http://purl.obolibrary.org/obo/NCBITaxon_121558
10741||10306||Partial deletion of the short arm of chromosome 5||http://www.orpha.net/ORDO/Orphanet_261893
10743||4122||Hypothalamic insufficiency-secondary microcephaly-visual impairment-urinary anomalies||http://www.orpha.net/ORDO/Orphanet_370006
10744||9900||ethmoid cartilage||http://purl.obolibrary.org/obo/UBERON_0011242
10745||10727||Genetic urogenital tract malformation||http://www.orpha.net/ORDO/Orphanet_156622
10746||13304||Focal palmoplantar keratoderma with joint keratoses||http://www.orpha.net/ORDO/Orphanet_370002
10747||1826||Senecio squalidus subsp. squalidus||http://purl.obolibrary.org/obo/NCBITaxon_121555
10748||10308||Partial deletion of the short arm of chromosome 4||http://www.orpha.net/ORDO/Orphanet_261884
10749||1276||Familial isolated hyperparathyroidism||http://www.orpha.net/ORDO/Orphanet_99879
10750||9607||Congenital disorder of glycosylation with cardiac malformation as a major feature||http://www.orpha.net/ORDO/Orphanet_371183
10751||15391||Congenital disorder of glycosylation with intestinal involvement||http://www.orpha.net/ORDO/Orphanet_371188
10752||11456||Partial duplication of the long arm of chromosome 13||http://www.orpha.net/ORDO/Orphanet_262932
10753||6087||Situs ambiguus||http://www.orpha.net/ORDO/Orphanet_157769
10754||10994||myxothiazol||http://purl.obolibrary.org/obo/CHEBI_25461
10755||1276||Familial parathyroid adenoma||http://www.orpha.net/ORDO/Orphanet_99877
10756||1276||Primary parathyroids hyperplasia||http://www.orpha.net/ORDO/Orphanet_99878
10757||3405||Ehlers-Danlos syndrome type 7A||http://www.orpha.net/ORDO/Orphanet_99875
10758||3405||Ehlers-Danlos syndrome type 7B||http://www.orpha.net/ORDO/Orphanet_99876
10759||10312||Partial deletion of the short arm of chromosome 3||http://www.orpha.net/ORDO/Orphanet_261875
10760||3573||Congenital disorder of glycosylation-related bone disorder||http://www.orpha.net/ORDO/Orphanet_371195
10761||7515||Partial duplication of the long arm of chromosome 11||http://www.orpha.net/ORDO/Orphanet_262923
10762||10994||3 ,5 -cyclic AMP||http://purl.obolibrary.org/obo/CHEBI_17489
10763||10994||mefloquine||http://purl.obolibrary.org/obo/CHEBI_63609
10764||1826||Gerbera hybrid cultivar||http://purl.obolibrary.org/obo/NCBITaxon_18101
10765||10314||Partial deletion of the short arm of chromosome 2||http://www.orpha.net/ORDO/Orphanet_261866
10766||4695||Familial syringomyelia||http://www.orpha.net/ORDO/Orphanet_370034
10767||10771||Idiopathic syringomyelia||http://www.orpha.net/ORDO/Orphanet_99858
10768||7500||Partial duplication of the long arm of chromosome 10||http://www.orpha.net/ORDO/Orphanet_262914
10769||3750||topoisomerase II inhibitor||http://purl.obolibrary.org/obo/CHEBI_50750
10770||9287||Methylcobalamin deficiency type cblDv1||http://www.orpha.net/ORDO/Orphanet_308380
10771||7992||Primary syringomyelia||http://www.orpha.net/ORDO/Orphanet_99856
10772||10573||Ovarioleukodystrophy||http://www.orpha.net/ORDO/Orphanet_99853
10773||10573||Cree leukoencephalopathy||http://www.orpha.net/ORDO/Orphanet_99854
10774||15549||RAVINE syndrome||http://www.orpha.net/ORDO/Orphanet_99852
10775||5700||Hypospadias - hypertelorism - coloboma and deafness||http://www.orpha.net/ORDO/Orphanet_157788
10777||4430||mutagen||http://purl.obolibrary.org/obo/CHEBI_25435
10776||10368||Partial deletion of the short arm of chromosome 1||http://www.orpha.net/ORDO/Orphanet_261857
10778||4929||Congenital disorder of glycosylation with dilated cardiomyopathy||http://www.orpha.net/ORDO/Orphanet_371176
10779||8191||bis(2-chloroethyl) sulfide||http://purl.obolibrary.org/obo/CHEBI_25434
10780||10837||Sulfite oxidase deficiency due to molybdenum cofactor deficiency type A||http://www.orpha.net/ORDO/Orphanet_308386
10781||12378||Autosomal dominant myoglobinuria||http://www.orpha.net/ORDO/Orphanet_99846
10782||6572||Glycogen storage disease due to muscle beta-enolase deficiency||http://www.orpha.net/ORDO/Orphanet_99849
10783||7497||Partial trisomy of the long arm of chromosome 9||http://www.orpha.net/ORDO/Orphanet_262905
10784||14642||Sterile multifocal osteomyelitis with periostitis and pustulosis||http://www.orpha.net/ORDO/Orphanet_210115
10785||4139||Alpha-thalassemia - intellectual disability syndrome linked to chromosome 16||http://www.orpha.net/ORDO/Orphanet_98791
10786||3560||Intermediate osteopetrosis||http://www.orpha.net/ORDO/Orphanet_210110
10788||3833||Hereditary mixed polyposis syndrome||http://www.orpha.net/ORDO/Orphanet_157794
10787||2409||Leukocyte adhesion deficiency type I||http://www.orpha.net/ORDO/Orphanet_99842
10789||2409||Leukocyte adhesion deficiency type II||http://www.orpha.net/ORDO/Orphanet_99843
10791||2409||Leukocyte adhesion deficiency type III||http://www.orpha.net/ORDO/Orphanet_99844
10790||9846||Isochromosomy Yq||http://www.orpha.net/ORDO/Orphanet_98798
10793||4191||Genetic recurrent myoglobinuria||http://www.orpha.net/ORDO/Orphanet_99845
10792||9846||Isochromosomy Yp||http://www.orpha.net/ORDO/Orphanet_98797
10796||3833||Hyperplastic polyposis syndrome||http://www.orpha.net/ORDO/Orphanet_157798
10795||2672||mouth mucosa||http://purl.obolibrary.org/obo/UBERON_0003729
10794||10837||Sulfite oxidase deficiency due to molybdenum cofactor deficiency type B||http://www.orpha.net/ORDO/Orphanet_308393
10797||2672||mediastinum||http://purl.obolibrary.org/obo/UBERON_0003728
10798||2506||Angelman syndrome due to paternal uniparental disomy of chromosome 15||http://www.orpha.net/ORDO/Orphanet_98795
10799||2506||Angelman syndrome due to maternal 15q11q13 deletion||http://www.orpha.net/ORDO/Orphanet_98794
10800||5462||Prader-Willi syndrome due to paternal 15q11q13 deletion||http://www.orpha.net/ORDO/Orphanet_98793
10801||6046||Amish lethal microcephaly||http://www.orpha.net/ORDO/Orphanet_99742
10802||4785||King-Denborough syndrome||http://www.orpha.net/ORDO/Orphanet_99741
10803||4706||Huntington disease-like syndrome||http://www.orpha.net/ORDO/Orphanet_158266
10804||10631||Partial monosomy of the short arm of chromosome 20||http://www.orpha.net/ORDO/Orphanet_261992
10805||1627||integumental system||http://purl.obolibrary.org/obo/UBERON_0002416
10806||2672||tail||http://purl.obolibrary.org/obo/UBERON_0002415
10807||1627||hepatobiliary system||http://purl.obolibrary.org/obo/UBERON_0002423
10808||2672||basal ganglion||http://purl.obolibrary.org/obo/UBERON_0002420
10809||8231||Trisomy 4p||http://www.orpha.net/ORDO/Orphanet_1738
10810||4803||Kostmann syndrome||http://www.orpha.net/ORDO/Orphanet_99749
10811||5502||Brevibacterium linens||http://purl.obolibrary.org/obo/NCBITaxon_1703
10812||5502||Bdellovibrio bacteriovorus HD100||http://purl.obolibrary.org/obo/NCBITaxon_264462
10813||8315||Atypical progressive supranuclear palsy||http://www.orpha.net/ORDO/Orphanet_99750
10814||13496||Australian bat lyssavirus||http://purl.obolibrary.org/obo/NCBITaxon_90961
10815||1627||immune system||http://purl.obolibrary.org/obo/UBERON_0002405
10816||2672||pericardium||http://purl.obolibrary.org/obo/UBERON_0002407
10817||8167||Trisomy 5p||http://www.orpha.net/ORDO/Orphanet_1742
10819||2672||vertebra||http://purl.obolibrary.org/obo/UBERON_0002412
10818||8132||Distal trisomy 6p||http://www.orpha.net/ORDO/Orphanet_1745
10821||11457||Mosaic trisomy 7||http://www.orpha.net/ORDO/Orphanet_1747
10820||799||cardiotonic drug||http://purl.obolibrary.org/obo/CHEBI_38147
10822||5502||Corynebacterium diphtheriae||http://purl.obolibrary.org/obo/NCBITaxon_1717
10823||5502||Corynebacterium glutamicum||http://purl.obolibrary.org/obo/NCBITaxon_1718
10824||10994||phorbol 13-acetate 12-myristate||http://purl.obolibrary.org/obo/CHEBI_37537
10825||13997||Familial esophageal achalasia||http://www.orpha.net/ORDO/Orphanet_99723
10826||1422||tumor grading||http://purl.obolibrary.org/obo/OBI_0600002
10827||10701||Distal trisomy 19q||http://www.orpha.net/ORDO/Orphanet_1717
10828||10370||Trisomy 18p||http://www.orpha.net/ORDO/Orphanet_1715
10830||13689||olfactory pit||http://purl.obolibrary.org/obo/UBERON_0005870
10829||5502||Streptococcus dysgalactiae subsp. equisimilis||http://purl.obolibrary.org/obo/NCBITaxon_119602
10831||10630||Distal trisomy 18q||http://www.orpha.net/ORDO/Orphanet_1716
10832||10374||17p11.2 microduplication syndrome||http://www.orpha.net/ORDO/Orphanet_1713
10833||11457||Mosaic trisomy 17||http://www.orpha.net/ORDO/Orphanet_1711
10834||9899||Inherited Creutzfeldt-Jakob disease||http://www.orpha.net/ORDO/Orphanet_282166
10836||1022||Anas platyrhynchos||http://purl.obolibrary.org/obo/NCBITaxon_8839
10835||10639||Partial deletion of the short arm of chromosome 18||http://www.orpha.net/ORDO/Orphanet_261974
10837||6316||Sulfite oxidase deficiency due to molybdenum cofactor deficiency||http://www.orpha.net/ORDO/Orphanet_99732
10839||1302||Combined dystonia||http://www.orpha.net/ORDO/Orphanet_98203
10838||9275||Myotonia permanens||http://www.orpha.net/ORDO/Orphanet_99735
10840||9275||Myotonia fluctuans||http://www.orpha.net/ORDO/Orphanet_99734
10841||6316||Isolated sulfite oxidase deficiency||http://www.orpha.net/ORDO/Orphanet_99731
10842||13883||group assignment||http://purl.obolibrary.org/obo/OBI_0600015
10843||2672||limb bone||http://purl.obolibrary.org/obo/UBERON_0002428
10845||4840||22q11.2 microduplication syndrome||http://www.orpha.net/ORDO/Orphanet_1727
10844||10994||sphingosine 1-phosphate||http://purl.obolibrary.org/obo/CHEBI_37550
10846||5502||Candidatus Phytoplasma asteris||http://purl.obolibrary.org/obo/NCBITaxon_85620
10847||11457||Mosaic trisomy 2||http://www.orpha.net/ORDO/Orphanet_1723
10848||11457||Mosaic trisomy 20||http://www.orpha.net/ORDO/Orphanet_1724
10849||13689||pectoral fin skeleton||http://purl.obolibrary.org/obo/UBERON_0010710
10850||9275||Acetazolamide-responsive myotonia||http://www.orpha.net/ORDO/Orphanet_99736
10851||11802||Rare familial disorder with hypertrophic cardiomyopathy||http://www.orpha.net/ORDO/Orphanet_99739
10852||10628||Partial deletion of the short arm of chromosome 19||http://www.orpha.net/ORDO/Orphanet_261983
10854||1531||mitochondrial envelope||http://purl.obolibrary.org/obo/GO_0005740
10853||4472||45,X/46,XY mixed gonadal dysgenesis||http://www.orpha.net/ORDO/Orphanet_1772
10856||11802||Left ventricular noncompaction||http://www.orpha.net/ORDO/Orphanet_54260
10855||3019||Gonadal dysgenesis, XY type - associated anomalies||http://www.orpha.net/ORDO/Orphanet_1770
10857||254||Dyskeratosis congenita||http://www.orpha.net/ORDO/Orphanet_1775
10858||1022||Enteromyxum leei||http://purl.obolibrary.org/obo/NCBITaxon_188704
10859||613||Neonatal epilepsy syndrome||http://www.orpha.net/ORDO/Orphanet_98257
10860||613||Childhood-onset epilepsy syndrome||http://www.orpha.net/ORDO/Orphanet_98259
10861||10272||Mesial temporal lobe epilepsy with hippocampal sclerosis||http://www.orpha.net/ORDO/Orphanet_99701
10862||613||Infantile epilepsy syndrome||http://www.orpha.net/ORDO/Orphanet_98258
10863||6054||Progeria-associated arthropathy||http://www.orpha.net/ORDO/Orphanet_99706
10864||5991||Gastrointestinal stromal tumor||http://www.orpha.net/ORDO/Orphanet_44890
10865||5502||Propionibacterium acnes||http://purl.obolibrary.org/obo/NCBITaxon_1747
10866||5300||Dysmorphism - cleft palate - loose skin||http://www.orpha.net/ORDO/Orphanet_1779
10867||2252||Facial dysmorphism - shawl scrotum - joint laxity||http://www.orpha.net/ORDO/Orphanet_1778
10868||10994||lithium atom||http://purl.obolibrary.org/obo/CHEBI_30145
10869||2252||Temtamy syndrome||http://www.orpha.net/ORDO/Orphanet_1777
10870||613||Adolescent-onset epilepsy syndrome||http://www.orpha.net/ORDO/Orphanet_98260
10871||3560||Dysosteosclerosis||http://www.orpha.net/ORDO/Orphanet_1782
10872||1171||Acro-fronto-facio-nasal dysostosis||http://www.orpha.net/ORDO/Orphanet_1784
10873||1171||Acrofacial dysostosis, Catania type||http://www.orpha.net/ORDO/Orphanet_1786
10875||1171||Acrofacial dysostosis, Palagonia type||http://www.orpha.net/ORDO/Orphanet_1787
10874||10860||Progressive myoclonic epilepsy||http://www.orpha.net/ORDO/Orphanet_98261
10876||15257||Genetic non-syndromic obesity||http://www.orpha.net/ORDO/Orphanet_98267
10877||1539||cytoplasm||http://purl.obolibrary.org/obo/GO_0005737
10878||2352||purine-containing compound biosynthetic process||http://purl.obolibrary.org/obo/GO_0072522
10879||1533||nucleolus||http://purl.obolibrary.org/obo/GO_0005730
10880||2307||purine-containing compound metabolic process||http://purl.obolibrary.org/obo/GO_0072521
10881||799||antibacterial drug||http://purl.obolibrary.org/obo/CHEBI_36047
10882||1560||mitochondrion||http://purl.obolibrary.org/obo/GO_0005739
10883||4266||Leber plus disease||http://www.orpha.net/ORDO/Orphanet_99718
10884||1171||Acrofacial dysostosis, Rodr guez type||http://www.orpha.net/ORDO/Orphanet_1788
10885||5502||Propionibacterium freudenreichii subsp. shermanii||http://purl.obolibrary.org/obo/NCBITaxon_1752
10886||10994||protein||http://purl.obolibrary.org/obo/CHEBI_36080
10887||10291||Trisomy 8q||http://www.orpha.net/ORDO/Orphanet_1752
10888||772||stationary phase culture||http://purl.obolibrary.org/obo/BTO_0001899
10889||4706||Posterior cortical atrophy||http://www.orpha.net/ORDO/Orphanet_54247
10890||2252||Multiple congenital anomalies-hypotonia-seizures syndrome type 2||http://www.orpha.net/ORDO/Orphanet_300496
10891||6770||Thoraco-abdominal enteric duplication||http://www.orpha.net/ORDO/Orphanet_1759
10892||13770||Fibular dimelia - diplopodia||http://www.orpha.net/ORDO/Orphanet_1757
10893||10633||Caudal duplication||http://www.orpha.net/ORDO/Orphanet_1756
10894||2252||Trisomy Xq28||http://www.orpha.net/ORDO/Orphanet_1762
10895||8191||apomorphine hydrochloride||http://purl.obolibrary.org/obo/CHEBI_31228
10896||5918||Familial dysautonomia||http://www.orpha.net/ORDO/Orphanet_1764
10897||7319||Dyschondrosteosis - nephritis||http://www.orpha.net/ORDO/Orphanet_1765
10898||2681||Ehlers-Danlos syndrome||http://www.orpha.net/ORDO/Orphanet_98249
10899||11831||Dysequilibrium syndrome||http://www.orpha.net/ORDO/Orphanet_1766
10900||5959||Familial caudal dysgenesis||http://www.orpha.net/ORDO/Orphanet_1768
10901||15608||LP.08 eight leaves visible stage||http://purl.obolibrary.org/obo/PO_0007095
10902||15608||LP.01 one leaf visible stage||http://purl.obolibrary.org/obo/PO_0007094
10903||14820||Syndromic X-linked ichthyosis||http://www.orpha.net/ORDO/Orphanet_281090
10904||1826||Triticum dicoccoides||http://purl.obolibrary.org/obo/NCBITaxon_85692
10905||2162||brain neoplasm||http://www.ebi.ac.uk/efo/EFO_0003833
10907||11037||Autosomal recessive congenital ichthyosis||http://www.orpha.net/ORDO/Orphanet_281097
10906||1403||gallbladder disease||http://www.ebi.ac.uk/efo/EFO_0003832
10908||10652||obsolete_chromosome disorder||http://www.ebi.ac.uk/efo/EFO_0003831
10909||1391||prostatitis||http://www.ebi.ac.uk/efo/EFO_0003830
10912||11618||calcification||http://www.ebi.ac.uk/efo/EFO_0003837
10911||5502||Dinoroseobacter shibae DFL 12||http://purl.obolibrary.org/obo/NCBITaxon_398580
10910||10335||Partial deletion of the short arm of chromosome 7||http://www.orpha.net/ORDO/Orphanet_261911
10913||15608||LP.02 two leaves visible stage||http://purl.obolibrary.org/obo/PO_0007098
10915||10994||lipoprotein||http://www.ebi.ac.uk/efo/EFO_0003836
10914||5502||Francisella tularensis subsp. holarctica LVS||http://purl.obolibrary.org/obo/NCBITaxon_376619
10916||2162||anal neoplasm||http://www.ebi.ac.uk/efo/EFO_0003835
10917||5103||cutaneous lupus erythematosus||http://www.ebi.ac.uk/efo/EFO_0003834
10918||10652||obsolete_inflammation||http://www.ebi.ac.uk/efo/EFO_0003838
10919||1391||retinopathy||http://www.ebi.ac.uk/efo/EFO_0003839
10920||5025||Arthroderma obtusum||http://purl.obolibrary.org/obo/NCBITaxon_119676
10921||1560||endoplasmic reticulum||http://purl.obolibrary.org/obo/GO_0005783
10922||8191||aluminium trichloride||http://purl.obolibrary.org/obo/CHEBI_30114
10924||1826||Citrus clementina||http://purl.obolibrary.org/obo/NCBITaxon_85681
10923||10684||Partial deletion of the short arm of chromosome 9||http://www.orpha.net/ORDO/Orphanet_261929
10925||10990||chronic progressive multiple sclerosis||http://www.ebi.ac.uk/efo/EFO_0003840
10926||10843||bone of lower extremity||http://www.ebi.ac.uk/efo/EFO_0003842
10927||2162||thyroid neoplasm||http://www.ebi.ac.uk/efo/EFO_0003841
10928||2162||ureteral neoplasm||http://www.ebi.ac.uk/efo/EFO_0003844
10929||11618||pain||http://www.ebi.ac.uk/efo/EFO_0003843
10931||2162||urethral neoplasm||http://www.ebi.ac.uk/efo/EFO_0003846
10930||10683||Partial deletion of the short arm of chromosome 8||http://www.orpha.net/ORDO/Orphanet_261920
10932||8970||kidney stone||http://www.ebi.ac.uk/efo/EFO_0003845
10933||10652||obsolete_cardiovascular abnormality||http://www.ebi.ac.uk/efo/EFO_0003848
10934||11618||mental retardation||http://www.ebi.ac.uk/efo/EFO_0003847
10935||2162||palatal neoplasm||http://www.ebi.ac.uk/efo/EFO_0003849
10936||11352||picoliter||http://purl.obolibrary.org/obo/UO_0000103
10937||11352||nanoliter||http://purl.obolibrary.org/obo/UO_0000102
10938||11352||microliter||http://purl.obolibrary.org/obo/UO_0000101
10939||1560||vacuole||http://purl.obolibrary.org/obo/GO_0005773
10940||1022||Parasteatoda tepidariorum||http://purl.obolibrary.org/obo/NCBITaxon_114398
10941||2162||meningeal neoplasm||http://www.ebi.ac.uk/efo/EFO_0003851
10942||2162||adrenal gland neoplasm||http://www.ebi.ac.uk/efo/EFO_0003850
10943||2162||uterine neoplasm||http://www.ebi.ac.uk/efo/EFO_0003859
10944||5502||Cronobacter dublinensis||http://purl.obolibrary.org/obo/NCBITaxon_413497
10946||11199||pressure unit||http://purl.obolibrary.org/obo/UO_0000109
10947||2672||skeleton structure||http://www.ebi.ac.uk/efo/EFO_0003858
10945||5502||Cronobacter||http://purl.obolibrary.org/obo/NCBITaxon_413496
10948||1391||arthrogryposis||http://www.ebi.ac.uk/efo/EFO_0003857
10949||14780||dissection||http://www.ebi.ac.uk/efo/EFO_0003856
10950||11352||femtoliter||http://purl.obolibrary.org/obo/UO_0000104
10951||2134||intestinal polyp||http://www.ebi.ac.uk/efo/EFO_0003855
10952||11005||postmenopausal osteoporosis||http://www.ebi.ac.uk/efo/EFO_0003854
10953||2162||respiratory system neoplasm||http://www.ebi.ac.uk/efo/EFO_0003853
10954||2165||developmental disability||http://www.ebi.ac.uk/efo/EFO_0003852
10955||10939||lysosome||http://purl.obolibrary.org/obo/GO_0005764
10956||12003||cellular response to pH||http://purl.obolibrary.org/obo/GO_0071467
10957||1524||chloroplast envelope||http://purl.obolibrary.org/obo/GO_0009941
10958||2162||pancreatic neoplasm||http://www.ebi.ac.uk/efo/EFO_0003860
10959||11618||dementia||http://www.ebi.ac.uk/efo/EFO_0003862
10960||1022||Globodera pallida||http://purl.obolibrary.org/obo/NCBITaxon_36090
10961||2672||pancreactic component||http://www.ebi.ac.uk/efo/EFO_0003861
10962||2672||epididymis||http://purl.obolibrary.org/obo/UBERON_0001301
10963||10348||Partial deletion of the short arm of chromosome 6||http://www.orpha.net/ORDO/Orphanet_261902
10964||1022||Helicoverpa armigera||http://purl.obolibrary.org/obo/NCBITaxon_29058
10965||2162||mouth neoplasm||http://www.ebi.ac.uk/efo/EFO_0003868
10966||1391||rhabdomyolysis||http://www.ebi.ac.uk/efo/EFO_0003867
10967||2162||breast neoplasm||http://www.ebi.ac.uk/efo/EFO_0003869
10968||10652||obsolete_genitourinary system||http://www.ebi.ac.uk/efo/EFO_0003864
10969||2162||urogenital neoplasm||http://www.ebi.ac.uk/efo/EFO_0003863
10970||11199||illuminance unit||http://purl.obolibrary.org/obo/UO_0000115
10971||2162||paranasal sinus neoplasm||http://www.ebi.ac.uk/efo/EFO_0003866
10973||2162||kidney neoplasm||http://www.ebi.ac.uk/efo/EFO_0003865
10972||10970||lux||http://purl.obolibrary.org/obo/UO_0000116
10974||11507||angle unit||http://purl.obolibrary.org/obo/UO_0000121
10975||1531||mitochondrial intermembrane space||http://purl.obolibrary.org/obo/GO_0005758
10976||10979||intermittent vascular claudication||http://www.ebi.ac.uk/efo/EFO_0003876
10977||1979||sleep apnea||http://www.ebi.ac.uk/efo/EFO_0003877
10978||15526||flatfoot||http://www.ebi.ac.uk/efo/EFO_0003874
10979||8288||peripheral vascular disease||http://www.ebi.ac.uk/efo/EFO_0003875
10980||10658||Partial deletion of the short arm of chromosome 16||http://www.orpha.net/ORDO/Orphanet_261956
10981||2700||urethritis||http://www.ebi.ac.uk/efo/EFO_0003878
10982||10652||obsolete_aortic valve||http://www.ebi.ac.uk/efo/EFO_0003879
10983||1022||Mucor circinelloides||http://purl.obolibrary.org/obo/NCBITaxon_36080
10984||1403||colitis||http://www.ebi.ac.uk/efo/EFO_0003872
10985||2672||prepuce of penis||http://purl.obolibrary.org/obo/UBERON_0001332
10986||2162||parotid neoplasm||http://www.ebi.ac.uk/efo/EFO_0003873
10987||11614||brain aneurysm||http://www.ebi.ac.uk/efo/EFO_0003870
10988||2162||tongue neoplasm||http://www.ebi.ac.uk/efo/EFO_0003871
10989||11458||Dentin dysplasia type I||http://www.orpha.net/ORDO/Orphanet_99789
10990||2165||multiple sclerosis||http://www.ebi.ac.uk/efo/EFO_0003885
10991||10652||obsolete_metacarpal bone||http://www.ebi.ac.uk/efo/EFO_0003886
10992||10652||obsolete_thrombophlebitis||http://www.ebi.ac.uk/efo/EFO_0003887
10993||11457||Mosaic trisomy 16||http://www.orpha.net/ORDO/Orphanet_1708
10995||2102||attention deficit hyperactivity disorder||http://www.ebi.ac.uk/efo/EFO_0003888
10994||4431||chemical compound||http://purl.obolibrary.org/obo/CHEBI_37577
10996||11618||functional laterality||http://www.ebi.ac.uk/efo/EFO_0003889
10997||10640||Partial monosomy of the short arm of chromosome 17||http://www.orpha.net/ORDO/Orphanet_261965
10999||11457||Mosaic trisomy 14||http://www.orpha.net/ORDO/Orphanet_1703
10998||2672||sciatic nerve||http://purl.obolibrary.org/obo/UBERON_0001322
11000||10752||Non-distal trisomy 13q||http://www.orpha.net/ORDO/Orphanet_1702
11001||2162||appendiceal neoplasm||http://www.ebi.ac.uk/efo/EFO_0003880
11003||14780||hysterectomy||http://www.ebi.ac.uk/efo/EFO_0003881
11002||10994||oxazepam||http://purl.obolibrary.org/obo/CHEBI_7823
11004||6017||Distal trisomy 15q||http://www.orpha.net/ORDO/Orphanet_1707
11005||15526||osteoporosis||http://www.ebi.ac.uk/efo/EFO_0003882
11006||11457||Mosaic trisomy 15||http://www.orpha.net/ORDO/Orphanet_1706
11007||1794||brain ischemia||http://www.ebi.ac.uk/efo/EFO_0003883
11008||6899||Distal trisomy 14q||http://www.orpha.net/ORDO/Orphanet_1705
11009||8970||chronic kidney disease||http://www.ebi.ac.uk/efo/EFO_0003884
11010||1596||Ehlers-Danlos syndrome due to tenascin-X deficiency||http://www.orpha.net/ORDO/Orphanet_230839
11011||15289||Dentin dysplasia - sclerotic bones||http://www.orpha.net/ORDO/Orphanet_99792
11012||11458||Dentin dysplasia type II||http://www.orpha.net/ORDO/Orphanet_99791
11014||2299||Venous thrombosis||http://purl.obolibrary.org/obo/HP_0004936
11013||1902||Subcortical band heterotopia||http://www.orpha.net/ORDO/Orphanet_99796
11015||1619||Anodontia||http://www.orpha.net/ORDO/Orphanet_99797
11016||1022||Leucoraja erinacea||http://purl.obolibrary.org/obo/NCBITaxon_7782
11017||1619||Oligodontia||http://www.orpha.net/ORDO/Orphanet_99798
11018||13496||Youcai mosaic virus||http://purl.obolibrary.org/obo/NCBITaxon_228578
11019||13689||vascular cord||http://purl.obolibrary.org/obo/UBERON_0006965
11020||2863||ankylosing spondylitis||http://www.ebi.ac.uk/efo/EFO_0003898
11021||2546||contracture||http://www.ebi.ac.uk/efo/EFO_0003899
11022||14656||left ventricular hypertrophy||http://www.ebi.ac.uk/efo/EFO_0003896
11023||2162||stomach neoplasm||http://www.ebi.ac.uk/efo/EFO_0003897
11024||2866||acne||http://www.ebi.ac.uk/efo/EFO_0003894
11025||2672||anal region||http://purl.obolibrary.org/obo/UBERON_0001353
11026||1015||epistaxis||http://www.ebi.ac.uk/efo/EFO_0003895
11027||14970||pulmonary function measurement||http://www.ebi.ac.uk/efo/EFO_0003892
11028||2162||ovarian neoplasm||http://www.ebi.ac.uk/efo/EFO_0003893
11030||2102||drug dependence||http://www.ebi.ac.uk/efo/EFO_0003890
11029||10672||Partial deletion of the short arm of chromosome 10||http://www.orpha.net/ORDO/Orphanet_261938
11031||2162||biliary tract neoplasm||http://www.ebi.ac.uk/efo/EFO_0003891
11032||2672||brown adipose tissue||http://purl.obolibrary.org/obo/UBERON_0001348
11033||1022||Onthophagus nigriventris||http://purl.obolibrary.org/obo/NCBITaxon_476074
11034||8141||Familial hyperreninemic hypoaldosteronism type 1||http://www.orpha.net/ORDO/Orphanet_99763
11035||8141||Familial hyperreninemic hypoaldosteronism type 2||http://www.orpha.net/ORDO/Orphanet_99764
11036||1022||Petromyzon marinus||http://purl.obolibrary.org/obo/NCBITaxon_7757
11037||5986||Inherited non-syndromic ichthyosis||http://www.orpha.net/ORDO/Orphanet_281082
11038||5986||Inherited ichthyosis syndromic form||http://www.orpha.net/ORDO/Orphanet_281085
11039||6264||Dihydropyrimidinuria||http://www.orpha.net/ORDO/Orphanet_38874
11040||11041||glycosyl compound biosynthetic process||http://purl.obolibrary.org/obo/GO_1901659
11041||195||glycosyl compound metabolic process||http://purl.obolibrary.org/obo/GO_1901657
11042||10671||Partial deletion of the short arm of chromosome 11||http://www.orpha.net/ORDO/Orphanet_261947
11043||2672||white adipose tissue||http://purl.obolibrary.org/obo/UBERON_0001347
11044||10921||smooth endoplasmic reticulum||http://purl.obolibrary.org/obo/GO_0005790
11045||10921||rough endoplasmic reticulum||http://purl.obolibrary.org/obo/GO_0005791
11046||1560||Golgi apparatus||http://purl.obolibrary.org/obo/GO_0005794
11047||5502||Thermotoga sp. RQ2||http://purl.obolibrary.org/obo/NCBITaxon_126740
11048||11457||Mosaic trisomy 9||http://www.orpha.net/ORDO/Orphanet_99776
11049||11056||micromolar||http://purl.obolibrary.org/obo/UO_0000064
11050||11056||millimolar||http://purl.obolibrary.org/obo/UO_0000063
11052||11056||picomolar||http://purl.obolibrary.org/obo/UO_0000066
11051||1022||Branchiostoma belcheri||http://purl.obolibrary.org/obo/NCBITaxon_7741
11053||11056||nanomolar||http://purl.obolibrary.org/obo/UO_0000065
11054||11056||molar||http://purl.obolibrary.org/obo/UO_0000062
11055||2672||cerebrospinal fluid||http://purl.obolibrary.org/obo/UBERON_0001359
11056||11067||unit of molarity||http://purl.obolibrary.org/obo/UO_0000061
11057||770||ovarian cancer cell lines||http://www.ebi.ac.uk/efo/EFO_0002394
11058||770||Y79||http://www.ebi.ac.uk/efo/EFO_0002392
11059||770||YPAC||http://www.ebi.ac.uk/efo/EFO_0002393
11060||1022||Hypomesus transpacificus||http://purl.obolibrary.org/obo/NCBITaxon_137520
11061||11172||seed imbibition stage||http://purl.obolibrary.org/obo/PO_0007022
11062||11088||FL.04 end of flowering stage||http://purl.obolibrary.org/obo/PO_0007024
11063||11088||FL.00 first flower(s) open stage||http://purl.obolibrary.org/obo/PO_0007026
11064||770||GM17209||http://purl.obolibrary.org/obo/CLO_0013875
11065||11199||molar mass unit||http://purl.obolibrary.org/obo/UO_0000055
11066||7629||Primary glaucoma||http://www.orpha.net/ORDO/Orphanet_156005
11067||11199||concentration unit||http://purl.obolibrary.org/obo/UO_0000051
11068||11228||erythrocyte differentiation||http://purl.obolibrary.org/obo/GO_0030218
11069||10652||obsolete_Wi38||http://www.ebi.ac.uk/efo/EFO_0002391
11070||770||WM115||http://www.ebi.ac.uk/efo/EFO_0002390
11072||7195||biceps femoris||http://purl.obolibrary.org/obo/UBERON_0001374
11071||10652||obsolete_THP1||http://www.ebi.ac.uk/efo/EFO_0002381
11074||770||GM17207||http://purl.obolibrary.org/obo/CLO_0013881
11073||770||TT||http://www.ebi.ac.uk/efo/EFO_0002382
11075||770||Toledo||http://www.ebi.ac.uk/efo/EFO_0002383
11076||770||U266B1||http://www.ebi.ac.uk/efo/EFO_0002384
11077||770||UACC893||http://www.ebi.ac.uk/efo/EFO_0002385
11078||770||UMC11||http://www.ebi.ac.uk/efo/EFO_0002386
11079||7195||quadriceps femoris||http://purl.obolibrary.org/obo/UBERON_0001377
11080||770||UMUC3||http://www.ebi.ac.uk/efo/EFO_0002387
11081||7195||vastus lateralis||http://purl.obolibrary.org/obo/UBERON_0001379
11082||770||WIDR||http://www.ebi.ac.uk/efo/EFO_0002389
11083||770||GM17216||http://purl.obolibrary.org/obo/CLO_0013888
11085||770||GM17217||http://purl.obolibrary.org/obo/CLO_0013887
11084||9746||whole plant fruit ripening stage||http://purl.obolibrary.org/obo/PO_0007010
11087||770||GM17214||http://purl.obolibrary.org/obo/CLO_0013886
11086||9746||sporophyte senescent stage||http://purl.obolibrary.org/obo/PO_0007017
11089||770||GM17215||http://purl.obolibrary.org/obo/CLO_0013885
11088||9746||whole plant flowering stage||http://purl.obolibrary.org/obo/PO_0007016
11090||11172||radicle emergence||http://purl.obolibrary.org/obo/PO_0007015
11091||770||GM17208||http://purl.obolibrary.org/obo/CLO_0013884
11092||14376||head mesenchyme from mesoderm||http://purl.obolibrary.org/obo/UBERON_0006904
11093||14126||growth phase culture||http://purl.obolibrary.org/obo/BTO_0001900
11094||4319||fast muscle tissue||http://purl.obolibrary.org/obo/UBERON_0006908
11095||7942||Ehlers-Danlos/osteogenesis imperfecta syndrome||http://www.orpha.net/ORDO/Orphanet_230857
11096||11200||square meter||http://purl.obolibrary.org/obo/UO_0000080
11097||772||logarithmic phase culture||http://purl.obolibrary.org/obo/BTO_0001903
11098||770||INC-2 cell||http://purl.obolibrary.org/obo/BTO_0004264
11099||7195||soleus muscle||http://purl.obolibrary.org/obo/UBERON_0001389
11102||770||COM-3 cell||http://purl.obolibrary.org/obo/BTO_0004263
11100||7195||gastrocnemius||http://purl.obolibrary.org/obo/UBERON_0001388
11101||9746||inflorescence emergence stage||http://purl.obolibrary.org/obo/PO_0007041
11104||770||GM17210||http://purl.obolibrary.org/obo/CLO_0013891
11103||1022||Ciona intestinalis||http://purl.obolibrary.org/obo/NCBITaxon_7719
11105||770||GM17211||http://purl.obolibrary.org/obo/CLO_0013890
11106||770||GM17213||http://purl.obolibrary.org/obo/CLO_0013893
11107||7195||tibialis anterior||http://purl.obolibrary.org/obo/UBERON_0001385
11108||2672||primary motor cortex||http://purl.obolibrary.org/obo/UBERON_0001384
11109||770||GM17212||http://purl.obolibrary.org/obo/CLO_0013895
11110||9746||3 inflorescence detectable stage||http://purl.obolibrary.org/obo/PO_0007047
11111||15609||cotyledon emergence stage||http://purl.obolibrary.org/obo/PO_0007049
11113||15609||hypocotyl emergence stage||http://purl.obolibrary.org/obo/PO_0007043
11112||9607||Ehlers-Danlos syndrome, cardiac valvular type||http://www.orpha.net/ORDO/Orphanet_230851
11114||11172||coleoptile emergence stage||http://purl.obolibrary.org/obo/PO_0007045
11115||4629||Ehlers-Danlos syndrome, vascular-like type||http://www.orpha.net/ORDO/Orphanet_230845
11116||5502||Prochlorococcus marinus subsp. pastoris str. CCMP1986||http://purl.obolibrary.org/obo/NCBITaxon_59919
11117||11056||femtomolar||http://purl.obolibrary.org/obo/UO_0000073
11118||10994||olanzapine||http://purl.obolibrary.org/obo/CHEBI_7735
11119||3072||brachial artery||http://purl.obolibrary.org/obo/UBERON_0001398
11120||11084||beginning of whole plant fruit ripening stage||http://purl.obolibrary.org/obo/PO_0007036
11121||6764||Congenital esophageal diverticulum||http://www.orpha.net/ORDO/Orphanet_91358
11122||6764||Duplication of the esophagus||http://www.orpha.net/ORDO/Orphanet_91357
11124||12151||trypanosomiasis||http://purl.obolibrary.org/obo/DOID_10113
11123||11505||microgram||http://purl.obolibrary.org/obo/UO_0000023
11125||11505||nanogram||http://purl.obolibrary.org/obo/UO_0000024
11126||11505||picogram||http://purl.obolibrary.org/obo/UO_0000025
11127||12498||sample treatment protocol||http://www.ebi.ac.uk/efo/EFO_0003809
11129||11505||femtogram||http://purl.obolibrary.org/obo/UO_0000026
11128||6854||Bietti crystalline dystrophy||http://www.orpha.net/ORDO/Orphanet_41751
11130||4335||labelling protocol||http://www.ebi.ac.uk/efo/EFO_0003808
11132||11506||picometer||http://purl.obolibrary.org/obo/UO_0000020
11131||9613||interleukin-33 (Rattus norvegicus)||http://www.ebi.ac.uk/efo/EFO_0003807
11134||11505||gram||http://purl.obolibrary.org/obo/UO_0000021
11133||9613||interleukin-26 (Homo sapiens)||http://www.ebi.ac.uk/efo/EFO_0003806
11136||11505||milligram||http://purl.obolibrary.org/obo/UO_0000022
11137||10994||acenocoumarol||http://purl.obolibrary.org/obo/CHEBI_53766
11135||9613||interleukin-24 (Homo sapiens)||http://www.ebi.ac.uk/efo/EFO_0003805
11138||15608||LP.05 five leaves visible stage||http://purl.obolibrary.org/obo/PO_0007065
11139||770||SW1116||http://www.ebi.ac.uk/efo/EFO_0002359
11140||9613||interleukin-20 (Homo sapiens)||http://www.ebi.ac.uk/efo/EFO_0003803
11142||770||SW1088||http://www.ebi.ac.uk/efo/EFO_0002358
11141||9613||interleukin-21 (Mus musculus)||http://www.ebi.ac.uk/efo/EFO_0003804
11143||15608||LP.17 seventeen leaves visible stage||http://purl.obolibrary.org/obo/PO_0007067
11144||770||SUDHL6||http://www.ebi.ac.uk/efo/EFO_0002357
11145||9613||interleukin-19 (Homo sapiens)||http://www.ebi.ac.uk/efo/EFO_0003801
11147||15302||mid rosette growth stage||http://purl.obolibrary.org/obo/PO_0007068
11146||770||SUDHL5||http://www.ebi.ac.uk/efo/EFO_0002356
11148||7911||refractory anemia||http://www.ebi.ac.uk/efo/EFO_0003802
11149||11506||micrometer||http://purl.obolibrary.org/obo/UO_0000017
11150||11506||millimeter||http://purl.obolibrary.org/obo/UO_0000016
11151||9613||interleukin-17 (Mus musculus)||http://www.ebi.ac.uk/efo/EFO_0003800
11152||11506||nanometer||http://purl.obolibrary.org/obo/UO_0000018
11153||770||SNU5||http://www.ebi.ac.uk/efo/EFO_0002351
11154||770||SNU475||http://www.ebi.ac.uk/efo/EFO_0002350
11155||14642||PFAPA syndrome||http://www.orpha.net/ORDO/Orphanet_42642
11156||770||ND04158||http://purl.obolibrary.org/obo/CLO_0032601
11157||770||SUDHL16||http://www.ebi.ac.uk/efo/EFO_0002355
11158||770||SUDHL10||http://www.ebi.ac.uk/efo/EFO_0002354
11160||15608||LP.07 seven leaves visible stage||http://purl.obolibrary.org/obo/PO_0007063
11159||770||ST486||http://www.ebi.ac.uk/efo/EFO_0002353
11161||15608||LP.12 twelve leaves visible stage||http://purl.obolibrary.org/obo/PO_0007064
11162||770||SR||http://www.ebi.ac.uk/efo/EFO_0002352
11163||11178||candela||http://purl.obolibrary.org/obo/UO_0000014
11164||11506||centimeter||http://purl.obolibrary.org/obo/UO_0000015
11165||1826||Silene latifolia||http://purl.obolibrary.org/obo/NCBITaxon_37657
11166||11182||kelvin||http://purl.obolibrary.org/obo/UO_0000012
11167||11181||mole||http://purl.obolibrary.org/obo/UO_0000013
11168||11504||second||http://purl.obolibrary.org/obo/UO_0000010
11169||11503||ampere||http://purl.obolibrary.org/obo/UO_0000011
11170||770||AG10941||http://purl.obolibrary.org/obo/CLO_0021459
11171||770||SNU387||http://www.ebi.ac.uk/efo/EFO_0002346
11173||770||SNU182||http://www.ebi.ac.uk/efo/EFO_0002345
11172||9746||0 seed germination stage||http://purl.obolibrary.org/obo/PO_0007057
11174||770||SNU423||http://www.ebi.ac.uk/efo/EFO_0002348
11175||11505||kilogram||http://purl.obolibrary.org/obo/UO_0000009
11176||770||SNU398||http://www.ebi.ac.uk/efo/EFO_0002347
11177||11506||meter||http://purl.obolibrary.org/obo/UO_0000008
11178||11198||luminous intensity unit||http://purl.obolibrary.org/obo/UO_0000007
11180||10994||oseltamivir||http://purl.obolibrary.org/obo/CHEBI_7798
11179||770||SNU449||http://www.ebi.ac.uk/efo/EFO_0002349
11181||11198||substance unit||http://purl.obolibrary.org/obo/UO_0000006
11182||11198||temperature unit||http://purl.obolibrary.org/obo/UO_0000005
11183||770||SKOV3||http://www.ebi.ac.uk/efo/EFO_0002340
11184||770||SNB19||http://www.ebi.ac.uk/efo/EFO_0002342
11185||11088||FL.02 1/2 of flowers open stage||http://purl.obolibrary.org/obo/PO_0007053
11186||770||SKUT1||http://www.ebi.ac.uk/efo/EFO_0002341
11187||770||SNU16||http://www.ebi.ac.uk/efo/EFO_0002344
11188||770||SNU1||http://www.ebi.ac.uk/efo/EFO_0002343
11189||770||TANOUE||http://www.ebi.ac.uk/efo/EFO_0002380
11190||11181||millimole||http://purl.obolibrary.org/obo/UO_0000040
11191||11181||nanomole||http://purl.obolibrary.org/obo/UO_0000041
11192||11181||picomole||http://purl.obolibrary.org/obo/UO_0000042
11193||11030||alcohol dependence||http://www.ebi.ac.uk/efo/EFO_0003829
11195||11181||femtomole||http://purl.obolibrary.org/obo/UO_0000043
11194||2162||spinal cord neoplasm||http://www.ebi.ac.uk/efo/EFO_0003828
11197||11181||attomole||http://purl.obolibrary.org/obo/UO_0000044
11196||1015||pulmonary embolism||http://www.ebi.ac.uk/efo/EFO_0003827
11198||11507||base unit||http://purl.obolibrary.org/obo/UO_0000045
11199||11507||derived unit||http://purl.obolibrary.org/obo/UO_0000046
11200||11199||area unit||http://purl.obolibrary.org/obo/UO_0000047
11201||11181||micromole||http://purl.obolibrary.org/obo/UO_0000039
11202||2165||migraine disorder||http://www.ebi.ac.uk/efo/EFO_0003821
11203||11618||hyperemia||http://www.ebi.ac.uk/efo/EFO_0003822
11204||2162||bone neoplasm||http://www.ebi.ac.uk/efo/EFO_0003820
11205||120||serous adenocarsinoma||http://www.ebi.ac.uk/efo/EFO_0003825
11206||2162||salivary gland neoplasm||http://www.ebi.ac.uk/efo/EFO_0003826
11207||770||SiHa||http://www.ebi.ac.uk/efo/EFO_0002379
11208||10652||obsolete_spinal muscular atrophy||http://www.ebi.ac.uk/efo/EFO_0003823
11211||2162||eye neoplasm||http://www.ebi.ac.uk/efo/EFO_0003824
11209||770||SW982||http://www.ebi.ac.uk/efo/EFO_0002378
11210||1022||Petrolisthes cinctipes||http://purl.obolibrary.org/obo/NCBITaxon_88211
11213||15608||LP.13 thirteen leaves visible stage||http://purl.obolibrary.org/obo/PO_0007083
11212||770||SW962||http://www.ebi.ac.uk/efo/EFO_0002377
11214||770||SW954||http://www.ebi.ac.uk/efo/EFO_0002376
11216||15608||LP.14 fourteen leaves visible stage||http://purl.obolibrary.org/obo/PO_0007085
11215||770||SW948||http://www.ebi.ac.uk/efo/EFO_0002375
11217||770||SW900||http://www.ebi.ac.uk/efo/EFO_0002374
11218||770||SW872||http://www.ebi.ac.uk/efo/EFO_0002373
11219||770||SW837||http://www.ebi.ac.uk/efo/EFO_0002372
11221||15302||early rosette growth stage||http://purl.obolibrary.org/obo/PO_0007081
11220||770||SW780||http://www.ebi.ac.uk/efo/EFO_0002371
11223||15608||LP.20 twenty or more leaves whorls visible stage||http://purl.obolibrary.org/obo/PO_0007082
11222||770||SW756||http://www.ebi.ac.uk/efo/EFO_0002370
11225||12528||hour||http://purl.obolibrary.org/obo/UO_0000032
11224||2162||laryngeal neoplasm||http://www.ebi.ac.uk/efo/EFO_0003817
11227||12528||day||http://purl.obolibrary.org/obo/UO_0000033
11226||11573||normalization data transformation protocol||http://www.ebi.ac.uk/efo/EFO_0003816
11229||1814||dental caries||http://www.ebi.ac.uk/efo/EFO_0003819
11228||5295||cellular process||http://purl.obolibrary.org/obo/GO_0009987
11230||12528||minute||http://purl.obolibrary.org/obo/UO_0000031
11231||1979||lung disease||http://www.ebi.ac.uk/efo/EFO_0003818
11232||12528||year||http://purl.obolibrary.org/obo/UO_0000036
11233||12528||week||http://purl.obolibrary.org/obo/UO_0000034
11234||12528||month||http://purl.obolibrary.org/obo/UO_0000035
11235||11504||microsecond||http://purl.obolibrary.org/obo/UO_0000029
11236||9613||interleukin-22 (Homo sapiens)||http://www.ebi.ac.uk/efo/EFO_0003810
11237||12563||degree celsius||http://purl.obolibrary.org/obo/UO_0000027
11238||7911||refractory anemia with excess blasts||http://www.ebi.ac.uk/efo/EFO_0003811
11239||15302||rosette growth complete stage||http://purl.obolibrary.org/obo/PO_0007078
11241||770||SW620||http://www.ebi.ac.uk/efo/EFO_0002368
11240||7911||refractory anemia with ringed sideroblasts||http://www.ebi.ac.uk/efo/EFO_0003812
11242||11130||nucleic acid labeling protocol||http://www.ebi.ac.uk/efo/EFO_0003813
11244||10994||omeprazole||http://purl.obolibrary.org/obo/CHEBI_7772
11243||770||SW48||http://www.ebi.ac.uk/efo/EFO_0002367
11246||15302||late rosette growth stage||http://purl.obolibrary.org/obo/PO_0007076
11245||11573||array scanning and feature extraction protocol||http://www.ebi.ac.uk/efo/EFO_0003814
11247||11409||nucleic acid hybridization to array protocol||http://www.ebi.ac.uk/efo/EFO_0003815
11248||770||SW684||http://www.ebi.ac.uk/efo/EFO_0002369
11249||770||SW1783||http://www.ebi.ac.uk/efo/EFO_0002364
11250||770||SW1573||http://www.ebi.ac.uk/efo/EFO_0002363
11253||15608||LP.18 eighteen leaves visible stage||http://purl.obolibrary.org/obo/PO_0007072
11252||770||SW403||http://www.ebi.ac.uk/efo/EFO_0002366
11251||772||corneal epithelial cell||http://purl.obolibrary.org/obo/BTO_0004298
11254||770||SW1990||http://www.ebi.ac.uk/efo/EFO_0002365
11255||770||SW1353||http://www.ebi.ac.uk/efo/EFO_0002360
11256||770||SW1463||http://www.ebi.ac.uk/efo/EFO_0002362
11257||770||SW1417||http://www.ebi.ac.uk/efo/EFO_0002361
11258||6897||Isolated cryptophthalmia||http://www.orpha.net/ORDO/Orphanet_91396
11259||6897||Isolated ankyloblepharon filiforme adnatum||http://www.orpha.net/ORDO/Orphanet_91397
11260||15368||estrogen receptor activity||http://purl.obolibrary.org/obo/GO_0030284
11261||5502||Bifidobacterium||http://purl.obolibrary.org/obo/NCBITaxon_1678
11262||770||OE33||http://www.ebi.ac.uk/efo/EFO_0002310
11263||770||OV90||http://www.ebi.ac.uk/efo/EFO_0002311
11264||770||P3HR1||http://www.ebi.ac.uk/efo/EFO_0002312
11265||770||PLB985||http://www.ebi.ac.uk/efo/EFO_0002313
11266||770||RCHACV||http://www.ebi.ac.uk/efo/EFO_0002314
11267||770||RD||http://www.ebi.ac.uk/efo/EFO_0002315
11268||770||RDES||http://www.ebi.ac.uk/efo/EFO_0002316
11269||770||REC1||http://www.ebi.ac.uk/efo/EFO_0002317
11270||770||RKOE6||http://www.ebi.ac.uk/efo/EFO_0002318
11271||770||RL||http://www.ebi.ac.uk/efo/EFO_0002319
11272||2415||Keratoconus||http://www.orpha.net/ORDO/Orphanet_156071
11273||5502||Bifidobacterium bifidum||http://purl.obolibrary.org/obo/NCBITaxon_1681
11274||5488||Autosomal recessive intermediate Charcot-Marie-Tooth disease type B||http://www.orpha.net/ORDO/Orphanet_254334
11275||770||NCI-H69||http://www.ebi.ac.uk/efo/EFO_0002300
11276||770||NCI-H747||http://www.ebi.ac.uk/efo/EFO_0002303
11277||770||NCI-H748||http://www.ebi.ac.uk/efo/EFO_0002304
11278||770||NCI-H716||http://www.ebi.ac.uk/efo/EFO_0002301
11279||770||NCI-H720||http://www.ebi.ac.uk/efo/EFO_0002302
11280||770||NCI-H838||http://www.ebi.ac.uk/efo/EFO_0002307
11281||770||OE19||http://www.ebi.ac.uk/efo/EFO_0002308
11282||770||NCI-H810||http://www.ebi.ac.uk/efo/EFO_0002305
11283||770||NCI-H82||http://www.ebi.ac.uk/efo/EFO_0002306
11284||770||OE21||http://www.ebi.ac.uk/efo/EFO_0002309
11285||2763||protein transport||http://purl.obolibrary.org/obo/GO_0015031
11286||7518||Trisomy 12p||http://www.orpha.net/ORDO/Orphanet_1699
11287||11457||Mosaic trisomy 12||http://www.orpha.net/ORDO/Orphanet_1698
11289||11457||Mosaic trisomy 1||http://www.orpha.net/ORDO/Orphanet_1692
11288||2603||Familial thoracic aortic aneurysm and aortic dissection||http://www.orpha.net/ORDO/Orphanet_91387
11290||10768||Non-distal trisomy 10q||http://www.orpha.net/ORDO/Orphanet_1695
11291||770||SJSA1||http://www.ebi.ac.uk/efo/EFO_0002330
11292||770||SKLMS1||http://www.ebi.ac.uk/efo/EFO_0002331
11293||770||SKMEL1||http://www.ebi.ac.uk/efo/EFO_0002332
11294||770||SKMEL3||http://www.ebi.ac.uk/efo/EFO_0002333
11295||5700||Tietz syndrome||http://www.orpha.net/ORDO/Orphanet_42665
11296||770||SKNFI||http://www.ebi.ac.uk/efo/EFO_0002338
11297||770||SKO007||http://www.ebi.ac.uk/efo/EFO_0002339
11298||11336||Mosaic genome-wide paternal uniparental disomy||http://www.orpha.net/ORDO/Orphanet_329813
11299||770||SKMES1||http://www.ebi.ac.uk/efo/EFO_0002334
11300||10652||obsolete_SKNAS||http://www.ebi.ac.uk/efo/EFO_0002335
11301||770||SKNDZ_11301||http://www.ebi.ac.uk/efo/EFO_0002336
11302||770||SKNEP1||http://www.ebi.ac.uk/efo/EFO_0002337
11303||770||GM17196||http://purl.obolibrary.org/obo/CLO_0013816
11304||770||GM17197||http://purl.obolibrary.org/obo/CLO_0013818
11305||1732||Hereditary angioedema||http://www.orpha.net/ORDO/Orphanet_91378
11306||6052||Distal 7q11.23 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_254351
11307||770||RPMI6666||http://www.ebi.ac.uk/efo/EFO_0002321
11308||5502||Listeria innocua||http://purl.obolibrary.org/obo/NCBITaxon_1642
11310||770||RPMI8226||http://www.ebi.ac.uk/efo/EFO_0002322
11309||8191||potassium bromate||http://purl.obolibrary.org/obo/CHEBI_38211
11311||770||RL952||http://www.ebi.ac.uk/efo/EFO_0002320
11312||770||SJRH30||http://www.ebi.ac.uk/efo/EFO_0002329
11313||2252||5p13 microduplication syndrome||http://www.orpha.net/ORDO/Orphanet_329802
11314||770||SH4||http://www.ebi.ac.uk/efo/EFO_0002327
11315||770||SHP77||http://www.ebi.ac.uk/efo/EFO_0002328
11316||770||SCaBER||http://www.ebi.ac.uk/efo/EFO_0002325
11318||770||SEM||http://www.ebi.ac.uk/efo/EFO_0002326
11317||799||calcium channel blocker||http://purl.obolibrary.org/obo/CHEBI_38215
11319||770||RWPE1||http://www.ebi.ac.uk/efo/EFO_0002323
11321||770||Raji||http://www.ebi.ac.uk/efo/EFO_0002324
11320||770||GM17198||http://purl.obolibrary.org/obo/CLO_0013823
11322||11325||Gonosome structural anomaly||http://www.orpha.net/ORDO/Orphanet_98157
11323||11322||Chromosome Y structural anomaly||http://www.orpha.net/ORDO/Orphanet_98158
11324||770||GM17199||http://purl.obolibrary.org/obo/CLO_0013826
11325||15364||Gonosome anomaly||http://www.orpha.net/ORDO/Orphanet_98155
11326||11325||Gonosome number anomaly||http://www.orpha.net/ORDO/Orphanet_98156
11327||11322||Chromosome X structural anomaly||http://www.orpha.net/ORDO/Orphanet_98159
11328||7992||Diastematomyelia||http://www.orpha.net/ORDO/Orphanet_1671
11329||3866||Chronic diarrhea with villous atrophy||http://www.orpha.net/ORDO/Orphanet_1670
11330||10852||19p13.12 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_254346
11331||11336||Uniparental disomy of maternal origin||http://www.orpha.net/ORDO/Orphanet_98153
11332||6264||Dihydropyrimidine dehydrogenase deficiency||http://www.orpha.net/ORDO/Orphanet_1675
11333||11336||Uniparental disomy of paternal origin||http://www.orpha.net/ORDO/Orphanet_98154
11335||11802||Familial idiopathic dilatation of the right atrium||http://www.orpha.net/ORDO/Orphanet_1677
11334||6432||Autosomal recessive spastic ataxia - optic atrophy - dysarthria||http://www.orpha.net/ORDO/Orphanet_254343
11336||11443||Autosomal uniparental disomy||http://www.orpha.net/ORDO/Orphanet_98152
11337||770||GM17205||http://purl.obolibrary.org/obo/CLO_0013834
11338||770||GM17204||http://purl.obolibrary.org/obo/CLO_0013835
11339||770||GM17206||http://purl.obolibrary.org/obo/CLO_0013833
11340||5025||Lachancea kluyveri NRRL Y-12651||http://purl.obolibrary.org/obo/NCBITaxon_226302
11341||5414||Exercise-induced hyperinsulinism||http://www.orpha.net/ORDO/Orphanet_165991
11342||770||GM17201||http://purl.obolibrary.org/obo/CLO_0013839
11343||1313||Selective pituitary resistance to thyroid hormone||http://www.orpha.net/ORDO/Orphanet_165994
11344||770||GM17202||http://purl.obolibrary.org/obo/CLO_0013837
11345||770||GM17203||http://purl.obolibrary.org/obo/CLO_0013836
11346||5502||Lactobacillus reuteri F275||http://purl.obolibrary.org/obo/NCBITaxon_299033
11347||9342||Diazoxide-sensitive diffuse hyperinsulinism||http://www.orpha.net/ORDO/Orphanet_165985
11348||9100||Diazoxide-resistant diffuse hyperinsulinism||http://www.orpha.net/ORDO/Orphanet_165988
11349||770||GM17200||http://purl.obolibrary.org/obo/CLO_0013840
11350||1022||Pimephales promelas||http://purl.obolibrary.org/obo/NCBITaxon_90988
11351||3655||juvenile leaf||http://purl.obolibrary.org/obo/BTO_0003147
11352||11199||volume unit||http://purl.obolibrary.org/obo/UO_0000095
11353||306||Anonychia with flexural pigmentation||http://www.orpha.net/ORDO/Orphanet_69125
11354||770||ND04424||http://purl.obolibrary.org/obo/CLO_0033747
11355||1022||Saccharina latissima||http://purl.obolibrary.org/obo/NCBITaxon_309358
11356||375||Pyogenic arthritis - pyoderma gangrenosum - acne||http://www.orpha.net/ORDO/Orphanet_69126
11357||11352||cubic centimeter||http://purl.obolibrary.org/obo/UO_0000097
11358||11352||milliliter||http://purl.obolibrary.org/obo/UO_0000098
11359||11352||liter||http://purl.obolibrary.org/obo/UO_0000099
11360||5502||Ralstonia solanacearum GMI1000||http://purl.obolibrary.org/obo/NCBITaxon_267608
11361||2672||stylopod||http://purl.obolibrary.org/obo/UBERON_0002472
11362||2672||zeugopod||http://purl.obolibrary.org/obo/UBERON_0002471
11363||9746||IL.00 inflorescence just visible stage||http://purl.obolibrary.org/obo/PO_0007006
11364||5085||Macrocephaly-autism syndrome||http://www.orpha.net/ORDO/Orphanet_210548
11365||5502||Salmonella enterica subsp. enterica serovar Montevideo||http://purl.obolibrary.org/obo/NCBITaxon_115981
11366||2021||Ulnar/fibula ray defect - brachydactyly||http://www.orpha.net/ORDO/Orphanet_52056
11367||6610||Craniosynostosis - intracranial calcifications||http://www.orpha.net/ORDO/Orphanet_52054
11368||2252||Agenesis of the corpus callosum - intellectual disability - coloboma - micrognathia||http://www.orpha.net/ORDO/Orphanet_52055
11369||5502||Bifidobacterium breve||http://purl.obolibrary.org/obo/NCBITaxon_1685
11370||4717||Malformation syndrome with hamartosis||http://www.orpha.net/ORDO/Orphanet_98196
11371||1022||Geospiza difficilis||http://purl.obolibrary.org/obo/NCBITaxon_87173
11372||11472||Partial deletion of chromosome 12||http://www.orpha.net/ORDO/Orphanet_282124
11373||9965||Late-onset retinal degeneration||http://www.orpha.net/ORDO/Orphanet_67042
11374||6597||Hyaluronidase deficiency||http://www.orpha.net/ORDO/Orphanet_67041
11375||426||Thrombocytopenia with congenital dyserythropoietic anemia||http://www.orpha.net/ORDO/Orphanet_67044
11376||12231||3-methylglutaconic aciduria type 1||http://www.orpha.net/ORDO/Orphanet_67046
11377||7682||X-linked intellectual disability with isolated growth hormone deficiency||http://www.orpha.net/ORDO/Orphanet_67045
11378||12231||3-methylglutaconic aciduria type 4||http://www.orpha.net/ORDO/Orphanet_67048
11379||1826||Alopecurus myosuroides||http://purl.obolibrary.org/obo/NCBITaxon_81473
11380||9710||3-methylglutaconic aciduria type 3||http://www.orpha.net/ORDO/Orphanet_67047
11381||5700||Nephrotic syndrome-deafness-pretibial epidermolysis bullosa syndrome||http://www.orpha.net/ORDO/Orphanet_300333
11382||10257||3q29 microduplication||http://www.orpha.net/ORDO/Orphanet_251038
11383||9690||Congenital blindness due to retinal non-attachment||http://www.orpha.net/ORDO/Orphanet_300337
11384||10994||mannose||http://purl.obolibrary.org/obo/CHEBI_37684
11385||4727||Hypoxanthine-guanine phosphoribosyltransferase deficiency||http://www.orpha.net/ORDO/Orphanet_206428
11386||10994||acetate||http://purl.obolibrary.org/obo/CHEBI_30089
11387||5573||Monosomy 18q||http://www.orpha.net/ORDO/Orphanet_1600
11388||10963||6p22 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_251046
11389||2405||Ring chromosome 5||http://www.orpha.net/ORDO/Orphanet_251043
11390||1022||Crotalus atrox||http://purl.obolibrary.org/obo/NCBITaxon_8730
11391||6054||Autosomal recessive systemic lupus erythematosus||http://www.orpha.net/ORDO/Orphanet_300345
11392||1826||Lycopersicon||http://purl.obolibrary.org/obo/NCBITaxon_49274
11394||4951||1p36 deletion syndrome||http://www.orpha.net/ORDO/Orphanet_1606
11393||10994||(1- 3)-beta-D-glucan||http://purl.obolibrary.org/obo/CHEBI_37671
11395||7090||Infantile Krabbe disease||http://www.orpha.net/ORDO/Orphanet_206436
11396||13448||pharyngeal arch||http://purl.obolibrary.org/obo/UBERON_0002539
11397||11433||hatching gland||http://purl.obolibrary.org/obo/UBERON_0002538
11398||2672||hermaphrodite gonad||http://purl.obolibrary.org/obo/UBERON_0002537
11399||10346||anterior silk gland||http://purl.obolibrary.org/obo/BTO_0001795
11400||2997||Autosomal dominant Charcot-Marie-Tooth disease type 2P||http://www.orpha.net/ORDO/Orphanet_300319
11401||5502||Leptospira interrogans serovar Lai||http://purl.obolibrary.org/obo/NCBITaxon_57678
11402||5864||2q31.1 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_251014
11403||9613||interleukin-13 (Mus musculus)||http://www.ebi.ac.uk/efo/EFO_0003798
11404||9613||interleukin-13 (Homo sapiens)||http://www.ebi.ac.uk/efo/EFO_0003797
11406||9613||interleukin-14 (Mus musculus)||http://www.ebi.ac.uk/efo/EFO_0003799
11405||9654||Congenital cataract-hearing loss-severe developmental delay syndrome||http://www.orpha.net/ORDO/Orphanet_300313
11407||5864||2q32q33 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_251019
11408||7090||Late-infantile/juvenile Krabbe disease||http://www.orpha.net/ORDO/Orphanet_206443
11410||10994||5-fluorouridine||http://purl.obolibrary.org/obo/CHEBI_185922
11409||4335||hybridization protocol||http://www.ebi.ac.uk/efo/EFO_0003790
11411||7090||Adult Krabbe disease||http://www.orpha.net/ORDO/Orphanet_206448
11412||9613||interleukin (Mus musculus)||http://www.ebi.ac.uk/efo/EFO_0003792
11413||2672||digit||http://purl.obolibrary.org/obo/UBERON_0002544
11414||9613||interleukin (Homo sapiens)||http://www.ebi.ac.uk/efo/EFO_0003791
11416||13448||germ ring||http://purl.obolibrary.org/obo/UBERON_0002541
11415||9613||interleukin-1 beta (Homo sapiens)||http://www.ebi.ac.uk/efo/EFO_0003794
11417||2672||scale||http://purl.obolibrary.org/obo/UBERON_0002542
11418||9613||interleukin (Rattus norvegicus)||http://www.ebi.ac.uk/efo/EFO_0003793
11419||9613||interleukin-1 beta (Rattus norvegicus)||http://www.ebi.ac.uk/efo/EFO_0003796
11422||14107||lateral line system||http://purl.obolibrary.org/obo/UBERON_0002540
11420||5864||2q24 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_1617
11421||9613||interleukin-1 beta (Mus musculus)||http://www.ebi.ac.uk/efo/EFO_0003795
11423||10759||Distal monosomy 3p||http://www.orpha.net/ORDO/Orphanet_1620
11424||5855||3q13 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_1621
11425||5502||Nitrosomonas europaea ATCC 19718||http://purl.obolibrary.org/obo/NCBITaxon_228410
11426||8846||Autosomal dominant optic atrophy and cataract||http://www.orpha.net/ORDO/Orphanet_67036
11427||13689||pronephric mesoderm||http://purl.obolibrary.org/obo/UBERON_0005721
11428||5864||2q33.1 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_251028
11429||1627||olfactory system||http://purl.obolibrary.org/obo/UBERON_0005725
11430||5502||Saccharopolyspora erythraea||http://purl.obolibrary.org/obo/NCBITaxon_1836
11431||2672||tail bud||http://purl.obolibrary.org/obo/UBERON_0002533
11432||6097||Distal monosomy 5q||http://www.orpha.net/ORDO/Orphanet_1627
11433||2672||gland||http://purl.obolibrary.org/obo/UBERON_0002530
11434||8142||8p23.1 microduplication syndrome||http://www.orpha.net/ORDO/Orphanet_251076
11435||10930||8p23.1 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_251071
11436||13689||otolith organ||http://purl.obolibrary.org/obo/UBERON_0002518
11438||14499||mediastinal lymph node||http://purl.obolibrary.org/obo/UBERON_0002524
11437||5061||Familial infantile gigantism||http://www.orpha.net/ORDO/Orphanet_300373
11439||6052||Distal monosomy 7q36||http://www.orpha.net/ORDO/Orphanet_1636
11440||10994||divanadium pentaoxide||http://purl.obolibrary.org/obo/CHEBI_30045
11441||770||GM15385||http://purl.obolibrary.org/obo/CLO_0026789
11442||770||GM15386||http://purl.obolibrary.org/obo/CLO_0026786
11443||15364||Autosomal anomaly||http://www.orpha.net/ORDO/Orphanet_98127
11444||3019||Distal monosomy 9p||http://www.orpha.net/ORDO/Orphanet_1642
11445||4887||Xp22.3 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_1643
11446||1123||Partial chromosome Y deletion||http://www.orpha.net/ORDO/Orphanet_1646
11447||6054||Progeroid and marfanoid aspect-lipodystrophy syndrome||http://www.orpha.net/ORDO/Orphanet_300382
11448||613||Oculocerebrocutaneous syndrome||http://www.orpha.net/ORDO/Orphanet_1647
11450||1491||intracellular||http://purl.obolibrary.org/obo/GO_0005622
11449||6039||6q25 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_251056
11451||3744||cell||http://purl.obolibrary.org/obo/GO_0005623
11453||11443||Autosomal trisomy||http://www.orpha.net/ORDO/Orphanet_98130
11452||4834||Natal teeth - intestinal pseudoobstruction - patent ductus||http://www.orpha.net/ORDO/Orphanet_1654
11454||5478||M llerian derivatives - lymphangiectasia - polydactyly||http://www.orpha.net/ORDO/Orphanet_1655
11456||11453||Partial autosomal trisomy/tetrasomy||http://www.orpha.net/ORDO/Orphanet_98132
11455||4810||Dent disease||http://www.orpha.net/ORDO/Orphanet_1652
11457||11453||Total autosomal trisomy||http://www.orpha.net/ORDO/Orphanet_98131
11458||1513||Dentin dysplasia||http://www.orpha.net/ORDO/Orphanet_1653
11460||2063||abnormality of the lung||http://purl.obolibrary.org/obo/HP_0002088
11459||325||Absence of fingerprints - congenital milia||http://www.orpha.net/ORDO/Orphanet_1658
11461||306||Dermatoosteolysis, Kirghizian type||http://www.orpha.net/ORDO/Orphanet_1657
11462||2063||abnormality of the respiratory system||http://purl.obolibrary.org/obo/HP_0002086
11463||5461||PLCG2-associated antibody deficiency and immune dysregulation||http://www.orpha.net/ORDO/Orphanet_300359
11464||11468||Immunoglobulin-mediated membranoproliferative glomerulonephritis||http://www.orpha.net/ORDO/Orphanet_329903
11465||11468||Non-immunoglobulin-mediated membranoproliferative glomerulonephritis||http://www.orpha.net/ORDO/Orphanet_329918
11466||10930||8p11.2 deletion syndrome||http://www.orpha.net/ORDO/Orphanet_251066
11468||3753||Primary membranoproliferative glomerulonephritis||http://www.orpha.net/ORDO/Orphanet_54370
11467||306||Dermo-odonto dysplasia||http://www.orpha.net/ORDO/Orphanet_1660
11469||9622||X-linked corneal dermoid||http://www.orpha.net/ORDO/Orphanet_1661
11470||5317||Lethal restrictive dermopathy||http://www.orpha.net/ORDO/Orphanet_1662
11471||6052||7q31 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_251061
11472||1400||Partial autosomal monosomy||http://www.orpha.net/ORDO/Orphanet_98142
11473||1400||Total autosomal monosomy||http://www.orpha.net/ORDO/Orphanet_98141
11474||5055||Wolcott-Rallison syndrome||http://www.orpha.net/ORDO/Orphanet_1667
11475||13297||RNA-seq of coding RNA||http://www.ebi.ac.uk/efo/EFO_0003738
11476||13297||RNA-seq of non coding RNA||http://www.ebi.ac.uk/efo/EFO_0003737
11477||10652||obsolete_lung (Sus scrofa)||http://www.ebi.ac.uk/efo/EFO_0003736
11479||1022||Strongylocentrotus purpuratus||http://purl.obolibrary.org/obo/NCBITaxon_7668
11478||10652||obsolete_lung (Rattus rattus)||http://www.ebi.ac.uk/efo/EFO_0003735
11480||10652||obsolete_lung (Rattus norvegicus)||http://www.ebi.ac.uk/efo/EFO_0003734
11481||10652||obsolete_lung (Mus musculus)||http://www.ebi.ac.uk/efo/EFO_0003733
11482||10652||obsolete_lung (Macaca fascicularis)||http://www.ebi.ac.uk/efo/EFO_0003732
11483||10652||obsolete_lung (Homo sapiens)||http://www.ebi.ac.uk/efo/EFO_0003731
11484||10652||obsolete_lung (Gallus gallus)||http://www.ebi.ac.uk/efo/EFO_0003730
11485||1627||skeletal system||http://purl.obolibrary.org/obo/UBERON_0001434
11486||8775||Mitochondrial DNA depletion syndrome, encephalomyopathic form with renal tubulopathy||http://www.orpha.net/ORDO/Orphanet_255235
11487||306||Dermotrichic syndrome||http://www.orpha.net/ORDO/Orphanet_99688
11488||1783||sequencer||http://www.ebi.ac.uk/efo/EFO_0003739
11489||4263||amplicon sequencing||http://www.ebi.ac.uk/efo/EFO_0003747
11491||10994||nickel chloride hexahydrate||http://purl.obolibrary.org/obo/CHEBI_53542
11490||4263||random exon sequencing||http://www.ebi.ac.uk/efo/EFO_0003746
11492||4263||MeDIP-seq||http://www.ebi.ac.uk/efo/EFO_0003749
11493||4263||MRE-seq||http://www.ebi.ac.uk/efo/EFO_0003748
11494||4263||clone end sequencing||http://www.ebi.ac.uk/efo/EFO_0003743
11495||4263||clone by clone sequencing||http://www.ebi.ac.uk/efo/EFO_0003742
11496||4263||random chromosome sequencing||http://www.ebi.ac.uk/efo/EFO_0003745
11497||4263||whole genome shotgun sequencing||http://www.ebi.ac.uk/efo/EFO_0003744
11498||4263||pooled clone sequencing||http://www.ebi.ac.uk/efo/EFO_0003741
11499||13301||sequencing assay||http://www.ebi.ac.uk/efo/EFO_0003740
11500||7551||Leigh syndrome with nephrotic syndrome||http://www.orpha.net/ORDO/Orphanet_255249
11503||11198||electric current unit||http://purl.obolibrary.org/obo/UO_0000004
11502||1022||Daphnia magna||http://purl.obolibrary.org/obo/NCBITaxon_35525
11501||6035||nucleus||http://purl.obolibrary.org/obo/GO_0005634
11504||11198||time unit||http://purl.obolibrary.org/obo/UO_0000003
11505||11198||mass unit||http://purl.obolibrary.org/obo/UO_0000002
11506||11198||length unit||http://purl.obolibrary.org/obo/UO_0000001
11507||15538||unit||http://purl.obolibrary.org/obo/UO_0000000
11508||1022||Daphnia pulicaria||http://purl.obolibrary.org/obo/NCBITaxon_35523
11509||7551||Leigh syndrome with leukodystrophy||http://www.orpha.net/ORDO/Orphanet_255241
11510||10652||obsolete_liver (Bos taurus)||http://www.ebi.ac.uk/efo/EFO_0003712
11511||13689||Rohon-Beard neuron||http://www.ebi.ac.uk/efo/EFO_0003711
11512||13689||anterior lateral line primordium||http://www.ebi.ac.uk/efo/EFO_0003710
11513||1826||Citrus trifoliata||http://purl.obolibrary.org/obo/NCBITaxon_37690
11514||10652||obsolete_liver (Macaca mulatta)||http://www.ebi.ac.uk/efo/EFO_0003716
11515||10652||obsolete_liver (Macaca fascicularis)||http://www.ebi.ac.uk/efo/EFO_0003715
11516||10652||obsolete_liver (Homo sapiens)||http://www.ebi.ac.uk/efo/EFO_0003714
11517||10652||obsolete_liver (Gallus gallus)||http://www.ebi.ac.uk/efo/EFO_0003713
11518||13689||swim bladder||http://purl.obolibrary.org/obo/UBERON_0006860
11519||1826||Marsilea quadrifolia||http://purl.obolibrary.org/obo/NCBITaxon_13816
11520||13249||Maternally-inherited Leigh syndrome||http://www.orpha.net/ORDO/Orphanet_255210
11521||10652||obsolete_liver (Pongo pygmaeus)||http://www.ebi.ac.uk/efo/EFO_0003719
11523||5502||Geobacter sulfurreducens||http://purl.obolibrary.org/obo/NCBITaxon_35554
11522||10652||obsolete_liver (Mus musculus)||http://www.ebi.ac.uk/efo/EFO_0003717
11524||772||cholangioma cell||http://purl.obolibrary.org/obo/BTO_0002842
11525||10652||obsolete_liver (Pan troglodytes)||http://www.ebi.ac.uk/efo/EFO_0003718
11526||772||breast invasive ductal carcinoma cell||http://purl.obolibrary.org/obo/BTO_0002844
11527||10652||obsolete_liver (Rattus rattus)||http://www.ebi.ac.uk/efo/EFO_0003721
11528||10652||obsolete_liver (Rattus norvegicus)||http://www.ebi.ac.uk/efo/EFO_0003720
11529||10652||obsolete_kidney (Homo sapiens)||http://www.ebi.ac.uk/efo/EFO_0003723
11530||10652||obsolete_kidney (Bos taurus)||http://www.ebi.ac.uk/efo/EFO_0003722
11531||10652||obsolete_kidney (Pan troglodytes)||http://www.ebi.ac.uk/efo/EFO_0003725
11532||1826||Aegilops tauschii||http://purl.obolibrary.org/obo/NCBITaxon_37682
11533||10652||obsolete_kidney (Mus musculus)||http://www.ebi.ac.uk/efo/EFO_0003724
11534||10652||obsolete_kidney (Rattus norvegicus)||http://www.ebi.ac.uk/efo/EFO_0003727
11535||10652||obsolete_kidney (Pongon pygmaeus)||http://www.ebi.ac.uk/efo/EFO_0003726
11536||8934||Navajo neurohepatopathy||http://www.orpha.net/ORDO/Orphanet_255229
11537||10994||phenol red||http://purl.obolibrary.org/obo/CHEBI_31991
11538||5295||developmental process||http://purl.obolibrary.org/obo/GO_0032502
11539||10652||obsolete_kidney (Rattus rattus)||http://www.ebi.ac.uk/efo/EFO_0003728
11540||10652||obsolete_lung (Bos taurus)||http://www.ebi.ac.uk/efo/EFO_0003729
11541||1826||Vitis riparia||http://purl.obolibrary.org/obo/NCBITaxon_96939
11542||2672||endocrine system component||http://www.ebi.ac.uk/efo/EFO_0003773
11543||11618||hyperlipidemia||http://www.ebi.ac.uk/efo/EFO_0003774
11544||10652||obsolete_abdominal fat||http://www.ebi.ac.uk/efo/EFO_0003771
11545||2672||lymphatic vessel||http://purl.obolibrary.org/obo/UBERON_0001473
11546||1485||diabetic retinopathy||http://www.ebi.ac.uk/efo/EFO_0003770
11547||2672||deltoid||http://purl.obolibrary.org/obo/UBERON_0001476
11548||5103||autoimmune thyroid disease||http://www.ebi.ac.uk/efo/EFO_0003779
11549||1015||heart disease||http://www.ebi.ac.uk/efo/EFO_0003777
11550||1790||psoriatic arthritis||http://www.ebi.ac.uk/efo/EFO_0003778
11551||1790||Job s syndrome||http://www.ebi.ac.uk/efo/EFO_0003775
11552||14780||coronary artery bypass||http://www.ebi.ac.uk/efo/EFO_0003776
11553||7946||Dappled diaphyseal dysplasia||http://www.orpha.net/ORDO/Orphanet_99645
11554||7966||Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria||http://www.orpha.net/ORDO/Orphanet_99646
11555||7966||Cheirospondyloenchondromatosis||http://www.orpha.net/ORDO/Orphanet_99647
11556||9918||Genetic dementia||http://www.orpha.net/ORDO/Orphanet_158124
11557||10143||Spondyloepimetaphyseal dysplasia, Handigodu type||http://www.orpha.net/ORDO/Orphanet_99642
11558||843||X-linked dystonia-parkinsonism||http://www.orpha.net/ORDO/Orphanet_53351
11559||2672||elbow||http://purl.obolibrary.org/obo/UBERON_0001461
11560||2165||motor neuron disease||http://www.ebi.ac.uk/efo/EFO_0003782
11561||2165||progressive bulbar palsy||http://www.ebi.ac.uk/efo/EFO_0003783
11562||2063||skin pigmentation||http://www.ebi.ac.uk/efo/EFO_0003784
11563||1790||allergy||http://www.ebi.ac.uk/efo/EFO_0003785
11564||2672||knee||http://purl.obolibrary.org/obo/UBERON_0001465
11565||2672||shoulder||http://purl.obolibrary.org/obo/UBERON_0001467
11566||5103||Behcet s syndrome||http://www.ebi.ac.uk/efo/EFO_0003780
11567||1015||carotid artery disease||http://www.ebi.ac.uk/efo/EFO_0003781
11568||11331||Maternal uniparental disomy of chromosome 1||http://www.orpha.net/ORDO/Orphanet_251009
11570||11333||Paternal uniparental disomy of chromosome 1||http://www.orpha.net/ORDO/Orphanet_251004
11569||10994||cytokine||http://www.ebi.ac.uk/efo/EFO_0003786
11572||2252||11p15.4 microduplication syndrome||http://www.orpha.net/ORDO/Orphanet_300305
11571||4430||cytokine role||http://www.ebi.ac.uk/efo/EFO_0003787
11573||4335||gene expression protocol||http://www.ebi.ac.uk/efo/EFO_0003788
11574||4335||growth protocol||http://www.ebi.ac.uk/efo/EFO_0003789
11575||5502||Streptococcus sanguinis SK36||http://purl.obolibrary.org/obo/NCBITaxon_388919
11576||3273||Primary dystonia, DYT2 type||http://www.orpha.net/ORDO/Orphanet_99657
11577||5005||freshwater sediment metagenome||http://purl.obolibrary.org/obo/NCBITaxon_556182
11578||2382||Brody myopathy||http://www.orpha.net/ORDO/Orphanet_53347
11579||2658||coelomic fluid||http://purl.obolibrary.org/obo/BTO_0001708
11580||770||HCT8||http://www.ebi.ac.uk/efo/EFO_0002189
11581||770||HCT15||http://www.ebi.ac.uk/efo/EFO_0002188
11582||770||HCC2218||http://www.ebi.ac.uk/efo/EFO_0002187
11584||4263||MNase-seq||http://www.ebi.ac.uk/efo/EFO_0003751
11583||770||HCC1599||http://www.ebi.ac.uk/efo/EFO_0002186
11586||4263||DNase-Hypersensitivity seq||http://www.ebi.ac.uk/efo/EFO_0003752
11585||770||HCC1395||http://www.ebi.ac.uk/efo/EFO_0002185
11587||770||H4||http://www.ebi.ac.uk/efo/EFO_0002184
11589||4263||MBD-seq||http://www.ebi.ac.uk/efo/EFO_0003750
11588||770||GDM1||http://www.ebi.ac.uk/efo/EFO_0002183
11590||4263||FL-cDNA||http://www.ebi.ac.uk/efo/EFO_0003755
11591||2165||autism spectrum disorder||http://www.ebi.ac.uk/efo/EFO_0003756
11592||4263||Bisulfite-seq||http://www.ebi.ac.uk/efo/EFO_0003753
11593||4263||EST sequencing||http://www.ebi.ac.uk/efo/EFO_0003754
11594||11591||pervasive developmental disorder - not otherwise specified||http://www.ebi.ac.uk/efo/EFO_0003759
11595||11591||Asperger syndrome||http://www.ebi.ac.uk/efo/EFO_0003757
11596||11591||autism||http://www.ebi.ac.uk/efo/EFO_0003758
11597||1022||Lytechinus pictus||http://purl.obolibrary.org/obo/NCBITaxon_7653
11598||770||HEC1B||http://www.ebi.ac.uk/efo/EFO_0002192
11599||770||HEL9217||http://www.ebi.ac.uk/efo/EFO_0002193
11600||9903||Hereditary geniospasm||http://www.orpha.net/ORDO/Orphanet_53372
11601||770||HDMYZ||http://www.ebi.ac.uk/efo/EFO_0002190
11602||770||HEC1A||http://www.ebi.ac.uk/efo/EFO_0002191
11603||10994||ochratoxin A||http://purl.obolibrary.org/obo/CHEBI_7719
11604||2672||chest||http://purl.obolibrary.org/obo/UBERON_0001443
11605||770||HSSultan||http://www.ebi.ac.uk/efo/EFO_0002199
11606||770||HPAFII||http://www.ebi.ac.uk/efo/EFO_0002198
11607||10926||fibula||http://purl.obolibrary.org/obo/UBERON_0001446
11608||2165||central nervous system cyst||http://www.ebi.ac.uk/efo/EFO_0003760
11609||770||HMCB||http://www.ebi.ac.uk/efo/EFO_0002195
11610||2102||unipolar depression||http://www.ebi.ac.uk/efo/EFO_0003761
11611||770||HH||http://www.ebi.ac.uk/efo/EFO_0002194
11612||12143||vitamin D deficiency||http://www.ebi.ac.uk/efo/EFO_0003762
11613||770||HPAC||http://www.ebi.ac.uk/efo/EFO_0002197
11615||770||HOS||http://www.ebi.ac.uk/efo/EFO_0002196
11614||1015||cerebrovascular disorder||http://www.ebi.ac.uk/efo/EFO_0003763
11616||11614||transient ischemic attack||http://www.ebi.ac.uk/efo/EFO_0003764
11617||3750||protein kinase inhibitor||http://purl.obolibrary.org/obo/CHEBI_37699
11618||2063||sign or symptom||http://www.ebi.ac.uk/efo/EFO_0003765
11619||10929||pain in abdomen||http://www.ebi.ac.uk/efo/EFO_0003766
11620||1403||inflammatory bowel disease||http://www.ebi.ac.uk/efo/EFO_0003767
11621||11030||nicotine dependence||http://www.ebi.ac.uk/efo/EFO_0003768
11622||2162||endocrine neoplasm||http://www.ebi.ac.uk/efo/EFO_0003769
11623||1022||Laternula elliptica||http://purl.obolibrary.org/obo/NCBITaxon_228457
11624||10994||azoxystrobin||http://purl.obolibrary.org/obo/CHEBI_40909
11625||306||Fried s tooth and nail syndrome||http://www.orpha.net/ORDO/Orphanet_99672
11626||770||GM17187||http://purl.obolibrary.org/obo/CLO_0013775
11627||770||GM17188||http://purl.obolibrary.org/obo/CLO_0013777
11628||770||NCI-H661||http://www.ebi.ac.uk/efo/EFO_0002299
11629||770||colonic epithelium cell line||http://purl.obolibrary.org/obo/BTO_0003250
11630||770||NCI-H630||http://www.ebi.ac.uk/efo/EFO_0002297
11631||770||NCI-H650||http://www.ebi.ac.uk/efo/EFO_0002298
11632||770||NCI-H522||http://www.ebi.ac.uk/efo/EFO_0002295
11633||770||NCI-H524||http://www.ebi.ac.uk/efo/EFO_0002296
11634||770||NCI-H446||http://www.ebi.ac.uk/efo/EFO_0002293
11635||770||NCI-H508||http://www.ebi.ac.uk/efo/EFO_0002294
11636||770||NCI-H322||http://www.ebi.ac.uk/efo/EFO_0002290
11637||6610||Muenke syndrome||http://www.orpha.net/ORDO/Orphanet_53271
11638||770||NCI-H441||http://www.ebi.ac.uk/efo/EFO_0002292
11639||770||NCI-H358||http://www.ebi.ac.uk/efo/EFO_0002291
11640||1491||cell envelope||http://purl.obolibrary.org/obo/GO_0030313
11641||1491||external encapsulating structure||http://purl.obolibrary.org/obo/GO_0030312
11642||5502||Streptomyces maritimus||http://purl.obolibrary.org/obo/NCBITaxon_115828
11643||770||GM17186||http://purl.obolibrary.org/obo/CLO_0013784
11644||770||NCI-H23||http://www.ebi.ac.uk/efo/EFO_0002286
11645||770||NCI-H2347||http://www.ebi.ac.uk/efo/EFO_0002287
11646||770||NCI-H2405||http://www.ebi.ac.uk/efo/EFO_0002288
11647||1826||Taraxacum officinale||http://purl.obolibrary.org/obo/NCBITaxon_50225
11648||770||NCI-H295R||http://www.ebi.ac.uk/efo/EFO_0002289
11649||770||NCI-H2171||http://www.ebi.ac.uk/efo/EFO_0002282
11650||770||NCI-H2195||http://www.ebi.ac.uk/efo/EFO_0002283
11652||770||NCI-H2228||http://www.ebi.ac.uk/efo/EFO_0002284
11651||770||GM17185||http://purl.obolibrary.org/obo/CLO_0013781
11653||770||NCI-H226||http://www.ebi.ac.uk/efo/EFO_0002285
11654||770||NCI-H2170||http://www.ebi.ac.uk/efo/EFO_0002281
11655||770||NCI-H2126||http://www.ebi.ac.uk/efo/EFO_0002280
11656||770||GM17181||http://purl.obolibrary.org/obo/CLO_0013755
11657||770||NCI-H2122||http://www.ebi.ac.uk/efo/EFO_0002279
11658||770||GM17184||http://purl.obolibrary.org/obo/CLO_0013752
11659||770||GM17180||http://purl.obolibrary.org/obo/CLO_0013751
11660||770||GM17182||http://purl.obolibrary.org/obo/CLO_0013754
11661||770||GM17183||http://purl.obolibrary.org/obo/CLO_0013753
11662||770||NCI-H2009||http://www.ebi.ac.uk/efo/EFO_0002273
11664||2672||knee joint||http://purl.obolibrary.org/obo/UBERON_0001485
11663||770||NCI-H2030||http://www.ebi.ac.uk/efo/EFO_0002274
11665||770||NCI-H1975||http://www.ebi.ac.uk/efo/EFO_0002271
11666||770||NCI-H1993||http://www.ebi.ac.uk/efo/EFO_0002272
11667||770||NCI-H2087||http://www.ebi.ac.uk/efo/EFO_0002277
11668||770||NCI-H2107||http://www.ebi.ac.uk/efo/EFO_0002278
11670||2672||ankle joint||http://purl.obolibrary.org/obo/UBERON_0001488
11669||770||NCI-H2052||http://www.ebi.ac.uk/efo/EFO_0002275
11671||770||NCI-H2081||http://www.ebi.ac.uk/efo/EFO_0002276
11672||770||NCI-H1930||http://www.ebi.ac.uk/efo/EFO_0002270
11673||2681||Familial cutaneous collagenoma||http://www.orpha.net/ORDO/Orphanet_53296
11675||13496||Cocksfoot streak virus||http://purl.obolibrary.org/obo/NCBITaxon_192452
11674||5502||Enterococcus casseliflavus||http://purl.obolibrary.org/obo/NCBITaxon_37734
11676||13496||Prunus necrotic ringspot virus||http://purl.obolibrary.org/obo/NCBITaxon_37733
11677||770||NCI-H1838||http://www.ebi.ac.uk/efo/EFO_0002268
11678||770||NCI-H187||http://www.ebi.ac.uk/efo/EFO_0002269
11680||4319||pectoral muscle||http://purl.obolibrary.org/obo/UBERON_0001495
11679||770||NCI-H1650||http://www.ebi.ac.uk/efo/EFO_0002260
11681||770||NCI-H1651||http://www.ebi.ac.uk/efo/EFO_0002261
11682||770||NCI-H1666||http://www.ebi.ac.uk/efo/EFO_0002262
11683||770||NCI-H1694||http://www.ebi.ac.uk/efo/EFO_0002263
11684||770||NCI-H1703||http://www.ebi.ac.uk/efo/EFO_0002264
11685||770||NCI-H1770||http://www.ebi.ac.uk/efo/EFO_0002265
11686||770||NCI-H1792||http://www.ebi.ac.uk/efo/EFO_0002266
11687||770||NCI-H1793||http://www.ebi.ac.uk/efo/EFO_0002267
11688||10652||obsolete_vascular cord||http://www.ebi.ac.uk/efo/EFO_0003709
11689||13689||primordial vasculature||http://www.ebi.ac.uk/efo/EFO_0003708
11690||13689||atrioventricular ring||http://www.ebi.ac.uk/efo/EFO_0003707
11691||13689||trabecular layer||http://www.ebi.ac.uk/efo/EFO_0003706
11692||770||NCI-H1573||http://www.ebi.ac.uk/efo/EFO_0002256
11693||770||NCI-H1563||http://www.ebi.ac.uk/efo/EFO_0002255
11694||770||NCI-H1437||http://www.ebi.ac.uk/efo/EFO_0002254
11695||770||NCI-H1436||http://www.ebi.ac.uk/efo/EFO_0002253
11696||770||NCI-H1395||http://www.ebi.ac.uk/efo/EFO_0002252
11697||770||NCI-H1355||http://www.ebi.ac.uk/efo/EFO_0002251
11698||770||NCI-H1155||http://www.ebi.ac.uk/efo/EFO_0002250
11700||13689||rostral blood island||http://www.ebi.ac.uk/efo/EFO_0003700
11699||770||GM15242||http://purl.obolibrary.org/obo/CLO_0027447
11701||13689||parachordal vessel||http://www.ebi.ac.uk/efo/EFO_0003701
11702||10994||(S)-azetidine-2-carboxylic acid||http://purl.obolibrary.org/obo/CHEBI_6198
11703||10652||obsolete_anterior lateral plate mesoderm||http://www.ebi.ac.uk/efo/EFO_0003704
11704||770||NCI-H1623||http://www.ebi.ac.uk/efo/EFO_0002259
11705||10652||obsolete_posterior lateral plate mesoderm||http://www.ebi.ac.uk/efo/EFO_0003705
11707||13689||anterior lateral mesoderm||http://www.ebi.ac.uk/efo/EFO_0003702
11706||770||NCI-H1618||http://www.ebi.ac.uk/efo/EFO_0002258
11708||13689||posterior lateral mesoderm||http://www.ebi.ac.uk/efo/EFO_0003703
11709||770||NCI-H1581||http://www.ebi.ac.uk/efo/EFO_0002257
11710||770||GM13649||http://purl.obolibrary.org/obo/CLO_0032713
11711||770||Malme3M||http://www.ebi.ac.uk/efo/EFO_0002243
11712||770||MV4II||http://www.ebi.ac.uk/efo/EFO_0002242
11713||770||NALM6||http://www.ebi.ac.uk/efo/EFO_0002245
11714||770||NALM1||http://www.ebi.ac.uk/efo/EFO_0002244
11715||770||MT3||http://www.ebi.ac.uk/efo/EFO_0002241
11716||10652||obsolete_MOLT4||http://www.ebi.ac.uk/efo/EFO_0002240
11717||770||NC37||http://www.ebi.ac.uk/efo/EFO_0002247
11718||770||NAMALWA||http://www.ebi.ac.uk/efo/EFO_0002246
11719||770||NCI-H1092||http://www.ebi.ac.uk/efo/EFO_0002249
11720||770||NCI-H1048||http://www.ebi.ac.uk/efo/EFO_0002248
11721||770||MCIXC||http://www.ebi.ac.uk/efo/EFO_0002230
11723||770||GM17191||http://purl.obolibrary.org/obo/CLO_0013793
11722||770||GM15236||http://purl.obolibrary.org/obo/CLO_0027467
11724||770||GM17190||http://purl.obolibrary.org/obo/CLO_0013794
11725||770||MG63||http://www.ebi.ac.uk/efo/EFO_0002234
11726||770||MESSA||http://www.ebi.ac.uk/efo/EFO_0002233
11727||770||MEG01||http://www.ebi.ac.uk/efo/EFO_0002232
11729||770||GM17189||http://purl.obolibrary.org/obo/CLO_0013790
11728||770||MEC1||http://www.ebi.ac.uk/efo/EFO_0002231
11730||770||ML2||http://www.ebi.ac.uk/efo/EFO_0002238
11731||770||MJ||http://www.ebi.ac.uk/efo/EFO_0002237
11732||770||MIA Paca-2||http://www.ebi.ac.uk/efo/EFO_0002236
11733||770||MHHPREB1||http://www.ebi.ac.uk/efo/EFO_0002235
11734||770||GM17193||http://purl.obolibrary.org/obo/CLO_0013795
11735||770||GM17192||http://purl.obolibrary.org/obo/CLO_0013796
11736||770||GM17195||http://purl.obolibrary.org/obo/CLO_0013797
11739||770||MOLT16||http://www.ebi.ac.uk/efo/EFO_0002239
11737||770||GM17194||http://purl.obolibrary.org/obo/CLO_0013798
11738||5502||Escherichia coli B||http://purl.obolibrary.org/obo/NCBITaxon_37762
11740||770||KPL1||http://www.ebi.ac.uk/efo/EFO_0002221
11741||770||KLE||http://www.ebi.ac.uk/efo/EFO_0002220
11742||770||KYSE30||http://www.ebi.ac.uk/efo/EFO_0002223
11743||770||KU812||http://www.ebi.ac.uk/efo/EFO_0002222
11744||770||L428||http://www.ebi.ac.uk/efo/EFO_0002225
11745||770||Kasumi2||http://www.ebi.ac.uk/efo/EFO_0002224
11746||770||LS174T||http://www.ebi.ac.uk/efo/EFO_0002227
11747||770||LS1034||http://www.ebi.ac.uk/efo/EFO_0002226
11748||770||MCCAR||http://www.ebi.ac.uk/efo/EFO_0002229
11749||770||MC116||http://www.ebi.ac.uk/efo/EFO_0002228
11750||770||KATOIII||http://www.ebi.ac.uk/efo/EFO_0002217
11751||1022||Coregonus clupeaformis||http://purl.obolibrary.org/obo/NCBITaxon_59861
11752||770||KG1||http://www.ebi.ac.uk/efo/EFO_0002218
11753||770||KHOS240S||http://www.ebi.ac.uk/efo/EFO_0002219
11754||770||JRT3T35||http://www.ebi.ac.uk/efo/EFO_0002213
11755||770||JVM3||http://www.ebi.ac.uk/efo/EFO_0002214
11756||770||Jiyoye||http://www.ebi.ac.uk/efo/EFO_0002215
11757||10652||obsolete_K562||http://www.ebi.ac.uk/efo/EFO_0002216
11758||770||GM15224||http://purl.obolibrary.org/obo/CLO_0027484
11759||770||J82||http://www.ebi.ac.uk/efo/EFO_0002210
11760||770||JAR||http://www.ebi.ac.uk/efo/EFO_0002211
11761||5961||X-linked intellectual disability - Dandy-Walker malformation - basal ganglia disease - Seizures||http://www.orpha.net/ORDO/Orphanet_1568
11762||770||JM1||http://www.ebi.ac.uk/efo/EFO_0002212
11763||770||GM15223||http://purl.obolibrary.org/obo/CLO_0027483
11764||5502||Mycobacterium smegmatis||http://purl.obolibrary.org/obo/NCBITaxon_1772
11765||5502||Mycobacterium tuberculosis||http://purl.obolibrary.org/obo/NCBITaxon_1773
11767||11465||C3 glomerulonephritis||http://www.orpha.net/ORDO/Orphanet_329931
11768||770||GM15226||http://purl.obolibrary.org/obo/CLO_0027486
11766||5502||Mycobacterium avium subsp. paratuberculosis||http://purl.obolibrary.org/obo/NCBITaxon_1770
11769||770||GM15221||http://purl.obolibrary.org/obo/CLO_0027487
11770||306||Dahlberg-Borer-Newcomer syndrome||http://www.orpha.net/ORDO/Orphanet_1563
11771||7943||Dacryocystitis - osteopoikilosis||http://www.orpha.net/ORDO/Orphanet_1562
11772||288||Fatal infantile cytochrome C oxidase deficiency||http://www.orpha.net/ORDO/Orphanet_1561
11773||770||GM15215||http://purl.obolibrary.org/obo/CLO_0027492
11774||13770||Dandy-Walker malformation - postaxial polydactyly||http://www.orpha.net/ORDO/Orphanet_1566
11775||770||GM15216||http://purl.obolibrary.org/obo/CLO_0027491
11776||770||HuPT4||http://www.ebi.ac.uk/efo/EFO_0002208
11777||770||HuT78||http://www.ebi.ac.uk/efo/EFO_0002209
11778||10652||obsolete_HepG2||http://www.ebi.ac.uk/efo/EFO_0002206
11779||770||HuNS1||http://www.ebi.ac.uk/efo/EFO_0002207
11781||770||HT3||http://www.ebi.ac.uk/efo/EFO_0002204
11780||8190||valproic acid||http://purl.obolibrary.org/obo/CHEBI_39867
11782||770||Hep3B||http://www.ebi.ac.uk/efo/EFO_0002205
11783||770||HT1197||http://www.ebi.ac.uk/efo/EFO_0002202
11784||5502||Mycobacterium leprae||http://purl.obolibrary.org/obo/NCBITaxon_1769
11785||770||HT1376||http://www.ebi.ac.uk/efo/EFO_0002203
11786||770||HT||http://www.ebi.ac.uk/efo/EFO_0002200
11787||5502||Mycobacterium avium||http://purl.obolibrary.org/obo/NCBITaxon_1764
11788||10652||obsolete_HT1080||http://www.ebi.ac.uk/efo/EFO_0002201
11789||770||GM15227||http://purl.obolibrary.org/obo/CLO_0027473
11790||5502||Mycobacterium bovis||http://purl.obolibrary.org/obo/NCBITaxon_1765
11791||7963||Currarino triad||http://www.orpha.net/ORDO/Orphanet_1552
11792||8646||Familial benign copper deficiency||http://www.orpha.net/ORDO/Orphanet_1551
11793||6610||Curry-Jones syndrome||http://www.orpha.net/ORDO/Orphanet_1553
11794||5918||Cutis gyrata - acanthosis nigricans - craniosynostosis||http://www.orpha.net/ORDO/Orphanet_1555
11795||9753||rectal prolapse||http://purl.obolibrary.org/obo/HP_0002035
11796||5457||Monosomy 13q14||http://www.orpha.net/ORDO/Orphanet_1587
11797||5962||Non-distal monosomy 10q||http://www.orpha.net/ORDO/Orphanet_1581
11798||11029||Distal monosomy 10p||http://www.orpha.net/ORDO/Orphanet_1580
11799||4907||Transient neonatal multiple acyl-CoA dehydrogenase deficiency||http://www.orpha.net/ORDO/Orphanet_329942
11800||770||GM15213||http://purl.obolibrary.org/obo/CLO_0027493
11801||4139||Infantile bilateral striatal necrosis||http://www.orpha.net/ORDO/Orphanet_1576
11802||1732||Rare genetic cardiac disease||http://www.orpha.net/ORDO/Orphanet_98054
11803||7749||Dehydratase deficiency||http://www.orpha.net/ORDO/Orphanet_1578
11804||260||Common variable immunodeficiency||http://www.orpha.net/ORDO/Orphanet_1572
11805||6899||Knobloch syndrome||http://www.orpha.net/ORDO/Orphanet_1571
11806||6897||Retinal degeneration - nanophthalmos - glaucoma||http://www.orpha.net/ORDO/Orphanet_1574
11807||306||Hypotrichosis with juvenile macular degeneration||http://www.orpha.net/ORDO/Orphanet_1573
11808||13824||Symbrachydactyly of hands and feet||http://www.orpha.net/ORDO/Orphanet_1570
11809||1732||Rare genetic renal disease||http://www.orpha.net/ORDO/Orphanet_98056
11810||2327||Generalized juvenile polyposis/juvenile polyposis coli||http://www.orpha.net/ORDO/Orphanet_329971
11811||10469||Nausea||http://purl.obolibrary.org/obo/HP_0002018
11812||1595||constipation||http://purl.obolibrary.org/obo/HP_0002019
11813||1595||diarrhea||http://purl.obolibrary.org/obo/HP_0002014
11814||3023||46,XY disorder of sex development due to a defect in testosterone metabolism by peripheral tissue||http://www.orpha.net/ORDO/Orphanet_98086
11815||3556||Syndrome with 46,XY disorder of sex development||http://www.orpha.net/ORDO/Orphanet_98087
11816||6054||Intermittent hydrarthrosis||http://www.orpha.net/ORDO/Orphanet_329967
11817||10929||abdominal pain||http://purl.obolibrary.org/obo/HP_0002027
11818||5457||Distal monosomy 13q||http://www.orpha.net/ORDO/Orphanet_1590
11819||2252||Premature chromosome condensation with microcephaly and intellectual disability||http://www.orpha.net/ORDO/Orphanet_52183
11820||5462||Distal monosomy 15q||http://www.orpha.net/ORDO/Orphanet_1596
11821||5483||Distal monosomy 17q||http://www.orpha.net/ORDO/Orphanet_1597
11822||10835||Monosomy 18p||http://www.orpha.net/ORDO/Orphanet_1598
11823||3042||Gonadal dysgenesis of gynecological interest||http://www.orpha.net/ORDO/Orphanet_98074
11824||10994||7,12-dimethylbenz(a)anthracene||http://purl.obolibrary.org/obo/CHEBI_254496
11825||770||HL-1 cell||http://purl.obolibrary.org/obo/BTO_0003264
11826||2672||postcentral gyrus||http://purl.obolibrary.org/obo/UBERON_0002581
11827||14145||Autosomal recessive syndromic cerebellar ataxia||http://www.orpha.net/ORDO/Orphanet_98099
11828||14145||Autosomal recessive degenerative and progressive cerebellar ataxia||http://www.orpha.net/ORDO/Orphanet_98098
11829||14145||Autosomal recessive cerebellar ataxia due to a DNA repair defect||http://www.orpha.net/ORDO/Orphanet_98097
11830||14145||Autosomal recessive metabolic cerebellar ataxia||http://www.orpha.net/ORDO/Orphanet_98096
11831||14145||Autosomal recessive congenital cerebellar ataxia||http://www.orpha.net/ORDO/Orphanet_98095
11832||5005||marine metagenome||http://purl.obolibrary.org/obo/NCBITaxon_408172
11833||2672||cerebral peduncle||http://purl.obolibrary.org/obo/UBERON_0002623
11834||4687||Craniosynostosis - Dandy-Walker malformation - hydrocephalus||http://www.orpha.net/ORDO/Orphanet_1538
11835||2672||brain ventricle||http://purl.obolibrary.org/obo/UBERON_0004086
11836||6610||Craniosynostosis - dysmorphism - brachydactyly||http://www.orpha.net/ORDO/Orphanet_1535
11837||6610||Craniosynostosis - cataract||http://www.orpha.net/ORDO/Orphanet_1530
11838||6610||Craniosynostosis - fibular aplasia||http://www.orpha.net/ORDO/Orphanet_1533
11840||4766||Craniosynostosis||http://www.orpha.net/ORDO/Orphanet_1531
11839||5893||Genetic neuromuscular junction disease||http://www.orpha.net/ORDO/Orphanet_98495
11841||4139||G mez-L pez-Hern ndez syndrome||http://www.orpha.net/ORDO/Orphanet_1532
11842||9918||Genetic peripheral neuropathy||http://www.orpha.net/ORDO/Orphanet_98497
11843||3485||right ventricle||http://purl.obolibrary.org/obo/BTO_0001630
11844||12386||Gyps fulvus||http://purl.obolibrary.org/obo/NCBITaxon_36247
11845||5005||human gut metagenome||http://purl.obolibrary.org/obo/NCBITaxon_408170
11846||13496||Synechococcus phage S-RSM2||http://purl.obolibrary.org/obo/NCBITaxon_264653
11847||12769||Cryptomicrotia - brachydactyly - excess fingertip arch||http://www.orpha.net/ORDO/Orphanet_1547
11848||2252||Cryptorchidism - arachnodactyly - intellectual disability||http://www.orpha.net/ORDO/Orphanet_1548
11849||6610||Jackson-Weiss syndrome||http://www.orpha.net/ORDO/Orphanet_1540
11850||6610||Craniosynostosis, Boston type||http://www.orpha.net/ORDO/Orphanet_1541
11851||12824||Crisponi syndrome||http://www.orpha.net/ORDO/Orphanet_1545
11852||6090||carbohydrate metabolic process||http://purl.obolibrary.org/obo/GO_0005975
11853||6294||Methylmalonic aciduria due to transcobalamin receptor defect||http://www.orpha.net/ORDO/Orphanet_280183
11854||13496||Bovine viral diarrhea virus 1||http://purl.obolibrary.org/obo/NCBITaxon_11099
11855||10140||Hypertelorism, Teebi type||http://www.orpha.net/ORDO/Orphanet_1519
11856||7962||Hypertrichotic osteochondrodysplasia, Cantu type||http://www.orpha.net/ORDO/Orphanet_1517
11857||4766||Craniofacial dyssynostosis||http://www.orpha.net/ORDO/Orphanet_1516
11858||306||Cranioectodermal dysplasia||http://www.orpha.net/ORDO/Orphanet_1515
11859||6299||Oscheius dolichura||http://purl.obolibrary.org/obo/NCBITaxon_473156
11860||2252||Craniodigital syndrome - intellectual disability||http://www.orpha.net/ORDO/Orphanet_1514
11861||4766||Craniodiaphyseal dysplasia||http://www.orpha.net/ORDO/Orphanet_1513
11862||5502||Streptomyces virginiae||http://purl.obolibrary.org/obo/NCBITaxon_1961
11863||2252||Crane-Heise syndrome||http://www.orpha.net/ORDO/Orphanet_1512
11864||12322||Muscular dystrophy||http://www.orpha.net/ORDO/Orphanet_98473
11866||14271||Septopreoptic holoprosencephaly||http://www.orpha.net/ORDO/Orphanet_280195
11865||13496||West Nile virus||http://purl.obolibrary.org/obo/NCBITaxon_11082
11867||13689||neuromast||http://purl.obolibrary.org/obo/UBERON_0008904
11868||13883||data transformation||http://purl.obolibrary.org/obo/OBI_0200000
11869||9753||Recurrent infection of the gastrointestinal tract||http://purl.obolibrary.org/obo/HP_0004798
11870||9753||gastrointestinal obstruction||http://purl.obolibrary.org/obo/HP_0004796
11871||5700||Craniofacial-deafness-hand syndrome||http://www.orpha.net/ORDO/Orphanet_1529
11872||1419||Craniotelencephalic dysplasia||http://www.orpha.net/ORDO/Orphanet_1528
11873||12458||biexponential transformation||http://purl.obolibrary.org/obo/OBI_0200006
11874||7739||Cranio-osteoarthropathy||http://www.orpha.net/ORDO/Orphanet_1525
11875||6610||Craniomicromelic syndrome||http://www.orpha.net/ORDO/Orphanet_1524
11876||6610||Craniosynostosis, Philadelphia type||http://www.orpha.net/ORDO/Orphanet_1527
11877||1171||Craniofrontonasal dysplasia||http://www.orpha.net/ORDO/Orphanet_1520
11878||10140||Craniofrontonasal dysplasia - Poland anomaly||http://www.orpha.net/ORDO/Orphanet_1521
11879||7943||Craniometaphyseal dysplasia||http://www.orpha.net/ORDO/Orphanet_1522
11880||13496||Yellow fever virus||http://purl.obolibrary.org/obo/NCBITaxon_11089
11881||12348||Metabolic myopathy||http://www.orpha.net/ORDO/Orphanet_98486
11882||10745||Syndromic urogenital tract malformation||http://www.orpha.net/ORDO/Orphanet_165707
11883||2672||superior frontal gyrus||http://purl.obolibrary.org/obo/UBERON_0002661
11884||1415||Autosomal recessive limb-girdle muscular dystrophy type 2O||http://www.orpha.net/ORDO/Orphanet_206564
11885||13496||Dengue virus 4||http://purl.obolibrary.org/obo/NCBITaxon_11070
11886||11901||Arabidopsis lyrata subsp. petraea||http://purl.obolibrary.org/obo/NCBITaxon_59691
11887||4406||Platelet storage pool disease||http://www.orpha.net/ORDO/Orphanet_98454
11888||11887||Alpha granule disease||http://www.orpha.net/ORDO/Orphanet_98455
11889||11887||Dense granule disease||http://www.orpha.net/ORDO/Orphanet_98456
11890||770||Th1-cell||http://purl.obolibrary.org/obo/BTO_0001678
11891||770||Th2-cell||http://purl.obolibrary.org/obo/BTO_0001679
11892||7973||Short rib-polydactyly syndrome||http://www.orpha.net/ORDO/Orphanet_1505
11893||7948||Thin ribs - tubular bones - dysmorphism||http://www.orpha.net/ORDO/Orphanet_1506
11894||8361||Autosomal recessive Robinow syndrome||http://www.orpha.net/ORDO/Orphanet_1507
11895||7949||Coxoauricular syndrome||http://www.orpha.net/ORDO/Orphanet_1508
11896||7955||Coxopodopatellar syndrome||http://www.orpha.net/ORDO/Orphanet_1509
11897||13496||Dengue virus 2||http://purl.obolibrary.org/obo/NCBITaxon_11060
11898||204||Complement component 3 deficiency||http://www.orpha.net/ORDO/Orphanet_280133
11899||4139||X-linked syndromic intellectual disability||http://www.orpha.net/ORDO/Orphanet_98464
11900||13496||Dengue virus 3||http://purl.obolibrary.org/obo/NCBITaxon_11069
11902||13155||Autosomal recessive lower motor neuron disease with childhood onset||http://www.orpha.net/ORDO/Orphanet_206580
11901||3352||Arabidopsis lyrata||http://purl.obolibrary.org/obo/NCBITaxon_59689
11903||15||Cardiodysrhythmic potassium-sensitive periodic paralysis||http://www.orpha.net/ORDO/Orphanet_37553
11904||1415||Autosomal recessive limb-girdle muscular dystrophy type 2L||http://www.orpha.net/ORDO/Orphanet_206549
11905||2323||Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers||http://www.orpha.net/ORDO/Orphanet_206546
11906||6768||Severe combined immunodeficiency due to LCK deficiency||http://www.orpha.net/ORDO/Orphanet_280142
11907||5502||Streptomyces rimosus||http://purl.obolibrary.org/obo/NCBITaxon_1927
11908||5502||Streptomyces rochei||http://purl.obolibrary.org/obo/NCBITaxon_1928
11911||13496||Dengue virus 1||http://purl.obolibrary.org/obo/NCBITaxon_11053
11910||2672||somatosensory cortex||http://purl.obolibrary.org/obo/UBERON_0008930
11909||6095||cilium||http://purl.obolibrary.org/obo/GO_0005929
11912||421||Hereditary combined deficiency of vitamin K-dependent clotting factors||http://www.orpha.net/ORDO/Orphanet_98434
11913||2654||bursa of Fabricius||http://purl.obolibrary.org/obo/BTO_0001699
11914||12747||response to topoisomerase inhibitor||http://purl.obolibrary.org/obo/GO_0072758
11915||1415||Autosomal recessive limb-girdle muscular dystrophy type 2N||http://www.orpha.net/ORDO/Orphanet_206559
11916||5502||Streptomyces scabiei||http://purl.obolibrary.org/obo/NCBITaxon_1930
11917||1415||Autosomal recessive limb-girdle muscular dystrophy type 2M||http://www.orpha.net/ORDO/Orphanet_206554
11918||770||LNCAP||http://www.ebi.ac.uk/efo/EFO_0002071
11919||770||MCF-7aro||http://www.ebi.ac.uk/efo/EFO_0002072
11920||770||LbetaT2||http://www.ebi.ac.uk/efo/EFO_0002070
11921||4994||Immunodeficiency due to interleukin-1 receptor-associated kinase-4 deficiency||http://www.orpha.net/ORDO/Orphanet_70592
11922||802||Vitamin B12- and folate-independent constitutional megaloblastic anemia||http://www.orpha.net/ORDO/Orphanet_98415
11923||8753||Sensory ataxic neuropathy - dysarthria - ophthalmoparesis||http://www.orpha.net/ORDO/Orphanet_70595
11924||8699||Dopa-responsive dystonia due to sepiapterin reductase deficiency||http://www.orpha.net/ORDO/Orphanet_70594
11925||6866||Immunodeficiency due to selective anti-polysaccharide antibody deficiency||http://www.orpha.net/ORDO/Orphanet_70593
11926||10994||isoniazide||http://purl.obolibrary.org/obo/CHEBI_6030
11927||5502||Streptomyces fradiae||http://purl.obolibrary.org/obo/NCBITaxon_1906
11928||5502||Streptomyces exfoliatus||http://purl.obolibrary.org/obo/NCBITaxon_1905
11929||5502||Streptomyces coelicolor||http://purl.obolibrary.org/obo/NCBITaxon_1902
11930||5502||Streptomyces clavuligerus||http://purl.obolibrary.org/obo/NCBITaxon_1901
11931||770||KELLY||http://www.ebi.ac.uk/efo/EFO_0002069
11932||770||Kc||http://www.ebi.ac.uk/efo/EFO_0002068
11933||770||K562||http://www.ebi.ac.uk/efo/EFO_0002067
11934||770||JEG3||http://www.ebi.ac.uk/efo/EFO_0002066
11935||770||ITV||http://www.ebi.ac.uk/efo/EFO_0002065
11936||770||ITM-ST||http://www.ebi.ac.uk/efo/EFO_0002064
11937||770||ITM-E6E7-ST||http://www.ebi.ac.uk/efo/EFO_0002063
11938||770||ITM-E6E7||http://www.ebi.ac.uk/efo/EFO_0002062
11939||770||SKMEL5_11939||http://www.ebi.ac.uk/efo/EFO_0002080
11940||12626||SN56.B5.G4||http://www.ebi.ac.uk/efo/EFO_0002081
11941||770||ssMCF7||http://www.ebi.ac.uk/efo/EFO_0002082
11942||770||SW480||http://www.ebi.ac.uk/efo/EFO_0002083
11943||12629||microgram per liter||http://purl.obolibrary.org/obo/UO_0000301
11944||5502||Streptomyces microflavus||http://purl.obolibrary.org/obo/NCBITaxon_1919
11946||15045||Secondary polycythemia||http://www.orpha.net/ORDO/Orphanet_98428
11945||5502||Streptomyces lividans||http://purl.obolibrary.org/obo/NCBITaxon_1916
11947||10994||isoflurane||http://purl.obolibrary.org/obo/CHEBI_6015
11948||5502||Streptomyces griseus||http://purl.obolibrary.org/obo/NCBITaxon_1911
11949||770||S1||http://www.ebi.ac.uk/efo/EFO_0002078
11950||770||Ramos||http://www.ebi.ac.uk/efo/EFO_0002077
11951||770||SK-MEL-2||http://www.ebi.ac.uk/efo/EFO_0002079
11952||770||PC-3||http://www.ebi.ac.uk/efo/EFO_0002074
11953||770||mIMCD-3||http://www.ebi.ac.uk/efo/EFO_0002073
11954||770||R1||http://www.ebi.ac.uk/efo/EFO_0002076
11955||770||PEL-5||http://www.ebi.ac.uk/efo/EFO_0002075
11956||1988||technical replicate||http://www.ebi.ac.uk/efo/EFO_0002090
11957||770||1A2||http://www.ebi.ac.uk/efo/EFO_0002094
11958||1988||biological replicate||http://www.ebi.ac.uk/efo/EFO_0002091
11959||1988||dye swap replicate||http://www.ebi.ac.uk/efo/EFO_0002092
11960||8191||N-(1-naphthyl)ethylenediamine dihydrochloride||http://purl.obolibrary.org/obo/CHEBI_53452
11961||2454||Adult polyglucosan body disease||http://www.orpha.net/ORDO/Orphanet_206583
11963||2672||intercostal muscle||http://purl.obolibrary.org/obo/UBERON_0001111
11962||2002||fibrosarcoma||http://www.ebi.ac.uk/efo/EFO_0002087
11964||770||TIVE||http://www.ebi.ac.uk/efo/EFO_0002086
11965||770||T98G||http://www.ebi.ac.uk/efo/EFO_0002085
11966||770||T84||http://www.ebi.ac.uk/efo/EFO_0002084
11967||2323||Isolated asymptomatic elevation of creatine phosphokinase||http://www.orpha.net/ORDO/Orphanet_206599
11968||10994||neuropeptide S||http://purl.obolibrary.org/obo/CHEBI_53461
11969||802||Constitutional megaloblastic anemia due to folate metabolism disorder||http://www.orpha.net/ORDO/Orphanet_98408
11971||770||5637||http://www.ebi.ac.uk/efo/EFO_0002096
11970||1022||Heterodera glycines||http://purl.obolibrary.org/obo/NCBITaxon_51029
11972||770||22Rv1||http://www.ebi.ac.uk/efo/EFO_0002095
11973||770||647V||http://www.ebi.ac.uk/efo/EFO_0002098
11974||770||639V||http://www.ebi.ac.uk/efo/EFO_0002097
11975||2672||diaphragm||http://purl.obolibrary.org/obo/UBERON_0001103
11976||770||769P||http://www.ebi.ac.uk/efo/EFO_0002099
11977||1414||Autosomal dominant limb-girdle muscular dystrophy type 1G||http://www.orpha.net/ORDO/Orphanet_55596
11978||12458||loess transformation||http://purl.obolibrary.org/obo/OBI_0200071
11979||1826||Pachycladon enysii||http://purl.obolibrary.org/obo/NCBITaxon_414717
11980||8024||Hypoinsulinemic hypoglycemia and body hemihypertrophy||http://www.orpha.net/ORDO/Orphanet_293964
11981||10994||calcineurin||http://purl.obolibrary.org/obo/CHEBI_53439
11982||1306||Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome||http://www.orpha.net/ORDO/Orphanet_293967
11983||1414||Autosomal dominant limb-girdle muscular dystrophy type 1F||http://www.orpha.net/ORDO/Orphanet_55595
11984||7529||bronchoalveolar lavage||http://purl.obolibrary.org/obo/BTO_0000155
11985||772||infected cell||http://purl.obolibrary.org/obo/BTO_0000152
11986||10994||isotretinoin||http://purl.obolibrary.org/obo/CHEBI_6067
11987||10994||methyl cellulose||http://purl.obolibrary.org/obo/CHEBI_53448
11989||9734||Childhood encephalopathy due to thiamine pyrophosphokinase deficiency||http://www.orpha.net/ORDO/Orphanet_293955
11988||9869||Juvenile amyotrophic lateral sclerosis||http://www.orpha.net/ORDO/Orphanet_300605
11990||5700||Hypertelorism-preauricular sinus-punctual pits-deafness syndrome||http://www.orpha.net/ORDO/Orphanet_293958
11991||5502||Rickettsia conorii str. Malish 7||http://purl.obolibrary.org/obo/NCBITaxon_272944
11992||5502||Rhodobacter sphaeroides 2.4.1||http://purl.obolibrary.org/obo/NCBITaxon_272943
11993||5025||Magnaporthe oryzae 70-15||http://purl.obolibrary.org/obo/NCBITaxon_242507
11994||770||Burkitt lymphoma cell||http://purl.obolibrary.org/obo/BTO_0000164
11995||8191||potassium dichromate||http://purl.obolibrary.org/obo/CHEBI_53444
11996||772||colorectal cancer cell||http://purl.obolibrary.org/obo/BTO_0001615
11997||4701||Rapid-onset childhood obesity - hypothalamic dysfunction - hypoventilation - autonomic dysregulation syndrome||http://www.orpha.net/ORDO/Orphanet_293987
11998||770||colorectal cancer cell line||http://purl.obolibrary.org/obo/BTO_0001616
11999||5502||Sphingomonas wittichii RW1||http://purl.obolibrary.org/obo/NCBITaxon_392499
12000||5502||Actinobacillus pleuropneumoniae serovar 1 str. 4074||http://purl.obolibrary.org/obo/NCBITaxon_228399
12001||10994||polysorbate 60||http://purl.obolibrary.org/obo/CHEBI_53425
12002||10994||polysorbate 20||http://purl.obolibrary.org/obo/CHEBI_53424
12003||4268||cellular response to abiotic stimulus||http://purl.obolibrary.org/obo/GO_0071214
12004||3485||left ventricle||http://purl.obolibrary.org/obo/BTO_0001629
12005||4122||Deficiency in anterior pituitary function-variable immunodeficiency syndrome||http://www.orpha.net/ORDO/Orphanet_293978
12006||1979||Bronchopulmonary dysplasia||http://www.orpha.net/ORDO/Orphanet_70589
12007||3854||Methanococcoides burtonii||http://purl.obolibrary.org/obo/NCBITaxon_29291
12008||770||BM1604||http://www.ebi.ac.uk/efo/EFO_0002117
12010||770||BHT101||http://www.ebi.ac.uk/efo/EFO_0002116
12009||5538||Rare genetic disorder with obstructive azoospermia||http://www.orpha.net/ORDO/Orphanet_400003
12011||770||BFTC905||http://www.ebi.ac.uk/efo/EFO_0002115
12012||770||BE2C_12012||http://www.ebi.ac.uk/efo/EFO_0002114
12015||2672||fundus of stomach||http://purl.obolibrary.org/obo/UBERON_0001160
12013||770||C32TG||http://www.ebi.ac.uk/efo/EFO_0002119
12014||4484||Rare genetic female infertility||http://www.orpha.net/ORDO/Orphanet_400008
12016||770||BV173||http://www.ebi.ac.uk/efo/EFO_0002118
12017||2672||pyloric antrum||http://purl.obolibrary.org/obo/UBERON_0001165
12018||770||BDCM||http://www.ebi.ac.uk/efo/EFO_0002113
12019||770||AsPC1||http://www.ebi.ac.uk/efo/EFO_0002112
12020||770||ARH77||http://www.ebi.ac.uk/efo/EFO_0002111
12021||770||AN3CA||http://www.ebi.ac.uk/efo/EFO_0002110
12022||770||A427||http://www.ebi.ac.uk/efo/EFO_0002104
12023||770||A375||http://www.ebi.ac.uk/efo/EFO_0002103
12024||770||A673||http://www.ebi.ac.uk/efo/EFO_0002106
12025||770||A498||http://www.ebi.ac.uk/efo/EFO_0002105
12026||770||ACHN||http://www.ebi.ac.uk/efo/EFO_0002108
12027||770||A7||http://www.ebi.ac.uk/efo/EFO_0002107
12028||12030||Rare female infertility due to adrenal disorder of genetic origin||http://www.orpha.net/ORDO/Orphanet_400018
12029||770||AGS||http://www.ebi.ac.uk/efo/EFO_0002109
12030||12014||Rare female infertility due to hypothalamic-pituitary-gonadal axis disorder of genetic origin||http://www.orpha.net/ORDO/Orphanet_400011
12031||770||A101D||http://www.ebi.ac.uk/efo/EFO_0002100
12032||770||A204||http://www.ebi.ac.uk/efo/EFO_0002102
12033||770||A172||http://www.ebi.ac.uk/efo/EFO_0002101
12034||770||GM13995||http://purl.obolibrary.org/obo/CLO_0033909
12035||3655||phyllid||http://www.ebi.ac.uk/efo/EFO_0001007
12036||3072||renal artery||http://purl.obolibrary.org/obo/UBERON_0001184
12037||2670||rhizome||http://www.ebi.ac.uk/efo/EFO_0001008
12039||10994||ivermectin||http://purl.obolibrary.org/obo/CHEBI_6078
12038||3645||apical root meristem||http://www.ebi.ac.uk/efo/EFO_0001009
12040||770||COLO704||http://www.ebi.ac.uk/efo/EFO_0002139
12041||3670||pollen tube||http://www.ebi.ac.uk/efo/EFO_0001004
12042||770||COLO668||http://www.ebi.ac.uk/efo/EFO_0002138
12043||3670||plant sperm||http://www.ebi.ac.uk/efo/EFO_0001005
12044||770||COLO320HSR||http://www.ebi.ac.uk/efo/EFO_0002137
12046||3670||thallus||http://www.ebi.ac.uk/efo/EFO_0001006
12045||770||COLO320DM||http://www.ebi.ac.uk/efo/EFO_0002136
12047||772||uterine smooth muscle cell||http://purl.obolibrary.org/obo/CL_0002601
12048||770||COLO201||http://www.ebi.ac.uk/efo/EFO_0002135
12049||770||CMLT1||http://www.ebi.ac.uk/efo/EFO_0002134
12050||770||CHP212||http://www.ebi.ac.uk/efo/EFO_0002133
12051||770||CHL1||http://www.ebi.ac.uk/efo/EFO_0002132
12052||770||CGTHW1||http://www.ebi.ac.uk/efo/EFO_0002131
12053||770||CESS||http://www.ebi.ac.uk/efo/EFO_0002130
12054||9288||hippocampal neuron||http://purl.obolibrary.org/obo/CL_0002608
12055||10652||obsolete_CEMC1||http://www.ebi.ac.uk/efo/EFO_0002129
12056||3370||blood serum||http://purl.obolibrary.org/obo/BTO_0000133
12057||770||CAL62||http://www.ebi.ac.uk/efo/EFO_0002126
12058||770||CAL54||http://www.ebi.ac.uk/efo/EFO_0002125
12059||770||CCRFCEM||http://www.ebi.ac.uk/efo/EFO_0002128
12061||770||CCFSTTG1||http://www.ebi.ac.uk/efo/EFO_0002127
12060||10994||atorvastatin||http://purl.obolibrary.org/obo/CHEBI_39548
12062||770||C4I||http://www.ebi.ac.uk/efo/EFO_0002122
12063||770||C3A||http://www.ebi.ac.uk/efo/EFO_0002121
12064||770||CA46||http://www.ebi.ac.uk/efo/EFO_0002124
12065||770||C4II||http://www.ebi.ac.uk/efo/EFO_0002123
12066||770||C33A||http://www.ebi.ac.uk/efo/EFO_0002120
12067||12629||microgram per milliliter||http://purl.obolibrary.org/obo/UO_0000274
12068||321||Hypotrichosis simplex||http://www.orpha.net/ORDO/Orphanet_55654
12069||12629||nanogram per milliliter||http://purl.obolibrary.org/obo/UO_0000275
12070||11067||milligram per liter||http://purl.obolibrary.org/obo/UO_0000273
12071||15129||adipocyte of breast||http://purl.obolibrary.org/obo/CL_0002617
12072||770||Calu6||http://www.ebi.ac.uk/efo/EFO_0002152
12073||770||Capan1||http://www.ebi.ac.uk/efo/EFO_0002153
12074||770||Caki2||http://www.ebi.ac.uk/efo/EFO_0002150
12075||770||Calu1||http://www.ebi.ac.uk/efo/EFO_0002151
12076||770||D283Med||http://www.ebi.ac.uk/efo/EFO_0002156
12077||770||D341Med||http://www.ebi.ac.uk/efo/EFO_0002157
12078||770||Capan2||http://www.ebi.ac.uk/efo/EFO_0002154
12080||2672||pectoral limb scapula||http://purl.obolibrary.org/obo/UBERON_0001124
12079||770||ChaGoK1||http://www.ebi.ac.uk/efo/EFO_0002155
12081||770||DB||http://www.ebi.ac.uk/efo/EFO_0002158
12082||770||DBTRG05MG||http://www.ebi.ac.uk/efo/EFO_0002159
12083||9857||Syndrome or malformation associated with head and neck malformations||http://www.orpha.net/ORDO/Orphanet_156237
12084||770||DG75||http://www.ebi.ac.uk/efo/EFO_0002160
12085||770||COLO829||http://www.ebi.ac.uk/efo/EFO_0002140
12086||770||CORL105||http://www.ebi.ac.uk/efo/EFO_0002141
12087||770||CORL23||http://www.ebi.ac.uk/efo/EFO_0002142
12088||770||CORL279||http://www.ebi.ac.uk/efo/EFO_0002143
12089||770||CORL88||http://www.ebi.ac.uk/efo/EFO_0002144
12090||770||CROAP2||http://www.ebi.ac.uk/efo/EFO_0002145
12092||2672||dorsum||http://purl.obolibrary.org/obo/UBERON_0001137
12091||770||CROAP5||http://www.ebi.ac.uk/efo/EFO_0002146
12093||770||CaHPV10||http://www.ebi.ac.uk/efo/EFO_0002147
12094||770||CaOv3||http://www.ebi.ac.uk/efo/EFO_0002148
12095||770||Caki1||http://www.ebi.ac.uk/efo/EFO_0002149
12096||5502||Bacteroides thetaiotaomicron VPI-5482||http://purl.obolibrary.org/obo/NCBITaxon_226186
12097||5502||Enterococcus faecalis V583||http://purl.obolibrary.org/obo/NCBITaxon_226185
12098||9857||Larynx anomaly||http://www.orpha.net/ORDO/Orphanet_156249
12099||5502||Neisseria meningitidis MC58||http://purl.obolibrary.org/obo/NCBITaxon_122586
12100||770||FaDu||http://www.ebi.ac.uk/efo/EFO_0002178
12101||770||G401||http://www.ebi.ac.uk/efo/EFO_0002179
12102||770||EM2||http://www.ebi.ac.uk/efo/EFO_0002176
12104||12030||Rare female infertility due to an anomaly of ovarian function of genetic origin||http://www.orpha.net/ORDO/Orphanet_400022
12103||770||ES2||http://www.ebi.ac.uk/efo/EFO_0002177
12105||770||EB3||http://www.ebi.ac.uk/efo/EFO_0002174
12106||770||EFM19||http://www.ebi.ac.uk/efo/EFO_0002175
12107||770||EB1||http://www.ebi.ac.uk/efo/EFO_0002172
12108||770||EB2||http://www.ebi.ac.uk/efo/EFO_0002173
12109||12014||Female infertility due to an implantation defect of genetic origin||http://www.orpha.net/ORDO/Orphanet_400025
12110||1022||Thalassiosira pseudonana||http://purl.obolibrary.org/obo/NCBITaxon_35128
12111||770||GCT||http://www.ebi.ac.uk/efo/EFO_0002182
12112||9857||Tracheal anomaly||http://www.orpha.net/ORDO/Orphanet_156252
12113||770||GA10||http://www.ebi.ac.uk/efo/EFO_0002181
12114||770||G402||http://www.ebi.ac.uk/efo/EFO_0002180
12117||10994||forskolin||http://purl.obolibrary.org/obo/CHEBI_42471
12116||2672||descending colon||http://purl.obolibrary.org/obo/UBERON_0001158
12115||770||DMS53||http://www.ebi.ac.uk/efo/EFO_0002165
12118||2672||transverse colon||http://purl.obolibrary.org/obo/UBERON_0001157
12119||770||DMS79||http://www.ebi.ac.uk/efo/EFO_0002166
12120||9923||host cell cytoplasm||http://purl.obolibrary.org/obo/GO_0030430
12122||770||DOHH2||http://www.ebi.ac.uk/efo/EFO_0002167
12121||5295||sleep||http://purl.obolibrary.org/obo/GO_0030431
12123||2672||sigmoid colon||http://purl.obolibrary.org/obo/UBERON_0001159
12124||770||DU4475||http://www.ebi.ac.uk/efo/EFO_0002168
12126||2672||vermiform appendix||http://purl.obolibrary.org/obo/UBERON_0001154
12125||770||DKMG||http://www.ebi.ac.uk/efo/EFO_0002161
12128||2672||caecum||http://purl.obolibrary.org/obo/UBERON_0001153
12127||770||DMS114||http://www.ebi.ac.uk/efo/EFO_0002162
12130||2672||ascending colon||http://purl.obolibrary.org/obo/UBERON_0001156
12129||770||DMS153||http://www.ebi.ac.uk/efo/EFO_0002163
12132||2672||colon||http://purl.obolibrary.org/obo/UBERON_0001155
12131||770||DMS273||http://www.ebi.ac.uk/efo/EFO_0002164
12133||770||Daudi||http://www.ebi.ac.uk/efo/EFO_0002169
12134||770||DoTc2||http://www.ebi.ac.uk/efo/EFO_0002171
12135||770||Detroit562||http://www.ebi.ac.uk/efo/EFO_0002170
12136||1006||lung carcinoma||http://www.ebi.ac.uk/efo/EFO_0001071
12137||12143||folate deficiency||http://www.ebi.ac.uk/efo/EFO_0001070
12138||4876||47,XYY syndrome||http://www.orpha.net/ORDO/Orphanet_8
12139||4898||Tetrasomy X||http://www.orpha.net/ORDO/Orphanet_9
12140||6306||Isolated 3-methylcrotonyl-CoA carboxylase deficiency||http://www.orpha.net/ORDO/Orphanet_6
12141||2252||3C syndrome||http://www.orpha.net/ORDO/Orphanet_7
12142||1211||Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency||http://www.orpha.net/ORDO/Orphanet_5
12143||1485||nutritional disorder||http://www.ebi.ac.uk/efo/EFO_0001069
12144||13448||pharyngeal pouch||http://purl.obolibrary.org/obo/UBERON_0004117
12145||2672||ventral tegmental area||http://purl.obolibrary.org/obo/UBERON_0002691
12147||3750||acetylcholinesterase inhibitor||http://purl.obolibrary.org/obo/CHEBI_38462
12146||9380||deafness||http://www.ebi.ac.uk/efo/EFO_0001063
12148||10652||obsolete_Down syndrome||http://www.ebi.ac.uk/efo/EFO_0001064
12149||1006||cervical carcinoma||http://www.ebi.ac.uk/efo/EFO_0001061
12150||2714||cytomegalovirus infection||http://www.ebi.ac.uk/efo/EFO_0001062
12151||5343||parasitic infection||http://www.ebi.ac.uk/efo/EFO_0001067
12152||12151||malaria||http://www.ebi.ac.uk/efo/EFO_0001068
12153||1761||endometriosis||http://www.ebi.ac.uk/efo/EFO_0001065
12154||14917||experimental autoimmune encephalomyelitis||http://www.ebi.ac.uk/efo/EFO_0001066
12155||2252||Intellectual disability - hypoplastic corpus callosum - preauricular tag||http://www.orpha.net/ORDO/Orphanet_1495
12157||2450||Corpus callosum agenesis - neuronopathy||http://www.orpha.net/ORDO/Orphanet_1496
12156||1403||celiac disease||http://www.ebi.ac.uk/efo/EFO_0001060
12158||7380||X-linked complicated corpus callosum dysgenesis||http://www.orpha.net/ORDO/Orphanet_1497
12159||5700||Corneal dystrophy - perceptive deafness||http://www.orpha.net/ORDO/Orphanet_1490
12160||238||Vici syndrome||http://www.orpha.net/ORDO/Orphanet_1493
12161||2165||sensory system disease||http://www.ebi.ac.uk/efo/EFO_0001058
12162||12161||cataract||http://www.ebi.ac.uk/efo/EFO_0001059
12163||10994||flavone||http://purl.obolibrary.org/obo/CHEBI_42491
12164||5502||Actinobacillus pleuropneumoniae serovar 2||http://purl.obolibrary.org/obo/NCBITaxon_34063
12165||2670||stamen||http://www.ebi.ac.uk/efo/EFO_0001050
12166||2670||carpel||http://www.ebi.ac.uk/efo/EFO_0001051
12167||2670||plant ovary||http://www.ebi.ac.uk/efo/EFO_0001052
12168||10994||acetonitrile||http://purl.obolibrary.org/obo/CHEBI_38472
12169||2670||stigma||http://www.ebi.ac.uk/efo/EFO_0001053
12171||2700||leprosy||http://www.ebi.ac.uk/efo/EFO_0001054
12170||1627||genitourinary system||http://purl.obolibrary.org/obo/UBERON_0004122
12172||12171||borderline leprosy||http://www.ebi.ac.uk/efo/EFO_0001055
12173||12171||tuberculoid leprosy||http://www.ebi.ac.uk/efo/EFO_0001056
12174||12171||lepromatous leprosy||http://www.ebi.ac.uk/efo/EFO_0001057
12175||10994||diltiazem||http://purl.obolibrary.org/obo/CHEBI_101278
12177||14963||Arthrogryposis - hyperkeratosis, lethal form||http://www.orpha.net/ORDO/Orphanet_1485
12176||770||BT474||http://www.ebi.ac.uk/efo/EFO_0001093
12178||5838||clinical modifier||http://purl.obolibrary.org/obo/HP_0012823
12180||770||BT20||http://www.ebi.ac.uk/efo/EFO_0001092
12179||6927||Lethal congenital contracture syndrome type 1||http://www.orpha.net/ORDO/Orphanet_1486
12181||770||BL41K3||http://www.ebi.ac.uk/efo/EFO_0001091
12182||770||BJABK3||http://www.ebi.ac.uk/efo/EFO_0001090
12183||306||Contractures - ectodermal dysplasia - cleft lip/palate||http://www.orpha.net/ORDO/Orphanet_1484
12184||307||Cooks syndrome||http://www.orpha.net/ORDO/Orphanet_1487
12185||12769||Cooper-Jabs syndrome||http://www.orpha.net/ORDO/Orphanet_1488
12186||6087||Ventricular septal defect||http://www.orpha.net/ORDO/Orphanet_1480
12187||5025||Saccharomyces bayanus x Saccharomyces cerevisiae||http://purl.obolibrary.org/obo/NCBITaxon_89981
12189||12463||acute inflammatory response||http://purl.obolibrary.org/obo/GO_0002526
12188||770||BEAS-2B||http://www.ebi.ac.uk/efo/EFO_0001089
12190||770||AU565||http://www.ebi.ac.uk/efo/EFO_0001087
12191||10652||obsolete_Beas2B||http://www.ebi.ac.uk/efo/EFO_0001088
12192||770||600MPE||http://www.ebi.ac.uk/efo/EFO_0001085
12193||5502||Salmonella enterica subsp. enterica serovar Choleraesuis||http://purl.obolibrary.org/obo/NCBITaxon_119912
12194||770||A549||http://www.ebi.ac.uk/efo/EFO_0001086
12195||770||293TsiLL||http://www.ebi.ac.uk/efo/EFO_0001083
12196||770||3T3-L1||http://www.ebi.ac.uk/efo/EFO_0001084
12197||770||267B1||http://www.ebi.ac.uk/efo/EFO_0001080
12198||2252||Uveal coloboma - cleft lip and palate - intellectual disability||http://www.orpha.net/ORDO/Orphanet_1473
12199||770||293T||http://www.ebi.ac.uk/efo/EFO_0001082
12200||1826||Curcuma longa||http://purl.obolibrary.org/obo/NCBITaxon_136217
12201||770||267B1 Ki-ras||http://www.ebi.ac.uk/efo/EFO_0001081
12202||6899||Renal coloboma syndrome||http://www.orpha.net/ORDO/Orphanet_1475
12203||6087||Interauricular communication||http://www.orpha.net/ORDO/Orphanet_1478
12204||15||Atrial septal defect - atrioventricular conduction defects||http://www.orpha.net/ORDO/Orphanet_1479
12205||9680||Coloboma of macula - brachydactyly type B||http://www.orpha.net/ORDO/Orphanet_1471
12206||2700||Pseudomonas infection||http://www.ebi.ac.uk/efo/EFO_0001076
12207||12206||Pseudomonas aeruginosa CF5 infection||http://www.ebi.ac.uk/efo/EFO_0001077
12208||12206||Pseudomonas aeruginosa PA14 infection||http://www.ebi.ac.uk/efo/EFO_0001078
12211||13448||heart tube||http://purl.obolibrary.org/obo/UBERON_0004141
12209||10251||mitochondrial NADH:ubiquinone reductase inhibitor||http://purl.obolibrary.org/obo/CHEBI_38498
12210||10652||obsolete_Rett syndrome||http://www.ebi.ac.uk/efo/EFO_0001079
12212||11618||memory impairment||http://www.ebi.ac.uk/efo/EFO_0001072
12213||12143||obesity||http://www.ebi.ac.uk/efo/EFO_0001073
12214||12213||morbid obesity||http://www.ebi.ac.uk/efo/EFO_0001074
12215||1006||ovarian carcinoma||http://www.ebi.ac.uk/efo/EFO_0001075
12216||8910||Isolated CoQ-cytochrome C reductase deficiency||http://www.orpha.net/ORDO/Orphanet_1460
12217||1022||Taeniopygia guttata||http://purl.obolibrary.org/obo/NCBITaxon_59729
12218||10153||COFS syndrome||http://www.orpha.net/ORDO/Orphanet_1466
12219||2021||Coffin-Siris syndrome||http://www.orpha.net/ORDO/Orphanet_1465
12220||3646||endosperm||http://www.ebi.ac.uk/efo/EFO_0001020
12221||2364||signal transduction by phosphorylation||http://purl.obolibrary.org/obo/GO_0023014
12223||13689||bulbus arteriosus||http://purl.obolibrary.org/obo/UBERON_0004152
12222||3654||flower structure||http://www.ebi.ac.uk/efo/EFO_0001024
12224||3654||bud||http://www.ebi.ac.uk/efo/EFO_0001023
12225||3654||cotyledon||http://www.ebi.ac.uk/efo/EFO_0001022
12226||3646||seed coat||http://www.ebi.ac.uk/efo/EFO_0001021
12227||3654||fruit||http://www.ebi.ac.uk/efo/EFO_0001028
12228||3654||tepal||http://www.ebi.ac.uk/efo/EFO_0001027
12229||3654||sepal||http://www.ebi.ac.uk/efo/EFO_0001026
12230||3654||petal||http://www.ebi.ac.uk/efo/EFO_0001025
12231||6306||3-methylglutaconic aciduria||http://www.orpha.net/ORDO/Orphanet_289902
12232||3654||inflorescence||http://www.ebi.ac.uk/efo/EFO_0001029
12233||1022||Plasmodium falciparum 3D7||http://purl.obolibrary.org/obo/NCBITaxon_36329
12234||1721||Joubert syndrome with hepatic defect||http://www.orpha.net/ORDO/Orphanet_1454
12235||41||CINCA syndrome||http://www.orpha.net/ORDO/Orphanet_1451
12236||2405||Ring chromosome 8||http://www.orpha.net/ORDO/Orphanet_1450
12237||7989||Cleidorhizomelic syndrome||http://www.orpha.net/ORDO/Orphanet_1453
12238||4766||Cleidocranial dysplasia||http://www.orpha.net/ORDO/Orphanet_1452
12239||12769||CODAS syndrome||http://www.orpha.net/ORDO/Orphanet_1458
12240||2670||taproot||http://www.ebi.ac.uk/efo/EFO_0001011
12241||3645||lateral root meristem||http://www.ebi.ac.uk/efo/EFO_0001010
12242||2670||root nodule||http://www.ebi.ac.uk/efo/EFO_0001013
12243||2670||root hair||http://www.ebi.ac.uk/efo/EFO_0001012
12244||2670||tuber||http://www.ebi.ac.uk/efo/EFO_0001015
12245||13701||root cap||http://www.ebi.ac.uk/efo/EFO_0001014
12246||3645||apical shoot meristem||http://www.ebi.ac.uk/efo/EFO_0001017
12247||2672||orbitofrontal cortex||http://purl.obolibrary.org/obo/UBERON_0004167
12248||3645||cambium||http://www.ebi.ac.uk/efo/EFO_0001016
12249||3645||radicle||http://www.ebi.ac.uk/efo/EFO_0001019
12250||3645||lateral shoot meristem||http://www.ebi.ac.uk/efo/EFO_0001018
12251||2405||Ring chromosome 18||http://www.orpha.net/ORDO/Orphanet_1442
12252||2405||Ring chromosome 17||http://www.orpha.net/ORDO/Orphanet_1441
12253||2681||Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency||http://www.orpha.net/ORDO/Orphanet_91135
12255||2405||Ring chromosome 14||http://www.orpha.net/ORDO/Orphanet_1440
12254||1826||Brachypodium distachyon||http://purl.obolibrary.org/obo/NCBITaxon_15368
12256||2405||Ring chromosome 22||http://www.orpha.net/ORDO/Orphanet_1446
12257||2405||Ring chromosome 21||http://www.orpha.net/ORDO/Orphanet_1445
12258||2405||Ring chromosome 20||http://www.orpha.net/ORDO/Orphanet_1444
12259||2405||Ring chromosome 19||http://www.orpha.net/ORDO/Orphanet_1443
12260||3656||nectar||http://www.ebi.ac.uk/efo/EFO_0001046
12262||2405||Ring chromosome 7||http://www.orpha.net/ORDO/Orphanet_1449
12261||1826||Rosa lucieae||http://purl.obolibrary.org/obo/NCBITaxon_74648
12263||3656||apoplasm||http://www.ebi.ac.uk/efo/EFO_0001045
12264||1826||Rosa chinensis||http://purl.obolibrary.org/obo/NCBITaxon_74649
12266||3654||phloem||http://www.ebi.ac.uk/efo/EFO_0001044
12265||2405||Ring chromosome 4||http://www.orpha.net/ORDO/Orphanet_1447
12269||12271||wood parenchyma||http://www.ebi.ac.uk/efo/EFO_0001043
12267||2405||Ring chromosome 6||http://www.orpha.net/ORDO/Orphanet_1448
12268||5502||Streptomyces bikiniensis||http://purl.obolibrary.org/obo/NCBITaxon_1896
12271||3654||xylem||http://www.ebi.ac.uk/efo/EFO_0001042
12270||321||Ichthyosis-hypotrichosis syndrome||http://www.orpha.net/ORDO/Orphanet_91132
12274||3654||bark||http://www.ebi.ac.uk/efo/EFO_0001041
12272||2252||Osteopenia - myopia - hearing loss - intellectual disability - facial dysmorphism||http://www.orpha.net/ORDO/Orphanet_91133
12273||5502||Streptomyces aureofaciens||http://purl.obolibrary.org/obo/NCBITaxon_1894
12276||4224||Cardiomyopathy - hypotonia - lactic acidosis||http://www.orpha.net/ORDO/Orphanet_91130
12275||3654||stem||http://www.ebi.ac.uk/efo/EFO_0001040
12277||7086||DK1-CDG||http://www.orpha.net/ORDO/Orphanet_91131
12278||3649||corm||http://www.ebi.ac.uk/efo/EFO_0001049
12279||3649||bulb||http://www.ebi.ac.uk/efo/EFO_0001048
12280||5025||Saccharomyces mikatae IFO 1815||http://purl.obolibrary.org/obo/NCBITaxon_226126
12281||3656||sap||http://www.ebi.ac.uk/efo/EFO_0001047
12282||5025||Saccharomyces bayanus MCYC 623||http://purl.obolibrary.org/obo/NCBITaxon_226127
12283||5025||Saccharomyces paradoxus NRRL Y-17217||http://purl.obolibrary.org/obo/NCBITaxon_226125
12284||1826||Eucalyptus grandis x Eucalyptus urophylla||http://purl.obolibrary.org/obo/NCBITaxon_192399
12285||5005||artificial sequences||http://purl.obolibrary.org/obo/NCBITaxon_81077
12286||914||Paroxysmal dyskinesia||http://www.orpha.net/ORDO/Orphanet_1431
12287||5502||Streptomyces antibioticus||http://purl.obolibrary.org/obo/NCBITaxon_1890
12288||306||Choroidal atrophy - alopecia||http://www.orpha.net/ORDO/Orphanet_1433
12289||802||Constitutional megaloblastic anemia due to vitamin B12 metabolism disorder||http://www.orpha.net/ORDO/Orphanet_98396
12290||4701||Choroideremia - deafness - obesity||http://www.orpha.net/ORDO/Orphanet_1435
12291||9677||Choroideremia - hypopituitarism||http://www.orpha.net/ORDO/Orphanet_1434
12293||13883||translation profiling||http://www.ebi.ac.uk/efo/EFO_0001033
12292||7984||Skeletal dysplasia - intellectual disability||http://www.orpha.net/ORDO/Orphanet_1436
12296||13883||transcription profiling||http://www.ebi.ac.uk/efo/EFO_0001032
12295||2405||Ring chromosome 1||http://www.orpha.net/ORDO/Orphanet_1437
12294||1826||Bromus inermis||http://purl.obolibrary.org/obo/NCBITaxon_15371
12297||12232||female inflorescence||http://www.ebi.ac.uk/efo/EFO_0001035
12298||2405||Ring chromosome 10||http://www.orpha.net/ORDO/Orphanet_1438
12299||5502||Crocosphaera watsonii WH 8501||http://purl.obolibrary.org/obo/NCBITaxon_165597
12300||12232||male inflorescence||http://www.ebi.ac.uk/efo/EFO_0001034
12301||2405||Ring chromosome 12||http://www.orpha.net/ORDO/Orphanet_1439
12302||13883||tiling path by array||http://www.ebi.ac.uk/efo/EFO_0001031
12303||9616||RNAi profiling by array||http://www.ebi.ac.uk/efo/EFO_0001030
12304||1826||Rosa gallica||http://purl.obolibrary.org/obo/NCBITaxon_74632
12305||3648||leaf vascular tissue||http://www.ebi.ac.uk/efo/EFO_0001037
12307||2448||Vitamin B12-unresponsive methylmalonic acidemia type mut0||http://www.orpha.net/ORDO/Orphanet_289916
12306||10652||obsolete_phyllid||http://www.ebi.ac.uk/efo/EFO_0001036
12308||3654||seedhead||http://www.ebi.ac.uk/efo/EFO_0001039
12309||3654||stomatal complex||http://www.ebi.ac.uk/efo/EFO_0001038
12310||1022||Scylla paramamosain||http://purl.obolibrary.org/obo/NCBITaxon_85552
12312||1022||Apis mellifera ligustica||http://purl.obolibrary.org/obo/NCBITaxon_7469
12311||5502||Streptomyces turgidiscabies||http://purl.obolibrary.org/obo/NCBITaxon_85558
12313||10272||Familial mesial temporal lobe epilepsy with febrile seizures||http://www.orpha.net/ORDO/Orphanet_165805
12314||770||GM08436||http://purl.obolibrary.org/obo/CLO_0010557
12315||13334||Autosomal recessive disease with focal palmoplantar keratoderma as a major feature||http://www.orpha.net/ORDO/Orphanet_98357
12316||13334||Autosomal dominant disease associated with focal palmoplantar keratoderma as a major feature||http://www.orpha.net/ORDO/Orphanet_98353
12317||10258||Autosomal recessive isolated diffuse palmoplantar keratoderma||http://www.orpha.net/ORDO/Orphanet_98356
12318||8997||Autosomal dominant disease with diffuse palmoplantar keratoderma as a major feature||http://www.orpha.net/ORDO/Orphanet_98352
12319||12460||response to osmotic stress||http://purl.obolibrary.org/obo/GO_0006970
12320||330||Hair defect - photosensitivity - intellectual disability||http://www.orpha.net/ORDO/Orphanet_1408
12321||330||Woolly hair - hypotrichosis - everted lower lip - outstanding ears||http://www.orpha.net/ORDO/Orphanet_1409
12322||5893||Genetic skeletal muscle disease||http://www.orpha.net/ORDO/Orphanet_206634
12323||3308||Charlie M syndrome||http://www.orpha.net/ORDO/Orphanet_1406
12324||13496||European bat lyssavirus 2||http://purl.obolibrary.org/obo/NCBITaxon_57483
12325||13496||European bat lyssavirus 1||http://purl.obolibrary.org/obo/NCBITaxon_57482
12326||4344||ALG11-CDG||http://www.orpha.net/ORDO/Orphanet_280071
12327||4624||Rare constitutional hemolytic anemia due to an enzyme disorder||http://www.orpha.net/ORDO/Orphanet_98369
12328||12330||Constitutional hemolytic anemia due to acanthocytosis||http://www.orpha.net/ORDO/Orphanet_98366
12329||12330||Hereditary stomatocytosis||http://www.orpha.net/ORDO/Orphanet_98365
12330||4624||Rare constitutional hemolytic anemia due to a red cell membrane anomaly||http://www.orpha.net/ORDO/Orphanet_98364
12331||5129||Constitutional sideroblastic anemia||http://www.orpha.net/ORDO/Orphanet_98362
12332||802||Constitutional anemia due to iron metabolism disorder||http://www.orpha.net/ORDO/Orphanet_98360
12333||5295||platelet aggregation||http://purl.obolibrary.org/obo/GO_0070527
12334||12335||Myotonic dystrophy||http://www.orpha.net/ORDO/Orphanet_206647
12335||11864||Progressive muscular dystrophy||http://www.orpha.net/ORDO/Orphanet_206644
12336||5478||Cholestasis-lymphedema syndrome||http://www.orpha.net/ORDO/Orphanet_1414
12337||9965||Pigmented paravenous retinochoroidal atrophy||http://www.orpha.net/ORDO/Orphanet_251295
12338||259||organelle organization||http://purl.obolibrary.org/obo/GO_0006996
12339||770||BA/F3 cell||http://purl.obolibrary.org/obo/BTO_0001516
12340||770||B-lymphoma cell line||http://purl.obolibrary.org/obo/BTO_0001518
12341||12327||Hemolytic anemia due to hexose monophosphate shunt and glutathione metabolism anomalies||http://www.orpha.net/ORDO/Orphanet_98370
12343||12327||Hemolytic anemia due to a disorder of glycolytic enzymes||http://www.orpha.net/ORDO/Orphanet_98372
12344||7953||Tarsal-carpal coalition syndrome||http://www.orpha.net/ORDO/Orphanet_1412
12342||7961||Parietal foramina with cleidocranial dysplasia||http://www.orpha.net/ORDO/Orphanet_251290
12346||12327||Hemolytic anemia due to an erythrocyte nucleotide metabolism disorder||http://www.orpha.net/ORDO/Orphanet_98374
12345||323||Uncombable hair syndrome||http://www.orpha.net/ORDO/Orphanet_1410
12347||6287||Greenberg dysplasia||http://www.orpha.net/ORDO/Orphanet_1426
12348||12322||Non-dystrophic myopathy||http://www.orpha.net/ORDO/Orphanet_206656
12350||2672||epithelium of pancreatic duct||http://purl.obolibrary.org/obo/UBERON_0009970
12349||5306||Desbuquois syndrome||http://www.orpha.net/ORDO/Orphanet_1425
12351||7955||Familial chondromalacia patellae||http://www.orpha.net/ORDO/Orphanet_1428
12352||7971||Otospondylomegaepiphyseal dysplasia||http://www.orpha.net/ORDO/Orphanet_1427
12353||2313||Non-dystrophic myopathy with collagen 6 anomaly||http://www.orpha.net/ORDO/Orphanet_206659
12354||7918||Benign familial chorea||http://www.orpha.net/ORDO/Orphanet_1429
12355||770||GM08388||http://purl.obolibrary.org/obo/CLO_0010521
12356||2187||rhombomere 7||http://purl.obolibrary.org/obo/UBERON_0005523
12357||770||GM08390||http://purl.obolibrary.org/obo/CLO_0010523
12358||8902||Autosomal dominant distal myopathy||http://www.orpha.net/ORDO/Orphanet_206650
12359||2187||rhombomere 8||http://purl.obolibrary.org/obo/UBERON_0005527
12360||8902||Autosomal recessive distal myopathy||http://www.orpha.net/ORDO/Orphanet_206653
12362||2187||rhombomere 6||http://purl.obolibrary.org/obo/UBERON_0005519
12361||6036||cytoskeleton||http://purl.obolibrary.org/obo/GO_0005856
12363||770||GM08398||http://purl.obolibrary.org/obo/CLO_0010526
12364||2672||entorhinal area||http://purl.obolibrary.org/obo/UBERON_0002728
12365||8026||Lethal chondrodysplasia, Moerman type||http://www.orpha.net/ORDO/Orphanet_1420
12366||8026||Lethal chondrodysplasia, Seller type||http://www.orpha.net/ORDO/Orphanet_1421
12367||1232||Chondrodysplasia - disorder of sex development||http://www.orpha.net/ORDO/Orphanet_1422
12368||8026||Lethal recessive chondrodysplasia||http://www.orpha.net/ORDO/Orphanet_1423
12370||11914||response to camptothecin||http://purl.obolibrary.org/obo/GO_1901563
12369||5967||Oligodontia - cancer predisposition syndrome||http://www.orpha.net/ORDO/Orphanet_300576
12371||2740||organonitrogen compound metabolic process||http://purl.obolibrary.org/obo/GO_1901564
12372||12348||Inclusion myopathy||http://www.orpha.net/ORDO/Orphanet_206662
12374||3035||Polymicrogyria due to TUBB2B mutation||http://www.orpha.net/ORDO/Orphanet_300573
12373||2187||rhombomere 5||http://purl.obolibrary.org/obo/UBERON_0005515
12375||798||Microphthalmia - retinitis pigmentosa - foveoschisis - optic disc drusen||http://www.orpha.net/ORDO/Orphanet_251279
12376||12371||organonitrogen compound biosynthetic process||http://purl.obolibrary.org/obo/GO_1901566
12377||2187||rhombomere 4||http://purl.obolibrary.org/obo/UBERON_0005511
12378||15571||Other metabolic disease||http://www.orpha.net/ORDO/Orphanet_91088
12379||1902||Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation||http://www.orpha.net/ORDO/Orphanet_300570
12380||1140||Male infertility due to gonadal dysgenesis||http://www.orpha.net/ORDO/Orphanet_98313
12381||11042||Potocki-Shaffer syndrome||http://www.orpha.net/ORDO/Orphanet_52022
12382||2187||rhombomere 3||http://purl.obolibrary.org/obo/UBERON_0005507
12383||6035||cis-Golgi network||http://purl.obolibrary.org/obo/GO_0005801
12385||1826||Zinnia violacea||http://purl.obolibrary.org/obo/NCBITaxon_34245
12384||451||Familial hyperaldosteronism type III||http://www.orpha.net/ORDO/Orphanet_251274
12386||1022||Gyps||http://purl.obolibrary.org/obo/NCBITaxon_8965
12387||7132||organic substance biosynthetic process||http://purl.obolibrary.org/obo/GO_1901576
12388||13691||neurogenic placode||http://purl.obolibrary.org/obo/UBERON_0009955
12389||8191||strontium chloride||http://purl.obolibrary.org/obo/CHEBI_36383
12390||9675||Benign concentric annular macular dystrophy||http://www.orpha.net/ORDO/Orphanet_251287
12391||10723||Autosomal dominant spastic ataxia type 1||http://www.orpha.net/ORDO/Orphanet_251282
12392||2672||phlegm||http://purl.obolibrary.org/obo/UBERON_0016552
12393||1560||cytosol||http://purl.obolibrary.org/obo/GO_0005829
12394||843||Dystonia 16||http://www.orpha.net/ORDO/Orphanet_210571
12395||12769||Braddock syndrome||http://www.orpha.net/ORDO/Orphanet_52047
12396||1526||spindle||http://purl.obolibrary.org/obo/GO_0005819
12397||10994||alpha-amanitin||http://purl.obolibrary.org/obo/CHEBI_37415
12398||2672||middle temporal gyrus||http://purl.obolibrary.org/obo/UBERON_0002771
12399||2672||superior temporal gyrus||http://purl.obolibrary.org/obo/UBERON_0002769
12400||3536||Familial osteochondritis dissecans||http://www.orpha.net/ORDO/Orphanet_251262
12401||10258||Autosomal dominant isolated diffuse palmoplantar keratoderma||http://www.orpha.net/ORDO/Orphanet_98349
12402||13496||Omsk hemorrhagic fever virus||http://purl.obolibrary.org/obo/NCBITaxon_12542
12403||4832||Paralytic facial malformation||http://www.orpha.net/ORDO/Orphanet_156224
12404||10994||parthenolide||http://purl.obolibrary.org/obo/CHEBI_7939
12405||4264||Very long chain acyl-CoA dehydrogenase deficiency||http://www.orpha.net/ORDO/Orphanet_26793
12406||4907||Short chain acyl-CoA dehydrogenase deficiency||http://www.orpha.net/ORDO/Orphanet_26792
12407||4264||Multiple acyl-CoA dehydrogenase deficiency||http://www.orpha.net/ORDO/Orphanet_26791
12408||2672||nephron tubule||http://purl.obolibrary.org/obo/UBERON_0001231
12409||2672||adrenal medulla||http://purl.obolibrary.org/obo/UBERON_0001236
12410||10994||paroxetine||http://purl.obolibrary.org/obo/CHEBI_7936
12411||2672||adrenal cortex||http://purl.obolibrary.org/obo/UBERON_0001235
12412||8713||Pseudohypoaldosteronism type 2E||http://www.orpha.net/ORDO/Orphanet_300530
12413||4344||DDOST-CDG||http://www.orpha.net/ORDO/Orphanet_300536
12414||12419||cells per milliliter||http://purl.obolibrary.org/obo/UO_0000201
12415||914||Paroxysmal dystonic choreathetosis with episodic ataxia and spasticity||http://www.orpha.net/ORDO/Orphanet_53583
12416||13496||Bluetongue virus 2||http://purl.obolibrary.org/obo/NCBITaxon_35328
12417||6373||Turner syndrome due to structural X chromosome anomalies||http://www.orpha.net/ORDO/Orphanet_99413
12419||11067||cell concentration unit||http://purl.obolibrary.org/obo/UO_0000200
12418||4832||Hypoglossia/aglossia||http://www.orpha.net/ORDO/Orphanet_156212
12420||12418||Oromandibular-limb anomalies syndrome||http://www.orpha.net/ORDO/Orphanet_156215
12421||13496||Mokola virus||http://purl.obolibrary.org/obo/NCBITaxon_12538
12423||3640||posterior lateral plate mesoderm||http://purl.obolibrary.org/obo/UBERON_0009910
12422||5037||Autosomal recessive infantile hypercalcemia||http://www.orpha.net/ORDO/Orphanet_300547
12424||13661||Otomandibular dysplasia associated with monogenic syndromes||http://www.orpha.net/ORDO/Orphanet_156202
12425||8193||D-penicillamine||http://purl.obolibrary.org/obo/CHEBI_7959
12426||1022||Protomelas similis||http://purl.obolibrary.org/obo/NCBITaxon_29149
12427||2672||Peyer s patch||http://purl.obolibrary.org/obo/UBERON_0001211
12428||8718||Complete androgen insensitivity syndrome||http://www.orpha.net/ORDO/Orphanet_99429
12429||1826||Euphorbia pulcherrima||http://purl.obolibrary.org/obo/NCBITaxon_37495
12431||4832||Macroglossia||http://www.orpha.net/ORDO/Orphanet_156207
12430||5785||apoptotic process||http://purl.obolibrary.org/obo/GO_0006915
12432||6250||Genetic lipodystrophy||http://www.orpha.net/ORDO/Orphanet_98305
12433||15363||Genetic tumor of hematopoietic and lymphoid tissues||http://www.orpha.net/ORDO/Orphanet_322126
12434||1022||Mytilus galloprovincialis||http://purl.obolibrary.org/obo/NCBITaxon_29158
12435||1022||Crassostrea gigas||http://purl.obolibrary.org/obo/NCBITaxon_29159
12436||4259||response to ribavirin||http://purl.obolibrary.org/obo/GO_1901559
12437||4259||response to metformin||http://purl.obolibrary.org/obo/GO_1901558
12439||12432||Familial partial lipodystrophy||http://www.orpha.net/ORDO/Orphanet_98306
12438||4259||response to fenofibrate||http://purl.obolibrary.org/obo/GO_1901557
12440||4259||response to candesartan||http://purl.obolibrary.org/obo/GO_1901556
12441||8713||Pseudohypoaldosteronism type 2D||http://www.orpha.net/ORDO/Orphanet_300525
12442||4188||response to paclitaxel||http://purl.obolibrary.org/obo/GO_1901555
12443||4259||response to acetaminophen||http://purl.obolibrary.org/obo/GO_1901554
12444||8190||flufenamic acid||http://purl.obolibrary.org/obo/CHEBI_42638
12445||1491||plasma membrane||http://purl.obolibrary.org/obo/GO_0005886
12446||1022||Nasonia vitripennis||http://purl.obolibrary.org/obo/NCBITaxon_7425
12447||770||ESHyb||http://www.ebi.ac.uk/efo/EFO_0003972
12448||770||MEL cell line||http://www.ebi.ac.uk/efo/EFO_0003971
12449||772||mouse erythroleukemia cell||http://www.ebi.ac.uk/efo/EFO_0003970
12450||2672||post-hyoid pharyngeal arch||http://purl.obolibrary.org/obo/UBERON_0008896
12451||2672||precentral gyrus||http://purl.obolibrary.org/obo/UBERON_0002703
12452||5502||Pasteurella multocida subsp. multocida str. Pm70||http://purl.obolibrary.org/obo/NCBITaxon_272843
12453||9803||pathogenicity||http://purl.obolibrary.org/obo/IDO_0000450
12454||9681||Goldmann-Favre syndrome||http://www.orpha.net/ORDO/Orphanet_53540
12455||13448||rhombomere 8 floor plate||http://purl.obolibrary.org/obo/UBERON_0005588
12456||13448||rhombomere 6 floor plate||http://purl.obolibrary.org/obo/UBERON_0005582
12457||13448||rhombomere 7 floor plate||http://purl.obolibrary.org/obo/UBERON_0005585
12458||11868||normalization data transformation||http://purl.obolibrary.org/obo/OBI_0200169
12459||1022||Neospora caninum||http://purl.obolibrary.org/obo/NCBITaxon_29176
12460||6476||response to stress||http://purl.obolibrary.org/obo/GO_0006950
12461||1732||Rare genetic hematologic disease||http://www.orpha.net/ORDO/Orphanet_158300
12462||1732||cleft lip||http://www.ebi.ac.uk/efo/EFO_0003959
12463||6476||inflammatory response||http://purl.obolibrary.org/obo/GO_0006954
12464||10652||obsolete_Treacher-Collins syndrome||http://www.ebi.ac.uk/efo/EFO_0003954
12465||14780||circumcision||http://www.ebi.ac.uk/efo/EFO_0003953
12467||13448||rhombomere 4 floor plate||http://purl.obolibrary.org/obo/UBERON_0005576
12466||11618||fever of unknown origin||http://www.ebi.ac.uk/efo/EFO_0003952
12468||14780||percutaneous transluminal coronary angioplasty||http://www.ebi.ac.uk/efo/EFO_0003951
12469||7944||Episodic ataxia type 1||http://www.orpha.net/ORDO/Orphanet_37612
12471||11067||milliliter per liter||http://purl.obolibrary.org/obo/UO_0000207
12470||2866||sunburn||http://www.ebi.ac.uk/efo/EFO_0003958
12472||12527||radius fracture||http://www.ebi.ac.uk/efo/EFO_0003957
12473||11563||seasonal allergic rhinitis||http://www.ebi.ac.uk/efo/EFO_0003956
12474||11352||deciliter||http://purl.obolibrary.org/obo/UO_0000209
12475||13448||rhombomere 5 floor plate||http://purl.obolibrary.org/obo/UBERON_0005579
12476||2700||bacterial sexually transmitted disease||http://www.ebi.ac.uk/efo/EFO_0003955
12477||13448||rhombomere 2 floor plate||http://purl.obolibrary.org/obo/UBERON_0005570
12478||10994||carboplatin||http://purl.obolibrary.org/obo/CHEBI_31355
12479||12527||ulna fracture||http://www.ebi.ac.uk/efo/EFO_0003950
12480||13448||rhombomere 3 floor plate||http://purl.obolibrary.org/obo/UBERON_0005573
12481||1826||Citrus reticulata||http://purl.obolibrary.org/obo/NCBITaxon_85571
12482||5502||Porphyromonas gingivalis W83||http://purl.obolibrary.org/obo/NCBITaxon_242619
12484||13496||California encephalitis virus||http://purl.obolibrary.org/obo/NCBITaxon_35305
12483||1022||Apis dorsata||http://purl.obolibrary.org/obo/NCBITaxon_7462
12485||1022||Apis florea||http://purl.obolibrary.org/obo/NCBITaxon_7463
12486||1022||Apis mellifera||http://purl.obolibrary.org/obo/NCBITaxon_7460
12487||11505||dalton||http://purl.obolibrary.org/obo/UO_0000221
12488||1022||Apis cerana||http://purl.obolibrary.org/obo/NCBITaxon_7461
12489||11562||freckles||http://www.ebi.ac.uk/efo/EFO_0003963
12491||13689||gonad primordium||http://purl.obolibrary.org/obo/UBERON_0005564
12490||8602||pulsed doppler echocardiography||http://www.ebi.ac.uk/efo/EFO_0003962
12492||8647||very low birth weight infant||http://www.ebi.ac.uk/efo/EFO_0003965
12493||13448||rhombomere 1 floor plate||http://purl.obolibrary.org/obo/UBERON_0005566
12494||12527||hip fracture||http://www.ebi.ac.uk/efo/EFO_0003964
12496||2187||rhombomere 2||http://purl.obolibrary.org/obo/UBERON_0005569
12495||2002||vascular sarcoma||http://www.ebi.ac.uk/efo/EFO_0003967
12497||1391||eye disease||http://www.ebi.ac.uk/efo/EFO_0003966
12498||4335||treatment protocol||http://www.ebi.ac.uk/efo/EFO_0003969
12499||12495||angiosarcoma||http://www.ebi.ac.uk/efo/EFO_0003968
12501||3805||trigeminal neural crest||http://purl.obolibrary.org/obo/UBERON_0005563
12500||2822||hormone replacement therapy||http://www.ebi.ac.uk/efo/EFO_0003961
12503||14970||computed tomography||http://www.ebi.ac.uk/efo/EFO_0003960
12502||13689||thymus primordium||http://purl.obolibrary.org/obo/UBERON_0005562
12504||6573||organization role||http://www.ebi.ac.uk/efo/EFO_0002012
12505||14780||heterologous transplantation||http://www.ebi.ac.uk/efo/EFO_0003942
12506||12527||humerus fracture||http://www.ebi.ac.uk/efo/EFO_0003943
12507||5295||physical activity||http://www.ebi.ac.uk/efo/EFO_0003940
12508||3974||sex hormone-binding globulin||http://www.ebi.ac.uk/efo/EFO_0003941
12509||1814||Fuchs  endothelial dystrophy||http://www.ebi.ac.uk/efo/EFO_0003946
12510||5838||personality||http://www.ebi.ac.uk/efo/EFO_0003947
12512||12527||tibia fracture||http://www.ebi.ac.uk/efo/EFO_0003944
12511||6299||Oscheius dolichuroides||http://purl.obolibrary.org/obo/NCBITaxon_96645
12513||11618||menorrhagia||http://www.ebi.ac.uk/efo/EFO_0003945
12514||12632||mass percent||http://purl.obolibrary.org/obo/UO_0000163
12516||2063||eye color||http://www.ebi.ac.uk/efo/EFO_0003949
12515||6476||response to virus||http://purl.obolibrary.org/obo/GO_0009615
12517||12632||volume percent||http://purl.obolibrary.org/obo/UO_0000165
12519||770||A-549 cell||http://purl.obolibrary.org/obo/BTO_0000018
12518||1403||gastroesophageal reflux disease||http://www.ebi.ac.uk/efo/EFO_0003948
12520||12633||part per million||http://purl.obolibrary.org/obo/UO_0000169
12521||12560||microeinstein per square meter per second||http://purl.obolibrary.org/obo/UO_0000160
12522||10994||3-(5-fluorouracil-1-yl)-L-alanine||http://purl.obolibrary.org/obo/CHEBI_42549
12523||6476||response to wounding||http://purl.obolibrary.org/obo/GO_0009611
12524||770||fibroblast derived cell line||http://www.ebi.ac.uk/efo/EFO_0002009
12526||11618||menarche||http://www.ebi.ac.uk/efo/EFO_0003930
12525||770||AG11364||http://purl.obolibrary.org/obo/CLO_0021597
12527||15526||bone fracture||http://www.ebi.ac.uk/efo/EFO_0003931
12528||11199||derived time unit||http://purl.obolibrary.org/obo/UO_0000149
12529||2700||bacterial vaginosis||http://www.ebi.ac.uk/efo/EFO_0003932
12530||10652||obsolete_mitral valve||http://www.ebi.ac.uk/efo/EFO_0003933
12531||1403||fatty liver||http://www.ebi.ac.uk/efo/EFO_0003934
12532||9803||mental health||http://www.ebi.ac.uk/efo/EFO_0003935
12533||10652||obsolete_physiological process||http://www.ebi.ac.uk/efo/EFO_0003936
12534||1391||aphthous ulcer||http://www.ebi.ac.uk/efo/EFO_0003938
12535||770||HEK-293 cell||http://purl.obolibrary.org/obo/BTO_0000007
12536||5295||energy intake||http://www.ebi.ac.uk/efo/EFO_0003939
12537||5502||Agrobacterium tumefaciens str. C58||http://purl.obolibrary.org/obo/NCBITaxon_176299
12538||6476||response to abiotic stimulus||http://purl.obolibrary.org/obo/GO_0009628
12539||193||Severe congenital neutropenia||http://www.orpha.net/ORDO/Orphanet_42738
12540||9350||Familial medullary thyroid carcinoma||http://www.orpha.net/ORDO/Orphanet_99361
12541||12808||Abnormality of muscle physiology||http://purl.obolibrary.org/obo/HP_0011804
12542||2063||hair color||http://www.ebi.ac.uk/efo/EFO_0003924
12543||8698||cognition||http://www.ebi.ac.uk/efo/EFO_0003925
12544||11618||menopause||http://www.ebi.ac.uk/efo/EFO_0003922
12545||14970||bone density||http://www.ebi.ac.uk/efo/EFO_0003923
12546||1732||cleft palate||http://www.ebi.ac.uk/efo/EFO_0003920
12547||1403||pouchitis||http://www.ebi.ac.uk/efo/EFO_0003921
12548||12432||Lipoatrophy with diabetes, leukomelanodermic papules, liver steatosis, and hypertrophic cardiomyopathy||http://www.orpha.net/ORDO/Orphanet_156156
12549||10990||relapsing-remitting multiple sclerosis||http://www.ebi.ac.uk/efo/EFO_0003929
12550||1403||necrotizing enterocolitis||http://www.ebi.ac.uk/efo/EFO_0003928
12551||12594||myopia||http://www.ebi.ac.uk/efo/EFO_0003927
12552||14970||neuropsychological test||http://www.ebi.ac.uk/efo/EFO_0003926
12553||1302||Isolated dystonia||http://www.orpha.net/ORDO/Orphanet_156159
12554||2672||myometrium||http://purl.obolibrary.org/obo/UBERON_0001296
12555||4081||atrial flutter||http://www.ebi.ac.uk/efo/EFO_0003911
12556||14970||ankle brachial index||http://www.ebi.ac.uk/efo/EFO_0003912
12557||11618||angina pectoris||http://www.ebi.ac.uk/efo/EFO_0003913
12558||1015||atherosclerosis||http://www.ebi.ac.uk/efo/EFO_0003914
12559||12560||absorbed dose unit||http://purl.obolibrary.org/obo/UO_0000129
12560||11199||radiation unit||http://purl.obolibrary.org/obo/UO_0000127
12563||11199||derived temperature unit||http://purl.obolibrary.org/obo/UO_0000126
12561||2672||endometrium||http://purl.obolibrary.org/obo/UBERON_0001295
12562||10652||obsolete_von Willebrand disease||http://www.ebi.ac.uk/efo/EFO_0003910
12564||12560||rad||http://purl.obolibrary.org/obo/UO_0000135
12565||9803||risk factor||http://www.ebi.ac.uk/efo/EFO_0003919
12566||12559||Gray||http://purl.obolibrary.org/obo/UO_0000134
12567||10652||obsolete_cerebral arteriovenous malformation||http://www.ebi.ac.uk/efo/EFO_0003916
12568||10652||obsolete_congenital abnormality||http://www.ebi.ac.uk/efo/EFO_0003915
12569||10977||obstructive sleep apnea||http://www.ebi.ac.uk/efo/EFO_0003918
12570||2063||premature birth||http://www.ebi.ac.uk/efo/EFO_0003917
12571||10652||obsolete_Wiskott-Aldrich syndrome||http://www.ebi.ac.uk/efo/EFO_0003903
12573||12527||spinal fracture||http://www.ebi.ac.uk/efo/EFO_0003902
12572||770||AG11498||http://purl.obolibrary.org/obo/CLO_0021565
12574||11618||dysuria||http://www.ebi.ac.uk/efo/EFO_0003901
12575||770||HT1080||http://www.ebi.ac.uk/efo/EFO_0002059
12576||1732||ciliopathy||http://www.ebi.ac.uk/efo/EFO_0003900
12577||770||HCC1008||http://www.ebi.ac.uk/efo/EFO_0002057
12578||10652||obsolete_HL60||http://www.ebi.ac.uk/efo/EFO_0002058
12579||12628||G1E-ER4||http://www.ebi.ac.uk/efo/EFO_0002055
12580||770||HaCaT||http://www.ebi.ac.uk/efo/EFO_0002056
12581||770||F9 mouse embryonal carcinoma cell line||http://www.ebi.ac.uk/efo/EFO_0002053
12583||770||Fu97||http://www.ebi.ac.uk/efo/EFO_0002054
12582||8193||4-hydroxyphenyl retinamide||http://purl.obolibrary.org/obo/CHEBI_42588
12586||2672||pancreas||http://purl.obolibrary.org/obo/UBERON_0001264
12585||770||D4 glioblastoma derived primary cell line||http://www.ebi.ac.uk/efo/EFO_0002051
12584||5025||Saccharomyces kudriavzevii||http://purl.obolibrary.org/obo/NCBITaxon_114524
12588||770||EcR-RKO/KLF4||http://www.ebi.ac.uk/efo/EFO_0002052
12587||5025||Saccharomyces mikatae||http://purl.obolibrary.org/obo/NCBITaxon_114525
12589||770||ITM||http://www.ebi.ac.uk/efo/EFO_0002061
12590||770||IBL4||http://www.ebi.ac.uk/efo/EFO_0002060
12591||14780||heart valve prosthesis||http://www.ebi.ac.uk/efo/EFO_0003906
12592||11014||deep vein thrombosis||http://www.ebi.ac.uk/efo/EFO_0003907
12593||10652||obsolete_venous thrombosis||http://www.ebi.ac.uk/efo/EFO_0003905
12594||1814||refractive error||http://www.ebi.ac.uk/efo/EFO_0003908
12595||14877||heart conduction system||http://www.ebi.ac.uk/efo/EFO_0003909
12596||2672||ilium||http://purl.obolibrary.org/obo/UBERON_0001273
12597||770||BCBL-1||http://www.ebi.ac.uk/efo/EFO_0002048
12598||770||BCKN-1||http://www.ebi.ac.uk/efo/EFO_0002049
12599||770||BC-1||http://www.ebi.ac.uk/efo/EFO_0002044
12600||770||BC-2||http://www.ebi.ac.uk/efo/EFO_0002045
12601||770||BC-3||http://www.ebi.ac.uk/efo/EFO_0002046
12602||770||BC-5||http://www.ebi.ac.uk/efo/EFO_0002047
12603||12625||B117H||http://www.ebi.ac.uk/efo/EFO_0002040
12604||12627||B117P||http://www.ebi.ac.uk/efo/EFO_0002041
12605||12625||B140H||http://www.ebi.ac.uk/efo/EFO_0002042
12606||2672||intestinal epithelium||http://purl.obolibrary.org/obo/UBERON_0001277
12607||12627||B140P||http://www.ebi.ac.uk/efo/EFO_0002043
12608||11899||Cerebellum agenesis - hydrocephaly||http://www.orpha.net/ORDO/Orphanet_1397
12609||770||BeWo||http://www.ebi.ac.uk/efo/EFO_0002050
12610||7319||Cerebro-reno-digital syndrome||http://www.orpha.net/ORDO/Orphanet_1396
12612||12633||fraction||http://purl.obolibrary.org/obo/UO_0000191
12611||4692||Richards-Rundle syndrome||http://www.orpha.net/ORDO/Orphanet_1399
12614||12769||Night blindness - skeletal anomalies - dysmorphism||http://www.orpha.net/ORDO/Orphanet_1390
12613||11067||milliliter per kilogram||http://purl.obolibrary.org/obo/UO_0000198
12615||12563||degree fahrenheit||http://purl.obolibrary.org/obo/UO_0000195
12616||2252||Cerebro-facio-thoracic dysplasia||http://www.orpha.net/ORDO/Orphanet_1394
12617||7963||Cerebro-costo-mandibular syndrome||http://www.orpha.net/ORDO/Orphanet_1393
12618||770||67NR||http://www.ebi.ac.uk/efo/EFO_0002039
12619||770||4T1||http://www.ebi.ac.uk/efo/EFO_0002037
12620||770||66cl4||http://www.ebi.ac.uk/efo/EFO_0002038
12621||770||GM17164||http://purl.obolibrary.org/obo/CLO_0013994
12622||770||GM17165||http://purl.obolibrary.org/obo/CLO_0013993
12623||770||GM17163||http://purl.obolibrary.org/obo/CLO_0013996
12624||770||GM17166||http://purl.obolibrary.org/obo/CLO_0013990
12625||770||Ara-C-resistant murine leukemia||http://www.ebi.ac.uk/efo/EFO_0002032
12626||770||murine neuroblastoma cholinergic cell line||http://www.ebi.ac.uk/efo/EFO_0002035
12627||770||Ara-C-sensitive parental cell line||http://www.ebi.ac.uk/efo/EFO_0002033
12628||770||G1E||http://www.ebi.ac.uk/efo/EFO_0002034
12629||11199||density unit||http://purl.obolibrary.org/obo/UO_0000182
12630||10994||fisetin||http://purl.obolibrary.org/obo/CHEBI_42567
12631||10974||degree||http://purl.obolibrary.org/obo/UO_0000185
12632||12633||percent||http://purl.obolibrary.org/obo/UO_0000187
12633||11199||dimensionless unit||http://purl.obolibrary.org/obo/UO_0000186
12634||1783||microarray wash station||http://www.ebi.ac.uk/efo/EFO_0002028
12635||15538||software||http://www.ebi.ac.uk/efo/EFO_0002029
12636||2672||urinary bladder||http://purl.obolibrary.org/obo/UBERON_0001255
12637||5502||Parabacteroides||http://purl.obolibrary.org/obo/NCBITaxon_375288
12638||12633||part per billion||http://purl.obolibrary.org/obo/UO_0000170
12639||12633||unit per milliliter||http://purl.obolibrary.org/obo/UO_0000178
12640||12629||milligram per milliliter||http://purl.obolibrary.org/obo/UO_0000176
12641||11067||gram per liter||http://purl.obolibrary.org/obo/UO_0000175
12642||5502||Campylobacter jejuni subsp. jejuni NCTC 11168||http://purl.obolibrary.org/obo/NCBITaxon_192222
12643||6275||Carnosinemia||http://www.orpha.net/ORDO/Orphanet_1361
12644||772||vascular smooth muscle cell||http://purl.obolibrary.org/obo/BTO_0004578
12645||4692||Cataract - ataxia - deafness||http://www.orpha.net/ORDO/Orphanet_1368
12646||4191||Congenital cataract - hypertrophic cardiomyopathy - mitochondrial myopathy||http://www.orpha.net/ORDO/Orphanet_1369
12647||306||Autosomal recessive palmoplantar keratoderma and congenital alopecia||http://www.orpha.net/ORDO/Orphanet_1366
12648||15||Heart-hand syndrome type 2||http://www.orpha.net/ORDO/Orphanet_1350
12649||6899||Atrioventricular defect - blepharophimosis -radial defects||http://www.orpha.net/ORDO/Orphanet_1352
12650||15059||response to cisplatin||http://purl.obolibrary.org/obo/GO_0072718
12651||12769||Heart defects - limb shortening||http://www.orpha.net/ORDO/Orphanet_1354
12652||2252||Heart defect - round face - congenital developmental delay||http://www.orpha.net/ORDO/Orphanet_1355
12653||5300||Carey-Fineman-Ziter  syndrome||http://www.orpha.net/ORDO/Orphanet_1358
12654||2897||Carney complex||http://www.orpha.net/ORDO/Orphanet_1359
12655||770||GM17161||http://purl.obolibrary.org/obo/CLO_0013982
12656||770||GM17162||http://purl.obolibrary.org/obo/CLO_0013983
12657||770||GM17160||http://purl.obolibrary.org/obo/CLO_0013984
12658||13448||caudal ganglionic eminence||http://purl.obolibrary.org/obo/UBERON_0004026
12659||770||GM17168||http://purl.obolibrary.org/obo/CLO_0013987
12660||770||GM17167||http://purl.obolibrary.org/obo/CLO_0013989
12661||2252||Cataract - deafness - hypogonadism||http://www.orpha.net/ORDO/Orphanet_1383
12662||4139||Cataract - nephropathy - encephalopathy||http://www.orpha.net/ORDO/Orphanet_1380
12663||2252||Cataract - intellectual disability - anal atresia - urinary defects||http://www.orpha.net/ORDO/Orphanet_1381
12664||2252||Catel-Manzke syndrome||http://www.orpha.net/ORDO/Orphanet_1388
12665||2252||Cortical blindness - intellectual disability - polydactyly||http://www.orpha.net/ORDO/Orphanet_1389
12666||1306||Cataract - intellectual disability - hypogonadism||http://www.orpha.net/ORDO/Orphanet_1387
12667||770||GM17150||http://purl.obolibrary.org/obo/CLO_0013956
12668||7159||Hereditary hypophosphatemic rickets with hypercalciuria||http://www.orpha.net/ORDO/Orphanet_157215
12669||6897||Cataract-microcornea syndrome||http://www.orpha.net/ORDO/Orphanet_1377
12670||6899||Cataract - aberrant oral frenula - growth delay||http://www.orpha.net/ORDO/Orphanet_1373
12671||306||Cataract - hypertrichosis - intellectual disability||http://www.orpha.net/ORDO/Orphanet_1375
12672||6899||Congenital cataract - ichthyosis||http://www.orpha.net/ORDO/Orphanet_1376
12673||10994||fenazaquin||http://purl.obolibrary.org/obo/CHEBI_38593
12674||770||GM17159||http://purl.obolibrary.org/obo/CLO_0013964
12675||770||GM17158||http://purl.obolibrary.org/obo/CLO_0013965
12676||1022||Columba livia||http://purl.obolibrary.org/obo/NCBITaxon_8932
12677||770||GM17155||http://purl.obolibrary.org/obo/CLO_0013960
12678||770||GM17154||http://purl.obolibrary.org/obo/CLO_0013961
12679||770||GM17157||http://purl.obolibrary.org/obo/CLO_0013962
12680||770||GM17156||http://purl.obolibrary.org/obo/CLO_0013963
12681||6246||Camptodactyly - taurinuria||http://www.orpha.net/ORDO/Orphanet_1325
12682||770||GM17143||http://purl.obolibrary.org/obo/CLO_0013937
12683||770||GM17142||http://purl.obolibrary.org/obo/CLO_0013938
12684||770||GM17140||http://purl.obolibrary.org/obo/CLO_0013935
12685||770||GM17144||http://purl.obolibrary.org/obo/CLO_0013936
12686||770||GM17141||http://purl.obolibrary.org/obo/CLO_0013939
12687||1826||Aloe vera||http://purl.obolibrary.org/obo/NCBITaxon_34199
12688||7943||Camurati-Engelmann disease||http://www.orpha.net/ORDO/Orphanet_1328
12689||12769||Camptodactyly syndrome, Guadalajara type 2||http://www.orpha.net/ORDO/Orphanet_1326
12690||12769||Camptodactyly syndrome, Guadalajara type 1||http://www.orpha.net/ORDO/Orphanet_1327
12691||7947||Caffey disease||http://www.orpha.net/ORDO/Orphanet_1310
12692||770||GM17149||http://purl.obolibrary.org/obo/CLO_0013947
12693||770||GM17147||http://purl.obolibrary.org/obo/CLO_0013941
12694||770||GM17148||http://purl.obolibrary.org/obo/CLO_0013940
12695||770||GM17145||http://purl.obolibrary.org/obo/CLO_0013943
12696||770||GM17146||http://purl.obolibrary.org/obo/CLO_0013942
12697||5478||Campomelia, Cumming type||http://www.orpha.net/ORDO/Orphanet_1318
12698||2021||Camptobrachydactyly||http://www.orpha.net/ORDO/Orphanet_1319
12699||5961||PHACE syndrome||http://www.orpha.net/ORDO/Orphanet_42775
12700||5502||Xanthomonas oryzae pv. oryzicola BLS256||http://purl.obolibrary.org/obo/NCBITaxon_383407
12701||4951||Cardiomyopathy - cataract - hip spine disease||http://www.orpha.net/ORDO/Orphanet_1345
12702||15||Atrial stand still||http://www.orpha.net/ORDO/Orphanet_1344
12703||15||Heart-hand syndrome type 3||http://www.orpha.net/ORDO/Orphanet_1342
12704||306||Cardiofaciocutaneous syndrome||http://www.orpha.net/ORDO/Orphanet_1340
12705||770||GM11840||http://purl.obolibrary.org/obo/CLO_0020019
12707||10994||rosuvastatin||http://purl.obolibrary.org/obo/CHEBI_38545
12706||5502||Lactococcus lactis subsp. cremoris MG1363||http://purl.obolibrary.org/obo/NCBITaxon_416870
12708||5502||Prochlorococcus marinus str. MIT 9312||http://purl.obolibrary.org/obo/NCBITaxon_74546
12709||5502||Prochlorococcus marinus str. MIT 9313||http://purl.obolibrary.org/obo/NCBITaxon_74547
12710||4266||Maternally-inherited cardiomyopathy and hearing loss||http://www.orpha.net/ORDO/Orphanet_1349
12711||4994||Chronic mucocutaneous candidosis||http://www.orpha.net/ORDO/Orphanet_1334
12712||13920||Familial pancreatic carcinoma||http://www.orpha.net/ORDO/Orphanet_1333
12713||5004||Hyperkeratosis-hyperpigmentation syndrome||http://www.orpha.net/ORDO/Orphanet_1336
12714||12769||Cantrell pentalogy||http://www.orpha.net/ORDO/Orphanet_1335
12715||6912||Autosomal recessive axonal Charcot-Marie-Tooth disease type 2||http://www.orpha.net/ORDO/Orphanet_91024
12716||5975||Familial prostate cancer||http://www.orpha.net/ORDO/Orphanet_1331
12717||770||GM17219||http://purl.obolibrary.org/obo/CLO_0013924
12718||770||GM17218||http://purl.obolibrary.org/obo/CLO_0013921
12719||10994||cytochrome P450||http://purl.obolibrary.org/obo/CHEBI_38559
12721||13448||anterior lateral plate mesoderm||http://purl.obolibrary.org/obo/UBERON_0009881
12720||12769||Heart defect-tongue hamartoma-polysyndactyly syndrome||http://www.orpha.net/ORDO/Orphanet_1338
12722||4864||Chudley-Lowry-Hoar syndrome||http://www.orpha.net/ORDO/Orphanet_93971
12723||4864||Holmes-Gang syndrome||http://www.orpha.net/ORDO/Orphanet_93970
12724||3072||ductus arteriosus||http://purl.obolibrary.org/obo/UBERON_0005440
12725||7984||Autosomal recessive spondylometaphyseal dysplasia, M garban  type||http://www.orpha.net/ORDO/Orphanet_401979
12726||4803||Anotia||http://www.orpha.net/ORDO/Orphanet_93976
12727||10994||fulvestrant||http://purl.obolibrary.org/obo/CHEBI_31638
12729||1022||Cryptopygus antarcticus||http://purl.obolibrary.org/obo/NCBITaxon_187623
12728||4864||Juberg-Marsidi syndrome||http://www.orpha.net/ORDO/Orphanet_93972
12731||4139||MEND syndrome||http://www.orpha.net/ORDO/Orphanet_401973
12730||4864||Carpenter-Waziri syndrome||http://www.orpha.net/ORDO/Orphanet_93973
12732||4864||Smith-Fineman-Myers syndrome||http://www.orpha.net/ORDO/Orphanet_93974
12733||4864||Renier-Gabreels-Jasper syndrome||http://www.orpha.net/ORDO/Orphanet_93975
12734||3670||megaspore||http://purl.obolibrary.org/obo/CL_0000250
12735||3670||microspore||http://purl.obolibrary.org/obo/CL_0000252
12736||10277||Basal epidermolysis bullosa simplex||http://www.orpha.net/ORDO/Orphanet_158665
12738||306||Epidermolysis bullosa simplex due to plakophilin deficiency||http://www.orpha.net/ORDO/Orphanet_158668
12737||8559||Myelomeningocele||http://www.orpha.net/ORDO/Orphanet_93969
12740||15059||response to carboplatin||http://purl.obolibrary.org/obo/GO_0097328
12739||15044||Blepharophimosis-intellectual disability syndrome, Verloes type||http://www.orpha.net/ORDO/Orphanet_293725
12741||4259||response to antimetabolite||http://purl.obolibrary.org/obo/GO_0097329
12742||10776||1p31p32 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_401986
12743||3273||Autosomal dominant focal dystonia, DYT7 type||http://www.orpha.net/ORDO/Orphanet_93963
12744||3273||Blepharospasm - oromandibular dystonia||http://www.orpha.net/ORDO/Orphanet_93964
12745||3273||Laryngeal dyskinesia||http://www.orpha.net/ORDO/Orphanet_93961
12747||4259||response to antineoplastic agent||http://purl.obolibrary.org/obo/GO_0097327
12746||3273||Autosomal dominant cervical dystonia||http://www.orpha.net/ORDO/Orphanet_93962
12748||10277||Suprabasal epidermolysis bullosa simplex||http://www.orpha.net/ORDO/Orphanet_158661
12749||760||Partial corpus callosum agenesis-cerebellar vermis hypoplasia with posterior fossa cysts syndrome||http://www.orpha.net/ORDO/Orphanet_401959
12750||15538||data item||http://purl.obolibrary.org/obo/IAO_0000027
12751||770||GM08931||http://purl.obolibrary.org/obo/CLO_0011234
12752||770||GM08930||http://purl.obolibrary.org/obo/CLO_0011235
12753||772||mesodermal cell||http://purl.obolibrary.org/obo/CL_0000222
12754||770||GM08928||http://purl.obolibrary.org/obo/CLO_0011237
12755||3273||Oromandibular dystonia||http://www.orpha.net/ORDO/Orphanet_93958
12756||1022||Teleopsis thaii||http://purl.obolibrary.org/obo/NCBITaxon_346187
12757||10275||Dystrophic epidermolysis bullosa, nails only||http://www.orpha.net/ORDO/Orphanet_158676
12758||10275||Acral dystrophic epidermolysis bullosa||http://www.orpha.net/ORDO/Orphanet_158673
12760||4876||49,XYYYY syndrome||http://www.orpha.net/ORDO/Orphanet_99330
12759||5917||X-linked intellectual disability, Sutherland-Haan type||http://www.orpha.net/ORDO/Orphanet_93950
12761||5632||X-linked dominant intellectual disability - epilepsy||http://www.orpha.net/ORDO/Orphanet_93951
12762||5632||X-linked intellectual disability, Hedera type||http://www.orpha.net/ORDO/Orphanet_93952
12763||3273||Benign essential blepharospasm||http://www.orpha.net/ORDO/Orphanet_93955
12764||3273||Truncal dystonia||http://www.orpha.net/ORDO/Orphanet_93956
12766||3273||Limb dystonia||http://www.orpha.net/ORDO/Orphanet_93957
12765||7944||Episodic ataxia with slurred speech||http://www.orpha.net/ORDO/Orphanet_401953
12767||5502||Caldicellulosiruptor lactoaceticus||http://purl.obolibrary.org/obo/NCBITaxon_52766
12768||5502||Caldicellulosiruptor kristjanssonii||http://purl.obolibrary.org/obo/NCBITaxon_52765
12769||4715||Genetic multiple congenital anomalies/dysmorphic syndrome without intellectual disability||http://www.orpha.net/ORDO/Orphanet_330206
12770||772||erythrocyte||http://purl.obolibrary.org/obo/CL_0000232
12771||772||macrophage||http://purl.obolibrary.org/obo/CL_0000235
12772||772||B cell||http://purl.obolibrary.org/obo/CL_0000236
12773||4876||48,XYYY syndrome||http://www.orpha.net/ORDO/Orphanet_99329
12775||10994||asbestos||http://purl.obolibrary.org/obo/CHEBI_46661
12774||7611||platelet||http://purl.obolibrary.org/obo/CL_0000233
12776||5917||X-linked intellectual disability, Golabi-Ito-Hall type||http://www.orpha.net/ORDO/Orphanet_93947
12777||12736||Epidermolysis bullosa simplex with pyloric atresia||http://www.orpha.net/ORDO/Orphanet_158684
12778||12748||Lethal acantholytic epidermolysis bullosa||http://www.orpha.net/ORDO/Orphanet_158687
12779||11333||Paternal uniparental disomy of chromosome 13||http://www.orpha.net/ORDO/Orphanet_99324
12780||12736||Epidermolysis bullosa simplex with circinate migratory erythema||http://www.orpha.net/ORDO/Orphanet_158681
12781||5917||X-linked intellectual disability, Porteous type||http://www.orpha.net/ORDO/Orphanet_93945
12782||2997||Autosomal dominant Charcot-Marie-Tooth disease type 2 with giant axons||http://www.orpha.net/ORDO/Orphanet_401964
12783||5917||Hamel cerebro-palato-cardiac syndrome||http://www.orpha.net/ORDO/Orphanet_93946
12784||15538||label||http://purl.obolibrary.org/obo/IAO_0000009
12785||13695||ventral midline neuron||http://www.ebi.ac.uk/efo/EFO_0003402
12786||13695||ventral nerve cord primordium||http://www.ebi.ac.uk/efo/EFO_0003401
12787||13695||embryonic tracheole||http://www.ebi.ac.uk/efo/EFO_0003404
12788||13695||ventral midline glia||http://www.ebi.ac.uk/efo/EFO_0003403
12789||772||cochlear hair cell||http://purl.obolibrary.org/obo/CL_0000202
12790||5475||Ataxia-telangiectasia-like disorder||http://www.orpha.net/ORDO/Orphanet_251347
12792||13695||embryonic proventriculus intermediate layer||http://www.ebi.ac.uk/efo/EFO_0003406
12791||10994||fluphenazine||http://purl.obolibrary.org/obo/CHEBI_5123
12793||13695||embryonic proventriculus inner layer||http://www.ebi.ac.uk/efo/EFO_0003405
12794||13695||larval labral segment||http://www.ebi.ac.uk/efo/EFO_0003408
12795||13695||embryonic proventriculus outer layer||http://www.ebi.ac.uk/efo/EFO_0003407
12796||5502||Cupriavidus metallidurans||http://purl.obolibrary.org/obo/NCBITaxon_119219
12797||13695||trunk mesoderm anlage||http://www.ebi.ac.uk/efo/EFO_0003400
12798||259||cell activation||http://purl.obolibrary.org/obo/GO_0001775
12799||13695||embryonic labial sensory complex||http://www.ebi.ac.uk/efo/EFO_0003409
12800||10994||N-benzyladenine||http://purl.obolibrary.org/obo/CHEBI_29022
12801||10994||flutamide||http://purl.obolibrary.org/obo/CHEBI_5132
12802||2187||rhombomere 1||http://purl.obolibrary.org/obo/UBERON_0005499
12803||772||electrically active cell||http://purl.obolibrary.org/obo/CL_0000211
12804||770||GM17733||http://purl.obolibrary.org/obo/CLO_0016995
12805||13689||hyoid muscle||http://purl.obolibrary.org/obo/UBERON_0005493
12806||5502||Marvinbryantia formatexigens DSM 14469||http://purl.obolibrary.org/obo/NCBITaxon_478749
12807||2672||non-neural ectoderm||http://purl.obolibrary.org/obo/UBERON_0005497
12808||2063||abnormality of the musculature||http://purl.obolibrary.org/obo/HP_0003011
12809||772||Schwann cell||http://purl.obolibrary.org/obo/CL_0000218
12810||15148||Sertoli cell||http://purl.obolibrary.org/obo/CL_0000216
12811||10652||obsolete_liver primordium||http://www.ebi.ac.uk/efo/EFO_0003428
12812||10652||obsolete_germ ring||http://www.ebi.ac.uk/efo/EFO_0003427
12813||10652||obsolete_otic placode||http://www.ebi.ac.uk/efo/EFO_0003429
12814||10652||obsolete_presumptive neural plate||http://www.ebi.ac.uk/efo/EFO_0003424
12815||13691||presumptive forebrain||http://www.ebi.ac.uk/efo/EFO_0003423
12816||13691||axial chorda mesoderm||http://www.ebi.ac.uk/efo/EFO_0003426
12817||13691||enveloping layer||http://www.ebi.ac.uk/efo/EFO_0003425
12818||10994||imatinib methanesulfonate||http://purl.obolibrary.org/obo/CHEBI_31690
12820||10994||cefalotin||http://purl.obolibrary.org/obo/CHEBI_124991
12819||10652||obsolete_olfactory placode||http://www.ebi.ac.uk/efo/EFO_0003420
12821||13691||polster||http://www.ebi.ac.uk/efo/EFO_0003422
12822||10652||obsolete_presumptive segmental plate||http://www.ebi.ac.uk/efo/EFO_0003421
12823||7377||Karyomegalic interstitial nephritis||http://www.orpha.net/ORDO/Orphanet_401996
12824||6900||Cold-induced sweating syndrome-hyperthermia spectrum||http://www.orpha.net/ORDO/Orphanet_401993
12825||10994||ceftriaxone||http://purl.obolibrary.org/obo/CHEBI_29007
12826||10994||selenate||http://purl.obolibrary.org/obo/CHEBI_15075
12827||12843||Sickle cell - hemoglobin C disease||http://www.orpha.net/ORDO/Orphanet_251365
12828||13691||forerunner cell group||http://www.ebi.ac.uk/efo/EFO_0003419
12829||13695||cibarium primordium||http://www.ebi.ac.uk/efo/EFO_0003418
12830||13695||ring gland primordium||http://www.ebi.ac.uk/efo/EFO_0003417
12831||13695||lateral cord surface glia||http://www.ebi.ac.uk/efo/EFO_0003416
12832||770||AG10049||http://purl.obolibrary.org/obo/CLO_0021875
12834||13695||embryonic ventral apodeme||http://www.ebi.ac.uk/efo/EFO_0003415
12833||12843||Sickle cell - beta-thalassemia disease||http://www.orpha.net/ORDO/Orphanet_251359
12835||13695||embryonic leading edge cell||http://www.ebi.ac.uk/efo/EFO_0003414
12836||13695||lateral cord neuron||http://www.ebi.ac.uk/efo/EFO_0003413
12837||13695||lateral cord glia||http://www.ebi.ac.uk/efo/EFO_0003412
12838||13695||embryonic hypocerebral ganglion||http://www.ebi.ac.uk/efo/EFO_0003411
12839||13695||embryonic midgut interstitial cell||http://www.ebi.ac.uk/efo/EFO_0003410
12840||1826||Populus balsamifera||http://purl.obolibrary.org/obo/NCBITaxon_73824
12841||10994||fluoxetine||http://purl.obolibrary.org/obo/CHEBI_5118
12842||5502||Haemophilus ducreyi 35000HP||http://purl.obolibrary.org/obo/NCBITaxon_233412
12843||4449||Sickle cell disease associated with an other hemoglobin anomaly||http://www.orpha.net/ORDO/Orphanet_251355
12845||4139||CK syndrome||http://www.orpha.net/ORDO/Orphanet_251383
12844||5025||Candida albicans WO-1||http://purl.obolibrary.org/obo/NCBITaxon_294748
12846||13218||hatching long-pec||http://www.ebi.ac.uk/efo/EFO_0002718
12847||14544||L2 larva||http://www.ebi.ac.uk/efo/EFO_0002719
12848||770||Pt45P1||http://www.ebi.ac.uk/efo/EFO_0002716
12849||770||SH-SY5Y||http://www.ebi.ac.uk/efo/EFO_0002717
12850||12843||Hereditary persistence of fetal hemoglobin - sickle cell disease||http://www.orpha.net/ORDO/Orphanet_251380
12851||10652||obsolete_presumptive hindbrain||http://www.ebi.ac.uk/efo/EFO_0003440
12852||10652||obsolete_presumptive paraxial mesoderm||http://www.ebi.ac.uk/efo/EFO_0003443
12853||10652||obsolete_presumptive shield||http://www.ebi.ac.uk/efo/EFO_0003444
12854||13691||presumptive telencephalon||http://www.ebi.ac.uk/efo/EFO_0003441
12855||1760||germline genotype||http://www.ebi.ac.uk/efo/EFO_0004973
12856||13691||presumptive diencephalon||http://www.ebi.ac.uk/efo/EFO_0003442
12857||1760||somatic genotype||http://www.ebi.ac.uk/efo/EFO_0004972
12858||770||PancTUI||http://www.ebi.ac.uk/efo/EFO_0002715
12859||1022||Oncorhynchus tshawytscha||http://purl.obolibrary.org/obo/NCBITaxon_74940
12860||10652||obsolete_presumptive rhombomere 7||http://www.ebi.ac.uk/efo/EFO_0003447
12861||770||Panc89||http://www.ebi.ac.uk/efo/EFO_0002714
12862||10652||obsolete_presumptive rhombomere 6||http://www.ebi.ac.uk/efo/EFO_0003448
12863||13691||posterior lateral line placode||http://www.ebi.ac.uk/efo/EFO_0003445
12864||770||Panc1||http://www.ebi.ac.uk/efo/EFO_0002713
12866||770||KIF5||http://www.ebi.ac.uk/efo/EFO_0002712
12865||10652||obsolete_presumptive midbrain hindbrain boundary||http://www.ebi.ac.uk/efo/EFO_0003446
12868||770||F13||http://www.ebi.ac.uk/efo/EFO_0002711
12869||8190||L-ascorbic acid||http://purl.obolibrary.org/obo/CHEBI_29073
12867||8579||comprehensive strength index||http://www.ebi.ac.uk/efo/EFO_0004979
12870||770||COLO357||http://www.ebi.ac.uk/efo/EFO_0002710
12871||10652||obsolete_presumptive rhombomere 5||http://www.ebi.ac.uk/efo/EFO_0003449
12872||770||BxPC-3||http://www.ebi.ac.uk/efo/EFO_0002709
12873||12843||Sickle cell - hemoglobin D disease||http://www.orpha.net/ORDO/Orphanet_251370
12875||12843||Sickle cell - hemoglobin E disease||http://www.orpha.net/ORDO/Orphanet_251375
12874||770||HPL1||http://www.ebi.ac.uk/efo/EFO_0002705
12877||2671||mycelium||http://purl.obolibrary.org/obo/BTO_0001436
12876||770||SM1||http://www.ebi.ac.uk/efo/EFO_0002706
12878||770||NT-1||http://www.ebi.ac.uk/efo/EFO_0002707
12879||770||SCN2.2||http://www.ebi.ac.uk/efo/EFO_0002708
12880||7918||Huntington disease-like syndrome due to C9ORF72 expansions||http://www.orpha.net/ORDO/Orphanet_401901
12881||13691||pectoral fin bud||http://www.ebi.ac.uk/efo/EFO_0003430
12883||13691||presumptive brain||http://www.ebi.ac.uk/efo/EFO_0003431
12882||13023||Clark level V||http://www.ebi.ac.uk/efo/EFO_0004961
12884||13023||Clark level IV||http://www.ebi.ac.uk/efo/EFO_0004960
12885||10652||obsolete_presumptive midbrain||http://www.ebi.ac.uk/efo/EFO_0003432
12886||10652||obsolete_trigeminal placode||http://www.ebi.ac.uk/efo/EFO_0003433
12887||13877||protein array||http://www.ebi.ac.uk/efo/EFO_0002702
12888||10652||obsolete_pancreas primordium||http://www.ebi.ac.uk/efo/EFO_0003434
12890||13877||DNA array||http://www.ebi.ac.uk/efo/EFO_0002701
12889||13691||presumptive dorsal mesoderm||http://www.ebi.ac.uk/efo/EFO_0003435
12891||13691||presumptive cephalic mesoderm||http://www.ebi.ac.uk/efo/EFO_0003436
12893||12890||tiling array||http://www.ebi.ac.uk/efo/EFO_0002704
12892||2770||total RNA||http://www.ebi.ac.uk/efo/EFO_0004964
12896||12890||SNP array||http://www.ebi.ac.uk/efo/EFO_0002703
12895||1766||gene knock in||http://www.ebi.ac.uk/efo/EFO_0004963
12894||10652||obsolete_presumptive endoderm||http://www.ebi.ac.uk/efo/EFO_0003437
12897||13691||presumptive spinal cord||http://www.ebi.ac.uk/efo/EFO_0003438
12898||11433||venom gland||http://purl.obolibrary.org/obo/BTO_0001440
12899||10652||obsolete_presumptive blood||http://www.ebi.ac.uk/efo/EFO_0003439
12900||10994||Alexa Fluor 555||http://www.ebi.ac.uk/efo/EFO_0004968
12901||10994||Alexa Fluor 647||http://www.ebi.ac.uk/efo/EFO_0004967
12902||1826||Piriqueta cistoides subsp. caroliniana||http://purl.obolibrary.org/obo/NCBITaxon_57329
12903||14730||B10.NOD_H2g7||http://www.ebi.ac.uk/efo/EFO_0002739
12904||10994||lisinopril||http://purl.obolibrary.org/obo/CHEBI_43755
12907||14970||serum IgM measurement||http://www.ebi.ac.uk/efo/EFO_0004993
12906||13691||posterior pancreatic bud||http://www.ebi.ac.uk/efo/EFO_0003465
12905||2672||presumptive endoderm||http://purl.obolibrary.org/obo/UBERON_0006595
12909||1814||Otitis media||http://www.ebi.ac.uk/efo/EFO_0004992
12908||10652||obsolete_presumptive ectoderm||http://www.ebi.ac.uk/efo/EFO_0003466
12910||8579||lean body mass||http://www.ebi.ac.uk/efo/EFO_0004995
12911||10652||obsolete_presumptive forebrain midbrain boundary||http://www.ebi.ac.uk/efo/EFO_0003463
12913||15526||lumbar disc degeneration||http://www.ebi.ac.uk/efo/EFO_0004994
12914||13691||anterior pancreatic bud||http://www.ebi.ac.uk/efo/EFO_0003464
12912||2672||presumptive blood||http://purl.obolibrary.org/obo/UBERON_0006596
12915||13691||anterior lateral line placode||http://www.ebi.ac.uk/efo/EFO_0003461
12916||10652||obsolete_presumptive enteric nervous system||http://www.ebi.ac.uk/efo/EFO_0003462
12918||5103||Myasthenia gravis||http://www.ebi.ac.uk/efo/EFO_0004991
12917||5502||Lactobacillus panis||http://purl.obolibrary.org/obo/NCBITaxon_47493
12920||770||J1||http://www.ebi.ac.uk/efo/EFO_0004990
12919||10652||obsolete_neurogenic placode||http://www.ebi.ac.uk/efo/EFO_0003460
12921||5502||Salmonella enterica subsp. enterica serovar Newport||http://purl.obolibrary.org/obo/NCBITaxon_108619
12923||13691||pelvic fin bud||http://www.ebi.ac.uk/efo/EFO_0003469
12924||2672||presumptive hypochord||http://purl.obolibrary.org/obo/UBERON_0006599
12922||1399||type 2 diabetes nephropathy||http://www.ebi.ac.uk/efo/EFO_0004997
12925||1399||type 1 diabetes nephropathy||http://www.ebi.ac.uk/efo/EFO_0004996
12927||12928||N-glycan measurement||http://www.ebi.ac.uk/efo/EFO_0004999
12926||10652||obsolete_presumptive mesoderm||http://www.ebi.ac.uk/efo/EFO_0003467
12928||14970||carbohydrate measurement||http://www.ebi.ac.uk/efo/EFO_0004998
12929||13691||fin bud||http://www.ebi.ac.uk/efo/EFO_0003468
12930||5585||Localized junctional epidermolysis bullosa, non-Herlitz type||http://www.orpha.net/ORDO/Orphanet_251393
12932||14970||complement C4 measurement||http://www.ebi.ac.uk/efo/EFO_0004984
12931||10652||obsolete_presumptive rhombomere 8||http://www.ebi.ac.uk/efo/EFO_0003452
12933||14970||complement C3 measurement||http://www.ebi.ac.uk/efo/EFO_0004983
12934||10652||obsolete_presumptive hypochord||http://www.ebi.ac.uk/efo/EFO_0003453
12936||4571||microbiome||http://www.ebi.ac.uk/efo/EFO_0004982
12935||10652||obsolete_presumptive floor plate||http://www.ebi.ac.uk/efo/EFO_0003454
12938||12936||peridontal microbiome||http://www.ebi.ac.uk/efo/EFO_0004981
12937||10652||obsolete_epibranchial placode||http://www.ebi.ac.uk/efo/EFO_0003455
12939||8579||appendicular lean mass||http://www.ebi.ac.uk/efo/EFO_0004980
12940||10652||obsolete_presumptive rhombomere 4||http://www.ebi.ac.uk/efo/EFO_0003450
12941||10652||obsolete_presumptive rhombomere 3||http://www.ebi.ac.uk/efo/EFO_0003451
12943||14544||L3 larva||http://www.ebi.ac.uk/efo/EFO_0002720
12942||13496||Rabies virus||http://purl.obolibrary.org/obo/NCBITaxon_11292
12944||1826||Cyclamen persicum||http://purl.obolibrary.org/obo/NCBITaxon_87530
12945||13131||postmenopausal||http://www.ebi.ac.uk/efo/EFO_0002721
12947||13691||vagal placode 1||http://www.ebi.ac.uk/efo/EFO_0003456
12946||13448||embryoid body||http://www.ebi.ac.uk/efo/EFO_0004988
12948||13691||vagal placode 2||http://www.ebi.ac.uk/efo/EFO_0003457
12949||772||embryonal carcinoma cell||http://www.ebi.ac.uk/efo/EFO_0004987
12950||13691||vagal placode 3||http://www.ebi.ac.uk/efo/EFO_0003458
12951||1006||embryonal carcinoma||http://www.ebi.ac.uk/efo/EFO_0004986
12952||14970||platelet reactivity measurement||http://www.ebi.ac.uk/efo/EFO_0004985
12953||13691||vagal placode 4||http://www.ebi.ac.uk/efo/EFO_0003459
12954||13689||cardinal system||http://www.ebi.ac.uk/efo/EFO_0003490
12955||6899||Autosomal dominant popliteal pterygium syndrome||http://www.orpha.net/ORDO/Orphanet_1300
12956||10652||obsolete_brain vasculature||http://www.ebi.ac.uk/efo/EFO_0003491
12957||12996||T2 tumor stage||http://www.ebi.ac.uk/efo/EFO_0004939
12958||12996||T1 tumor stage||http://www.ebi.ac.uk/efo/EFO_0004938
12959||13008||M1 distant metastasis stage||http://www.ebi.ac.uk/efo/EFO_0004930
12960||13008||MX distant metastasis stage||http://www.ebi.ac.uk/efo/EFO_0004931
12961||12999||N0 lymph node stage||http://www.ebi.ac.uk/efo/EFO_0004932
12962||12999||N1 lymph node stage||http://www.ebi.ac.uk/efo/EFO_0004933
12963||10652||obsolete_blood island||http://www.ebi.ac.uk/efo/EFO_0003489
12965||12999||N2 lymph node stage||http://www.ebi.ac.uk/efo/EFO_0004934
12964||10994||malathion||http://purl.obolibrary.org/obo/CHEBI_6651
12967||12999||N3 lymph node stage||http://www.ebi.ac.uk/efo/EFO_0004935
12966||772||hyphal cell||http://purl.obolibrary.org/obo/CL_0000286
12969||12999||NX lymph node stage||http://www.ebi.ac.uk/efo/EFO_0004936
12968||5502||Streptococcus sp.  group A ||http://purl.obolibrary.org/obo/NCBITaxon_36470
12970||12996||T0 stage||http://www.ebi.ac.uk/efo/EFO_0004937
12971||2672||ventral striatum||http://purl.obolibrary.org/obo/UBERON_0005403
12972||10652||obsolete_trigeminal neural crest||http://www.ebi.ac.uk/efo/EFO_0003484
12973||2021||Feingold syndrome||http://www.orpha.net/ORDO/Orphanet_1305
12974||10652||obsolete_swim bladder||http://www.ebi.ac.uk/efo/EFO_0003483
12975||13689||somite 5||http://www.ebi.ac.uk/efo/EFO_0003482
12976||2681||Buschke-Ollendorff syndrome||http://www.orpha.net/ORDO/Orphanet_1306
12978||13689||somite 1||http://www.ebi.ac.uk/efo/EFO_0003481
12977||10768||Distal limb deficiencies - micrognathia syndrome||http://www.orpha.net/ORDO/Orphanet_1307
12980||13689||apical ectodermal ridge dorsal fin||http://www.ebi.ac.uk/efo/EFO_0003488
12979||2252||C syndrome||http://www.orpha.net/ORDO/Orphanet_1308
12982||13689||apical ectodermal ridge pectoral fin bud||http://www.ebi.ac.uk/efo/EFO_0003487
12983||2252||14q24.1q24.3 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_401935
12981||742||Medullary sponge kidney||http://www.orpha.net/ORDO/Orphanet_1309
12984||13689||ventral mesoderm||http://www.ebi.ac.uk/efo/EFO_0003486
12985||2658||seminal fluid||http://purl.obolibrary.org/obo/UBERON_0006530
12986||10652||obsolete_trunk mesenchyme||http://www.ebi.ac.uk/efo/EFO_0003485
12987||4705||Moyamoya disease with early-onset achalasia||http://www.orpha.net/ORDO/Orphanet_401945
12988||4832||Familial median cleft of the upper and lower lips||http://www.orpha.net/ORDO/Orphanet_401942
12989||5961||Permanent neonatal diabetes mellitus - pancreatic and cerebellar agenesis||http://www.orpha.net/ORDO/Orphanet_65288
12990||6264||Beta-ureidopropionase deficiency||http://www.orpha.net/ORDO/Orphanet_65287
12991||10652||obsolete_rhombomere 6||http://www.ebi.ac.uk/efo/EFO_0003480
12992||5855||3q29 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_65286
12993||6249||Bipartite talus||http://www.orpha.net/ORDO/Orphanet_364198
12994||13008||M0 distant metastasis stage||http://www.ebi.ac.uk/efo/EFO_0004929
12995||5961||Lhermitte-Duclos disease||http://www.orpha.net/ORDO/Orphanet_65285
12996||13007||T stage||http://www.ebi.ac.uk/efo/EFO_0004928
12997||2672||gastrointestinal system||http://purl.obolibrary.org/obo/UBERON_0005409
12998||9734||Biotin-responsive basal ganglia disease||http://www.orpha.net/ORDO/Orphanet_65284
12999||13007||N stage||http://www.ebi.ac.uk/efo/EFO_0004927
13000||8737||Timothy syndrome||http://www.orpha.net/ORDO/Orphanet_65283
13001||4951||Woolly hair-palmoplantar keratoderma-dilated cardiomyopathy syndrome||http://www.orpha.net/ORDO/Orphanet_65282
13002||770||GM00038||http://www.ebi.ac.uk/efo/EFO_0004921
13003||10652||obsolete_pronephric mesoderm||http://www.ebi.ac.uk/efo/EFO_0003479
13005||770||GM00719||http://www.ebi.ac.uk/efo/EFO_0004922
13004||10652||obsolete_postoptic commissure||http://www.ebi.ac.uk/efo/EFO_0003478
13006||1388||progression free survival||http://www.ebi.ac.uk/efo/EFO_0004920
13007||1422||tumor stage||http://www.ebi.ac.uk/efo/EFO_0004925
13008||13007||M stage||http://www.ebi.ac.uk/efo/EFO_0004926
13009||3074||peripheral vein||http://www.ebi.ac.uk/efo/EFO_0004923
13010||10652||obsolete_ataxia telangiectasia||http://www.ebi.ac.uk/efo/EFO_0004924
13012||13691||presumptive ventral fin fold||http://www.ebi.ac.uk/efo/EFO_0003471
13011||772||guard cell||http://purl.obolibrary.org/obo/CL_0000292
13013||10652||obsolete_pancreatic bud||http://www.ebi.ac.uk/efo/EFO_0003470
13014||10652||obsolete_floor plate||http://www.ebi.ac.uk/efo/EFO_0003473
13015||10652||obsolete_caudal artery||http://www.ebi.ac.uk/efo/EFO_0003472
13016||10652||obsolete_hypochord||http://www.ebi.ac.uk/efo/EFO_0003475
13017||13689||macula utricle||http://www.ebi.ac.uk/efo/EFO_0003474
13018||6290||Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency||http://www.orpha.net/ORDO/Orphanet_401948
13019||13689||median fin fold||http://www.ebi.ac.uk/efo/EFO_0003477
13020||13689||intermediate cell mass of mesoderm||http://www.ebi.ac.uk/efo/EFO_0003476
13021||450||AXIN2-related attenuated familial adenomatous polyposis||http://www.orpha.net/ORDO/Orphanet_401911
13022||1022||Haematobia irritans||http://purl.obolibrary.org/obo/NCBITaxon_7368
13023||13030||Clark level||http://www.ebi.ac.uk/efo/EFO_0004956
13024||13023||Clark level I||http://www.ebi.ac.uk/efo/EFO_0004957
13026||13023||Clark level II||http://www.ebi.ac.uk/efo/EFO_0004958
13025||6246||Arthrogryposis syndrome||http://www.orpha.net/ORDO/Orphanet_109007
13027||13023||Clark level III||http://www.ebi.ac.uk/efo/EFO_0004959
13028||13036||disease recurrence||http://www.ebi.ac.uk/efo/EFO_0004952
13029||2813||date of diagnosis||http://www.ebi.ac.uk/efo/EFO_0004953
13030||1422||melanoma staging||http://www.ebi.ac.uk/efo/EFO_0004954
13031||13030||Breslow thickness||http://www.ebi.ac.uk/efo/EFO_0004955
13032||2813||date of birth||http://www.ebi.ac.uk/efo/EFO_0004950
13033||13036||alive at endpoint||http://www.ebi.ac.uk/efo/EFO_0004951
13034||1022||Moniliophthora perniciosa||http://purl.obolibrary.org/obo/NCBITaxon_153609
13035||2252||9q31.1q31.3 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_401923
13036||2842||clinical temporal measurement||http://www.ebi.ac.uk/efo/EFO_0004949
13037||12996||Tis||http://www.ebi.ac.uk/efo/EFO_0004947
13038||13044||TX||http://www.ebi.ac.uk/efo/EFO_0004948
13039||13448||definitive endoderm||http://purl.obolibrary.org/obo/UBERON_0005439
13040||13043||T4a tumor stage||http://www.ebi.ac.uk/efo/EFO_0004945
13041||13043||T4b tumor stage||http://www.ebi.ac.uk/efo/EFO_0004946
13042||13048||T3c tumor stage||http://www.ebi.ac.uk/efo/EFO_0004943
13043||12996||T4 tumor stage||http://www.ebi.ac.uk/efo/EFO_0004944
13044||13048||T3a tumor stage||http://www.ebi.ac.uk/efo/EFO_0004941
13045||13048||T3b tumor stage||http://www.ebi.ac.uk/efo/EFO_0004942
13046||4719||Non-syndromic limb malformation||http://www.orpha.net/ORDO/Orphanet_109011
13047||10652||obsolete_neural keel||http://www.ebi.ac.uk/efo/EFO_0003497
13048||12996||T3 tumor stage||http://www.ebi.ac.uk/efo/EFO_0004940
13049||10652||obsolete_olfactory pit||http://www.ebi.ac.uk/efo/EFO_0003496
13050||13689||otic lateral line neuromast||http://www.ebi.ac.uk/efo/EFO_0003499
13051||10652||obsolete_neural rod||http://www.ebi.ac.uk/efo/EFO_0003498
13052||13689||lateral line ganglion||http://www.ebi.ac.uk/efo/EFO_0003493
13053||10652||obsolete_head mesenchyme||http://www.ebi.ac.uk/efo/EFO_0003492
13054||13689||mandibular lateral line neuromast||http://www.ebi.ac.uk/efo/EFO_0003495
13055||10652||obsolete_lens placode||http://www.ebi.ac.uk/efo/EFO_0003494
13056||13695||pole plasm||http://www.ebi.ac.uk/efo/EFO_0003399
13057||10652||obsolete_chorion||http://www.ebi.ac.uk/efo/EFO_0002780
13058||13695||hypopharyngeal sense organ||http://www.ebi.ac.uk/efo/EFO_0003397
13059||770||TERV-AntiSenseB56||http://www.ebi.ac.uk/efo/EFO_0001250
13060||13695||capitellum||http://www.ebi.ac.uk/efo/EFO_0003398
13061||770||TERV-ST||http://www.ebi.ac.uk/efo/EFO_0001251
13064||13695||ring gland||http://www.ebi.ac.uk/efo/EFO_0003395
13063||13155||Spinal atrophy - ophthalmoplegia - pyramidal syndrome||http://www.orpha.net/ORDO/Orphanet_1217
13062||770||TERV-ST110||http://www.ebi.ac.uk/efo/EFO_0001252
13065||770||GM12878||http://www.ebi.ac.uk/efo/EFO_0002784
13067||13695||prothoracic gland||http://www.ebi.ac.uk/efo/EFO_0003396
13068||770||THP-1||http://www.ebi.ac.uk/efo/EFO_0001253
13069||770||GM06990||http://www.ebi.ac.uk/efo/EFO_0002783
13066||6928||Autosomal dominant congenital benign spinal muscular atrophy||http://www.orpha.net/ORDO/Orphanet_1216
13070||13678||hypopharyngeal sense organ primordium||http://www.ebi.ac.uk/efo/EFO_0003393
13073||770||glioblastoma H54||http://www.ebi.ac.uk/efo/EFO_0002782
13071||770||U266_13071||http://www.ebi.ac.uk/efo/EFO_0001254
13072||5502||Rhodococcus jostii||http://purl.obolibrary.org/obo/NCBITaxon_132919
13074||13695||embryonic stomatogastric nervous system||http://www.ebi.ac.uk/efo/EFO_0003394
13077||2672||hindbrain||http://purl.obolibrary.org/obo/UBERON_0002028
13076||770||U373||http://www.ebi.ac.uk/efo/EFO_0001255
13075||770||chorion cell line||http://www.ebi.ac.uk/efo/EFO_0002781
13079||770||U87||http://www.ebi.ac.uk/efo/EFO_0001256
13078||770||GM19238||http://www.ebi.ac.uk/efo/EFO_0002788
13081||770||U937||http://www.ebi.ac.uk/efo/EFO_0001257
13080||770||GM18507||http://www.ebi.ac.uk/efo/EFO_0002787
13083||770||UACC812||http://www.ebi.ac.uk/efo/EFO_0001258
13082||770||GM12892||http://www.ebi.ac.uk/efo/EFO_0002786
13085||770||GM12891||http://www.ebi.ac.uk/efo/EFO_0002785
13084||770||UBOC1||http://www.ebi.ac.uk/efo/EFO_0001259
13086||10994||rofecoxib||http://purl.obolibrary.org/obo/CHEBI_8887
13087||2672||occipital lobe||http://purl.obolibrary.org/obo/UBERON_0002021
13088||770||GM19239||http://www.ebi.ac.uk/efo/EFO_0002789
13089||1826||Macroptilium atropurpureum||http://purl.obolibrary.org/obo/NCBITaxon_90550
13091||13496||Human echovirus 18||http://purl.obolibrary.org/obo/NCBITaxon_47506
13090||1022||Trichoplax adhaerens||http://purl.obolibrary.org/obo/NCBITaxon_10228
13092||6917||Autosomal dominant optic atrophy plus syndrome||http://www.orpha.net/ORDO/Orphanet_1215
13093||770||ZF4||http://www.ebi.ac.uk/efo/EFO_0001261
13094||770||ZR751||http://www.ebi.ac.uk/efo/EFO_0001262
13096||3072||pulmonary artery||http://purl.obolibrary.org/obo/UBERON_0002012
13095||770||HeLa-S3||http://www.ebi.ac.uk/efo/EFO_0002791
13098||770||WI38||http://www.ebi.ac.uk/efo/EFO_0001260
13097||770||GM19240||http://www.ebi.ac.uk/efo/EFO_0002790
13099||1997||female||http://www.ebi.ac.uk/efo/EFO_0001265
13100||770||HL-60||http://www.ebi.ac.uk/efo/EFO_0002793
13103||1997||male||http://www.ebi.ac.uk/efo/EFO_0001266
13101||770||HGF||http://www.ebi.ac.uk/efo/EFO_0002792
13102||9918||Congenital intrauterine infection-like syndrome||http://www.orpha.net/ORDO/Orphanet_1229
13106||770||HUVEC cell line||http://www.ebi.ac.uk/efo/EFO_0002795
13104||770||ZR7530||http://www.ebi.ac.uk/efo/EFO_0001263
13105||7953||Banki syndrome||http://www.orpha.net/ORDO/Orphanet_1228
13108||770||HRE||http://www.ebi.ac.uk/efo/EFO_0002794
13107||770||ZR75B||http://www.ebi.ac.uk/efo/EFO_0001264
13109||5146||Bangstad syndrome||http://www.orpha.net/ORDO/Orphanet_1227
13110||13115||mating type h minus||http://www.ebi.ac.uk/efo/EFO_0001269
13111||770||LHSR||http://www.ebi.ac.uk/efo/EFO_0002797
13112||770||Jurkat||http://www.ebi.ac.uk/efo/EFO_0002796
13113||1997||hermaphrodite||http://www.ebi.ac.uk/efo/EFO_0001267
13114||770||NHEK||http://www.ebi.ac.uk/efo/EFO_0002799
13116||4173||risperidone||http://purl.obolibrary.org/obo/CHEBI_8871
13117||770||NB4||http://www.ebi.ac.uk/efo/EFO_0002798
13115||5838||mating type||http://www.ebi.ac.uk/efo/EFO_0001268
13118||1022||Dicentrarchus labrax||http://purl.obolibrary.org/obo/NCBITaxon_13489
13119||6610||Baller-Gerold syndrome||http://www.orpha.net/ORDO/Orphanet_1225
13120||5300||Bamforth-Lazarus syndrome||http://www.orpha.net/ORDO/Orphanet_1226
13121||15449||blastula 1k-cell||http://www.ebi.ac.uk/efo/EFO_0001274
13122||2672||vasculature||http://purl.obolibrary.org/obo/UBERON_0002049
13124||13115||mating type a||http://www.ebi.ac.uk/efo/EFO_0001275
13123||2672||lung||http://purl.obolibrary.org/obo/UBERON_0002048
13126||15449||blastula 256-cell||http://www.ebi.ac.uk/efo/EFO_0001276
13125||9869||Bulbospinal muscular atrophy||http://www.orpha.net/ORDO/Orphanet_206701
13127||15449||blastula 30%-epiboly||http://www.ebi.ac.uk/efo/EFO_0001277
13128||13115||mating type alpha||http://www.ebi.ac.uk/efo/EFO_0001270
13129||13125||Bulbospinal muscular atrophy of children||http://www.orpha.net/ORDO/Orphanet_206704
13130||4571||mixed sex population||http://www.ebi.ac.uk/efo/EFO_0001271
13131||618||adult||http://www.ebi.ac.uk/efo/EFO_0001272
13132||15449||blastula 128-cell||http://www.ebi.ac.uk/efo/EFO_0001273
13133||11433||thyroid gland||http://purl.obolibrary.org/obo/UBERON_0002046
13134||13367||intraepithelial lymphocyte||http://purl.obolibrary.org/obo/CL_0002496
13135||1676||alveolus||http://purl.obolibrary.org/obo/UBERON_0003215
13137||2672||dorsal raphe nucleus||http://purl.obolibrary.org/obo/UBERON_0002043
13136||7485||Yoruba||http://www.ebi.ac.uk/efo/EFO_0004900
13138||15449||blastula 512-cell||http://www.ebi.ac.uk/efo/EFO_0001278
13139||770||European HapMap cell line||http://www.ebi.ac.uk/efo/EFO_0004902
13141||15449||blastula dome||http://www.ebi.ac.uk/efo/EFO_0001279
13140||203||Northern and Western European||http://www.ebi.ac.uk/efo/EFO_0004901
13142||10652||obsolete_hereditary genetic disorder||http://www.ebi.ac.uk/efo/EFO_0004904
13143||1783||probe design element||http://www.ebi.ac.uk/efo/EFO_0004903
13144||2564||induced pluripotent stem cell||http://www.ebi.ac.uk/efo/EFO_0004905
13146||1006||metastasis to lymph node||http://www.ebi.ac.uk/efo/EFO_0004906
13145||5502||Streptomyces hygroscopicus subsp. jinggangensis||http://purl.obolibrary.org/obo/NCBITaxon_311982
13147||14970||testosterone measurement||http://www.ebi.ac.uk/efo/EFO_0004908
13148||14970||dihydrotestosterone measurement||http://www.ebi.ac.uk/efo/EFO_0004909
13149||13125||Bulbospinal muscular atrophy of adult||http://www.orpha.net/ORDO/Orphanet_206707
13150||15449||blastula high||http://www.ebi.ac.uk/efo/EFO_0001280
13152||15448||cleavage 4-cell||http://www.ebi.ac.uk/efo/EFO_0001287
13151||8997||Autosomal recessive disease with diffuse palmoplantar keratoderma as a major feature||http://www.orpha.net/ORDO/Orphanet_307804
13154||15448||cleavage 64-cell||http://www.ebi.ac.uk/efo/EFO_0001288
13153||9869||Distal spinal muscular atrophy||http://www.orpha.net/ORDO/Orphanet_206713
13157||15448||cleavage 2-cell||http://www.ebi.ac.uk/efo/EFO_0001285
13155||13125||Generalized bulbospinal muscular atrophy||http://www.orpha.net/ORDO/Orphanet_206710
13156||2672||substantia nigra||http://purl.obolibrary.org/obo/UBERON_0002038
13159||15448||cleavage 32-cell||http://www.ebi.ac.uk/efo/EFO_0001286
13158||2672||cerebellum||http://purl.obolibrary.org/obo/UBERON_0002037
13160||15449||blastula sphere||http://www.ebi.ac.uk/efo/EFO_0001283
13161||15448||cleavage 16-cell||http://www.ebi.ac.uk/efo/EFO_0001284
13162||15449||blastula oblong||http://www.ebi.ac.uk/efo/EFO_0001281
13163||2672||suprachiasmatic nucleus||http://purl.obolibrary.org/obo/UBERON_0002034
13164||10652||obsolete_blastula stage||http://www.ebi.ac.uk/efo/EFO_0001282
13165||1485||familial hypercholesterolemia||http://www.ebi.ac.uk/efo/EFO_0004911
13166||14970||CYP3A4 activity||http://www.ebi.ac.uk/efo/EFO_0004910
13167||14970||vaspin measurement||http://www.ebi.ac.uk/efo/EFO_0004915
13168||14970||facial neural processing||http://www.ebi.ac.uk/efo/EFO_0004914
13169||6573||chemical role||http://purl.obolibrary.org/obo/CHEBI_51086
13171||15448||cleavage 8-cell||http://www.ebi.ac.uk/efo/EFO_0001289
13170||14970||lentiform nucleus measurement||http://www.ebi.ac.uk/efo/EFO_0004913
13172||14970||serum IgA measurement||http://www.ebi.ac.uk/efo/EFO_0004912
13173||10206||double negative thymocyte||http://purl.obolibrary.org/obo/CL_0002489
13174||13036||age at diagnosis||http://www.ebi.ac.uk/efo/EFO_0004918
13175||1194||metastasis free survival||http://www.ebi.ac.uk/efo/EFO_0004919
13176||9698||Nuclear oculomotor paralysis||http://www.orpha.net/ORDO/Orphanet_100932
13177||11573||high throughput sequence alignment protocol||http://www.ebi.ac.uk/efo/EFO_0004917
13178||13496||Influenza A virus||http://purl.obolibrary.org/obo/NCBITaxon_11320
13179||15442||gastrula 50%-epiboly||http://www.ebi.ac.uk/efo/EFO_0001291
13181||5700||Choanal atresia-deafness-cardiac defects-dysmorphism syndrome||http://www.orpha.net/ORDO/Orphanet_1200
13180||10652||obsolete_cleavage stage||http://www.ebi.ac.uk/efo/EFO_0001290
13182||6775||Duodenal atresia||http://www.orpha.net/ORDO/Orphanet_1203
13183||6771||Atresia of small intestine||http://www.orpha.net/ORDO/Orphanet_1201
13184||12098||Larynx atresia||http://www.orpha.net/ORDO/Orphanet_1202
13185||13188||F4/80-negative adipose macrophage||http://purl.obolibrary.org/obo/CL_0002478
13186||2206||C57BL/6-scid||http://www.ebi.ac.uk/efo/EFO_0002743
13187||14730||NOD.B10||http://www.ebi.ac.uk/efo/EFO_0002744
13188||10187||adipose macrophage||http://purl.obolibrary.org/obo/CL_0002477
13189||14730||B10.NOD_H2g7_Idd3||http://www.ebi.ac.uk/efo/EFO_0002741
13190||13188||F4/80-positive adipose macrophage||http://purl.obolibrary.org/obo/CL_0002479
13191||2206||B6.H2_g7||http://www.ebi.ac.uk/efo/EFO_0002742
13192||13587||ObOb||http://www.ebi.ac.uk/efo/EFO_0002747
13193||13228||lymphoid MHC-II-negative classical monocyte||http://purl.obolibrary.org/obo/CL_0002474
13196||363||MHC-II-high non-classical monocyte||http://purl.obolibrary.org/obo/CL_0002473
13195||1022||Caenorhabditis||http://purl.obolibrary.org/obo/NCBITaxon_6237
13194||10652||obsolete_tail bud||http://www.ebi.ac.uk/efo/EFO_0002748
13198||14730||NOD.B6||http://www.ebi.ac.uk/efo/EFO_0002745
13199||13195||Caenorhabditis briggsae||http://purl.obolibrary.org/obo/NCBITaxon_6238
13197||10187||bone marrow macrophage||http://purl.obolibrary.org/obo/CL_0002476
13201||13211||lymphoid MHC-II-negative non-classical monocyte||http://purl.obolibrary.org/obo/CL_0002475
13202||13195||Caenorhabditis elegans||http://purl.obolibrary.org/obo/NCBITaxon_6239
13200||2182||IR (lox/lox)||http://www.ebi.ac.uk/efo/EFO_0002746
13204||15442||gastrula 90%-epiboly||http://www.ebi.ac.uk/efo/EFO_0001293
13205||15436||MHC-II-positive classical monocyte||http://purl.obolibrary.org/obo/CL_0002470
13203||1022||Anolis carolinensis||http://purl.obolibrary.org/obo/NCBITaxon_28377
13207||15442||gastrula 75%-epiboly||http://www.ebi.ac.uk/efo/EFO_0001292
13206||13409||Mitochondrial oxidative phosphorylation disorder due to a large-scale single deletion of mitochondrial DNA||http://www.orpha.net/ORDO/Orphanet_254767
13208||15442||gastrula germ-ring||http://www.ebi.ac.uk/efo/EFO_0001295
13209||363||MHC-II-low non-classical monocyte||http://purl.obolibrary.org/obo/CL_0002472
13210||15442||gastrula bud||http://www.ebi.ac.uk/efo/EFO_0001294
13212||10994||2- {[(2E)-3-iodoprop-2-en-1-yl](propyl)amino }tetralin-7-ol maleate||http://purl.obolibrary.org/obo/CHEBI_64134
13211||363||MHC-II-negative non-classical monocyte||http://purl.obolibrary.org/obo/CL_0002471
13214||15442||gastrula shield||http://www.ebi.ac.uk/efo/EFO_0001297
13213||3072||aortic arch||http://purl.obolibrary.org/obo/UBERON_0004363
13215||14730||NOD.scid||http://www.ebi.ac.uk/efo/EFO_0002740
13216||10652||obsolete_gastrula stage||http://www.ebi.ac.uk/efo/EFO_0001296
13217||13218||hatching pec-fin||http://www.ebi.ac.uk/efo/EFO_0001299
13219||592||Focal palmoplantar keratoderma||http://www.orpha.net/ORDO/Orphanet_307837
13218||618||hatching stage||http://www.ebi.ac.uk/efo/EFO_0001298
13220||6899||Blepharophimosis - radioulnar synostosis||http://www.orpha.net/ORDO/Orphanet_1256
13221||6897||Blepharoptosis - myopia - ectopia lentis||http://www.orpha.net/ORDO/Orphanet_1259
13222||4834||Blepharoptosis - cleft palate - ectrodactyly - dental anomalies||http://www.orpha.net/ORDO/Orphanet_1258
13223||5317||Ascher syndrome||http://www.orpha.net/ORDO/Orphanet_1253
13224||2252||Blepharonasofacial malformation syndrome||http://www.orpha.net/ORDO/Orphanet_1252
13225||8191||(2R,3S)-EHNA hydrochloride||http://purl.obolibrary.org/obo/CHEBI_64139
13226||4509||Porphyria due to ALA dehydratase deficiency||http://www.orpha.net/ORDO/Orphanet_100924
13227||3052||undisturbed flow regions||http://www.ebi.ac.uk/efo/EFO_0002749
13228||15436||MHC-II-negative classical monocyte||http://purl.obolibrary.org/obo/CL_0002469
13229||1422||aggressive||http://www.ebi.ac.uk/efo/EFO_0002752
13230||10237||Gr1-low myeloid suppressor cell||http://purl.obolibrary.org/obo/CL_0002468
13231||10237||Gr1-high myeloid suppressor cell||http://purl.obolibrary.org/obo/CL_0002467
13232||13234||small intestine serosal dendritic cell||http://purl.obolibrary.org/obo/CL_0002466
13233||711||diet||http://www.ebi.ac.uk/efo/EFO_0002755
13235||3068||fasting||http://www.ebi.ac.uk/efo/EFO_0002756
13234||10580||CD11b-positive dendritic cell||http://purl.obolibrary.org/obo/CL_0002465
13237||13241||SIRPa-negative adipose dendritic cell||http://purl.obolibrary.org/obo/CL_0002464
13236||13233||high fat diet||http://www.ebi.ac.uk/efo/EFO_0002757
13239||13241||SIRPa-positive adipose dendritic cell||http://purl.obolibrary.org/obo/CL_0002463
13238||13233||low fat diet||http://www.ebi.ac.uk/efo/EFO_0002758
13240||2743||methylation profiling by array||http://www.ebi.ac.uk/efo/EFO_0002759
13241||10580||adipose dendritic cell||http://purl.obolibrary.org/obo/CL_0002462
13242||10580||CD103-positive dendritic cell||http://purl.obolibrary.org/obo/CL_0002461
13244||8191||NAN 190 hydrobromide||http://purl.obolibrary.org/obo/CHEBI_64123
13243||10541||CD8alpha-negative thymic conventional dendritic cell||http://purl.obolibrary.org/obo/CL_0002460
13245||2672||orbit||http://purl.obolibrary.org/obo/BTO_0004687
13246||3052||disturbed flow regions||http://www.ebi.ac.uk/efo/EFO_0002750
13247||1422||benign||http://www.ebi.ac.uk/efo/EFO_0002751
13249||13409||Mitochondrial oxidative phosphorylation disorder due to a point mutation of mitochondrial DNA||http://www.orpha.net/ORDO/Orphanet_254776
13248||12769||Dermato-cardio-skeletal syndrome, Borrone type||http://www.orpha.net/ORDO/Orphanet_1266
13250||306||Tricho-retino-dento-digital syndrome||http://www.orpha.net/ORDO/Orphanet_1264
13251||7949||Boomerang dysplasia||http://www.orpha.net/ORDO/Orphanet_1263
13252||306||B k syndrome||http://www.orpha.net/ORDO/Orphanet_1262
13253||2252||Bonnemann-Meinecke-Reich syndrome||http://www.orpha.net/ORDO/Orphanet_1261
13254||15||Sino-auricular heart block||http://www.orpha.net/ORDO/Orphanet_1260
13255||12296||transcription profiling by tiling array||http://www.ebi.ac.uk/efo/EFO_0002769
13256||13234||Cd4-negative, CD8_alpha-negative, CD11b-positive dendritic cell||http://purl.obolibrary.org/obo/CL_0002454
13257||2742||genotyping by array||http://www.ebi.ac.uk/efo/EFO_0002767
13258||12296||transcription profiling by array||http://www.ebi.ac.uk/efo/EFO_0002768
13259||2756||proteomic profiling by array||http://www.ebi.ac.uk/efo/EFO_0002765
13260||10614||CD8_alpha-positive plasmactyoid dendritic cell||http://purl.obolibrary.org/obo/CL_0002456
13262||2756||proteomic profiling by mass spectrometer||http://www.ebi.ac.uk/efo/EFO_0002766
13263||6573||phase-transfer catalyst role||http://purl.obolibrary.org/obo/CHEBI_63060
13261||10614||CD8_alpha-negative plasmactyoid dendritic cell||http://purl.obolibrary.org/obo/CL_0002455
13265||14103||langerin-positive dermal dendritic cell||http://purl.obolibrary.org/obo/CL_0002458
13264||10652||obsolete_ChIP-seq by high throughput sequencing||http://www.ebi.ac.uk/efo/EFO_0002763
13266||2761||ChIP-chip by SNP array||http://www.ebi.ac.uk/efo/EFO_0002764
13267||8616||epidermal Langerhans cell||http://purl.obolibrary.org/obo/CL_0002457
13268||2743||methylation profiling by high throughput sequencing||http://www.ebi.ac.uk/efo/EFO_0002761
13269||8191||GR 127935 hydrochloride||http://purl.obolibrary.org/obo/CHEBI_64111
13270||10994||4,4 ,4 -(4-propylpyrazole-1,3,5-triyl)trisphenol||http://purl.obolibrary.org/obo/CHEBI_64110
13273||2761||ChIP-chip by tiling array||http://www.ebi.ac.uk/efo/EFO_0002762
13272||1627||enteric nervous system||http://purl.obolibrary.org/obo/UBERON_0002005
13271||9710||Behr syndrome||http://www.orpha.net/ORDO/Orphanet_1239
13274||13496||Ralstonia phage RSL1||http://purl.obolibrary.org/obo/NCBITaxon_482058
13275||2761||ChIP-chip by array||http://www.ebi.ac.uk/efo/EFO_0002760
13276||13249||Maternally-inherited mitochondrial myopathy||http://www.orpha.net/ORDO/Orphanet_254788
13277||8191||(1S,2R)-5-methoxy-1-methyl-2-(propylamino)tetralin hydrochloride||http://purl.obolibrary.org/obo/CHEBI_64115
13278||322||Barber-Say syndrome||http://www.orpha.net/ORDO/Orphanet_1231
13279||10994||(S)-(-)-sulpiride||http://purl.obolibrary.org/obo/CHEBI_64119
13280||306||Bartsocas-Papas syndrome||http://www.orpha.net/ORDO/Orphanet_1234
13281||12769||Beemer-Ertbruggen syndrome||http://www.orpha.net/ORDO/Orphanet_1237
13282||14103||langerin-negative dermal  dendritic cell||http://purl.obolibrary.org/obo/CL_0002459
13283||13320||Ly49CI-positive natural killer cell||http://purl.obolibrary.org/obo/CL_0002443
13284||770||BG02ES||http://www.ebi.ac.uk/efo/EFO_0002778
13285||13320||CD94-negative, Ly49CI-negative natural killer cell||http://purl.obolibrary.org/obo/CL_0002442
13286||770||BJ||http://www.ebi.ac.uk/efo/EFO_0002779
13287||13320||CD94-positive natural killer cell||http://purl.obolibrary.org/obo/CL_0002441
13288||13320||Ly49D-positive natural killer cell||http://purl.obolibrary.org/obo/CL_0002440
13289||13320||CD94-negative natural killer cell||http://purl.obolibrary.org/obo/CL_0002447
13290||13301||mass spectrometry assay||http://www.ebi.ac.uk/efo/EFO_0002774
13291||13320||Ly49CI-negative natural killer cell||http://purl.obolibrary.org/obo/CL_0002446
13292||3218||aorta smooth muscle||http://www.ebi.ac.uk/efo/EFO_0002775
13294||13320||Ly49D-negative natural killer cell||http://purl.obolibrary.org/obo/CL_0002445
13293||770||H0287||http://www.ebi.ac.uk/efo/EFO_0002776
13296||13320||Ly49H-positive natural killer cell||http://purl.obolibrary.org/obo/CL_0002444
13295||770||Normal Human Astrocytes||http://www.ebi.ac.uk/efo/EFO_0002777
13297||12296||transcription profiling by high throughput sequencing||http://www.ebi.ac.uk/efo/EFO_0002770
13298||2742||genotyping by high throughput sequencing||http://www.ebi.ac.uk/efo/EFO_0002771
13299||4263||assay by molecule||http://www.ebi.ac.uk/efo/EFO_0002772
13301||4263||assay by instrument||http://www.ebi.ac.uk/efo/EFO_0002773
13300||1022||Falco chicquera||http://purl.obolibrary.org/obo/NCBITaxon_495941
13302||10994||sodium 8-bromo-3 ,5 -cyclic GMP||http://purl.obolibrary.org/obo/CHEBI_64104
13304||13219||Isolated focal palmoplantar keratoderma||http://www.orpha.net/ORDO/Orphanet_307846
13303||8191||sodium butyrate||http://purl.obolibrary.org/obo/CHEBI_64103
13305||9675||Best vitelliform macular dystrophy||http://www.orpha.net/ORDO/Orphanet_1243
13306||4715||Genetic multiple congenital anomalies/dysmorphic syndrome - variable intellectual disability||http://www.orpha.net/ORDO/Orphanet_330197
13307||5300||Bencze syndrome||http://www.orpha.net/ORDO/Orphanet_1241
13308||5700||Maxillonasal dysplasia||http://www.orpha.net/ORDO/Orphanet_1248
13309||13409||Mitochondrial oxidative phosphorylation disorder due to a duplication of mitochondrial DNA||http://www.orpha.net/ORDO/Orphanet_254793
13310||2252||Brachydactyly - nystagmus - cerebellar ataxia||http://www.orpha.net/ORDO/Orphanet_1246
13311||13320||Ly49H-negative natural killer cell||http://purl.obolibrary.org/obo/CL_0002448
13312||13320||CD94-positive Ly49CI-positive natural killer cell||http://purl.obolibrary.org/obo/CL_0002449
13313||8001||Metaphyseal acroscyphodysplasia||http://www.orpha.net/ORDO/Orphanet_1240
13314||1022||Haemonchus contortus||http://purl.obolibrary.org/obo/NCBITaxon_6289
13315||2021||Brachytelephalangy - dysmorphism - Kallmann syndrome||http://www.orpha.net/ORDO/Orphanet_1295
13317||2021||Brachymorphism - onychodysplasia - dysphalangism||http://www.orpha.net/ORDO/Orphanet_1292
13316||1022||Dirofilaria immitis||http://purl.obolibrary.org/obo/NCBITaxon_6287
13318||7984||Brachyolmia||http://www.orpha.net/ORDO/Orphanet_1293
13319||13320||NKGA2-positive natural killer cell||http://purl.obolibrary.org/obo/CL_0002439
13321||2672||crypt||http://purl.obolibrary.org/obo/BTO_0000305
13320||10110||NK1.1-positive natural killer cell||http://purl.obolibrary.org/obo/CL_0002438
13323||1523||plastid envelope||http://purl.obolibrary.org/obo/GO_0009526
13322||7037||mature CD8 single-positive thymocyte||http://purl.obolibrary.org/obo/CL_0002437
13324||1022||Brugia pahangi||http://purl.obolibrary.org/obo/NCBITaxon_6280
13325||2252||Branchio-skeleto-genital syndrome||http://www.orpha.net/ORDO/Orphanet_1299
13326||2252||Lambert syndrome||http://www.orpha.net/ORDO/Orphanet_1296
13327||10994||propofol||http://purl.obolibrary.org/obo/CHEBI_44915
13328||5300||Branchio-oculo-facial syndrome||http://www.orpha.net/ORDO/Orphanet_1297
13329||5204||Congenital sucrase-isomaltase deficiency without starch intolerance||http://www.orpha.net/ORDO/Orphanet_306462
13330||10994||potassium nitrate||http://purl.obolibrary.org/obo/CHEBI_63043
13331||10051||CD69-positive, CD8-positive single-positive thymocyte||http://purl.obolibrary.org/obo/CL_0002435
13332||7036||mature CD4 single-positive thymocyte||http://purl.obolibrary.org/obo/CL_0002436
13334||13219||Disease with focal palmoplantar keratoderma as a major feature||http://www.orpha.net/ORDO/Orphanet_307871
13333||10047||CD69-positive, CD4-positive single-positive thymocyte||http://purl.obolibrary.org/obo/CL_0002433
13335||10051||CD24-positive, CD8 single-positive thymocyte||http://purl.obolibrary.org/obo/CL_0002434
13336||5025||Sordaria macrospora||http://purl.obolibrary.org/obo/NCBITaxon_5147
13337||10068||CD4-positive, CD8-intermediate double-positive thymocyte||http://purl.obolibrary.org/obo/CL_0002431
13338||10047||CD24-positive, CD4 single-positive thymocyte||http://purl.obolibrary.org/obo/CL_0002432
13339||10068||CD4-intermediate, CD8-positive double-positive thymocyte||http://purl.obolibrary.org/obo/CL_0002430
13340||13496||Human herpesvirus 1||http://purl.obolibrary.org/obo/NCBITaxon_10298
13341||10068||resting double-positive thymocyte||http://purl.obolibrary.org/obo/CL_0002427
13342||13320||CD11b-positive, CD27-positive natural killer cell||http://purl.obolibrary.org/obo/CL_0002426
13343||10068||CD69-positive double-positive thymocyte||http://purl.obolibrary.org/obo/CL_0002429
13345||2672||postcranial axial skeleton||http://purl.obolibrary.org/obo/UBERON_0002090
13344||10068||double-positive blast||http://purl.obolibrary.org/obo/CL_0002428
13346||8191||ammonium nitrate||http://purl.obolibrary.org/obo/CHEBI_63038
13347||8191||caesium chloride||http://purl.obolibrary.org/obo/CHEBI_63039
13348||770||GM14382||http://purl.obolibrary.org/obo/CLO_0031198
13349||8191||clobenpropit dihydrobromide||http://purl.obolibrary.org/obo/CHEBI_64165
13350||10994||diquat||http://purl.obolibrary.org/obo/CHEBI_64163
13351||5502||Pectobacterium atrosepticum||http://purl.obolibrary.org/obo/NCBITaxon_29471
13352||9268||enucleated reticulocyte||http://purl.obolibrary.org/obo/CL_0002422
13354||2672||appendicular skeleton||http://purl.obolibrary.org/obo/UBERON_0002091
13355||10071||DN2a thymocyte||http://purl.obolibrary.org/obo/CL_0002423
13353||10994||N-methylquipazine dimaleate||http://purl.obolibrary.org/obo/CHEBI_64162
13357||2672||interventricular septum||http://purl.obolibrary.org/obo/UBERON_0002094
13356||10071||DN2b thymocyte||http://purl.obolibrary.org/obo/CL_0002424
13358||10113||early T lineage precursor||http://purl.obolibrary.org/obo/CL_0002425
13359||14549||immature T cell||http://purl.obolibrary.org/obo/CL_0002420
13360||2672||skin of body||http://purl.obolibrary.org/obo/UBERON_0002097
13361||9268||nucleated reticulocyte||http://purl.obolibrary.org/obo/CL_0002421
13362||7606||primitive erythroid lineage cell||http://purl.obolibrary.org/obo/CL_0002417
13363||13386||mature Vgamma1.1-positive, Vdelta6.3-positive thymocyte||http://purl.obolibrary.org/obo/CL_0002416
13364||13386||immature Vgamma1.1-positive, Vdelta6.3-positive thymocyte||http://purl.obolibrary.org/obo/CL_0002415
13365||2252||Fine-Lubinsky syndrome||http://www.orpha.net/ORDO/Orphanet_1272
13366||2252||Bowen-Conradi syndrome||http://www.orpha.net/ORDO/Orphanet_1270
13367||14549||mature T cell||http://purl.obolibrary.org/obo/CL_0002419
13368||2021||Brachydactyly - arterial hypertension||http://www.orpha.net/ORDO/Orphanet_1276
13369||2252||Brachydactyly - mesomelia - intellectual disability - heart defects||http://www.orpha.net/ORDO/Orphanet_1277
13370||2021||Brachydactyly - elbow wrist dysplasia||http://www.orpha.net/ORDO/Orphanet_1275
13371||2021||Brachydactyly - preaxial hallux varus||http://www.orpha.net/ORDO/Orphanet_1278
13372||9762||Hyperglycemia||http://purl.obolibrary.org/obo/HP_0003074
13374||3733||hypoalbuminemia||http://purl.obolibrary.org/obo/HP_0003073
13373||10994||tanespimycin||http://purl.obolibrary.org/obo/CHEBI_64153
13376||6570||Tricarboxylic acid cycle disorder||http://www.orpha.net/ORDO/Orphanet_254749
13375||10994||radicicol||http://purl.obolibrary.org/obo/CHEBI_556075
13377||770||GM14381||http://purl.obolibrary.org/obo/CLO_0031189
13378||6570||Pyruvate metabolism disorder||http://www.orpha.net/ORDO/Orphanet_254746
13379||5204||Congenital sucrase-isomaltase deficiency without sucrose intolerance||http://www.orpha.net/ORDO/Orphanet_306486
13380||8191||2-methyl-6-(phenylethynyl)pyridine hydrochloride||http://purl.obolibrary.org/obo/CHEBI_64158
13381||5025||Gibberella fujikuroi||http://purl.obolibrary.org/obo/NCBITaxon_5127
13382||5025||Gibberella pulicaris||http://purl.obolibrary.org/obo/NCBITaxon_5128
13383||13385||mature Vgamma1.1-positive, Vdelta6.3-negative thymocyte||http://purl.obolibrary.org/obo/CL_0002413
13384||13385||immature Vgamma1.1-positive, Vdelta6.3-negative thymocyte||http://purl.obolibrary.org/obo/CL_0002414
13385||13388||Vgamma1.1-positive, Vdelta6.3-negative thymocyte||http://purl.obolibrary.org/obo/CL_0002411
13386||13388||Vgamma1.1-positive, Vdelta6.3-positive thymocyte||http://purl.obolibrary.org/obo/CL_0002412
13387||8191||imetit dihydrobromide||http://purl.obolibrary.org/obo/CHEBI_64151
13389||1560||plastid||http://purl.obolibrary.org/obo/GO_0009536
13388||10206||gamma-delta thymocyte||http://purl.obolibrary.org/obo/CL_0002405
13392||13389||proplastid||http://purl.obolibrary.org/obo/GO_0009537
13393||770||RBA-2 cell||http://purl.obolibrary.org/obo/BTO_0002599
13391||5025||Neurospora crassa||http://purl.obolibrary.org/obo/NCBITaxon_5141
13390||10206||fetal thymocyte||http://purl.obolibrary.org/obo/CL_0002404
13394||13388||mature Vgamma2-positive thymocyte||http://purl.obolibrary.org/obo/CL_0002407
13395||13388||immature Vgamma2-positive thymocyte||http://purl.obolibrary.org/obo/CL_0002406
13396||13388||mature Vgamma2-negative thymocyte||http://purl.obolibrary.org/obo/CL_0002409
13399||13388||immature Vgamma2-negative thymocyte||http://purl.obolibrary.org/obo/CL_0002408
13397||770||MDAMB231||http://www.ebi.ac.uk/efo/EFO_0001209
13398||5025||Podospora anserina||http://purl.obolibrary.org/obo/NCBITaxon_5145
13400||1813||culture condition:dark-grown cell||http://purl.obolibrary.org/obo/BTO_0000332
13401||1022||Brugia malayi||http://purl.obolibrary.org/obo/NCBITaxon_6279
13402||5502||Brucella melitensis||http://purl.obolibrary.org/obo/NCBITaxon_29459
13403||10994||depudecin||http://purl.obolibrary.org/obo/CHEBI_64143
13404||10994||1-[1-(1-benzothiophen-2-yl)cyclohexyl]piperidine maleate||http://purl.obolibrary.org/obo/CHEBI_64144
13405||770||MCF 10A||http://www.ebi.ac.uk/efo/EFO_0001200
13406||10994||tropanyl 3,5-dimethylbenzoate||http://purl.obolibrary.org/obo/CHEBI_64142
13407||10994||5-nonyloxytryptamine oxalate||http://purl.obolibrary.org/obo/CHEBI_64147
13408||5204||Congenital sucrase-isomaltase deficiency with starch and lactose intolerance||http://www.orpha.net/ORDO/Orphanet_306474
13409||21||Mitochondrial oxidative phosphorylation disorder due to mitochondrial DNA anomalies||http://www.orpha.net/ORDO/Orphanet_254758
13410||770||MDAMB134VI||http://www.ebi.ac.uk/efo/EFO_0001205
13411||770||MDAMB157||http://www.ebi.ac.uk/efo/EFO_0001206
13412||10652||obsolete_MDAMB-157||http://www.ebi.ac.uk/efo/EFO_0001207
13414||770||MDAMB175VII||http://www.ebi.ac.uk/efo/EFO_0001208
13413||5502||Caulobacter vibrioides||http://purl.obolibrary.org/obo/NCBITaxon_155892
13415||10058||Fraction B/C precursor B cell||http://purl.obolibrary.org/obo/CL_0002400
13416||13390||mature dendritic epithelial T cell precursor||http://purl.obolibrary.org/obo/CL_0002401
13417||770||MCF12A||http://www.ebi.ac.uk/efo/EFO_0001202
13419||770||MCF-7||http://www.ebi.ac.uk/efo/EFO_0001203
13418||8239||Peyer s patch B cell||http://purl.obolibrary.org/obo/CL_0002402
13420||13390||mature Vgamma2-positive fetal thymocyte||http://purl.obolibrary.org/obo/CL_0002403
13421||13025||Distal arthrogryposis||http://www.orpha.net/ORDO/Orphanet_97120
13422||5025||Claviceps purpurea||http://purl.obolibrary.org/obo/NCBITaxon_5111
13423||770||MDAMB453||http://www.ebi.ac.uk/efo/EFO_0001215
13424||770||MDAMB436||http://www.ebi.ac.uk/efo/EFO_0001214
13425||770||MDAMB435||http://www.ebi.ac.uk/efo/EFO_0001213
13426||770||MDAMB415||http://www.ebi.ac.uk/efo/EFO_0001212
13427||770||MM1||http://www.ebi.ac.uk/efo/EFO_0001219
13428||770||Met5A||http://www.ebi.ac.uk/efo/EFO_0001218
13430||770||MDAMB468||http://www.ebi.ac.uk/efo/EFO_0001216
13429||4430||tyrosine kinase inhibitor||http://purl.obolibrary.org/obo/CHEBI_38637
13431||3273||Autosomal dominant focal dystonia, DYT25||http://www.orpha.net/ORDO/Orphanet_329466
13432||3074||umbilical vein||http://purl.obolibrary.org/obo/UBERON_0002066
13433||2672||dermis||http://purl.obolibrary.org/obo/UBERON_0002067
13435||4259||response to bronchodilator||http://purl.obolibrary.org/obo/GO_0097366
13434||770||MDAMB361||http://www.ebi.ac.uk/efo/EFO_0001211
13436||1754||Lipoprotein glomerulopathy||http://www.orpha.net/ORDO/Orphanet_329481
13437||533||X-linked spastic paraplegia type 16||http://www.orpha.net/ORDO/Orphanet_100997
13438||6928||Autosomal dominant spastic paraplegia type 17||http://www.orpha.net/ORDO/Orphanet_100998
13439||13471||Autosomal dominant spastic paraplegia type 19||http://www.orpha.net/ORDO/Orphanet_100999
13441||586||Autosomal dominant spastic paraplegia type 13||http://www.orpha.net/ORDO/Orphanet_100994
13440||770||PAC2||http://www.ebi.ac.uk/efo/EFO_0001224
13443||13471||Autosomal dominant spastic paraplegia type 12||http://www.orpha.net/ORDO/Orphanet_100993
13442||770||NIH3T3-L1||http://www.ebi.ac.uk/efo/EFO_0001223
13445||13470||Autosomal recessive spastic paraplegia type 15||http://www.orpha.net/ORDO/Orphanet_100996
13444||770||R18||http://www.ebi.ac.uk/efo/EFO_0001226
13448||2672||embryonic structure||http://purl.obolibrary.org/obo/UBERON_0002050
13449||583||Autosomal recessive spastic paraplegia type 14||http://www.orpha.net/ORDO/Orphanet_100995
13447||770||PC12||http://www.ebi.ac.uk/efo/EFO_0001225
13446||799||dopamine agonist||http://purl.obolibrary.org/obo/CHEBI_51065
13450||13501||Autosomal dominant spastic paraplegia type 9||http://www.orpha.net/ORDO/Orphanet_100990
13451||770||R43||http://www.ebi.ac.uk/efo/EFO_0001228
13453||13496||Vaccinia virus Lister||http://purl.obolibrary.org/obo/NCBITaxon_10252
13452||770||R28||http://www.ebi.ac.uk/efo/EFO_0001227
13455||770||R46||http://www.ebi.ac.uk/efo/EFO_0001229
13454||586||Autosomal dominant spastic paraplegia type 10||http://www.orpha.net/ORDO/Orphanet_100991
13456||12358||Adult-onset distal myopathy due to VCP mutation||http://www.orpha.net/ORDO/Orphanet_329478
13457||14513||ciliary ganglion||http://purl.obolibrary.org/obo/UBERON_0002058
13458||770||MOLT-4||http://www.ebi.ac.uk/efo/EFO_0001220
13459||7966||Spastic paraplegia - Paget disease of bone||http://www.orpha.net/ORDO/Orphanet_329475
13460||770||NIH3T3||http://www.ebi.ac.uk/efo/EFO_0001222
13461||770||NCI-H929||http://www.ebi.ac.uk/efo/EFO_0001221
13462||2477||Congenital dyserythropoietic anemia type IV||http://www.orpha.net/ORDO/Orphanet_293825
13463||8190||kainic acid||http://purl.obolibrary.org/obo/CHEBI_31746
13464||1491||cell periphery||http://purl.obolibrary.org/obo/GO_0071944
13465||586||Autosomal dominant spastic paraplegia type 6||http://www.orpha.net/ORDO/Orphanet_100988
13466||13471||Autosomal dominant spastic paraplegia type 8||http://www.orpha.net/ORDO/Orphanet_100989
13467||583||Autosomal recessive spastic paraplegia type 5A||http://www.orpha.net/ORDO/Orphanet_100986
13468||4803||MITF-related melanoma and renal cell carcinoma predisposition syndrome||http://www.orpha.net/ORDO/Orphanet_293822
13469||13389||chloroplast||http://purl.obolibrary.org/obo/GO_0009507
13470||1418||Autosomal recessive complex spastic paraplegia||http://www.orpha.net/ORDO/Orphanet_100981
13471||1417||Autosomal dominant pure spastic paraplegia||http://www.orpha.net/ORDO/Orphanet_100980
13472||770||SUM1315MO2||http://www.ebi.ac.uk/efo/EFO_0001239
13473||10994||nafadotride||http://purl.obolibrary.org/obo/CHEBI_64191
13475||2672||cardiac ventricle||http://purl.obolibrary.org/obo/UBERON_0002082
13474||770||SKGT4||http://www.ebi.ac.uk/efo/EFO_0001237
13476||586||Autosomal dominant spastic paraplegia type 4||http://www.orpha.net/ORDO/Orphanet_100985
13478||770||SKBR3||http://www.ebi.ac.uk/efo/EFO_0001236
13477||586||Autosomal dominant spastic paraplegia type 3||http://www.orpha.net/ORDO/Orphanet_100984
13479||10994||ritanserin||http://purl.obolibrary.org/obo/CHEBI_64195
13484||10994||paroxetine maleate||http://purl.obolibrary.org/obo/CHEBI_64194
13483||2672||cardiac atrium||http://purl.obolibrary.org/obo/UBERON_0002081
13482||770||S49||http://www.ebi.ac.uk/efo/EFO_0001234
13480||1417||Autosomal recessive pure spastic paraplegia||http://www.orpha.net/ORDO/Orphanet_100982
13481||5502||Escherichia coli O157:H7 str. EDL933||http://purl.obolibrary.org/obo/NCBITaxon_155864
13485||770||S2||http://www.ebi.ac.uk/efo/EFO_0001233
13486||770||RKO||http://www.ebi.ac.uk/efo/EFO_0001232
13487||1732||Genetic hyperferritinemia without iron overload||http://www.orpha.net/ORDO/Orphanet_254704
13489||770||RAW264.7||http://www.ebi.ac.uk/efo/EFO_0001231
13488||8191||carmoxirole hydrochloride||http://purl.obolibrary.org/obo/CHEBI_64199
13491||10994||dimercaprol||http://purl.obolibrary.org/obo/CHEBI_64198
13492||770||R8||http://www.ebi.ac.uk/efo/EFO_0001230
13490||5204||Congenital sucrase-isomaltase deficiency with minimal starch tolerance||http://www.orpha.net/ORDO/Orphanet_306446
13493||13516||response to risperidone||http://purl.obolibrary.org/obo/GO_0097336
13494||13516||response to quetiapine||http://purl.obolibrary.org/obo/GO_0097335
13495||13516||response to clozapine||http://purl.obolibrary.org/obo/GO_0097338
13498||13516||response to ziprasidone||http://purl.obolibrary.org/obo/GO_0097337
13497||4740||Adamantinoma||http://www.orpha.net/ORDO/Orphanet_55881
13496||5005||Virus||http://purl.obolibrary.org/obo/NCBITaxon_10239
13499||10907||Bathing suit ichthyosis||http://www.orpha.net/ORDO/Orphanet_100976
13500||6610||Cloverleaf skull - asphyxiating thoracic dysplasia||http://www.orpha.net/ORDO/Orphanet_100978
13501||1418||Autosomal dominant complex spastic paraplegia||http://www.orpha.net/ORDO/Orphanet_100979
13502||2672||elementary body||http://purl.obolibrary.org/obo/BTO_0000377
13503||2672||hair follicle||http://purl.obolibrary.org/obo/UBERON_0002073
13504||770||TERV||http://www.ebi.ac.uk/efo/EFO_0001249
13505||1669||renal cell carcinoma cell line||http://purl.obolibrary.org/obo/BTO_0000383
13506||2672||embryonic blood||http://purl.obolibrary.org/obo/BTO_0000381
13507||770||SUM52PE||http://www.ebi.ac.uk/efo/EFO_0001246
13508||770||SUM44PE||http://www.ebi.ac.uk/efo/EFO_0001245
13510||1732||FRAXF syndrome||http://www.orpha.net/ORDO/Orphanet_100974
13509||5204||Congenital sucrase-isomaltase deficiency with starch intolerance||http://www.orpha.net/ORDO/Orphanet_306436
13511||11899||FRAXE intellectual disability||http://www.orpha.net/ORDO/Orphanet_100973
13512||770||T47D||http://www.ebi.ac.uk/efo/EFO_0001247
13514||12747||response to cytarabine||http://purl.obolibrary.org/obo/GO_0097331
13515||10994||nilotinib||http://purl.obolibrary.org/obo/CHEBI_52172
13513||770||SUM185PE||http://www.ebi.ac.uk/efo/EFO_0001242
13516||4259||response to antipsychotic drug||http://purl.obolibrary.org/obo/GO_0097332
13517||770||SUM159PT||http://www.ebi.ac.uk/efo/EFO_0001241
13518||10994||benserazide||http://purl.obolibrary.org/obo/CHEBI_64187
13519||13516||response to olanzapine||http://purl.obolibrary.org/obo/GO_0097333
13520||770||SUM225CWN||http://www.ebi.ac.uk/efo/EFO_0001244
13522||13516||response to perphenazine||http://purl.obolibrary.org/obo/GO_0097334
13521||770||SUM190PT||http://www.ebi.ac.uk/efo/EFO_0001243
13523||13421||Distal arthrogryposis type 5D||http://www.orpha.net/ORDO/Orphanet_329457
13524||770||SUM149PT||http://www.ebi.ac.uk/efo/EFO_0001240
13525||12741||response to 5-fluoro-2 -deoxyuridine||http://purl.obolibrary.org/obo/GO_0097330
13526||10994||polyethylene glycol||http://purl.obolibrary.org/obo/CHEBI_46793
13527||772||hair follicle dermal papilla cell||http://purl.obolibrary.org/obo/CL_0000346
13528||1826||Nicotiana langsdorffii x Nicotiana sanderae||http://purl.obolibrary.org/obo/NCBITaxon_164110
13529||13470||Autosomal recessive spastic paraplegia type 69||http://www.orpha.net/ORDO/Orphanet_401830
13530||13470||Autosomal recessive spastic paraplegia type 70||http://www.orpha.net/ORDO/Orphanet_401835
13531||772||extraembryonic cell||http://purl.obolibrary.org/obo/CL_0000349
13532||15322||epiblast cell||http://purl.obolibrary.org/obo/CL_0000352
13534||1826||Brassica rapa subsp. pekinensis||http://purl.obolibrary.org/obo/NCBITaxon_51351
13533||1022||Notophthalmus viridescens||http://purl.obolibrary.org/obo/NCBITaxon_8316
13535||13531||trophoblast cell||http://purl.obolibrary.org/obo/CL_0000351
13536||13471||Autosomal recessive spastic paraplegia type 72||http://www.orpha.net/ORDO/Orphanet_401849
13537||13480||Autosomal recessive spastic paraplegia type 71||http://www.orpha.net/ORDO/Orphanet_401840
13538||6770||Hypoplastic pancreas-intestinal atresia-hypoplastic gallbalder syndrome||http://www.orpha.net/ORDO/Orphanet_293864
13539||618||zygote||http://purl.obolibrary.org/obo/CL_0000365
13541||13543||Drosophila ananassae||http://purl.obolibrary.org/obo/NCBITaxon_7217
13540||2671||conidiophore||http://purl.obolibrary.org/obo/BTO_0000281
13542||14614||epidermal cell||http://purl.obolibrary.org/obo/CL_0000362
13543||1022||Drosophila||http://purl.obolibrary.org/obo/NCBITaxon_7215
13544||13547||Lipoic acid synthetase deficiency||http://www.orpha.net/ORDO/Orphanet_401859
13545||10994||calcium(2 )||http://purl.obolibrary.org/obo/CHEBI_29108
13546||1022||Onthophagus taurus||http://purl.obolibrary.org/obo/NCBITaxon_166361
13547||15483||Lipoic acid biosynthesis defect||http://www.orpha.net/ORDO/Orphanet_401854
13548||3854||Methanococcus maripaludis S2||http://purl.obolibrary.org/obo/NCBITaxon_267377
13549||770||ND00022||http://purl.obolibrary.org/obo/CLO_0030105
13550||1022||Xenopus laevis||http://purl.obolibrary.org/obo/NCBITaxon_8355
13551||5129||Constitutional dyserythropoietic anemia||http://www.orpha.net/ORDO/Orphanet_293830
13552||13543||Drosophila erecta||http://purl.obolibrary.org/obo/NCBITaxon_7220
13553||772||protoplast||http://purl.obolibrary.org/obo/CL_0000371
13554||15121||Fatal multiple mitochondrial dysfunction syndrome type 1||http://www.orpha.net/ORDO/Orphanet_401869
13555||10716||Spasticity-ataxia-gait anomalies syndrome||http://www.orpha.net/ORDO/Orphanet_401866
13556||10036||Right temporal lobar atrophy||http://www.orpha.net/ORDO/Orphanet_293848
13557||13547||Lipoyl transferase 1 deficiency||http://www.orpha.net/ORDO/Orphanet_401862
13558||1022||Ceratitis capitata||http://purl.obolibrary.org/obo/NCBITaxon_7213
13559||6373||Monosomy X||http://www.orpha.net/ORDO/Orphanet_99226
13560||2252||Craniofacial-ulnar-renal syndrome||http://www.orpha.net/ORDO/Orphanet_293843
13561||6373||Mosaic monosomy X||http://www.orpha.net/ORDO/Orphanet_99228
13562||770||ND00268||http://purl.obolibrary.org/obo/CLO_0026399
13563||2672||caudate-putamen||http://purl.obolibrary.org/obo/UBERON_0005383
13564||10886||heregulin B1||http://www.ebi.ac.uk/efo/EFO_0003308
13565||10886||hepatocyte growth factor||http://www.ebi.ac.uk/efo/EFO_0003303
13566||10886||anti-CD28||http://www.ebi.ac.uk/efo/EFO_0003304
13568||10994||Bandrowski s base||http://purl.obolibrary.org/obo/CHEBI_53109
13567||5186||Familial isolated arrhythmogenic ventricular dysplasia, biventricular form||http://www.orpha.net/ORDO/Orphanet_293899
13569||15121||Fatal multiple mitochondrial dysfunction syndrome type 2||http://www.orpha.net/ORDO/Orphanet_401874
13570||1749||Hypobetalipoproteinemia||http://www.orpha.net/ORDO/Orphanet_31154
13571||10994||1,10-phenanthroline||http://purl.obolibrary.org/obo/CHEBI_44975
13572||1749||Hypoalphalipoproteinemia||http://www.orpha.net/ORDO/Orphanet_31153
13573||772||keratinocyte||http://purl.obolibrary.org/obo/CL_0000312
13574||2454||Tangier disease||http://www.orpha.net/ORDO/Orphanet_31150
13575||5502||Methylobacterium extorquens AM1||http://purl.obolibrary.org/obo/NCBITaxon_272630
13576||1022||Xenopus (Silurana) tropicalis||http://purl.obolibrary.org/obo/NCBITaxon_8364
13577||13579||Mus caroli||http://purl.obolibrary.org/obo/NCBITaxon_10089
13578||13496||Cucumber mosaic virus||http://purl.obolibrary.org/obo/NCBITaxon_12305
13579||1022||Mus||http://purl.obolibrary.org/obo/NCBITaxon_10088
13580||1022||Locusta migratoria manilensis||http://purl.obolibrary.org/obo/NCBITaxon_229990
13581||5502||Dickeya dadantii||http://purl.obolibrary.org/obo/NCBITaxon_204038
13582||10994||3 -amino-3 -deoxy-N(6),N(6)-dimethyladenosine||http://purl.obolibrary.org/obo/CHEBI_42839
13583||13496||Cucumber mosaic virus (strain FNY)||http://purl.obolibrary.org/obo/NCBITaxon_12307
13584||3068||callous character||http://www.ebi.ac.uk/efo/EFO_0004891
13585||7529||Sasang constitutional medicine||http://www.ebi.ac.uk/efo/EFO_0004892
13587||13579||Mus musculus||http://purl.obolibrary.org/obo/NCBITaxon_10090
13586||3068||anti-social behavior||http://www.ebi.ac.uk/efo/EFO_0004890
13588||1391||Tourette syndrome||http://www.ebi.ac.uk/efo/EFO_0004895
13589||1761||testicular dysgenesis syndrome||http://www.ebi.ac.uk/efo/EFO_0004893
13590||1732||tetralogy of fallot||http://www.ebi.ac.uk/efo/EFO_0004894
13591||2672||olfactory lobe||http://purl.obolibrary.org/obo/UBERON_0005366
13592||7391||Mus spretus||http://purl.obolibrary.org/obo/NCBITaxon_10096
13593||5502||Streptococcus gordonii str. Challis||http://purl.obolibrary.org/obo/NCBITaxon_29390
13595||10994||fenoldopam||http://purl.obolibrary.org/obo/CHEBI_5002
13594||7391||Mus musculus castaneus||http://purl.obolibrary.org/obo/NCBITaxon_10091
13597||10994||fenofibrate||http://purl.obolibrary.org/obo/CHEBI_5001
13596||7391||Mus musculus domesticus||http://purl.obolibrary.org/obo/NCBITaxon_10092
13598||5502||Ralstonia eutropha H16||http://purl.obolibrary.org/obo/NCBITaxon_381666
13599||5502||Lactococcus lactis subsp. lactis Il1403||http://purl.obolibrary.org/obo/NCBITaxon_272623
13600||5502||Legionella pneumophila subsp. pneumophila str. Philadelphia 1||http://purl.obolibrary.org/obo/NCBITaxon_272624
13601||14970||urinary arsenic measurement||http://www.ebi.ac.uk/efo/EFO_0004880
13602||1826||Brassica carinata||http://purl.obolibrary.org/obo/NCBITaxon_52824
13604||4259||asparaginase hypersensitivity||http://www.ebi.ac.uk/efo/EFO_0004881
13603||5502||Staphylococcus saprophyticus||http://purl.obolibrary.org/obo/NCBITaxon_29385
13605||10652||obsolete_avelline corneal dystrophy||http://www.ebi.ac.uk/efo/EFO_0004882
13606||10652||obsolete_Blepharophimosis-Ptosis-Epicanthus inversus syndrome||http://www.ebi.ac.uk/efo/EFO_0004883
13607||8700||breast size||http://www.ebi.ac.uk/efo/EFO_0004884
13608||14970||early cardiac repolarization measurement||http://www.ebi.ac.uk/efo/EFO_0004885
13610||14970||intra cranial volume||http://www.ebi.ac.uk/efo/EFO_0004886
13609||8193||4,5-dianilinophthalimide||http://purl.obolibrary.org/obo/CHEBI_53110
13611||14970||maximal oxygen uptake measurement||http://www.ebi.ac.uk/efo/EFO_0004887
13612||4050||post operative nausea and vomiting||http://www.ebi.ac.uk/efo/EFO_0004888
13613||772||neural crest cell||http://purl.obolibrary.org/obo/CL_0000333
13614||1391||postoperative ventricular dysfunction||http://www.ebi.ac.uk/efo/EFO_0004889
13615||10994||8-(3-chlorostyryl) caffeine||http://purl.obolibrary.org/obo/CHEBI_53115
13616||4929||Familial dilated cardiomyopathy with conduction defect due to LMNA mutation||http://www.orpha.net/ORDO/Orphanet_300751
13617||1733||Hyperlipoproteinemia type 5||http://www.orpha.net/ORDO/Orphanet_70470
13618||7551||Leigh syndrome with cardiomyopathy||http://www.orpha.net/ORDO/Orphanet_70474
13619||1022||Bufo marinus||http://purl.obolibrary.org/obo/NCBITaxon_8386
13620||11433||adrenal gland||http://purl.obolibrary.org/obo/CL_0000336
13621||7551||Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type||http://www.orpha.net/ORDO/Orphanet_70472
13622||14490||neuroblast (sensu Vertebrata)||http://purl.obolibrary.org/obo/CL_0000337
13623||5186||Familial isolated arrhythmogenic ventricular dysplasia, left dominant form||http://www.orpha.net/ORDO/Orphanet_293888
13624||10994||(S)-alpha-methyl-4-carboxyphenylglycine||http://purl.obolibrary.org/obo/CHEBI_43876
13625||9812||Coloboma of superior eyelid||http://www.orpha.net/ORDO/Orphanet_155884
13626||10652||obsolete_pituitary adenoma||http://www.ebi.ac.uk/efo/EFO_0002619
13627||13822||Congenital absence/hypoplasia of thumb||http://www.orpha.net/ORDO/Orphanet_294988
13628||2737||metastatic melanoma||http://www.ebi.ac.uk/efo/EFO_0002617
13630||13799||Apodia||http://www.orpha.net/ORDO/Orphanet_294986
13629||1006||pancreatic carcinoma||http://www.ebi.ac.uk/efo/EFO_0002618
13631||13799||Acheiria||http://www.orpha.net/ORDO/Orphanet_294983
13632||2714||human herpesvirus 8 infection||http://www.ebi.ac.uk/efo/EFO_0002612
13633||13799||Congenital absence of both lower leg and foot||http://www.orpha.net/ORDO/Orphanet_294981
13634||10652||obsolete_hereditary breast and ovarian cancer||http://www.ebi.ac.uk/efo/EFO_0002611
13635||13496||Human adenovirus 40||http://purl.obolibrary.org/obo/NCBITaxon_28284
13636||11030||cocaine dependence||http://www.ebi.ac.uk/efo/EFO_0002610
13637||13693||pericardial cell primordium||http://www.ebi.ac.uk/efo/EFO_0003348
13638||96||macroglobulinemia||http://www.ebi.ac.uk/efo/EFO_0002616
13640||13693||visceral muscle primordium||http://www.ebi.ac.uk/efo/EFO_0003349
13639||12543||mathematical ability||http://www.ebi.ac.uk/efo/EFO_0004875
13641||11614||internal carotid artery stenosis||http://www.ebi.ac.uk/efo/EFO_0002615
13644||13693||visual anlage||http://www.ebi.ac.uk/efo/EFO_0003346
13642||13496||Human adenovirus 4||http://purl.obolibrary.org/obo/NCBITaxon_28280
13643||11618||insulin resistance||http://www.ebi.ac.uk/efo/EFO_0002614
13647||13693||hypopharynx anlage||http://www.ebi.ac.uk/efo/EFO_0003347
13645||10994||loxtidine||http://purl.obolibrary.org/obo/CHEBI_6550
13646||1796||iatrogenic Kaposi s sarcoma||http://www.ebi.ac.uk/efo/EFO_0002613
13650||14970||inflammatory marker measurement||http://www.ebi.ac.uk/efo/EFO_0004872
13648||13693||tracheal primordium||http://www.ebi.ac.uk/efo/EFO_0003344
13649||9812||Coloboma of inferior eyelid||http://www.orpha.net/ORDO/Orphanet_155889
13651||13693||foregut anlage||http://www.ebi.ac.uk/efo/EFO_0003345
13653||14970||memory performance||http://www.ebi.ac.uk/efo/EFO_0004874
13652||13693||hindgut anlage||http://www.ebi.ac.uk/efo/EFO_0003342
13655||14970||cytokine measurement||http://www.ebi.ac.uk/efo/EFO_0004873
13654||13693||ventral ectoderm anlage||http://www.ebi.ac.uk/efo/EFO_0003343
13656||13693||posterior endoderm anlage||http://www.ebi.ac.uk/efo/EFO_0003340
13657||13693||ventral thoracic disc||http://www.ebi.ac.uk/efo/EFO_0003341
13658||13496||Human adenovirus 5||http://purl.obolibrary.org/obo/NCBITaxon_28285
13659||14970||sleep measurement||http://www.ebi.ac.uk/efo/EFO_0004870
13660||5502||Thermoanaerobacter sp. X514||http://purl.obolibrary.org/obo/NCBITaxon_399726
13661||9857||Otomandibular dysplasia||http://www.orpha.net/ORDO/Orphanet_155896
13662||13824||Brachydactyly of toes||http://www.orpha.net/ORDO/Orphanet_294998
13663||10652||obsolete_gene||http://www.ebi.ac.uk/efo/EFO_0002606
13664||10652||obsolete_experiment||http://www.ebi.ac.uk/efo/EFO_0002607
13665||10959||AIDS dementia||http://www.ebi.ac.uk/efo/EFO_0002608
13666||1980||chronic childhood arthritis||http://www.ebi.ac.uk/efo/EFO_0002609
13667||13823||Split foot||http://www.orpha.net/ORDO/Orphanet_294994
13668||13824||Brachydactyly of fingers||http://www.orpha.net/ORDO/Orphanet_294996
13669||13693||posterior spiracle primordium||http://www.ebi.ac.uk/efo/EFO_0003339
13670||13822||Congenital absence/hypoplasia of fingers excluding thumb||http://www.orpha.net/ORDO/Orphanet_294990
13671||770||ND00259||http://purl.obolibrary.org/obo/CLO_0026349
13673||14970||YKL40 measurement||http://www.ebi.ac.uk/efo/EFO_0004869
13672||3446||proximal portion of anterior interventricular branch of left coronary artery||http://www.ebi.ac.uk/efo/EFO_0002601
13675||14970||volumetric brain MRI||http://www.ebi.ac.uk/efo/EFO_0004868
13676||13823||Split hand||http://www.orpha.net/ORDO/Orphanet_294992
13674||3446||distal portion of right coronary artery||http://www.ebi.ac.uk/efo/EFO_0002600
13677||14574||vitamin E measurement||http://www.ebi.ac.uk/efo/EFO_0004867
13678||13695||Drosophila embryonic structure||http://www.ebi.ac.uk/efo/EFO_0003335
13679||3446||proximal portion of right coronary artery||http://www.ebi.ac.uk/efo/EFO_0002603
13680||14970||autoantibody measurement||http://www.ebi.ac.uk/efo/EFO_0004866
13682||13693||mesectoderm anlage||http://www.ebi.ac.uk/efo/EFO_0003336
13681||3446||proximal portion of circumflex branch of left coronary artery||http://www.ebi.ac.uk/efo/EFO_0002602
13684||15538||gene name||http://www.ebi.ac.uk/efo/EFO_0002605
13683||14970||thyroid volume||http://www.ebi.ac.uk/efo/EFO_0004865
13685||13693||head mesoderm||http://www.ebi.ac.uk/efo/EFO_0003337
13687||14970||renal sinus adipose tissue measurement||http://www.ebi.ac.uk/efo/EFO_0004864
13686||13693||embryonic optic lobe primordium||http://www.ebi.ac.uk/efo/EFO_0003338
13688||14970||recombination rate||http://www.ebi.ac.uk/efo/EFO_0004863
13689||2672||zebrafish component||http://www.ebi.ac.uk/efo/EFO_0003331
13692||14970||phytosterol measurement||http://www.ebi.ac.uk/efo/EFO_0004862
13691||13689||zebrafish embryonic structure||http://www.ebi.ac.uk/efo/EFO_0003332
13690||13661||Mandibulofacial dysostosis||http://www.orpha.net/ORDO/Orphanet_155899
13694||14970||phosphorus measurement||http://www.ebi.ac.uk/efo/EFO_0004861
13693||13695||Drosophila developmental tissue||http://www.ebi.ac.uk/efo/EFO_0003333
13696||14970||common carotid intimal medial thickness||http://www.ebi.ac.uk/efo/EFO_0004860
13695||2672||Drosophila component||http://www.ebi.ac.uk/efo/EFO_0003334
13697||13797||Amelia of lower limb||http://www.orpha.net/ORDO/Orphanet_294969
13698||12083||Popliteal pterygium syndrome||http://www.orpha.net/ORDO/Orphanet_294963
13699||13797||Amelia of upper limb||http://www.orpha.net/ORDO/Orphanet_294967
13700||13025||Lethal congenital contracture syndrome||http://www.orpha.net/ORDO/Orphanet_294965
13702||14605||vitamin A measurement||http://www.ebi.ac.uk/efo/EFO_0004857
13701||2670||root tip||http://purl.obolibrary.org/obo/PO_0000025
13703||11618||abdominal aortic artery calcification||http://www.ebi.ac.uk/efo/EFO_0004859
13704||8191||fasudil hydrochloride||http://purl.obolibrary.org/obo/CHEBI_31593
13705||13799||Congenital absence of both forearm and hand||http://www.orpha.net/ORDO/Orphanet_294979
13706||13797||Tetra-amelia||http://www.orpha.net/ORDO/Orphanet_294971
13707||7957||Humeral agenesis/hypoplasia||http://www.orpha.net/ORDO/Orphanet_294973
13708||13796||Congenital absence of upper arm and forearm with hand present||http://www.orpha.net/ORDO/Orphanet_294975
13709||13796||Congenital absence of thigh and lower leg with foot present||http://www.orpha.net/ORDO/Orphanet_294977
13710||14970||magnesium measurement||http://www.ebi.ac.uk/efo/EFO_0004845
13711||8700||hip bone size||http://www.ebi.ac.uk/efo/EFO_0004844
13712||14970||vitamin B measurement||http://www.ebi.ac.uk/efo/EFO_0004843
13714||14970||eosinophil count||http://www.ebi.ac.uk/efo/EFO_0004842
13713||10886||basic fibroblast growth factor||http://www.ebi.ac.uk/efo/EFO_0003316
13715||10886||anti-CD3||http://www.ebi.ac.uk/efo/EFO_0003317
13716||27||age at onset||http://www.ebi.ac.uk/efo/EFO_0004847
13717||14970||serotonin measurement||http://www.ebi.ac.uk/efo/EFO_0004846
13718||770||C2C12||http://www.ebi.ac.uk/efo/EFO_0001098
13719||770||Caco-2||http://www.ebi.ac.uk/efo/EFO_0001099
13720||770||BT549||http://www.ebi.ac.uk/efo/EFO_0001096
13721||8700||digit length ratio||http://www.ebi.ac.uk/efo/EFO_0004841
13722||14970||cortical thickness||http://www.ebi.ac.uk/efo/EFO_0004840
13723||770||BT483||http://www.ebi.ac.uk/efo/EFO_0001095
13725||13543||Drosophila simulans||http://purl.obolibrary.org/obo/NCBITaxon_7240
13724||13046||Congenital deformities of limbs||http://www.orpha.net/ORDO/Orphanet_294944
13726||1826||Cichorium intybus||http://purl.obolibrary.org/obo/NCBITaxon_13427
13727||2169||Postaxial polydactyly of fingers||http://www.orpha.net/ORDO/Orphanet_294942
13728||13543||Drosophila teissieri||http://purl.obolibrary.org/obo/NCBITaxon_7243
13729||13543||Drosophila virilis||http://purl.obolibrary.org/obo/NCBITaxon_7244
13730||14970||CD4:CD8 lymphocyte ratio||http://www.ebi.ac.uk/efo/EFO_0004839
13731||13543||Drosophila yakuba||http://purl.obolibrary.org/obo/NCBITaxon_7245
13732||13678||embryonic outer optic lobe primordium||http://www.ebi.ac.uk/efo/EFO_0003391
13733||13678||hypopharynx anlage in statu nascendi||http://www.ebi.ac.uk/efo/EFO_0003392
13734||13678||embryonic Malpighian tubule tip cell||http://www.ebi.ac.uk/efo/EFO_0003390
13735||6249||Joint formation defects||http://www.orpha.net/ORDO/Orphanet_294949
13736||13724||Congenital deformities of fingers||http://www.orpha.net/ORDO/Orphanet_294947
13737||13678||embryonic hindgut||http://www.ebi.ac.uk/efo/EFO_0003389
13738||13678||embryonic maxillary sensory complex||http://www.ebi.ac.uk/efo/EFO_0003388
13740||13678||ventral midline neuroblast||http://www.ebi.ac.uk/efo/EFO_0003387
13741||10994||pristane||http://purl.obolibrary.org/obo/CHEBI_53181
13739||10994||tamoxifen||http://purl.obolibrary.org/obo/CHEBI_41774
13742||14970||caudate nucleus volume||http://www.ebi.ac.uk/efo/EFO_0004830
13743||13678||central brain primordium||http://www.ebi.ac.uk/efo/EFO_0003386
13744||13678||stomatogastric nervous system primordium||http://www.ebi.ac.uk/efo/EFO_0003385
13745||13678||ventral epidermis primordium||http://www.ebi.ac.uk/efo/EFO_0003384
13746||13678||midline primordium||http://www.ebi.ac.uk/efo/EFO_0003383
13747||13678||somatic muscle primordium||http://www.ebi.ac.uk/efo/EFO_0003382
13748||13543||Drosophila sechellia||http://purl.obolibrary.org/obo/NCBITaxon_7238
13749||13778||prohemocyte (sensu Nematoda and Protostomia)||http://purl.obolibrary.org/obo/CL_0000385
13752||13689||blastema||http://purl.obolibrary.org/obo/UBERON_0005306
13751||13543||Drosophila pseudoobscura||http://purl.obolibrary.org/obo/NCBITaxon_7237
13750||10652||obsolete_alcohol consumption||http://www.ebi.ac.uk/efo/EFO_0004836
13753||772||ligament cell||http://purl.obolibrary.org/obo/CL_0000384
13755||14970||calcium measurement||http://www.ebi.ac.uk/efo/EFO_0004838
13754||9795||Iminoglycinuria||http://www.orpha.net/ORDO/Orphanet_42062
13756||14970||RR interval||http://www.ebi.ac.uk/efo/EFO_0004831
13757||14970||optic disc size measurement||http://www.ebi.ac.uk/efo/EFO_0004832
13759||14970||neutrophil count||http://www.ebi.ac.uk/efo/EFO_0004833
13758||2672||connective tissue||http://purl.obolibrary.org/obo/CL_0000388
13760||772||hemocyte||http://purl.obolibrary.org/obo/CL_0000387
13761||13046||Limb overgrowth||http://www.orpha.net/ORDO/Orphanet_294953
13762||13543||Drosophila mojavensis||http://purl.obolibrary.org/obo/NCBITaxon_7230
13764||13046||Congenital joint dislocations||http://www.orpha.net/ORDO/Orphanet_294951
13763||12747||response to irinotecan||http://www.ebi.ac.uk/efo/EFO_0004829
13766||15538||genetic variation||http://www.ebi.ac.uk/efo/EFO_0004828
13765||13543||Drosophila persimilis||http://purl.obolibrary.org/obo/NCBITaxon_7234
13767||13678||pars intercerebralis primordium||http://www.ebi.ac.uk/efo/EFO_0003380
13768||13678||salivary gland body primordium||http://www.ebi.ac.uk/efo/EFO_0003381
13769||6246||Dysostosis with combined reduction defects of upper and lower limbs||http://www.orpha.net/ORDO/Orphanet_294957
13770||6246||Syndrome with limb duplication, polydactyly, syndactyly, and/or hyperphalangy||http://www.orpha.net/ORDO/Orphanet_294959
13771||13470||Autosomal recessive spastic paraplegia type 60||http://www.orpha.net/ORDO/Orphanet_401800
13772||13678||Malpighian tubule main body primordium||http://www.ebi.ac.uk/efo/EFO_0003376
13774||13678||visual anlage in statu nascendi||http://www.ebi.ac.uk/efo/EFO_0003375
13773||13470||Autosomal recessive spastic paraplegia type 63||http://www.orpha.net/ORDO/Orphanet_401805
13775||13678||large intestine primordium||http://www.ebi.ac.uk/efo/EFO_0003378
13776||13678||small intestine primordium||http://www.ebi.ac.uk/efo/EFO_0003377
13777||13678||visual primordium||http://www.ebi.ac.uk/efo/EFO_0003372
13778||14556||blood cell (sensu Nematoda and Protostomia)||http://purl.obolibrary.org/obo/CL_0000390
13779||13678||embryonic inner optic lobe primordium||http://www.ebi.ac.uk/efo/EFO_0003371
13780||13678||hindgut anlage in statu nascendi||http://www.ebi.ac.uk/efo/EFO_0003374
13782||13678||fat body primordium||http://www.ebi.ac.uk/efo/EFO_0003373
13781||2656||crystal cell||http://purl.obolibrary.org/obo/CL_0000392
13783||5103||anti-neutrophil antibody associated vasculitis||http://www.ebi.ac.uk/efo/EFO_0004826
13784||5838||economic and social preference||http://www.ebi.ac.uk/efo/EFO_0004827
13786||13543||Drosophila melanogaster||http://purl.obolibrary.org/obo/NCBITaxon_7227
13785||10652||obsolete_behavior or behavioral disorder measurement||http://www.ebi.ac.uk/efo/EFO_0004824
13787||14970||temperament and character inventory||http://www.ebi.ac.uk/efo/EFO_0004825
13788||13543||Drosophila mauritiana||http://purl.obolibrary.org/obo/NCBITaxon_7226
13789||13678||rectum primordium||http://www.ebi.ac.uk/efo/EFO_0003379
13790||12543||perception of facial expression||http://www.ebi.ac.uk/efo/EFO_0004823
13791||14970||sex ratio||http://www.ebi.ac.uk/efo/EFO_0004820
13792||14970||transforming growth factor beta measurement||http://www.ebi.ac.uk/efo/EFO_0004818
13793||1826||Coffea arabica||http://purl.obolibrary.org/obo/NCBITaxon_13443
13794||14970||resistin measurement||http://www.ebi.ac.uk/efo/EFO_0004819
13795||13470||Autosomal recessive spastic paraplegia type 64||http://www.orpha.net/ORDO/Orphanet_401810
13796||7957||Intercalary limb defects||http://www.orpha.net/ORDO/Orphanet_294927
13797||7957||Amelia||http://www.orpha.net/ORDO/Orphanet_294925
13798||13678||posterior midgut proper primordium||http://www.ebi.ac.uk/efo/EFO_0003370
13799||7957||Terminal limb defects||http://www.orpha.net/ORDO/Orphanet_294929
13800||13693||amnioserosa primordium||http://www.ebi.ac.uk/efo/EFO_0003363
13801||13693||central brain anlage||http://www.ebi.ac.uk/efo/EFO_0003362
13802||13693||head visceral muscle primordium||http://www.ebi.ac.uk/efo/EFO_0003361
13803||13693||ventral imaginal precursor||http://www.ebi.ac.uk/efo/EFO_0003360
13804||13693||oenocyte primordium||http://www.ebi.ac.uk/efo/EFO_0003367
13805||13470||Autosomal recessive spastic paraplegia type 66||http://www.orpha.net/ORDO/Orphanet_401815
13806||13693||primary segmental branch primordium||http://www.ebi.ac.uk/efo/EFO_0003366
13807||13693||longitudinal visceral muscle primordium||http://www.ebi.ac.uk/efo/EFO_0003365
13808||13693||visceral branch primordium||http://www.ebi.ac.uk/efo/EFO_0003364
13809||14970||interleukin-6 measurement||http://www.ebi.ac.uk/efo/EFO_0004810
13810||14970||interleukin-8 measurement||http://www.ebi.ac.uk/efo/EFO_0004811
13811||13678||Malpighian tubule primordium||http://www.ebi.ac.uk/efo/EFO_0003369
13812||14970||interleukin-1 beta measurement||http://www.ebi.ac.uk/efo/EFO_0004812
13813||13678||hindgut proper primordium||http://www.ebi.ac.uk/efo/EFO_0003368
13815||14970||alpha globulin measurement||http://www.ebi.ac.uk/efo/EFO_0004813
13814||1826||Coffea||http://purl.obolibrary.org/obo/NCBITaxon_13442
13816||14970||interleukin-6 receptor measurement||http://www.ebi.ac.uk/efo/EFO_0004814
13817||14970||alpha macroglobulin measurement||http://www.ebi.ac.uk/efo/EFO_0004815
13818||14970||fructose-bisphosphate aldolase measurement||http://www.ebi.ac.uk/efo/EFO_0004809
13819||14970||L lactate dehydrogenase measurement||http://www.ebi.ac.uk/efo/EFO_0004808
13820||2842||short sleep||http://www.ebi.ac.uk/efo/EFO_0004807
13821||14970||asbestos exposure measurement||http://www.ebi.ac.uk/efo/EFO_0004806
13822||13799||Adactyly of hand||http://www.orpha.net/ORDO/Orphanet_294931
13823||13799||Split hand or/and split foot malformation||http://www.orpha.net/ORDO/Orphanet_294935
13824||13799||Brachydactyly||http://www.orpha.net/ORDO/Orphanet_294937
13825||2169||Preaxial polydactyly of fingers||http://www.orpha.net/ORDO/Orphanet_294939
13826||13470||Autosomal recessive spastic paraplegia type 67||http://www.orpha.net/ORDO/Orphanet_401820
13828||13693||inclusive hindgut primordium||http://www.ebi.ac.uk/efo/EFO_0003350
13827||1826||Zea mays subsp. parviglumis||http://purl.obolibrary.org/obo/NCBITaxon_76912
13829||13693||foregut primordium||http://www.ebi.ac.uk/efo/EFO_0003352
13830||770||GM14405||http://purl.obolibrary.org/obo/CLO_0031201
13831||13693||gnathal primordium||http://www.ebi.ac.uk/efo/EFO_0003351
13832||13693||labial sensory complex primordium||http://www.ebi.ac.uk/efo/EFO_0003354
13833||13693||maxillary sensory complex primordium||http://www.ebi.ac.uk/efo/EFO_0003353
13834||13693||head mesoderm anlage||http://www.ebi.ac.uk/efo/EFO_0003356
13836||13693||labral sensory complex primordium||http://www.ebi.ac.uk/efo/EFO_0003355
13835||13470||Autosomal recessive spastic paraplegia type 68||http://www.orpha.net/ORDO/Orphanet_401825
13838||14970||frontal theta oscillation measurement||http://www.ebi.ac.uk/efo/EFO_0004800
13837||13693||sensory nervous system primordium||http://www.ebi.ac.uk/efo/EFO_0003358
13839||13693||proventriculus primordium||http://www.ebi.ac.uk/efo/EFO_0003357
13841||13693||ventral sensory complex primordium||http://www.ebi.ac.uk/efo/EFO_0003359
13840||10994||flucloxacillin||http://purl.obolibrary.org/obo/CHEBI_5098
13842||14970||birth rate||http://www.ebi.ac.uk/efo/EFO_0004804
13843||11618||formal thought disorder||http://www.ebi.ac.uk/efo/EFO_0004805
13845||14970||family size||http://www.ebi.ac.uk/efo/EFO_0004802
13844||10994||losartan||http://purl.obolibrary.org/obo/CHEBI_6541
13846||2063||male fertility||http://www.ebi.ac.uk/efo/EFO_0004803
13847||5502||Streptococcus pseudopneumoniae||http://purl.obolibrary.org/obo/NCBITaxon_257758
13849||770||GM12814||http://www.ebi.ac.uk/efo/EFO_0001157
13848||5103||primary antiphospholipid syndrome||http://www.ebi.ac.uk/efo/EFO_0002689
13851||770||GM12815||http://www.ebi.ac.uk/efo/EFO_0001158
13850||10652||obsolete_myelodysplastic syndrome (MDS)-like||http://www.ebi.ac.uk/efo/EFO_0002688
13853||770||GM12872||http://www.ebi.ac.uk/efo/EFO_0001159
13852||1015||ischemia reperfusion injury||http://www.ebi.ac.uk/efo/EFO_0002687
13854||11563||atopy||http://www.ebi.ac.uk/efo/EFO_0002686
13856||770||GM12762||http://www.ebi.ac.uk/efo/EFO_0001153
13855||9613||interleukin-4 (Homo sapiens)||http://www.ebi.ac.uk/efo/EFO_0003296
13857||10652||obsolete_rosette stage||http://www.ebi.ac.uk/efo/EFO_0002685
13859||770||GM12763||http://www.ebi.ac.uk/efo/EFO_0001154
13858||10652||obsolete_pupa||http://www.ebi.ac.uk/efo/EFO_0002684
13864||770||GM12812||http://www.ebi.ac.uk/efo/EFO_0001155
13861||770||GM14409||http://purl.obolibrary.org/obo/CLO_0031226
13860||306||Hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome||http://www.orpha.net/ORDO/Orphanet_307936
13863||618||floral transition||http://www.ebi.ac.uk/efo/EFO_0002683
13862||10886||listeriolysin||http://www.ebi.ac.uk/efo/EFO_0003294
13867||770||GM12813||http://www.ebi.ac.uk/efo/EFO_0001156
13866||770||GM14414||http://purl.obolibrary.org/obo/CLO_0031225
13865||6681||third instar larva stage||http://www.ebi.ac.uk/efo/EFO_0002682
13868||2672||endocardium||http://purl.obolibrary.org/obo/UBERON_0002165
13870||770||GM12751||http://www.ebi.ac.uk/efo/EFO_0001150
13869||10886||urocortin II||http://www.ebi.ac.uk/efo/EFO_0002680
13872||770||GM12760||http://www.ebi.ac.uk/efo/EFO_0001151
13871||10886||epidermal growth factor||http://www.ebi.ac.uk/efo/EFO_0003298
13873||770||GM12761||http://www.ebi.ac.uk/efo/EFO_0001152
13874||770||GM14408||http://purl.obolibrary.org/obo/CLO_0031227
13875||770||GM14406||http://purl.obolibrary.org/obo/CLO_0031228
13876||5025||Nectria rigidiuscula||http://purl.obolibrary.org/obo/NCBITaxon_57161
13877||1783||array||http://www.ebi.ac.uk/efo/EFO_0002698
13878||13301||high throughput sequencing assay||http://www.ebi.ac.uk/efo/EFO_0002697
13880||770||HCC1007||http://www.ebi.ac.uk/efo/EFO_0001168
13879||10994||chlorphenamine||http://purl.obolibrary.org/obo/CHEBI_52010
13881||11488||high throughput sequencer||http://www.ebi.ac.uk/efo/EFO_0002699
13882||770||HCC1143||http://www.ebi.ac.uk/efo/EFO_0001169
13884||770||H720||http://www.ebi.ac.uk/efo/EFO_0001166
13883||7529||experimental process||http://www.ebi.ac.uk/efo/EFO_0002694
13885||13883||DNA-seq||http://www.ebi.ac.uk/efo/EFO_0002693
13886||770||HBL100||http://www.ebi.ac.uk/efo/EFO_0001167
13888||13301||array assay||http://www.ebi.ac.uk/efo/EFO_0002696
13887||10652||obsolete_GM12892||http://www.ebi.ac.uk/efo/EFO_0001164
13890||770||H209||http://www.ebi.ac.uk/efo/EFO_0001165
13889||10652||obsolete_RNA-seq||http://www.ebi.ac.uk/efo/EFO_0002695
13892||770||GM12875||http://www.ebi.ac.uk/efo/EFO_0001162
13891||5103||systemic lupus erythematosus||http://www.ebi.ac.uk/efo/EFO_0002690
13893||10652||obsolete_GM12891||http://www.ebi.ac.uk/efo/EFO_0001163
13896||2672||early telencephalic vesicle||http://purl.obolibrary.org/obo/UBERON_0009676
13894||770||GM12873||http://www.ebi.ac.uk/efo/EFO_0001160
13895||4738||ChIP-seq||http://www.ebi.ac.uk/efo/EFO_0002692
13897||14513||retinal ganglion||http://www.ebi.ac.uk/efo/EFO_0002691
13898||770||GM12874||http://www.ebi.ac.uk/efo/EFO_0001161
13899||770||HCC1187||http://www.ebi.ac.uk/efo/EFO_0001170
13900||770||GM12057||http://www.ebi.ac.uk/efo/EFO_0001135
13901||770||GM12144||http://www.ebi.ac.uk/efo/EFO_0001136
13902||772||monocyte-derived osteoclast||http://www.ebi.ac.uk/efo/EFO_0002666
13903||770||GM12145||http://www.ebi.ac.uk/efo/EFO_0001137
13904||772||monocyte-derived intermediate cell||http://www.ebi.ac.uk/efo/EFO_0002665
13905||5502||Burkholderia mallei||http://purl.obolibrary.org/obo/NCBITaxon_13373
13907||2672||skeleton||http://purl.obolibrary.org/obo/UBERON_0004288
13906||770||GM12146||http://www.ebi.ac.uk/efo/EFO_0001138
13908||770||GM12154||http://www.ebi.ac.uk/efo/EFO_0001139
13909||10994||ENBREL||http://www.ebi.ac.uk/efo/EFO_0002669
13910||10886||vascular endothelial growth factor||http://www.ebi.ac.uk/efo/EFO_0003276
13911||770||GM12005||http://www.ebi.ac.uk/efo/EFO_0001130
13912||2672||locus ceruleus||http://purl.obolibrary.org/obo/UBERON_0002148
13913||770||GM12006||http://www.ebi.ac.uk/efo/EFO_0001131
13915||770||GM12043||http://www.ebi.ac.uk/efo/EFO_0001132
13914||772||dendritic cell-derived osteoclast||http://www.ebi.ac.uk/efo/EFO_0002662
13917||770||GM12044||http://www.ebi.ac.uk/efo/EFO_0001133
13916||772||dendritic cell-derived intermediate cell||http://www.ebi.ac.uk/efo/EFO_0002661
13918||770||GM12056||http://www.ebi.ac.uk/efo/EFO_0001134
13919||773||primary cell||http://www.ebi.ac.uk/efo/EFO_0002660
13920||14001||Genetic pancreatic disease||http://www.orpha.net/ORDO/Orphanet_165661
13921||770||GM12717||http://www.ebi.ac.uk/efo/EFO_0001148
13922||770||GM12750||http://www.ebi.ac.uk/efo/EFO_0001149
13924||770||GM12249||http://www.ebi.ac.uk/efo/EFO_0001146
13923||10994||tempol||http://www.ebi.ac.uk/efo/EFO_0002678
13925||10994||phosmet||http://purl.obolibrary.org/obo/CHEBI_38786
13926||2685||micturition||http://purl.obolibrary.org/obo/GO_0060073
13928||770||GM12716||http://www.ebi.ac.uk/efo/EFO_0001147
13927||10994||saline||http://www.ebi.ac.uk/efo/EFO_0002677
13929||10886||urocortin I||http://www.ebi.ac.uk/efo/EFO_0002679
13930||2672||mitral valve||http://purl.obolibrary.org/obo/UBERON_0002135
13931||770||GM12155||http://www.ebi.ac.uk/efo/EFO_0001140
13932||15140||urine||http://purl.obolibrary.org/obo/UBERON_0001088
13934||770||GM12156||http://www.ebi.ac.uk/efo/EFO_0001141
13933||770||AG08904||http://purl.obolibrary.org/obo/CLO_0031232
13935||770||GM12239||http://www.ebi.ac.uk/efo/EFO_0001144
13938||10994||iberin||http://www.ebi.ac.uk/efo/EFO_0002671
13937||770||GM14433||http://purl.obolibrary.org/obo/CLO_0031236
13936||770||GM12248||http://www.ebi.ac.uk/efo/EFO_0001145
13941||2672||aortic valve||http://purl.obolibrary.org/obo/UBERON_0002137
13939||770||GM12234||http://www.ebi.ac.uk/efo/EFO_0001142
13940||10994||ovalbumin||http://www.ebi.ac.uk/efo/EFO_0002674
13942||10994||antiprogestin||http://www.ebi.ac.uk/efo/EFO_0002673
13944||770||GM14439||http://purl.obolibrary.org/obo/CLO_0031234
13943||770||GM12236||http://www.ebi.ac.uk/efo/EFO_0001143
13945||6899||Microphthalmia with limb anomalies||http://www.orpha.net/ORDO/Orphanet_1106
13946||12769||Anophthalmia plus syndrome||http://www.orpha.net/ORDO/Orphanet_1104
13947||770||GM14432||http://purl.obolibrary.org/obo/CLO_0031238
13949||770||GM14417||http://purl.obolibrary.org/obo/CLO_0031239
13948||9613||interleukin-2 (Mus musculus)||http://www.ebi.ac.uk/efo/EFO_0003292
13950||12769||Anophthalmia - megalocornea - cardiopathy - skeletal anomalies||http://www.orpha.net/ORDO/Orphanet_1101
13951||10994||quetiapine||http://purl.obolibrary.org/obo/CHEBI_8707
13953||770||L3055||http://www.ebi.ac.uk/efo/EFO_0001198
13952||5317||Aplasia cutis - myopia||http://www.orpha.net/ORDO/Orphanet_1117
13955||13769||Fibular aplasia - ectrodactyly||http://www.orpha.net/ORDO/Orphanet_1118
13954||770||Kin-S49||http://www.ebi.ac.uk/efo/EFO_0001197
13956||5005||uncultured organism||http://purl.obolibrary.org/obo/NCBITaxon_155900
13957||770||LY2||http://www.ebi.ac.uk/efo/EFO_0001199
13959||770||IB3-1||http://www.ebi.ac.uk/efo/EFO_0001194
13958||770||GM14452||http://purl.obolibrary.org/obo/CLO_0031263
13961||770||HT-29||http://www.ebi.ac.uk/efo/EFO_0001193
13960||5502||Cupriavidus metallidurans CH34||http://purl.obolibrary.org/obo/NCBITaxon_266264
13962||770||IMR-90||http://www.ebi.ac.uk/efo/EFO_0001196
13964||2672||medulla of thymus||http://purl.obolibrary.org/obo/UBERON_0002124
13963||770||IMR-32||http://www.ebi.ac.uk/efo/EFO_0001195
13965||2672||alveolar bone||http://purl.obolibrary.org/obo/BTO_0001383
13966||770||GM14447||http://purl.obolibrary.org/obo/CLO_0031260
13967||770||GM14448||http://purl.obolibrary.org/obo/CLO_0031261
13968||13986||pronephros||http://purl.obolibrary.org/obo/UBERON_0002120
13969||1125||tissue culture||http://purl.obolibrary.org/obo/BTO_0001384
13970||5025||Eurotium amstelodami||http://purl.obolibrary.org/obo/NCBITaxon_5054
13971||5025||Aspergillus clavatus||http://purl.obolibrary.org/obo/NCBITaxon_5057
13972||5795||Disorder of lysine and hydroxylysine metabolism||http://www.orpha.net/ORDO/Orphanet_289832
13973||2252||Aortic arch anomaly - peculiar facies - intellectual disability||http://www.orpha.net/ORDO/Orphanet_1110
13974||6244||Aphalangy - hemivertebrae - urogenital-intestinal dysgenesis||http://www.orpha.net/ORDO/Orphanet_1112
13975||5865||Circumscribed cutaneous aplasia of the vertex||http://www.orpha.net/ORDO/Orphanet_1114
13976||6244||Aphalangy - syndactyly - microcephaly||http://www.orpha.net/ORDO/Orphanet_1113
13977||5317||Aplasia cutis congenita - intestinal lymphangiectasia||http://www.orpha.net/ORDO/Orphanet_1116
13978||5317||Recessive aplasia cutis congenita of limbs||http://www.orpha.net/ORDO/Orphanet_1115
13979||2672||ileum||http://purl.obolibrary.org/obo/UBERON_0002116
13980||2672||duodenum||http://purl.obolibrary.org/obo/UBERON_0002114
13981||770||GM14455||http://purl.obolibrary.org/obo/CLO_0031256
13982||2672||jejunum||http://purl.obolibrary.org/obo/UBERON_0002115
13984||2252||Arachnodactyly - abnormal ossification - intellectual disability||http://www.orpha.net/ORDO/Orphanet_1129
13983||770||GM14440||http://purl.obolibrary.org/obo/CLO_0031257
13985||770||GM14454||http://purl.obolibrary.org/obo/CLO_0031254
13986||2672||kidney||http://purl.obolibrary.org/obo/UBERON_0002113
13987||2672||gallbladder||http://purl.obolibrary.org/obo/UBERON_0002110
13989||770||GM14453||http://purl.obolibrary.org/obo/CLO_0031253
13988||592||Punctate palmoplantar keratoderma||http://www.orpha.net/ORDO/Orphanet_307967
13992||15538||protocol parameter||http://www.ebi.ac.uk/efo/EFO_0002658
13991||2672||cranium||http://purl.obolibrary.org/obo/UBERON_0003128
13990||5025||Aspergillus flavus||http://purl.obolibrary.org/obo/NCBITaxon_5059
13993||770||MDCC-MSB1||http://www.ebi.ac.uk/efo/EFO_0002659
13995||2672||trachea||http://purl.obolibrary.org/obo/UBERON_0003126
13994||2467||Glutathione synthetase deficiency with 5-oxoprolinuria||http://www.orpha.net/ORDO/Orphanet_289846
13997||14001||Genetic gastro-esophageal disease||http://www.orpha.net/ORDO/Orphanet_165658
13996||2672||chorion||http://purl.obolibrary.org/obo/UBERON_0003124
13999||14001||Genetic intestinal disease||http://www.orpha.net/ORDO/Orphanet_165655
13998||2467||Glutathione synthetase deficiency without 5-oxoprolinuria||http://www.orpha.net/ORDO/Orphanet_289849
14000||5025||Aspergillus oryzae||http://purl.obolibrary.org/obo/NCBITaxon_5062
14001||1732||Rare genetic gastroenterological disease||http://www.orpha.net/ORDO/Orphanet_165652
14002||5025||Aspergillus parasiticus||http://purl.obolibrary.org/obo/NCBITaxon_5067
14003||5795||Disorder of glutamine metabolism||http://www.orpha.net/ORDO/Orphanet_289841
14004||2252||Caudal appendage - deafness||http://www.orpha.net/ORDO/Orphanet_1123
14005||13769||Ulnar hypoplasia - split foot||http://www.orpha.net/ORDO/Orphanet_1122
14006||13769||Radial deficiency - tibial hypoplasia||http://www.orpha.net/ORDO/Orphanet_1121
14007||5053||Lung agenesis - heart defect - thumb anomalies||http://www.orpha.net/ORDO/Orphanet_1120
14008||7404||Aprosencephaly cerebellar dysgenesis||http://www.orpha.net/ORDO/Orphanet_1126
14009||2672||small intestine||http://purl.obolibrary.org/obo/UBERON_0002108
14010||9691||Ocular motor apraxia, Cogan type||http://www.orpha.net/ORDO/Orphanet_1125
14011||11433||liver||http://purl.obolibrary.org/obo/UBERON_0002107
14012||5025||Aspergillus niger||http://purl.obolibrary.org/obo/NCBITaxon_5061
14013||770||HCC1500||http://www.ebi.ac.uk/efo/EFO_0001172
14014||2672||trunk||http://purl.obolibrary.org/obo/UBERON_0002100
14015||770||HCC1428||http://www.ebi.ac.uk/efo/EFO_0001171
14017||14759||limb||http://purl.obolibrary.org/obo/UBERON_0002101
14016||770||HCC1937||http://www.ebi.ac.uk/efo/EFO_0001174
14019||14017||forelimb||http://purl.obolibrary.org/obo/UBERON_0002102
14018||770||HCC1569||http://www.ebi.ac.uk/efo/EFO_0001173
14020||14017||hindlimb||http://purl.obolibrary.org/obo/UBERON_0002103
14021||770||HCC202||http://www.ebi.ac.uk/efo/EFO_0001176
14022||770||HCC1954||http://www.ebi.ac.uk/efo/EFO_0001175
14023||770||HCC2185||http://www.ebi.ac.uk/efo/EFO_0001178
14025||2672||spleen||http://purl.obolibrary.org/obo/UBERON_0002106
14024||770||HCC2157||http://www.ebi.ac.uk/efo/EFO_0001177
14027||13689||olfactory region||http://purl.obolibrary.org/obo/UBERON_0003112
14026||2714||rotavirus infection||http://www.ebi.ac.uk/efo/EFO_0002622
14029||15238||bronchial smooth muscle cell||http://purl.obolibrary.org/obo/CL_0002598
14030||2700||septic peritonitis||http://www.ebi.ac.uk/efo/EFO_0002623
14028||770||HCC3153||http://www.ebi.ac.uk/efo/EFO_0001179
14031||10652||obsolete_primary hyperparathyroidism||http://www.ebi.ac.uk/efo/EFO_0002620
14032||1644||prostate intraepithelial neoplasia||http://www.ebi.ac.uk/efo/EFO_0002621
14033||770||GM14474||http://purl.obolibrary.org/obo/CLO_0031280
14034||2162||thymus neoplasm||http://www.ebi.ac.uk/efo/EFO_0002626
14035||770||GM14468||http://purl.obolibrary.org/obo/CLO_0031281
14036||2162||vulvar intraepithelial neoplasia||http://www.ebi.ac.uk/efo/EFO_0002627
14037||10652||obsolete_spinocerebellar ataxia||http://www.ebi.ac.uk/efo/EFO_0002624
14038||1761||teratozoospermia||http://www.ebi.ac.uk/efo/EFO_0002625
14039||13496||Vesicular stomatitis Indiana virus||http://purl.obolibrary.org/obo/NCBITaxon_11277
14041||13306||Arachnodactyly - intellectual disability - dysmorphism||http://www.orpha.net/ORDO/Orphanet_1130
14040||1392||viral cardiomyopathy||http://www.ebi.ac.uk/efo/EFO_0002629
14042||1392||peripartum cardiomyopathy||http://www.ebi.ac.uk/efo/EFO_0002628
14043||5025||Penicillium chrysogenum||http://purl.obolibrary.org/obo/NCBITaxon_5076
14044||3854||Methanobacterium congolense||http://purl.obolibrary.org/obo/NCBITaxon_118062
14045||8559||Arnold-Chiari malformation type II||http://www.orpha.net/ORDO/Orphanet_1136
14046||12769||Arrhinia - choanal atresia - microphthalmia||http://www.orpha.net/ORDO/Orphanet_1135
14047||12741||response to methotrexate||http://purl.obolibrary.org/obo/GO_0031427
14048||1171||X-linked mandibulofacial dysostosis||http://www.orpha.net/ORDO/Orphanet_1131
14049||770||HCC38||http://www.ebi.ac.uk/efo/EFO_0001180
14050||770||HCC70||http://www.ebi.ac.uk/efo/EFO_0001181
14051||306||AREDYLD syndrome||http://www.orpha.net/ORDO/Orphanet_1133
14053||770||GM14467||http://purl.obolibrary.org/obo/CLO_0031276
14052||770||HeLa||http://www.ebi.ac.uk/efo/EFO_0001185
14055||770||HEK293T||http://www.ebi.ac.uk/efo/EFO_0001184
14054||8191||N-allyl-6-chloro-1-(3-methylphenyl)-2,3,4,5-tetrahydro-3-benzazepine-7,8-diol hydrobromide||http://purl.obolibrary.org/obo/CHEBI_64002
14057||770||HEK-293H||http://www.ebi.ac.uk/efo/EFO_0001183
14056||770||GM14476||http://purl.obolibrary.org/obo/CLO_0031274
14059||770||HEK293||http://www.ebi.ac.uk/efo/EFO_0001182
14058||770||GM14465||http://purl.obolibrary.org/obo/CLO_0031275
14060||770||HMEC S1||http://www.ebi.ac.uk/efo/EFO_0001189
14061||1560||cytoplasmic vesicle||http://purl.obolibrary.org/obo/GO_0031410
14062||770||HMEC||http://www.ebi.ac.uk/efo/EFO_0001188
14064||770||GM14464||http://purl.obolibrary.org/obo/CLO_0031278
14063||770||HepG2||http://www.ebi.ac.uk/efo/EFO_0001187
14065||770||HepaRG||http://www.ebi.ac.uk/efo/EFO_0001186
14066||1016||restrictive cardiomyopathy||http://www.ebi.ac.uk/efo/EFO_0002630
14067||13496||Human respiratory syncytial virus A strain Long||http://purl.obolibrary.org/obo/NCBITaxon_11260
14068||5795||Disorder of tryptophan metabolism||http://www.orpha.net/ORDO/Orphanet_289829
14069||10652||obsolete_arrhythmogenic right ventricular cardiomyopathy||http://www.ebi.ac.uk/efo/EFO_0002631
14070||10652||obsolete_left ventricular noncompaction||http://www.ebi.ac.uk/efo/EFO_0002632
14072||615||Late-onset primary lymphedema||http://www.orpha.net/ORDO/Orphanet_289825
14071||770||GM14475||http://purl.obolibrary.org/obo/CLO_0031272
14073||5025||Neosartorya fischeri||http://purl.obolibrary.org/obo/NCBITaxon_36630
14074||1022||Acropora palmata||http://purl.obolibrary.org/obo/NCBITaxon_6131
14075||14963||Arthrogryposis-like syndrome||http://www.orpha.net/ORDO/Orphanet_1149
14076||13421||Sheldon-Hall syndrome||http://www.orpha.net/ORDO/Orphanet_1147
14077||12769||Digitotalar dysmorphism||http://www.orpha.net/ORDO/Orphanet_1146
14079||770||HMT3522S1||http://www.ebi.ac.uk/efo/EFO_0001191
14078||9869||X-linked distal arthrogryposis multiplex congenita||http://www.orpha.net/ORDO/Orphanet_1145
14081||770||HS578T||http://www.ebi.ac.uk/efo/EFO_0001192
14080||5700||Arthrogryposis-like hand anomaly - sensorineural deafness||http://www.orpha.net/ORDO/Orphanet_1144
14082||14963||Neurogenic arthrogryposis multiplex congenita||http://www.orpha.net/ORDO/Orphanet_1143
14083||770||HMEC184||http://www.ebi.ac.uk/efo/EFO_0001190
14084||8793||Arthrogryposis due to muscular dystrophy||http://www.orpha.net/ORDO/Orphanet_1155
14085||5502||Aggregatibacter actinomycetemcomitans HK1651||http://purl.obolibrary.org/obo/NCBITaxon_272556
14086||13421||Arthrogryposis with oculomotor limitation and electroretinal anomalies||http://www.orpha.net/ORDO/Orphanet_1154
14087||10143||Progressive pseudorheumatoid arthropathy of childhood||http://www.orpha.net/ORDO/Orphanet_1159
14088||5502||Bacteroides fragilis NCTC 9343||http://purl.obolibrary.org/obo/NCBITaxon_272559
14090||9946||Epiblepharon||http://www.orpha.net/ORDO/Orphanet_99169
14089||10580||interstitial dendritic cell||http://purl.obolibrary.org/obo/CL_0001007
14091||14543||Kit and Sca1-positive hematopoietic stem cell||http://purl.obolibrary.org/obo/CL_0001008
14092||14103||immature dermal dendritic cell||http://purl.obolibrary.org/obo/CL_0001009
14093||12083||Arthrogryposis multiplex congenita - whistling face||http://www.orpha.net/ORDO/Orphanet_1150
14095||14125||immature CD1a-positive dermal dendritic cell||http://purl.obolibrary.org/obo/CL_0002530
14094||10580||CD8_alpha-positive CD11b-negative dendritic cell||http://purl.obolibrary.org/obo/CL_0001000
14096||14125||mature CD1a-positive dermal dendritic cell||http://purl.obolibrary.org/obo/CL_0002531
14097||10592||mature CD8_alpha-negative CD11b-negative dendritic cell||http://purl.obolibrary.org/obo/CL_0001002
14098||10592||immature CD8_alpha-negative CD11b-negative dendritic cell||http://purl.obolibrary.org/obo/CL_0001001
14100||14102||mature CD16-positive myeloid dendritic cell||http://purl.obolibrary.org/obo/CL_0002534
14099||14094||immature CD8_alpha-positive CD11b-negative dendritic cell||http://purl.obolibrary.org/obo/CL_0001004
14101||10591||mature CD8_alpha-negative CD11b-positive dendritic cell||http://purl.obolibrary.org/obo/CL_0001003
14102||8236||CD16-positive myeloid dendritic cell||http://purl.obolibrary.org/obo/CL_0002532
14103||10580||dermal dendritic cell||http://purl.obolibrary.org/obo/CL_0001006
14104||14102||immature CD16-positive myeloid dendritic cell||http://purl.obolibrary.org/obo/CL_0002533
14105||14094||mature CD8_alpha-positive CD11b-negative dendritic cell||http://purl.obolibrary.org/obo/CL_0001005
14106||2672||chordotonal organ||http://purl.obolibrary.org/obo/UBERON_0001038
14107||1627||sensory system||http://purl.obolibrary.org/obo/UBERON_0001032
14108||1627||gustatory system||http://purl.obolibrary.org/obo/UBERON_0001033
14109||9949||Tarsal kink syndrome||http://www.orpha.net/ORDO/Orphanet_99170
14110||9928||Isolated congenital ectropion||http://www.orpha.net/ORDO/Orphanet_99171
14111||13306||Congenital unilateral hypoplasia of depressor anguli oris||http://www.orpha.net/ORDO/Orphanet_1166
14112||9928||Euryblepharon||http://www.orpha.net/ORDO/Orphanet_99172
14113||6543||Ataxia - oculomotor apraxia type 1||http://www.orpha.net/ORDO/Orphanet_1168
14114||9933||Congenital eyelid retraction||http://www.orpha.net/ORDO/Orphanet_99176
14116||12460||response to water deprivation||http://purl.obolibrary.org/obo/GO_0009414
14115||9606||Isolated distichiasis||http://www.orpha.net/ORDO/Orphanet_99177
14117||14103||CD14-positive dermal dendritic cell||http://purl.obolibrary.org/obo/CL_0002526
14118||12538||response to water stimulus||http://purl.obolibrary.org/obo/GO_0009415
14119||5502||Burkholderia pseudomallei K96243||http://purl.obolibrary.org/obo/NCBITaxon_272560
14120||6854||Kandori fleck retina||http://www.orpha.net/ORDO/Orphanet_99179
14121||14117||mature CD14-positive dermal dendritic cell||http://purl.obolibrary.org/obo/CL_0002528
14122||14117||immature CD14-positive dermal dendritic cell||http://purl.obolibrary.org/obo/CL_0002527
14123||5502||Clostridium difficile 630||http://purl.obolibrary.org/obo/NCBITaxon_272563
14125||14103||CD1a-positive dermal dendritic cell||http://purl.obolibrary.org/obo/CL_0002529
14126||1125||cell culture||http://purl.obolibrary.org/obo/BTO_0000214
14124||8027||Isolated encephalocele||http://www.orpha.net/ORDO/Orphanet_199647
14127||1022||Ambystoma mexicanum||http://purl.obolibrary.org/obo/NCBITaxon_8296
14128||5025||Leptosphaeria maculans||http://purl.obolibrary.org/obo/NCBITaxon_5022
14129||5502||Clostridium acetobutylicum ATCC 824||http://purl.obolibrary.org/obo/NCBITaxon_272562
14130||1813||cell suspension culture||http://purl.obolibrary.org/obo/BTO_0000221
14131||5984||Isolated congenital microcephaly||http://www.orpha.net/ORDO/Orphanet_199642
14132||13496||Tobacco rattle virus||http://purl.obolibrary.org/obo/NCBITaxon_12295
14133||10994||nebivolol||http://purl.obolibrary.org/obo/CHEBI_64022
14134||13496||Synechococcus phage S-IO21||http://purl.obolibrary.org/obo/NCBITaxon_375052
14135||1627||digestive system||http://purl.obolibrary.org/obo/UBERON_0001007
14136||7858||Benign paroxysmal tonic upgaze of childhood with ataxia||http://www.orpha.net/ORDO/Orphanet_1179
14137||11828||Early-onset cerebellar ataxia with retained tendon reflexes||http://www.orpha.net/ORDO/Orphanet_1177
14138||4692||Ataxia - tapetoretinal degeneration||http://www.orpha.net/ORDO/Orphanet_1178
14141||13496||Synechococcus phage S-IO17||http://purl.obolibrary.org/obo/NCBITaxon_375050
14139||3114||X-linked progressive cerebellar ataxia||http://www.orpha.net/ORDO/Orphanet_1175
14140||770||C1R cell||http://purl.obolibrary.org/obo/BTO_0003699
14142||1306||Cerebellar ataxia - hypogonadism||http://www.orpha.net/ORDO/Orphanet_1173
14143||306||Cerebellar ataxia - ectodermal dysplasia||http://www.orpha.net/ORDO/Orphanet_1174
14144||5700||Cerebellar ataxia - areflexia - pes cavus - optic atrophy - sensorineural hearing loss||http://www.orpha.net/ORDO/Orphanet_1171
14146||12460||response to cold||http://purl.obolibrary.org/obo/GO_0009409
14145||4692||Autosomal recessive cerebellar ataxia||http://www.orpha.net/ORDO/Orphanet_1172
14147||872||common dendritic progenitor||http://purl.obolibrary.org/obo/CL_0001029
14148||13496||Influenza A virus (A/Texas/36/1991(H1N1))||http://purl.obolibrary.org/obo/NCBITaxon_380964
14149||11831||Autosomal recessive cerebelloparenchymal disorder type 3||http://www.orpha.net/ORDO/Orphanet_1170
14150||14488||CD34-positive, CD38-positive common myeloid progenitor||http://purl.obolibrary.org/obo/CL_0001026
14151||14512||Kit-positive, Sca1-positive common lymphoid progenitor||http://purl.obolibrary.org/obo/CL_0001025
14152||10994||N-desmethylclozapine||http://purl.obolibrary.org/obo/CHEBI_64050
14153||14512||CD7-positive lymphoid progenitor cell||http://purl.obolibrary.org/obo/CL_0001028
14154||14512||CD7-negative lymphoid progenitor cell||http://purl.obolibrary.org/obo/CL_0001027
14155||1022||Heterocephalus glaber||http://purl.obolibrary.org/obo/NCBITaxon_10181
14156||9247||CD115-positive monocyte||http://purl.obolibrary.org/obo/CL_0001022
14159||14512||CD34-positive, CD38-positive common lymphoid progenitor||http://purl.obolibrary.org/obo/CL_0001021
14157||14503||lung fibroblast||http://purl.obolibrary.org/obo/CL_0002553
14158||1564||Marginal papular palmoplantar keratoderma||http://www.orpha.net/ORDO/Orphanet_307995
14161||14543||CD34-positive, CD38-negative hematopoietic stem cell||http://purl.obolibrary.org/obo/CL_0001024
14160||8091||Neonatal glycine encephalopathy||http://www.orpha.net/ORDO/Orphanet_289857
14162||14488||Kit-positive, CD34-positive common myeloid progenitor||http://purl.obolibrary.org/obo/CL_0001023
14163||8191||3-[4-(3-chlorophenyl)piperazin-1-yl]-1,1-diphenylpropan-2-ol hydrochloride||http://purl.obolibrary.org/obo/CHEBI_64057
14164||14188||mature CD8_alpha-low Langerhans cell||http://purl.obolibrary.org/obo/CL_0001020
14165||2672||adipose tissue||http://purl.obolibrary.org/obo/UBERON_0001013
14166||2672||extraembryonic tissue||http://purl.obolibrary.org/obo/UBERON_0005292
14168||5502||Clostridium argentinense||http://purl.obolibrary.org/obo/NCBITaxon_29341
14167||10994||4-(4-methylpiperazin-1-yl)-7-(trifluoromethyl)pyrrolo[1,2-a]quinoxaline dimaleate||http://purl.obolibrary.org/obo/CHEBI_64053
14169||2672||musculature||http://purl.obolibrary.org/obo/UBERON_0001015
14171||1627||nervous system||http://purl.obolibrary.org/obo/UBERON_0001016
14170||1022||Scophthalmus maximus||http://purl.obolibrary.org/obo/NCBITaxon_52904
14172||1627||central nervous system||http://purl.obolibrary.org/obo/UBERON_0001017
14173||8934||Infantile onset spinocerebellar ataxia||http://www.orpha.net/ORDO/Orphanet_1186
14174||3114||Lethal ataxia with deafness and optic atrophy||http://www.orpha.net/ORDO/Orphanet_1187
14175||3114||Ataxia-deafness-intellectual disability syndrome||http://www.orpha.net/ORDO/Orphanet_1188
14177||8091||Atypical glycine encephalopathy||http://www.orpha.net/ORDO/Orphanet_289863
14176||10723||Spastic ataxia with congenital miosis||http://www.orpha.net/ORDO/Orphanet_1182
14178||4692||Spinocerebellar ataxia - dysmorphism||http://www.orpha.net/ORDO/Orphanet_1185
14179||6269||Disorder of proline metabolism||http://www.orpha.net/ORDO/Orphanet_289866
14180||8091||Infantile glycine encephalopathy||http://www.orpha.net/ORDO/Orphanet_289860
14182||14188||immature CD8_alpha-low Langerhans cell||http://purl.obolibrary.org/obo/CL_0001018
14181||1306||Ataxia - hypogonadism - choroidal dystrophy||http://www.orpha.net/ORDO/Orphanet_1180
14184||561||Atypical autism||http://www.orpha.net/ORDO/Orphanet_199627
14183||872||CD115-positive monocyte OR common dendritic progenitor||http://purl.obolibrary.org/obo/CL_0001019
14185||14190||mature CD1a-positive Langerhans cell||http://purl.obolibrary.org/obo/CL_0001017
14187||14190||immature CD1a-positive Langerhans cell||http://purl.obolibrary.org/obo/CL_0001016
14186||8193||N-octylhomovanillamide||http://purl.obolibrary.org/obo/CHEBI_64041
14189||5991||Familial gastric cancer||http://www.orpha.net/ORDO/Orphanet_26106
14188||8616||CD8_alpha-low Langerhans cell||http://purl.obolibrary.org/obo/CL_0001015
14190||8616||CD1a-positive Langerhans cell||http://purl.obolibrary.org/obo/CL_0001014
14191||14089||mature interstitial dendritic cell||http://purl.obolibrary.org/obo/CL_0001013
14192||871||CD7-negative lymphoid progenitor OR granulocyte monocyte progenitor||http://purl.obolibrary.org/obo/CL_0001012
14193||14089||immature interstitial dendritic cell||http://purl.obolibrary.org/obo/CL_0001011
14194||5025||Ajellomyces capsulatus||http://purl.obolibrary.org/obo/NCBITaxon_5037
14195||14103||mature dermal dendritic cell||http://purl.obolibrary.org/obo/CL_0001010
14196||6269||Disorder of ornithine metabolism||http://www.orpha.net/ORDO/Orphanet_289869
14197||2672||chitin-based cuticle||http://purl.obolibrary.org/obo/UBERON_0001001
14198||2672||vas deferens||http://purl.obolibrary.org/obo/UBERON_0001000
14199||10994||isoquinoline-1,5-diol||http://purl.obolibrary.org/obo/CHEBI_64044
14201||13689||brain vasculature||http://purl.obolibrary.org/obo/UBERON_0005284
14200||10994||amisulpride||http://purl.obolibrary.org/obo/CHEBI_64045
14203||13496||Synechococcus phage S-IO9||http://purl.obolibrary.org/obo/NCBITaxon_375033
14204||2672||epidermis||http://purl.obolibrary.org/obo/UBERON_0001003
14205||7195||plantaris||http://purl.obolibrary.org/obo/UBERON_0011905
14202||10994||3-aminobenzamide||http://purl.obolibrary.org/obo/CHEBI_64042
14207||1627||respiratory system||http://purl.obolibrary.org/obo/UBERON_0001004
14206||618||pupa||http://purl.obolibrary.org/obo/UBERON_0003143
14208||613||Atherosclerosis - deafness - diabetes - epilepsy - nephropathy||http://www.orpha.net/ORDO/Orphanet_1192
14209||5767||Atelosteogenesis type I||http://www.orpha.net/ORDO/Orphanet_1190
14210||8636||Congenital atransferrinemia||http://www.orpha.net/ORDO/Orphanet_1195
14211||4987||Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency||http://www.orpha.net/ORDO/Orphanet_1194
14212||2252||Atkin-Flaitz syndrome||http://www.orpha.net/ORDO/Orphanet_1193
14213||5085||1p21.3 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_293948
14214||6771||Colonic atresia||http://www.orpha.net/ORDO/Orphanet_1198
14215||1022||Schistosoma mansoni||http://purl.obolibrary.org/obo/NCBITaxon_6183
14216||1022||Schistosoma japonicum||http://purl.obolibrary.org/obo/NCBITaxon_6182
14217||10717||Low phospholipid associated cholelithiasis||http://www.orpha.net/ORDO/Orphanet_69663
14218||770||GM07034||http://www.ebi.ac.uk/efo/EFO_0001112
14219||770||GM07022||http://www.ebi.ac.uk/efo/EFO_0001111
14221||770||GM07000||http://www.ebi.ac.uk/efo/EFO_0001110
14220||8191||(1R,3S)-3-(adamantan-1-yl)-1-(aminomethyl)-3,4-dihydroisochromene-5,6-diol hydrochloride||http://purl.obolibrary.org/obo/CHEBI_64078
14222||13496||Bean pod mottle virus||http://purl.obolibrary.org/obo/NCBITaxon_12260
14223||770||GM11831||http://www.ebi.ac.uk/efo/EFO_0001119
14224||770||GM11830||http://www.ebi.ac.uk/efo/EFO_0001118
14225||770||GM11829||http://www.ebi.ac.uk/efo/EFO_0001117
14226||770||GM07357||http://www.ebi.ac.uk/efo/EFO_0001116
14228||770||GM07345||http://www.ebi.ac.uk/efo/EFO_0001115
14227||5611||Hereditary persistence of fetal hemoglobin - beta-thalassemia||http://www.orpha.net/ORDO/Orphanet_46532
14229||770||GM07056||http://www.ebi.ac.uk/efo/EFO_0001114
14231||10994||exendin-4||http://purl.obolibrary.org/obo/CHEBI_64073
14230||3072||external carotid artery||http://purl.obolibrary.org/obo/UBERON_0001070
14232||770||GM07055||http://www.ebi.ac.uk/efo/EFO_0001113
14234||14236||Rattus rattus||http://purl.obolibrary.org/obo/NCBITaxon_10117
14233||12341||6-phosphogluconate dehydrogenase deficiency||http://www.orpha.net/ORDO/Orphanet_99135
14235||14236||Rattus norvegicus||http://purl.obolibrary.org/obo/NCBITaxon_10116
14236||1022||Rattus||http://purl.obolibrary.org/obo/NCBITaxon_10114
14237||1022||Mastomys natalensis||http://purl.obolibrary.org/obo/NCBITaxon_10112
14238||6266||Hemolytic anemia due to erythrocyte adenosine deaminase overproduction||http://www.orpha.net/ORDO/Orphanet_99138
14239||770||myoblast cell line||http://purl.obolibrary.org/obo/BTO_0000256
14240||9626||EDICT syndrome||http://www.orpha.net/ORDO/Orphanet_293936
14241||5209||Distal Xq28 microduplication syndrome||http://www.orpha.net/ORDO/Orphanet_293939
14243||770||GM11839||http://www.ebi.ac.uk/efo/EFO_0001121
14242||8191||SB 224289 hydrochloride||http://purl.obolibrary.org/obo/CHEBI_64067
14244||770||GM11832||http://www.ebi.ac.uk/efo/EFO_0001120
14246||770||GM11882||http://www.ebi.ac.uk/efo/EFO_0001123
14245||8191||CGP 78608 hydrochloride||http://purl.obolibrary.org/obo/CHEBI_64065
14247||770||GM11881||http://www.ebi.ac.uk/efo/EFO_0001122
14249||2672||neurohypophysis||http://purl.obolibrary.org/obo/UBERON_0002198
14248||871||CD117-positive common myeloid progenitor OR CD217-positive common lymphoid progenitor||http://purl.obolibrary.org/obo/CL_0001030
14250||2672||intervertebral disk||http://purl.obolibrary.org/obo/UBERON_0001066
14252||10994||ranitidine||http://purl.obolibrary.org/obo/CHEBI_8776
14251||770||GM12004||http://www.ebi.ac.uk/efo/EFO_0001129
14253||770||GM12003||http://www.ebi.ac.uk/efo/EFO_0001128
14254||2672||adenohypophysis||http://purl.obolibrary.org/obo/UBERON_0002196
14255||10994||raloxifene||http://purl.obolibrary.org/obo/CHEBI_8772
14256||770||GM11993||http://www.ebi.ac.uk/efo/EFO_0001125
14257||770||GM11992||http://www.ebi.ac.uk/efo/EFO_0001124
14258||770||GM11995||http://www.ebi.ac.uk/efo/EFO_0001127
14259||770||GM11994||http://www.ebi.ac.uk/efo/EFO_0001126
14261||5795||Organic aciduria||http://www.orpha.net/ORDO/Orphanet_289899
14260||6072||Midline interhemispheric variant of holoprosencephaly||http://www.orpha.net/ORDO/Orphanet_93926
14262||6072||Alobar holoprosencephaly||http://www.orpha.net/ORDO/Orphanet_93925
14263||7727||Epispadias||http://www.orpha.net/ORDO/Orphanet_93928
14264||7727||Cloacal exstrophy||http://www.orpha.net/ORDO/Orphanet_93929
14265||10067||Vgamma5-negative CD8alpha alpha positive gamma-delta intraepithelial T cell||http://purl.obolibrary.org/obo/CL_0002514
14266||770||uterine leiomyosarcoma cell line||http://purl.obolibrary.org/obo/BTO_0002488
14267||6325||Hypermethioninemia due to glycine N-methyltransferase deficiency||http://www.orpha.net/ORDO/Orphanet_289891
14268||4803||Neurofibromatosis type 3||http://www.orpha.net/ORDO/Orphanet_93921
14270||6610||Lethal occipital encephalocele-skeletal dysplasia syndrome||http://www.orpha.net/ORDO/Orphanet_293925
14269||8191||ferric ammonium citrate||http://purl.obolibrary.org/obo/CHEBI_31604
14271||6072||Lobar holoprosencephaly||http://www.orpha.net/ORDO/Orphanet_93924
14272||2672||Malpighian tubule||http://purl.obolibrary.org/obo/UBERON_0001054
14273||11433||corpus allatum||http://purl.obolibrary.org/obo/UBERON_0001057
14275||11433||corpus cardiacum||http://purl.obolibrary.org/obo/UBERON_0001056
14274||5502||Streptomyces cattleya||http://purl.obolibrary.org/obo/NCBITaxon_29303
14276||13695||pars intercerebralis||http://purl.obolibrary.org/obo/UBERON_0001059
14277||8191||N-(2,3-dihydro-1,4-benzodioxin-2-ylmethyl)-2-(2,6-dimethoxyphenoxy)ethanamine||http://purl.obolibrary.org/obo/CHEBI_64098
14278||14513||mushroom body||http://purl.obolibrary.org/obo/UBERON_0001058
14279||8191||4-fluoro-N- {2-[4-(7-methoxynaphthalen-1-yl)piperazin-1-yl]ethyl }benzamide hydrochloride||http://purl.obolibrary.org/obo/CHEBI_64099
14280||10067||Vgamma5-positive CD8alpha alpha positive gamma-delta intraepithelial T cell||http://purl.obolibrary.org/obo/CL_0002513
14281||14295||CD11b-high, CD103-negative, langerin-negative lymph node dendritic cell||http://purl.obolibrary.org/obo/CL_0002512
14282||14288||main bronchus||http://purl.obolibrary.org/obo/UBERON_0002182
14283||13496||Flock house virus||http://purl.obolibrary.org/obo/NCBITaxon_12287
14284||14295||CD11b-low, CD103-negative, langerin-negative lymph node dendritic cell||http://purl.obolibrary.org/obo/CL_0002511
14285||14294||CD103-negative, langerin-positive lymph node dendritic cell||http://purl.obolibrary.org/obo/CL_0002510
14287||13496||Tobacco ringspot virus||http://purl.obolibrary.org/obo/NCBITaxon_12282
14286||10994||tert-butyl hydroperoxide||http://purl.obolibrary.org/obo/CHEBI_64090
14289||2672||hypopharynx||http://purl.obolibrary.org/obo/UBERON_0001051
14288||2672||bronchus||http://purl.obolibrary.org/obo/UBERON_0002185
14290||13496||Tomato ringspot virus||http://purl.obolibrary.org/obo/NCBITaxon_12280
14291||2672||neurohemal organ||http://purl.obolibrary.org/obo/UBERON_0001053
14293||2672||rectum||http://purl.obolibrary.org/obo/UBERON_0001052
14292||8191||1-[2-(benzhydryloxy)ethyl]-4-(3-phenylpropyl)piperazine dihydrochloride||http://purl.obolibrary.org/obo/CHEBI_64091
14294||10580||langerin-positive lymph node dendritic cell||http://purl.obolibrary.org/obo/CL_0002507
14295||10580||langerin-negative, CD103-negative lymph node dendritic cell||http://purl.obolibrary.org/obo/CL_0002508
14297||14954||Terminal transverse defects of arm||http://www.orpha.net/ORDO/Orphanet_93937
14296||14294||CD103-positive, langerin-positive lymph node dendritic cell||http://purl.obolibrary.org/obo/CL_0002509
14298||5186||Familial isolated arrhythmogenic ventricular dysplasia, right dominant form||http://www.orpha.net/ORDO/Orphanet_293910
14300||13256||liver CD103-negative dendritic cell||http://purl.obolibrary.org/obo/CL_0002505
14299||772||cerebrovascular endothelial cell||http://purl.obolibrary.org/obo/BTO_0000238
14301||13256||liver CD103-positive dendritic cell||http://purl.obolibrary.org/obo/CL_0002506
14302||7727||Bladder exstrophy||http://www.orpha.net/ORDO/Orphanet_93930
14303||2672||midgut||http://purl.obolibrary.org/obo/UBERON_0001045
14304||11433||salivary gland||http://purl.obolibrary.org/obo/UBERON_0001044
14305||2672||esophagus||http://purl.obolibrary.org/obo/UBERON_0001043
14306||258||secretion by cell||http://purl.obolibrary.org/obo/GO_0032940
14308||1678||primordium||http://purl.obolibrary.org/obo/UBERON_0001048
14307||770||CC531||http://www.ebi.ac.uk/efo/EFO_0001101
14309||770||CAMA1||http://www.ebi.ac.uk/efo/EFO_0001100
14310||8191||vanoxerine dihydrochloride||http://purl.obolibrary.org/obo/CHEBI_64086
14311||770||CSBwt-rescued fibroblasts||http://www.ebi.ac.uk/efo/EFO_0001103
14312||770||CFT-2||http://www.ebi.ac.uk/efo/EFO_0001102
14313||770||GLI60||http://www.ebi.ac.uk/efo/EFO_0001105
14314||770||GLI56||http://www.ebi.ac.uk/efo/EFO_0001104
14317||2672||chordate pharynx||http://purl.obolibrary.org/obo/UBERON_0001042
14315||770||GM06985||http://www.ebi.ac.uk/efo/EFO_0001107
14316||8191||RS 39604 hydrochloride||http://purl.obolibrary.org/obo/CHEBI_64081
14318||770||GLI72||http://www.ebi.ac.uk/efo/EFO_0001106
14319||13496||Arabis mosaic virus||http://purl.obolibrary.org/obo/NCBITaxon_12271
14321||2672||yolk sac||http://purl.obolibrary.org/obo/UBERON_0001040
14322||770||GM06994||http://www.ebi.ac.uk/efo/EFO_0001109
14320||1022||Trialeurodes vaporariorum||http://purl.obolibrary.org/obo/NCBITaxon_88556
14323||770||GM06993||http://www.ebi.ac.uk/efo/EFO_0001108
14324||10994||polidocanol||http://purl.obolibrary.org/obo/CHEBI_46859
14325||1355||abnormality of the lymphatic system||http://purl.obolibrary.org/obo/HP_0100763
14327||7529||self rated health||http://www.ebi.ac.uk/efo/EFO_0004778
14326||9558||Cerebral arteriovenous malformation||http://www.orpha.net/ORDO/Orphanet_46724
14328||10652||obsolete_pelvic fin||http://www.ebi.ac.uk/efo/EFO_0003644
14330||14970||CHAOS measure||http://www.ebi.ac.uk/efo/EFO_0004779
14329||13689||non neural ectoderm||http://www.ebi.ac.uk/efo/EFO_0003643
14332||13689||corpuscles of Stannius||http://www.ebi.ac.uk/efo/EFO_0003646
14331||11030||alcohol and nicotine codependence||http://www.ebi.ac.uk/efo/EFO_0004776
14333||11030||alcohol withdrawal||http://www.ebi.ac.uk/efo/EFO_0004777
14334||10652||obsolete_cranial neural crest||http://www.ebi.ac.uk/efo/EFO_0003645
14335||13689||epibranchial 5||http://www.ebi.ac.uk/efo/EFO_0003648
14336||10994||beta amyloid||http://purl.obolibrary.org/obo/CHEBI_53002
14338||1536||organelle membrane||http://purl.obolibrary.org/obo/GO_0031090
14339||8193||naphthalene-1,5-diamine||http://purl.obolibrary.org/obo/CHEBI_53003
14337||10652||obsolete_axial mesoderm||http://www.ebi.ac.uk/efo/EFO_0003647
14341||13689||lateral floor plate||http://www.ebi.ac.uk/efo/EFO_0003649
14340||10994||lipoxin A4||http://purl.obolibrary.org/obo/CHEBI_6498
14342||14970||ovarian reserve||http://www.ebi.ac.uk/efo/EFO_0004770
14343||14970||visual cortical surface area measurement||http://www.ebi.ac.uk/efo/EFO_0004771
14344||13689||tooth 3V||http://www.ebi.ac.uk/efo/EFO_0003640
14345||3068||chewing tobacco behavior||http://www.ebi.ac.uk/efo/EFO_0004774
14346||2866||toxic epidermal necrolysis||http://www.ebi.ac.uk/efo/EFO_0004775
14348||13689||anal fin||http://www.ebi.ac.uk/efo/EFO_0003642
14347||1825||early onset hypertension||http://www.ebi.ac.uk/efo/EFO_0004772
14349||13689||posterior lateral line primordium||http://www.ebi.ac.uk/efo/EFO_0003641
14350||12361||microtubule cytoskeleton||http://purl.obolibrary.org/obo/GO_0015630
14351||7963||Tall stature - scoliosis - macrodactyly of the great toes||http://www.orpha.net/ORDO/Orphanet_329191
14353||15549||Hypomyelinating leukodystrophy with or without oligondontia and/or hypogonadism||http://www.orpha.net/ORDO/Orphanet_289494
14352||5085||Developmental delay with autism spectrum disorder and gait instability||http://www.orpha.net/ORDO/Orphanet_329195
14354||5502||Streptococcus pyogenes M49 591||http://purl.obolibrary.org/obo/NCBITaxon_294934
14355||9654||Congenital cataract microcornea with corneal opacity||http://www.orpha.net/ORDO/Orphanet_289499
14357||14970||visceral adipose tissue measurement||http://www.ebi.ac.uk/efo/EFO_0004765
14356||10652||obsolete_pharyngeal pouch 6||http://www.ebi.ac.uk/efo/EFO_0003635
14358||14970||subcutaneous adipose tissue||http://www.ebi.ac.uk/efo/EFO_0004766
14359||10652||obsolete_pharyngeal pouch 3||http://www.ebi.ac.uk/efo/EFO_0003634
14360||14970||visceral:subcutaneous adipose tissue ratio||http://www.ebi.ac.uk/efo/EFO_0004767
14361||10652||obsolete_pharyngeal pouch 2||http://www.ebi.ac.uk/efo/EFO_0003633
14363||14970||follicle stimulating hormone measurement||http://www.ebi.ac.uk/efo/EFO_0004768
14362||13689||pharyngeal pouches 2-6||http://www.ebi.ac.uk/efo/EFO_0003632
14364||13689||trunk mesenchyme||http://purl.obolibrary.org/obo/UBERON_0005256
14365||14970||anti-Mullerian hormone measurement||http://www.ebi.ac.uk/efo/EFO_0004769
14366||13689||tooth 4V||http://www.ebi.ac.uk/efo/EFO_0003639
14367||13689||tooth 5V||http://www.ebi.ac.uk/efo/EFO_0003638
14368||1022||Cryptococcus gattii||http://purl.obolibrary.org/obo/NCBITaxon_552467
14369||10652||obsolete_pharyngeal pouch 4||http://www.ebi.ac.uk/efo/EFO_0003637
14370||10652||obsolete_pharyngeal pouch 5||http://www.ebi.ac.uk/efo/EFO_0003636
14371||14970||t-tau measurement||http://www.ebi.ac.uk/efo/EFO_0004760
14373||14970||uric acid measurement||http://www.ebi.ac.uk/efo/EFO_0004761
14372||10652||obsolete_pharyngeal pouch 1||http://www.ebi.ac.uk/efo/EFO_0003631
14375||14970||vascular endothelial growth factor measurement||http://www.ebi.ac.uk/efo/EFO_0004762
14374||13689||urogenital papilla||http://www.ebi.ac.uk/efo/EFO_0003630
14377||14970||p-tau measurement||http://www.ebi.ac.uk/efo/EFO_0004763
14376||13689||head mesenchyme||http://purl.obolibrary.org/obo/UBERON_0005253
14378||8579||adipose tissue measurement||http://www.ebi.ac.uk/efo/EFO_0004764
14379||10652||obsolete_ankle||http://www.ebi.ac.uk/efo/EFO_0001409
14380||10652||obsolete_placenta||http://www.ebi.ac.uk/efo/EFO_0001407
14381||2672||cervical neck region||http://www.ebi.ac.uk/efo/EFO_0001408
14382||10652||obsolete_trigeminal nerve||http://www.ebi.ac.uk/efo/EFO_0001402
14383||13689||facial ganglion||http://www.ebi.ac.uk/efo/EFO_0003669
14384||10652||obsolete_tonsil||http://www.ebi.ac.uk/efo/EFO_0001401
14385||10652||obsolete_scapula||http://www.ebi.ac.uk/efo/EFO_0001400
14387||13689||renal tubule||http://www.ebi.ac.uk/efo/EFO_0003666
14386||10652||obsolete_extraembryonic tissue||http://www.ebi.ac.uk/efo/EFO_0001406
14389||13689||caudal vein plexus||http://www.ebi.ac.uk/efo/EFO_0003665
14388||10652||obsolete_back||http://www.ebi.ac.uk/efo/EFO_0001405
14392||14970||copy number variation||http://www.ebi.ac.uk/efo/EFO_0004798
14390||2672||seminiferous tubules||http://www.ebi.ac.uk/efo/EFO_0001404
14391||10652||obsolete_ciliary marginal zone||http://www.ebi.ac.uk/efo/EFO_0003668
14393||10994||lincomycin||http://purl.obolibrary.org/obo/CHEBI_6472
14396||2672||corneal limbus||http://www.ebi.ac.uk/efo/EFO_0001403
14395||1391||cholelithiasis||http://www.ebi.ac.uk/efo/EFO_0004799
14394||10652||obsolete_renal glomerulus||http://www.ebi.ac.uk/efo/EFO_0003667
14397||13689||branchiostegal ray 3||http://www.ebi.ac.uk/efo/EFO_0003662
14398||10652||obsolete_freckling||http://www.ebi.ac.uk/efo/EFO_0004796
14399||13689||branchiostegal ray 1||http://www.ebi.ac.uk/efo/EFO_0003661
14400||10652||obsolete_Li-Fraumeni syndrome||http://www.ebi.ac.uk/efo/EFO_0004797
14401||13689||intersegmental vessel||http://www.ebi.ac.uk/efo/EFO_0003664
14402||13689||branchiostegal ray 2||http://www.ebi.ac.uk/efo/EFO_0003663
14403||1391||skin sensitivity to sun||http://www.ebi.ac.uk/efo/EFO_0004795
14404||14970||plasminogen activator inhibitor 1 measurement||http://www.ebi.ac.uk/efo/EFO_0004792
14405||14970||CD40 ligand measurement||http://www.ebi.ac.uk/efo/EFO_0004790
14406||13689||ventral mandibular arch||http://www.ebi.ac.uk/efo/EFO_0003660
14407||14970||tissue plasminogen activator measurement||http://www.ebi.ac.uk/efo/EFO_0004791
14408||5894||Congenital muscular dystrophy with intellectual disability and severe epilepsy||http://www.orpha.net/ORDO/Orphanet_329178
14409||5025||Naumovozyma||http://purl.obolibrary.org/obo/NCBITaxon_278028
14410||10652||obsolete_palatoquadrate arch||http://www.ebi.ac.uk/efo/EFO_0003659
14411||10652||obsolete_blastema||http://www.ebi.ac.uk/efo/EFO_0003658
14412||13689||regenerating fin||http://www.ebi.ac.uk/efo/EFO_0003657
14413||13689||cranial vasculature||http://www.ebi.ac.uk/efo/EFO_0003656
14414||14970||atrial natriuretic factor measurement||http://www.ebi.ac.uk/efo/EFO_0004789
14415||13689||ovarian follicle stage III||http://www.ebi.ac.uk/efo/EFO_0003655
14416||13689||ovarian follicle stage II||http://www.ebi.ac.uk/efo/EFO_0003654
14418||14970||TEMPS-A questionnaire||http://www.ebi.ac.uk/efo/EFO_0004783
14417||13689||ovarian follicle stage IV||http://www.ebi.ac.uk/efo/EFO_0003653
14420||14970||self reported educational attainment||http://www.ebi.ac.uk/efo/EFO_0004784
14419||13689||ovarian follicle stage I||http://www.ebi.ac.uk/efo/EFO_0003652
14422||14970||South Texas Assessment of Neurocognition||http://www.ebi.ac.uk/efo/EFO_0004785
14421||10652||obsolete_gonad primordium||http://www.ebi.ac.uk/efo/EFO_0003651
14424||14970||Mini-International Neuropsychiatric Interview||http://www.ebi.ac.uk/efo/EFO_0004786
14423||13689||ventricular system||http://www.ebi.ac.uk/efo/EFO_0003650
14426||14970||DSM-IV-based social scale||http://www.ebi.ac.uk/efo/EFO_0004780
14425||1595||abdominal distention||http://purl.obolibrary.org/obo/HP_0003270
14427||14970||DSM-IV-based  non-social scale||http://www.ebi.ac.uk/efo/EFO_0004781
14428||14970||behavior or behavioral disorder measurement||http://www.ebi.ac.uk/efo/EFO_0004782
14429||5317||Isolated adermatoglyphia||http://www.orpha.net/ORDO/Orphanet_289465
14430||10652||obsolete_rhombomere 1||http://www.ebi.ac.uk/efo/EFO_0003608
14431||10652||obsolete_supraorbital lateral line neuromast||http://www.ebi.ac.uk/efo/EFO_0003607
14432||10652||obsolete_rhombomere 4||http://www.ebi.ac.uk/efo/EFO_0003609
14434||15323||early embryonic cell||http://purl.obolibrary.org/obo/CL_0000007
14433||13496||Pepper mild mottle virus||http://purl.obolibrary.org/obo/NCBITaxon_12239
14435||5278||function||http://www.ifomis.org/bfo/1.1/snap#Function
14436||770||immortal cell line cell||http://purl.obolibrary.org/obo/CL_0000002
14437||13689||slow muscle cell somite 7||http://www.ebi.ac.uk/efo/EFO_0003600
14438||13689||somite 13||http://www.ebi.ac.uk/efo/EFO_0003601
14440||13689||lateral wall spinal cord||http://www.ebi.ac.uk/efo/EFO_0003602
14439||9104||Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement||http://www.orpha.net/ORDO/Orphanet_31043
14441||13689||mesenchyme derived from head mesoderm||http://www.ebi.ac.uk/efo/EFO_0003603
14442||10652||obsolete_mesenchyme pectoral fin||http://www.ebi.ac.uk/efo/EFO_0003604
14443||13496||Turnip mosaic virus||http://purl.obolibrary.org/obo/NCBITaxon_12230
14444||10652||obsolete_trunk neural crest||http://www.ebi.ac.uk/efo/EFO_0003605
14445||10652||obsolete_occipital lateral line neuromast||http://www.ebi.ac.uk/efo/EFO_0003606
14446||4259||response to reverse transcriptase inhibitor||http://purl.obolibrary.org/obo/GO_0061479
14447||12203||Atrial septal defect, ostium secundum type||http://www.orpha.net/ORDO/Orphanet_99103
14448||12203||Atrial septal defect, coronary sinus type||http://www.orpha.net/ORDO/Orphanet_99104
14449||12203||Atrial septal defect, sinus venosus type||http://www.orpha.net/ORDO/Orphanet_99105
14450||12203||Atrial septal defect, ostium primum type||http://www.orpha.net/ORDO/Orphanet_99106
14451||4259||response to anticoagulant||http://purl.obolibrary.org/obo/GO_0061476
14452||2672||sperm||http://purl.obolibrary.org/obo/CL_0000019
14453||4259||response to aromatase inhibitor||http://purl.obolibrary.org/obo/GO_0061477
14454||4259||response to platelet aggregation inhibitor||http://purl.obolibrary.org/obo/GO_0061478
14455||4775||Mandibulofacial dysostosis - macroblepharon - macrostomia||http://www.orpha.net/ORDO/Orphanet_357158
14456||1826||Populus euphratica||http://purl.obolibrary.org/obo/NCBITaxon_75702
14457||10994||S-[2,3-bis(palmitoyloxy)propyl]-Cys-Ser-Lys-Lys-Lys-Lys||http://purl.obolibrary.org/obo/CHEBI_46889
14458||8190||N-methyl-D-aspartic acid||http://purl.obolibrary.org/obo/CHEBI_31882
14459||9382||male germ cell||http://purl.obolibrary.org/obo/CL_0000015
14460||5025||Hypocrea jecorina||http://purl.obolibrary.org/obo/NCBITaxon_51453
14462||13496||Tobacco mosaic virus||http://purl.obolibrary.org/obo/NCBITaxon_12242
14461||10652||obsolete_cell line cell||http://purl.obolibrary.org/obo/CL_0000010
14463||13689||thecal cell layer||http://www.ebi.ac.uk/efo/EFO_0003629
14464||13496||Plum pox virus||http://purl.obolibrary.org/obo/NCBITaxon_12211
14465||4139||Intellectual disability - alacrima - achalasia||http://www.orpha.net/ORDO/Orphanet_289483
14466||10994||nemonapride||http://purl.obolibrary.org/obo/CHEBI_31899
14467||13689||axial vasculature||http://www.ebi.ac.uk/efo/EFO_0003620
14468||13689||myoseptum||http://www.ebi.ac.uk/efo/EFO_0003625
14469||13689||pharyngeal endoderm||http://www.ebi.ac.uk/efo/EFO_0003626
14470||10652||obsolete_pharyngeal pouch||http://www.ebi.ac.uk/efo/EFO_0003627
14471||13689||granulosa cell layer||http://www.ebi.ac.uk/efo/EFO_0003628
14472||13689||intestinal bulb||http://www.ebi.ac.uk/efo/EFO_0003621
14473||10652||obsolete_thymus primordium||http://www.ebi.ac.uk/efo/EFO_0003622
14474||10652||obsolete_chordo neural hinge||http://www.ebi.ac.uk/efo/EFO_0003623
14475||10652||obsolete_ventricular zone||http://www.ebi.ac.uk/efo/EFO_0003624
14476||2252||Short ulna - dysmorphism - hypotonia - intellectual disability||http://www.orpha.net/ORDO/Orphanet_357175
14478||1826||Saccharum sp.||http://purl.obolibrary.org/obo/NCBITaxon_15819
14477||10652||obsolete_presumptive pronephric mesoderm||http://www.ebi.ac.uk/efo/EFO_0003619
14479||10652||obsolete_neural arch||http://www.ebi.ac.uk/efo/EFO_0003618
14480||13689||posterior caudal vein||http://www.ebi.ac.uk/efo/EFO_0003616
14481||10652||obsolete_rhombomere||http://www.ebi.ac.uk/efo/EFO_0003617
14482||13689||cranial division of the internal carotid artery||http://www.ebi.ac.uk/efo/EFO_0003614
14483||10652||obsolete_primitive mesencephalic artery||http://www.ebi.ac.uk/efo/EFO_0003615
14484||13689||primitive internal carotid artery||http://www.ebi.ac.uk/efo/EFO_0003612
14485||13689||lateral dorsal aorta||http://www.ebi.ac.uk/efo/EFO_0003613
14486||13689||slow muscle cell somite 10||http://www.ebi.ac.uk/efo/EFO_0003610
14487||13689||caudal division of the internal carotid artery||http://www.ebi.ac.uk/efo/EFO_0003611
14488||871||common myeloid progenitor||http://purl.obolibrary.org/obo/CL_0000049
14489||14537||multipotent stem cell||http://purl.obolibrary.org/obo/CL_0000048
14490||14537||neuronal stem cell||http://purl.obolibrary.org/obo/CL_0000047
14491||7590||mature basophil||http://purl.obolibrary.org/obo/CL_0000043
14494||2672||presumptive midbrain||http://purl.obolibrary.org/obo/UBERON_0009616
14492||770||AG08048||http://purl.obolibrary.org/obo/CLO_0033570
14493||10089||neutrophilic myeloblast||http://purl.obolibrary.org/obo/CL_0000042
14496||2672||head||http://purl.obolibrary.org/obo/UBERON_0000033
14495||7630||mature eosinophil||http://purl.obolibrary.org/obo/CL_0000041
14497||14514||monoblast||http://purl.obolibrary.org/obo/CL_0000040
14498||770||AG08046||http://purl.obolibrary.org/obo/CLO_0033577
14499||2672||lymph node||http://purl.obolibrary.org/obo/UBERON_0000029
14500||11641||fungal-type cell wall||http://purl.obolibrary.org/obo/GO_0009277
14501||1490||cell outer membrane||http://purl.obolibrary.org/obo/GO_0009279
14502||1022||Choristoneura fumiferana||http://purl.obolibrary.org/obo/NCBITaxon_7141
14503||772||fibroblast||http://purl.obolibrary.org/obo/CL_0000057
14504||772||myoblast||http://purl.obolibrary.org/obo/CL_0000056
14505||772||blast cell||http://purl.obolibrary.org/obo/CL_0000055
14506||5502||Vibrio harveyi ATCC BAA-1116||http://purl.obolibrary.org/obo/NCBITaxon_338187
14508||772||myelocyte||http://purl.obolibrary.org/obo/CL_0002193
14507||871||megakaryocyte-erythroid progenitor cell||http://purl.obolibrary.org/obo/CL_0000050
14509||14510||metamyelocyte||http://purl.obolibrary.org/obo/CL_0002192
14511||14513||dorsal root ganglion||http://purl.obolibrary.org/obo/UBERON_0000044
14510||10085||granulocytopoietic cell||http://purl.obolibrary.org/obo/CL_0002191
14513||2672||ganglion||http://purl.obolibrary.org/obo/UBERON_0000045
14512||871||common lymphoid progenitor||http://purl.obolibrary.org/obo/CL_0000051
14514||10085||monopoietic cell||http://purl.obolibrary.org/obo/CL_0002194
14515||1022||Manduca sexta||http://purl.obolibrary.org/obo/NCBITaxon_7130
14516||11618||sexual dysfunction||http://www.ebi.ac.uk/efo/EFO_0004714
14517||9382||oocyte||http://purl.obolibrary.org/obo/CL_0000023
14518||1391||MRI defined brain infarct||http://www.ebi.ac.uk/efo/EFO_0004715
14519||10652||obsolete_thyrotoxic periodic paralysis||http://www.ebi.ac.uk/efo/EFO_0004716
14520||1761||pelvic organ prolapse||http://www.ebi.ac.uk/efo/EFO_0004710
14522||1790||elephantiasis||http://www.ebi.ac.uk/efo/EFO_0004711
14521||770||GM09581||http://purl.obolibrary.org/obo/CLO_0011436
14524||14522||podoconiosis||http://www.ebi.ac.uk/efo/EFO_0004712
14523||3670||plant egg||http://purl.obolibrary.org/obo/CL_0000025
14525||14970||FEV/FEC ratio||http://www.ebi.ac.uk/efo/EFO_0004713
14526||2672||large intestine||http://purl.obolibrary.org/obo/UBERON_0000059
14527||2672||urethra||http://purl.obolibrary.org/obo/UBERON_0000057
14528||2672||vessel||http://purl.obolibrary.org/obo/UBERON_0000055
14529||2672||ureter||http://purl.obolibrary.org/obo/UBERON_0000056
14530||770||GM09579||http://purl.obolibrary.org/obo/CLO_0011438
14531||5103||pemphigus vulgaris||http://www.ebi.ac.uk/efo/EFO_0004719
14532||2165||vasuclar dementia||http://www.ebi.ac.uk/efo/EFO_0004718
14533||1022||Spodoptera frugiperda||http://purl.obolibrary.org/obo/NCBITaxon_7108
14534||1391||hypothyroidism||http://www.ebi.ac.uk/efo/EFO_0004705
14535||2351||cachexia||http://purl.obolibrary.org/obo/HP_0004326
14536||27||age at menarche||http://www.ebi.ac.uk/efo/EFO_0004703
14537||772||stem cell||http://purl.obolibrary.org/obo/CL_0000034
14538||27||age at menopause||http://www.ebi.ac.uk/efo/EFO_0004704
14539||11030||metamphetamine dependence||http://www.ebi.ac.uk/efo/EFO_0004701
14540||1729||abnormality of body weight||http://purl.obolibrary.org/obo/HP_0004323
14541||10652||obsolete_response to iloperidone||http://www.ebi.ac.uk/efo/EFO_0004702
14542||7606||erythroid progenitor cell||http://purl.obolibrary.org/obo/CL_0000038
14543||772||hematopoietic stem cell||http://purl.obolibrary.org/obo/CL_0000037
14544||618||larval stage||http://purl.obolibrary.org/obo/UBERON_0000069
14545||10994||celecoxib||http://purl.obolibrary.org/obo/CHEBI_41423
14546||10652||obsolete_orofacial cleft||http://www.ebi.ac.uk/efo/EFO_0004709
14547||7930||nodular sclerosis Hodgkin lymphoma||http://www.ebi.ac.uk/efo/EFO_0004708
14548||1403||infantile hypertrophic pyloric stenosis||http://www.ebi.ac.uk/efo/EFO_0004707
14550||13689||apical ectodermal ridge pelvic fin bud||http://www.ebi.ac.uk/efo/EFO_0003681
14549||9294||T cell||http://purl.obolibrary.org/obo/CL_0000084
14551||13689||regeneration epithelium||http://www.ebi.ac.uk/efo/EFO_0003682
14552||13689||axial hypoblast||http://www.ebi.ac.uk/efo/EFO_0003680
14553||772||exocrine pancreas cell||http://purl.obolibrary.org/obo/CL_0000083
14554||772||circulating cell||http://purl.obolibrary.org/obo/CL_0000080
14555||10652||obsolete_ethmoid cartilage||http://www.ebi.ac.uk/efo/EFO_0003685
14557||13689||hyosymplectic cartilage||http://www.ebi.ac.uk/efo/EFO_0003686
14556||772||blood cell||http://purl.obolibrary.org/obo/CL_0000081
14558||14970||eye measurement||http://www.ebi.ac.uk/efo/EFO_0004731
14559||13689||anterior lateral line ganglion||http://www.ebi.ac.uk/efo/EFO_0003683
14560||14970||hormone measurement||http://www.ebi.ac.uk/efo/EFO_0004730
14562||13689||ventral hyoid arch||http://www.ebi.ac.uk/efo/EFO_0003684
14561||3020||male reproductive system||http://purl.obolibrary.org/obo/UBERON_0000079
14563||14970||anti-cyclic citrullinated peptide antibody measurement||http://www.ebi.ac.uk/efo/EFO_0004733
14564||10652||obsolete_pharyngeal arch cartilage||http://www.ebi.ac.uk/efo/EFO_0003689
14565||14970||lipoprotein measurement||http://www.ebi.ac.uk/efo/EFO_0004732
14566||14970||serum alanine aminotransferase measurement||http://www.ebi.ac.uk/efo/EFO_0004735
14567||13689||primitive olfactory epithelium||http://www.ebi.ac.uk/efo/EFO_0003687
14568||13689||floor plate neural tube||http://www.ebi.ac.uk/efo/EFO_0003688
14571||14970||carotenoid measurement||http://www.ebi.ac.uk/efo/EFO_0004737
14570||13689||renal glomerulus||http://purl.obolibrary.org/obo/UBERON_0000074
14569||10994||1-fluoro-2,4-dinitrobenzene||http://purl.obolibrary.org/obo/CHEBI_53049
14572||14970||aspartate aminotransferase measurement||http://www.ebi.ac.uk/efo/EFO_0004736
14573||14970||circulating cell free DNA measurement||http://www.ebi.ac.uk/efo/EFO_0004739
14574||14970||tocopherol measurement||http://www.ebi.ac.uk/efo/EFO_0004738
14575||2658||saliva||http://purl.obolibrary.org/obo/BTO_0001202
14576||770||RT4-D6P2T cell||http://purl.obolibrary.org/obo/BTO_0001205
14577||13448||inner cell mass||http://purl.obolibrary.org/obo/UBERON_0000087
14578||772||granulocyte||http://purl.obolibrary.org/obo/CL_0000094
14579||13689||vagal ganglion 1||http://www.ebi.ac.uk/efo/EFO_0003670
14580||13689||vagal ganglion 2||http://www.ebi.ac.uk/efo/EFO_0003671
14581||7637||mature neutrophil||http://purl.obolibrary.org/obo/CL_0000096
14582||13689||vagal ganglion 3||http://www.ebi.ac.uk/efo/EFO_0003672
14583||2165||prion disease||http://www.ebi.ac.uk/efo/EFO_0004720
14584||13689||vagal ganglion 4||http://www.ebi.ac.uk/efo/EFO_0003673
14585||10187||Kupffer cell||http://purl.obolibrary.org/obo/CL_0000091
14586||10652||obsolete_dorsal anterior lateral line ganglion||http://www.ebi.ac.uk/efo/EFO_0003674
14587||13689||ventral anterior lateral line ganglion||http://www.ebi.ac.uk/efo/EFO_0003675
14588||7589||osteoclast||http://purl.obolibrary.org/obo/CL_0000092
14590||14970||carotid-femoral pulse wave velocity||http://www.ebi.ac.uk/efo/EFO_0004724
14589||13689||posterior lateral line ganglion||http://www.ebi.ac.uk/efo/EFO_0003676
14592||11618||coronary artery calcification||http://www.ebi.ac.uk/efo/EFO_0004723
14591||10652||obsolete_neurocranial trabecula||http://www.ebi.ac.uk/efo/EFO_0003677
14593||10652||obsolete_terminal nerve||http://www.ebi.ac.uk/efo/EFO_0003678
14594||13986||mesonephros||http://purl.obolibrary.org/obo/UBERON_0000080
14595||13689||pineal complex||http://www.ebi.ac.uk/efo/EFO_0003679
14597||10994||creatine||http://purl.obolibrary.org/obo/CHEBI_16919
14596||10652||obsolete_Gaucher disease||http://www.ebi.ac.uk/efo/EFO_0004721
14598||14970||serum amyloid A protein measurement||http://www.ebi.ac.uk/efo/EFO_0004728
14599||7589||mast cell||http://purl.obolibrary.org/obo/CL_0000097
14600||10994||metabolite||http://www.ebi.ac.uk/efo/EFO_0004727
14601||9288||interneuron||http://purl.obolibrary.org/obo/CL_0000099
14602||14970||metabolite measurement||http://www.ebi.ac.uk/efo/EFO_0004725
14603||3854||Pyrobaculum aerophilum||http://purl.obolibrary.org/obo/NCBITaxon_13773
14604||8190||salicylic acid||http://purl.obolibrary.org/obo/CHEBI_16914
14605||14970||vitamin measurement||http://www.ebi.ac.uk/efo/EFO_0004729
14606||1022||Culex quinquefasciatus||http://purl.obolibrary.org/obo/NCBITaxon_7176
14607||1022||Anopheles arabiensis||http://purl.obolibrary.org/obo/NCBITaxon_7173
14608||14970||CCL4 measurement||http://www.ebi.ac.uk/efo/EFO_0004751
14609||14970||interleukin 10 measurement||http://www.ebi.ac.uk/efo/EFO_0004750
14610||14970||interleukin 12 measurement||http://www.ebi.ac.uk/efo/EFO_0004753
14611||14970||parathyroid hormone measurement||http://www.ebi.ac.uk/efo/EFO_0004752
14612||772||osteoblast||http://purl.obolibrary.org/obo/CL_0000062
14613||10994||levetiracetam||http://purl.obolibrary.org/obo/CHEBI_6437
14614||772||epithelial cell||http://purl.obolibrary.org/obo/CL_0000066
14615||14970||interleukin 1 receptor antagonist measurement||http://www.ebi.ac.uk/efo/EFO_0004754
14616||1022||Anopheles gambiae||http://purl.obolibrary.org/obo/NCBITaxon_7165
14617||1022||Aedes albopictus||http://purl.obolibrary.org/obo/NCBITaxon_7160
14618||14970||renal system measurement||http://www.ebi.ac.uk/efo/EFO_0004742
14619||13689||pharyngeal arch 3-7||http://www.ebi.ac.uk/efo/EFO_0003694
14620||14970||blood urea nitrogen measurement||http://www.ebi.ac.uk/efo/EFO_0004741
14621||10652||obsolete_aortic arch||http://www.ebi.ac.uk/efo/EFO_0003695
14622||13689||mid cerebral vein||http://www.ebi.ac.uk/efo/EFO_0003696
14623||13689||primordial midbrain channel||http://www.ebi.ac.uk/efo/EFO_0003697
14625||15087||blood vessel endothelial cell||http://purl.obolibrary.org/obo/CL_0000071
14624||13689||chondrocranium cartilage||http://www.ebi.ac.uk/efo/EFO_0003690
14626||13689||anterior lateral line system||http://www.ebi.ac.uk/efo/EFO_0003691
14628||13689||posterior lateral line system||http://www.ebi.ac.uk/efo/EFO_0003692
14627||2672||vasculature of eye||http://purl.obolibrary.org/obo/UBERON_0002203
14629||13689||superficial blastomere||http://www.ebi.ac.uk/efo/EFO_0003693
14630||14970||CCL2 measurement||http://www.ebi.ac.uk/efo/EFO_0004749
14633||14970||thyroid stimulating hormone measurement||http://www.ebi.ac.uk/efo/EFO_0004748
14631||772||mesothelial cell||http://purl.obolibrary.org/obo/CL_0000077
14632||5502||Salmonella enterica subsp. enterica serovar Senftenberg||http://purl.obolibrary.org/obo/NCBITaxon_28150
14634||14970||protein measurement||http://www.ebi.ac.uk/efo/EFO_0004747
14635||14970||lipoprotein-associated phospholipase A(2) measurement||http://www.ebi.ac.uk/efo/EFO_0004746
14636||13689||dorsal longitudinal anastomotic vessel||http://www.ebi.ac.uk/efo/EFO_0003698
14638||14970||NT-proBNP measurement||http://www.ebi.ac.uk/efo/EFO_0004745
14637||13689||ventral wall of dorsal aorta||http://www.ebi.ac.uk/efo/EFO_0003699
14639||14970||matrix metalloproteinase measurement||http://www.ebi.ac.uk/efo/EFO_0004744
14640||2063||facial morphology||http://www.ebi.ac.uk/efo/EFO_0004743
14641||1022||Aedes aegypti||http://purl.obolibrary.org/obo/NCBITaxon_7159
14642||194||Autoinflammatory syndrome with immune deficiency||http://www.orpha.net/ORDO/Orphanet_290839
14643||1826||Lotus corniculatus||http://purl.obolibrary.org/obo/NCBITaxon_47247
14644||321||Alopecia - intellectual disability - hypergonadotropic hypogonadism||http://www.orpha.net/ORDO/Orphanet_1014
14645||1022||Bombyx mori||http://purl.obolibrary.org/obo/NCBITaxon_7091
14646||306||Autosomal dominant palmoplantar keratoderma and congenital alopecia||http://www.orpha.net/ORDO/Orphanet_1010
14647||12161||progressive external ophthalmoplegia||http://www.ebi.ac.uk/efo/EFO_0002509
14648||2165||Parkinson s disease||http://www.ebi.ac.uk/efo/EFO_0002508
14649||109||ovarian adenoma benign||http://www.ebi.ac.uk/efo/EFO_0002507
14650||2228||anaplastic oligodendroglioma||http://www.ebi.ac.uk/efo/EFO_0002501
14651||1790||benign insulitis||http://www.ebi.ac.uk/efo/EFO_0002502
14652||2225||anaplastic oligoastrocytoma||http://www.ebi.ac.uk/efo/EFO_0002500
14653||10652||obsolete_multiple system atrophy||http://www.ebi.ac.uk/efo/EFO_0002505
14654||14614||epithelial cell of prostate||http://purl.obolibrary.org/obo/CL_0002231
14655||5315||osteoarthritis||http://www.ebi.ac.uk/efo/EFO_0002506
14656||15525||cardiac hypertrophy||http://www.ebi.ac.uk/efo/EFO_0002503
14657||109||serous cystadenoma||http://www.ebi.ac.uk/efo/EFO_0002504
14658||5466||Paternal 14q32.2 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_254525
14659||9753||gastrointestinal inflammation||http://purl.obolibrary.org/obo/HP_0004386
14661||14964||Maternal 14q32.2 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_254528
14660||5216||X-linked diffuse leiomyomatosis - Alport syndrome||http://www.orpha.net/ORDO/Orphanet_1018
14662||306||Amelo-onycho-hypohidrotic syndrome||http://www.orpha.net/ORDO/Orphanet_1028
14664||6244||Autosomal recessive amelia||http://www.orpha.net/ORDO/Orphanet_1027
14663||6476||response to radiation||http://purl.obolibrary.org/obo/GO_0009314
14665||14964||Maternal 14q32.2 hypermethylation syndrome||http://www.orpha.net/ORDO/Orphanet_254534
14666||1257||Congenital generalized hypertrichosis, Ambras type||http://www.orpha.net/ORDO/Orphanet_1023
14668||14966||Paternal 14q32.2 hypomethylation syndrome||http://www.orpha.net/ORDO/Orphanet_254531
14667||9965||Amaurosis - hypertrichosis||http://www.orpha.net/ORDO/Orphanet_1021
14670||15185||Early-onset autosomal dominant Alzheimer disease||http://www.orpha.net/ORDO/Orphanet_1020
14669||2670||vegetative apex||http://www.ebi.ac.uk/efo/EFO_0002519
14671||3043||raphe magnus||http://www.ebi.ac.uk/efo/EFO_0002518
14672||2671||haustorium||http://purl.obolibrary.org/obo/BTO_0000515
14673||15413||serous cystadenofibroma||http://www.ebi.ac.uk/efo/EFO_0002510
14674||109||simple cystadenoma||http://www.ebi.ac.uk/efo/EFO_0002511
14675||10652||obsolete_supranuclear palsy, progressive||http://www.ebi.ac.uk/efo/EFO_0002512
14676||10652||obsolete_alveolus||http://www.ebi.ac.uk/efo/EFO_0002513
14677||2672||corneal stroma||http://www.ebi.ac.uk/efo/EFO_0002514
14678||10652||obsolete_ductus arteriosus||http://www.ebi.ac.uk/efo/EFO_0002515
14679||14513||inferior ganglion of vagus nerve||http://www.ebi.ac.uk/efo/EFO_0002516
14680||120||pancreatic ductal adenocarcinoma||http://www.ebi.ac.uk/efo/EFO_0002517
14682||1022||Palaemonetes pugio||http://purl.obolibrary.org/obo/NCBITaxon_221654
14681||5502||Salmonella enterica subsp. enterica serovar Oranienburg||http://purl.obolibrary.org/obo/NCBITaxon_28147
14683||3733||abnormality of temperature regulation||http://purl.obolibrary.org/obo/HP_0004370
14684||1022||Tribolium castaneum||http://purl.obolibrary.org/obo/NCBITaxon_7070
14685||13535||intermediate trophoblast cell||http://purl.obolibrary.org/obo/CL_0002217
14686||13390||immature dendritic epithelial T cell precursor||http://purl.obolibrary.org/obo/CL_0002218
14687||770||INS-1||http://www.ebi.ac.uk/efo/EFO_0002529
14688||10652||obsolete_descending thoracic aorta||http://www.ebi.ac.uk/efo/EFO_0002527
14689||13156||substantia nigra and ventral tegmental area||http://www.ebi.ac.uk/efo/EFO_0002528
14690||2672||spinal cord||http://purl.obolibrary.org/obo/UBERON_0002240
14691||10652||obsolete_thoracic aorta||http://www.ebi.ac.uk/efo/EFO_0002525
14693||3229||Tumor necrosis factor receptor 1 associated periodic syndrome||http://www.orpha.net/ORDO/Orphanet_32960
14692||10652||obsolete_preoptic area||http://www.ebi.ac.uk/efo/EFO_0002523
14694||10652||obsolete_abdominal aorta||http://www.ebi.ac.uk/efo/EFO_0002524
14695||10652||obsolete_cerebral hemisphere||http://www.ebi.ac.uk/efo/EFO_0002521
14696||13587||BTBR mouse||http://www.ebi.ac.uk/efo/EFO_0002522
14697||3043||neurointermediate lobe||http://www.ebi.ac.uk/efo/EFO_0002520
14698||13448||spinal cord lateral wall||http://purl.obolibrary.org/obo/UBERON_0009582
14699||6036||bacterial thylakoid||http://purl.obolibrary.org/obo/GO_0030075
14701||12186||Interventricular septum aneurysm||http://www.orpha.net/ORDO/Orphanet_99092
14700||5502||Bacteroides ovatus||http://purl.obolibrary.org/obo/NCBITaxon_28116
14702||12186||Multiple ventricular septal defects||http://www.orpha.net/ORDO/Orphanet_99096
14704||12186||Gerbode defect||http://www.orpha.net/ORDO/Orphanet_99095
14703||2021||2q37 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_1001
14706||12186||Laubry-Pezzi syndrome||http://www.orpha.net/ORDO/Orphanet_99094
14705||1827||Ocular albinism with late-onset sensorineural deafness||http://www.orpha.net/ORDO/Orphanet_1000
14707||321||Alopecia antibody deficiency||http://www.orpha.net/ORDO/Orphanet_1006
14708||306||Alopecia-contractures-dwarfism-intellectual disability syndrome||http://www.orpha.net/ORDO/Orphanet_1005
14710||12186||Single ventricular septal defect||http://www.orpha.net/ORDO/Orphanet_99097
14709||5865||Scalp defects - postaxial polydactyly||http://www.orpha.net/ORDO/Orphanet_1003
14711||14556||fetal blood cell||http://www.ebi.ac.uk/efo/EFO_0002534
14712||321||Alopecia - epilepsy - pyorrhea - intellectual disability||http://www.orpha.net/ORDO/Orphanet_1008
14713||9838||Peptic ulcer||http://purl.obolibrary.org/obo/HP_0004398
14714||13496||Hantaan virus||http://purl.obolibrary.org/obo/NCBITaxon_11599
14715||10994||bilirubin||http://purl.obolibrary.org/obo/CHEBI_16990
14716||8047||DNA||http://purl.obolibrary.org/obo/CHEBI_16991
14717||2672||olfactory apparatus||http://purl.obolibrary.org/obo/UBERON_0000004
14718||2672||uterine cervix||http://purl.obolibrary.org/obo/UBERON_0000002
14719||15148||islet cell||http://www.ebi.ac.uk/efo/EFO_0002542
14720||772||nestin positive islet-derived progenitor cell||http://www.ebi.ac.uk/efo/EFO_0002540
14721||14775||Mitochondrial myopathy||http://www.orpha.net/ORDO/Orphanet_206966
14722||11618||abnormal glucose tolerance||http://www.ebi.ac.uk/efo/EFO_0002546
14723||10652||obsolete_endoderm||http://www.ebi.ac.uk/efo/EFO_0002545
14724||618||plasmodium parasite stage||http://www.ebi.ac.uk/efo/EFO_0002544
14726||13496||Toscana virus||http://purl.obolibrary.org/obo/NCBITaxon_11590
14725||618||mouse prenatal||http://www.ebi.ac.uk/efo/EFO_0002543
14727||10652||obsolete_vagus nerve||http://www.ebi.ac.uk/efo/EFO_0002549
14728||13496||Crimean-Congo hemorrhagic fever virus||http://purl.obolibrary.org/obo/NCBITaxon_11593
14729||10652||obsolete_endothelium||http://www.ebi.ac.uk/efo/EFO_0002548
14730||13587||NOD mouse||http://www.ebi.ac.uk/efo/EFO_0002547
14731||10994||nitrofurantoin||http://purl.obolibrary.org/obo/CHEBI_7591
14732||13496||Rift Valley fever virus||http://purl.obolibrary.org/obo/NCBITaxon_11588
14733||2672||vomeronasal organ||http://purl.obolibrary.org/obo/UBERON_0002255
14734||10652||obsolete_coronary artery||http://www.ebi.ac.uk/efo/EFO_0002551
14735||10652||obsolete_brachiocephalic artery||http://www.ebi.ac.uk/efo/EFO_0002550
14736||10652||obsolete_tongue mucosa||http://www.ebi.ac.uk/efo/EFO_0002553
14738||1022||Cryptococcus neoformans var. grubii H99||http://purl.obolibrary.org/obo/NCBITaxon_235443
14737||10652||obsolete_renal artery||http://www.ebi.ac.uk/efo/EFO_0002552
14739||10652||obsolete_pyloric antrum||http://www.ebi.ac.uk/efo/EFO_0002555
14740||14742||Congenital myotonia||http://www.orpha.net/ORDO/Orphanet_206973
14741||10652||obsolete_gastric fundus||http://www.ebi.ac.uk/efo/EFO_0002554
14742||12322||Myotonic syndrome||http://www.orpha.net/ORDO/Orphanet_206970
14743||2672||pancreatic mesenchyme||http://www.ebi.ac.uk/efo/EFO_0002557
14744||2672||pancreatic duct epithelium||http://www.ebi.ac.uk/efo/EFO_0002556
14745||10652||obsolete_ciliary ganglion||http://www.ebi.ac.uk/efo/EFO_0002559
14746||10652||obsolete_parotid gland||http://www.ebi.ac.uk/efo/EFO_0002558
14747||13496||La Crosse virus||http://purl.obolibrary.org/obo/NCBITaxon_11577
14748||4803||Constitutional mismatch repair deficiency syndrome||http://www.orpha.net/ORDO/Orphanet_252202
14749||10994||benzene-1,2,4-triol||http://purl.obolibrary.org/obo/CHEBI_16979
14751||15511||embryonic day 13.5||http://www.ebi.ac.uk/efo/EFO_0002564
14750||14759||wing||http://purl.obolibrary.org/obo/UBERON_0000023
14753||15511||embryonic day 12.5||http://www.ebi.ac.uk/efo/EFO_0002563
14752||2672||feather||http://purl.obolibrary.org/obo/UBERON_0000022
14754||15511||embryonic day 11.5||http://www.ebi.ac.uk/efo/EFO_0002562
14755||15511||embryonic day 8.25||http://www.ebi.ac.uk/efo/EFO_0002561
14756||7111||site||http://www.ifomis.org/bfo/1.1/snap#Site
14757||15442||gastrula 80%-epiboly||http://www.ebi.ac.uk/efo/EFO_0002560
14758||5295||neurodegeneration||http://purl.obolibrary.org/obo/HP_0002180
14759||2672||appendage||http://purl.obolibrary.org/obo/UBERON_0000026
14761||10994||nimodipine||http://purl.obolibrary.org/obo/CHEBI_7575
14760||772||epithelial cell of large intestine||http://purl.obolibrary.org/obo/CL_0002253
14762||15511||embryonic day 18||http://www.ebi.ac.uk/efo/EFO_0002569
14763||15511||embryonic day 17.5||http://www.ebi.ac.uk/efo/EFO_0002568
14764||15511||embryonic day 16.5||http://www.ebi.ac.uk/efo/EFO_0002567
14765||15511||embryonic day 15.5||http://www.ebi.ac.uk/efo/EFO_0002566
14766||15511||embryonic day 14.5||http://www.ebi.ac.uk/efo/EFO_0002565
14767||8938||Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome||http://www.orpha.net/ORDO/Orphanet_281201
14768||2672||islet of Langerhans||http://purl.obolibrary.org/obo/UBERON_0000006
14769||11433||pituitary gland||http://purl.obolibrary.org/obo/UBERON_0000007
14770||15129||small adipocyte||http://www.ebi.ac.uk/efo/EFO_0002573
14771||1627||peripheral nervous system||http://purl.obolibrary.org/obo/UBERON_0000010
14772||15129||large adipocyte||http://www.ebi.ac.uk/efo/EFO_0002572
14773||3639||esophageal endoderm||http://www.ebi.ac.uk/efo/EFO_0002575
14775||11881||Muscular lipidosis||http://www.orpha.net/ORDO/Orphanet_206953
14776||1627||parasympathetic nervous system||http://purl.obolibrary.org/obo/UBERON_0000011
14774||10652||obsolete_definitive endoderm||http://www.ebi.ac.uk/efo/EFO_0002574
14777||11881||Muscular glycogenosis||http://www.orpha.net/ORDO/Orphanet_206959
14778||1627||sympathetic nervous system||http://purl.obolibrary.org/obo/UBERON_0000013
14780||13883||medical procedure||http://www.ebi.ac.uk/efo/EFO_0002571
14779||2672||endocrine pancreas||http://purl.obolibrary.org/obo/UBERON_0000016
14781||15511||embryonic day 18.5||http://www.ebi.ac.uk/efo/EFO_0002570
14782||10994||nifedipine||http://purl.obolibrary.org/obo/CHEBI_7565
14783||3639||liver endoderm||http://www.ebi.ac.uk/efo/EFO_0002577
14784||7704||pluripotent stem cell||http://purl.obolibrary.org/obo/CL_0002248
14785||3639||intestinal endoderm||http://www.ebi.ac.uk/efo/EFO_0002576
14786||14543||peripheral blood stem cell||http://purl.obolibrary.org/obo/CL_0002246
14788||3639||pancreatic endoderm||http://www.ebi.ac.uk/efo/EFO_0002579
14787||5502||Salmonella enterica subsp. enterica serovar Paratyphi C||http://purl.obolibrary.org/obo/NCBITaxon_57046
14791||3639||lung endoderm||http://www.ebi.ac.uk/efo/EFO_0002578
14790||5502||Salmonella enterica subsp. enterica serovar Paratyphi B||http://purl.obolibrary.org/obo/NCBITaxon_57045
14789||10187||pleural macrophage||http://purl.obolibrary.org/obo/CL_0002247
14793||14725||Theiler stage 26||http://www.ebi.ac.uk/efo/EFO_0002587
14792||13299||RNA assay||http://www.ebi.ac.uk/efo/EFO_0001457
14795||13299||DNA assay||http://www.ebi.ac.uk/efo/EFO_0001456
14794||799||intravenous anaesthetic||http://purl.obolibrary.org/obo/CHEBI_38877
14796||7785||Theiler stage 28||http://www.ebi.ac.uk/efo/EFO_0002588
14798||14724||hepatic schizont||http://www.ebi.ac.uk/efo/EFO_0002589
14797||13689||floor plate||http://purl.obolibrary.org/obo/UBERON_0003079
14799||12388||epibranchial placode||http://purl.obolibrary.org/obo/UBERON_0003078
14801||4803||BAP1-related tumor predisposition syndrome||http://www.orpha.net/ORDO/Orphanet_289539
14800||5025||Saccharomyces cerevisiae x Saccharomyces kudriavzevii||http://purl.obolibrary.org/obo/NCBITaxon_332112
14802||2318||Microcephalic primordial dwarfism due to ZNF335 deficiency||http://www.orpha.net/ORDO/Orphanet_329228
14803||13299||protein assay||http://www.ebi.ac.uk/efo/EFO_0001458
14805||13689||lens placode||http://purl.obolibrary.org/obo/UBERON_0003073
14804||8193||glucosamine||http://purl.obolibrary.org/obo/CHEBI_5417
14807||3639||stomach endoderm||http://www.ebi.ac.uk/efo/EFO_0002580
14806||2252||Intellectual disability - craniofacial dysmorphism - cryptorchidism||http://www.orpha.net/ORDO/Orphanet_329224
14808||14780||pancreatectomy||http://www.ebi.ac.uk/efo/EFO_0002581
14809||14725||Theiler stage 11||http://www.ebi.ac.uk/efo/EFO_0002582
14810||12388||trigeminal placode||http://purl.obolibrary.org/obo/UBERON_0003070
14811||14725||Theiler stage 17||http://www.ebi.ac.uk/efo/EFO_0002583
14812||13448||paraxial mesoderm||http://purl.obolibrary.org/obo/UBERON_0003077
14813||14725||Theiler stage 21||http://www.ebi.ac.uk/efo/EFO_0002584
14816||15538||instrument design||http://www.ebi.ac.uk/efo/EFO_0001451
14814||14725||Theiler stage 22||http://www.ebi.ac.uk/efo/EFO_0002585
14815||799||inhalation anaesthetic||http://purl.obolibrary.org/obo/CHEBI_38870
14817||14725||Theiler stage 24||http://www.ebi.ac.uk/efo/EFO_0002586
14818||6625||Niemann-Pick disease type E||http://www.orpha.net/ORDO/Orphanet_99022
14819||2446||Methylmalonic acidemia with homocystinuria, type cblX||http://www.orpha.net/ORDO/Orphanet_369962
14821||12769||Anonychia - microcephaly||http://www.orpha.net/ORDO/Orphanet_1094
14820||11038||X-linked ichthyosis syndrome||http://www.orpha.net/ORDO/Orphanet_281210
14823||11038||Autosomal ichthyosis syndrome||http://www.orpha.net/ORDO/Orphanet_281217
14822||9749||Adult-onset autosomal dominant leukodystrophy||http://www.orpha.net/ORDO/Orphanet_99027
14824||7319||Renal-genital-middle ear anomalies||http://www.orpha.net/ORDO/Orphanet_1092
14825||1022||Cricetulus griseus||http://purl.obolibrary.org/obo/NCBITaxon_10029
14826||13689||axial mesoderm||http://purl.obolibrary.org/obo/UBERON_0003068
14827||3446||distal portion of anterior interventricular branch of left coronary artery||http://www.ebi.ac.uk/efo/EFO_0002598
14829||12388||otic placode||http://purl.obolibrary.org/obo/UBERON_0003069
14828||10994||tetrafluoroethene||http://purl.obolibrary.org/obo/CHEBI_38866
14830||3446||distal portion of circumflex branch of left coronary artery||http://www.ebi.ac.uk/efo/EFO_0002599
14831||212||Inherited isolated adrenal insufficiency due to CYP11A1 deficiency||http://www.orpha.net/ORDO/Orphanet_289548
14832||1627||biliary system||http://purl.obolibrary.org/obo/UBERON_0002294
14833||14724||trophozoite||http://www.ebi.ac.uk/efo/EFO_0002592
14835||12036||distal renal artery||http://www.ebi.ac.uk/efo/EFO_0002593
14834||2672||brainstem||http://purl.obolibrary.org/obo/UBERON_0002298
14837||14724||ring stage trophozoite||http://www.ebi.ac.uk/efo/EFO_0002590
14836||9803||uninfected||http://www.ebi.ac.uk/efo/EFO_0001460
14840||14724||erythrocytic schizont||http://www.ebi.ac.uk/efo/EFO_0002591
14838||13689||blood island||http://purl.obolibrary.org/obo/UBERON_0003061
14839||6989||X-linked central congenital hypothyroidism with late-onset testicular enlargement||http://www.orpha.net/ORDO/Orphanet_329235
14841||1711||carotid artery endothelium||http://www.ebi.ac.uk/efo/EFO_0002596
14842||6573||control||http://www.ebi.ac.uk/efo/EFO_0001461
14843||10652||obsolete_aorta endothelium||http://www.ebi.ac.uk/efo/EFO_0002597
14844||12036||proximal renal artery||http://www.ebi.ac.uk/efo/EFO_0002594
14845||13689||ciliary marginal zone||http://purl.obolibrary.org/obo/UBERON_0003065
14846||2794||renal branch of vagus nerve||http://www.ebi.ac.uk/efo/EFO_0002595
14847||4454||oxygen||http://purl.obolibrary.org/obo/CHEBI_15379
14848||13770||Finger hyperphalangy-toe anomalies-severe pectus excavatum syndrome||http://www.orpha.net/ORDO/Orphanet_369979
14849||14823||Autosomal ichthyosis syndrome with prominent hair abnormalities||http://www.orpha.net/ORDO/Orphanet_281222
14850||10994||5,6,7,8-tetrahydrobiopterin||http://purl.obolibrary.org/obo/CHEBI_15372
14851||4750||Microcornea-myopic chorioretinal atrophy-telecanthus syndrome||http://www.orpha.net/ORDO/Orphanet_369970
14852||10994||water||http://purl.obolibrary.org/obo/CHEBI_15377
14853||1528||46,XY partial gonadal dysgenesis||http://www.orpha.net/ORDO/Orphanet_251510
14854||13421||Distal arthrogryposis type 10||http://www.orpha.net/ORDO/Orphanet_251515
14855||13496||Cymbidium ringspot virus||http://purl.obolibrary.org/obo/NCBITaxon_12144
14856||13448||cranial neural crest||http://purl.obolibrary.org/obo/UBERON_0003099
14857||2021||Thumb stiffness - brachydactyly - intellectual disability||http://www.orpha.net/ORDO/Orphanet_1078
14858||1619||Dental ankylosis||http://www.orpha.net/ORDO/Orphanet_1077
14859||553||Butterfly-shaped pigment dystrophy||http://www.orpha.net/ORDO/Orphanet_99001
14860||5292||organic substance metabolic process||http://purl.obolibrary.org/obo/GO_0071704
14861||9675||Adult-onset foveomacular vitelliform dystrophy||http://www.orpha.net/ORDO/Orphanet_99000
14862||5366||all-trans-retinoic acid||http://purl.obolibrary.org/obo/CHEBI_15367
14863||10994||acrolein||http://purl.obolibrary.org/obo/CHEBI_15368
14864||306||Ankyloblepharon - ectodermal defects - cleft lip/palate||http://www.orpha.net/ORDO/Orphanet_1071
14865||8190||acetylsalicylic acid||http://purl.obolibrary.org/obo/CHEBI_15365
14867||14823||Autosomal ichthyosis syndrome with prominent neurologics signs||http://www.orpha.net/ORDO/Orphanet_281238
14868||553||Fundus pulverulentus||http://www.orpha.net/ORDO/Orphanet_99004
14866||5700||Dysmorphism - conductive hearing loss - heart defect||http://www.orpha.net/ORDO/Orphanet_289553
14869||8190||acetic acid||http://purl.obolibrary.org/obo/CHEBI_15366
14870||553||Multifocal pattern dystrophy simulating fundus flavimaculatus||http://www.orpha.net/ORDO/Orphanet_99003
14871||553||Reticular dystrophy of the retinal pigment epithelium||http://www.orpha.net/ORDO/Orphanet_99002
14872||6899||Ankyloblepharon filiforme - imperforate anus||http://www.orpha.net/ORDO/Orphanet_1074
14873||5300||Ankyloblepharon filiforme adnatum - cleft palate||http://www.orpha.net/ORDO/Orphanet_1072
14874||5191||Recurrent infections - inflammatory syndrome due to zinc metabolism disorder||http://www.orpha.net/ORDO/Orphanet_251523
14875||14823||Autosomal ichthyosis syndrome with fatal disease course||http://www.orpha.net/ORDO/Orphanet_281241
14877||1627||cardiovascular system||http://purl.obolibrary.org/obo/UBERON_0004535
14876||1022||Heterorhabditis bacteriophora||http://purl.obolibrary.org/obo/NCBITaxon_37862
14878||3072||caudal artery||http://purl.obolibrary.org/obo/UBERON_0003086
14879||9719||Autosomal dominant neovascular inflammatory vitreoretinopathy||http://www.orpha.net/ORDO/Orphanet_329211
14880||1826||Zostera marina||http://purl.obolibrary.org/obo/NCBITaxon_29655
14881||13448||trunk neural crest||http://purl.obolibrary.org/obo/UBERON_0003083
14882||13306||Short stature-heart defect-craniofacial anomalies syndrome||http://www.orpha.net/ORDO/Orphanet_1088
14883||12401||Diffuse palmoplantar keratoderma with painful fissures||http://www.orpha.net/ORDO/Orphanet_369999
14884||9711||Autosomal recessive optic atrophy, OPA6 type||http://www.orpha.net/ORDO/Orphanet_99012
14885||7675||Neurodegeneration with brain iron accumulation due to C19orf12 mutation||http://www.orpha.net/ORDO/Orphanet_289560
14886||2996||X-linked Charcot-Marie-Tooth disease type 5||http://www.orpha.net/ORDO/Orphanet_99014
14887||583||Autosomal recessive spastic paraplegia type 7||http://www.orpha.net/ORDO/Orphanet_99013
14888||325||Severe dermatitis-multiple allergies-metabolic wasting syndrome||http://www.orpha.net/ORDO/Orphanet_369992
14889||533||Spastic paraplegia type 2||http://www.orpha.net/ORDO/Orphanet_99015
14891||14823||Autosomal ichthyosis syndrome with other associated signs||http://www.orpha.net/ORDO/Orphanet_281244
14890||13496||Southern bean mosaic virus||http://purl.obolibrary.org/obo/NCBITaxon_12139
14892||1433||Isolated lissencephaly type 1 without known genetic defects||http://www.orpha.net/ORDO/Orphanet_1084
14893||2683||Microlissencephaly||http://www.orpha.net/ORDO/Orphanet_1083
14894||4259||response to tamsulosin||http://purl.obolibrary.org/obo/GO_1901905
14895||3049||Aldosterone-producing adenoma with seizures and neurological abnormalities||http://www.orpha.net/ORDO/Orphanet_369929
14896||10652||obsolete_deltoid||http://www.ebi.ac.uk/efo/EFO_0001412
14897||10652||obsolete_gastrocnemius||http://www.ebi.ac.uk/efo/EFO_0001413
14898||14017||arm||http://www.ebi.ac.uk/efo/EFO_0001410
14899||14017||leg||http://www.ebi.ac.uk/efo/EFO_0001411
14900||120||cervical adenocarcinoma||http://www.ebi.ac.uk/efo/EFO_0001416
14901||10652||obsolete_sciatic nerve||http://www.ebi.ac.uk/efo/EFO_0001417
14902||13448||embryonic gonadal ridge||http://www.ebi.ac.uk/efo/EFO_0001414
14903||772||lung cancer cell||http://purl.obolibrary.org/obo/BTO_0000551
14904||10652||obsolete_umbilical cord||http://www.ebi.ac.uk/efo/EFO_0001415
14905||5967||Mosaic variegated aneuploidy syndrome||http://www.orpha.net/ORDO/Orphanet_1052
14907||2252||Ramos-Arroyo syndrome||http://www.orpha.net/ORDO/Orphanet_1051
14906||10652||obsolete_biceps femoris||http://www.ebi.ac.uk/efo/EFO_0001418
14909||1839||Tyrosinemia type 3||http://www.orpha.net/ORDO/Orphanet_69723
14908||10994||acetaldehyde||http://purl.obolibrary.org/obo/CHEBI_15343
14910||9894||Pontocerebellar hypoplasia type 9||http://www.orpha.net/ORDO/Orphanet_369920
14911||10994||acetone||http://purl.obolibrary.org/obo/CHEBI_15347
14912||4803||Blue rubber bleb nevus||http://www.orpha.net/ORDO/Orphanet_1059
14913||4139||Severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome||http://www.orpha.net/ORDO/Orphanet_369939
14914||1355||sepsis||http://www.ebi.ac.uk/efo/EFO_0001420
14915||1391||liver disease||http://www.ebi.ac.uk/efo/EFO_0001421
14916||14915||cirrhosis of liver||http://www.ebi.ac.uk/efo/EFO_0001422
14917||2165||encephalomyelitis||http://www.ebi.ac.uk/efo/EFO_0001423
14918||10652||obsolete_masseter muscle||http://www.ebi.ac.uk/efo/EFO_0001424
14919||2672||cingulate cortex||http://purl.obolibrary.org/obo/UBERON_0003027
14920||1016||ischemic cardiomyopathy||http://www.ebi.ac.uk/efo/EFO_0001425
14922||4335||study design||http://www.ebi.ac.uk/efo/EFO_0001426
14924||1022||Amphimedon queenslandica||http://purl.obolibrary.org/obo/NCBITaxon_400682
14921||5700||Athabaskan brainstem dysgenesis syndrome||http://www.orpha.net/ORDO/Orphanet_69739
14923||6306||Combined malonic and methylmalonic acidemia||http://www.orpha.net/ORDO/Orphanet_289504
14925||15020||case control design||http://www.ebi.ac.uk/efo/EFO_0001427
14926||15020||cross sectional design||http://www.ebi.ac.uk/efo/EFO_0001428
14927||5478||Hypotrichosis - lymphedema - telangiectasia||http://www.orpha.net/ORDO/Orphanet_69735
14929||15020||family based design||http://www.ebi.ac.uk/efo/EFO_0001429
14930||733||Hereditary neurocutaneous angioma||http://www.orpha.net/ORDO/Orphanet_1062
14928||4605||non ionic surfactant role||http://purl.obolibrary.org/obo/CHEBI_38828
14932||5700||Bosley-Salih-Alorainy syndrome||http://www.orpha.net/ORDO/Orphanet_69737
14931||10694||Tufted angioma||http://www.orpha.net/ORDO/Orphanet_1063
14933||2252||Aniridia - renal agenesis - psychomotor retardation||http://www.orpha.net/ORDO/Orphanet_1064
14934||6899||Aniridia - absent patella||http://www.orpha.net/ORDO/Orphanet_1069
14935||4139||Aniridia - cerebellar ataxia - intellectual disability||http://www.orpha.net/ORDO/Orphanet_1065
14936||4139||Aniridia - ptosis - intellectual disability - familial obesity||http://www.orpha.net/ORDO/Orphanet_1067
14937||4139||Aniridia-intellectual disability syndrome||http://www.orpha.net/ORDO/Orphanet_1068
14938||15020||population based design||http://www.ebi.ac.uk/efo/EFO_0001430
14939||14929||twin design||http://www.ebi.ac.uk/efo/EFO_0001431
14940||13689||ventricular zone||http://purl.obolibrary.org/obo/UBERON_0003053
14941||13448||olfactory placode||http://purl.obolibrary.org/obo/UBERON_0003050
14942||2002||Dermatofibrosarcoma protuberans||http://www.orpha.net/ORDO/Orphanet_31112
14943||5025||Cordyceps militaris||http://purl.obolibrary.org/obo/NCBITaxon_73501
14944||13496||Potato virus X||http://purl.obolibrary.org/obo/NCBITaxon_12183
14945||13448||hypochord||http://purl.obolibrary.org/obo/UBERON_0003058
14946||2672||presomitic mesoderm||http://purl.obolibrary.org/obo/UBERON_0003059
14947||10652||obsolete_race||http://www.ebi.ac.uk/efo/EFO_0001432
14948||7023||Double outlet right ventricle with non-committed subpulmonary ventricular septal defect||http://www.orpha.net/ORDO/Orphanet_99046
14950||11285||protein secretion||http://purl.obolibrary.org/obo/GO_0009306
14949||7023||Double outlet right ventricle with doubly committed ventricular septal defect||http://www.orpha.net/ORDO/Orphanet_99047
14951||1022||Phodopus sungorus||http://purl.obolibrary.org/obo/NCBITaxon_10044
14952||10659||12q15q21.1 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_289513
14953||4834||Amelogenesis imperfecta - nephrocalcinosis||http://www.orpha.net/ORDO/Orphanet_1031
14954||13799||Amniotic bands||http://www.orpha.net/ORDO/Orphanet_1034
14955||4706||Encephalopathy due to beta-mercaptolactate-cysteine disulfiduria||http://www.orpha.net/ORDO/Orphanet_1035
14956||6305||Hyperdibasic aminoaciduria type 1||http://www.orpha.net/ORDO/Orphanet_1032
14959||266||CADDS||http://www.orpha.net/ORDO/Orphanet_369942
14958||7023||Double outlet right ventricle with subaortic ventricular septal defect||http://www.orpha.net/ORDO/Orphanet_99044
14957||10994||oxaliplatin||http://purl.obolibrary.org/obo/CHEBI_31941
14960||7023||Double outlet right ventricle with subpulmonary ventricular septal defect||http://www.orpha.net/ORDO/Orphanet_99045
14961||6262||Congenitally uncorrected transposition of the great arteries with coarctation||http://www.orpha.net/ORDO/Orphanet_99042
14963||13025||Arthrogryposis multiplex congenita||http://www.orpha.net/ORDO/Orphanet_1037
14962||7023||Double outlet right ventricle, Fallot type||http://www.orpha.net/ORDO/Orphanet_99043
14964||2252||Multiple congenital anomalies due to 14q32.2 maternally expressed gene defect||http://www.orpha.net/ORDO/Orphanet_254519
14965||13543||Drosophila pseudoobscura bogotana||http://purl.obolibrary.org/obo/NCBITaxon_46244
14966||4139||Motor developmental delay due to 14q32.2 paternally expressed gene defect||http://www.orpha.net/ORDO/Orphanet_254516
14967||4266||Fatal infantile hypertrophic cardiomyopathy due to mitochondrial complex I deficiency||http://www.orpha.net/ORDO/Orphanet_289527
14968||772||bone marrow cancer cell||http://purl.obolibrary.org/obo/BTO_0000583
14969||9934||Char syndrome||http://www.orpha.net/ORDO/Orphanet_46627
14970||15538||measurement||http://www.ebi.ac.uk/efo/EFO_0001444
14971||2252||Microtriplication 11q24.1||http://www.orpha.net/ORDO/Orphanet_289522
14973||1022||Mesocricetus auratus||http://purl.obolibrary.org/obo/NCBITaxon_10036
14972||8001||Metaphyseal anadysplasia||http://www.orpha.net/ORDO/Orphanet_1040
14974||2446||Methylmalonic acidemia with homocystinuria, type cblJ||http://www.orpha.net/ORDO/Orphanet_369955
14975||6266||Anemia due to adenosine triphosphatase deficiency||http://www.orpha.net/ORDO/Orphanet_1044
14976||4624||Lethal hemolytic anemia - genital anomalies||http://www.orpha.net/ORDO/Orphanet_1046
14977||2252||Isolated anencephaly/exencephaly||http://www.orpha.net/ORDO/Orphanet_1048
14978||2252||Intellectual disability-seizures-macrocephaly-obesity syndrome||http://www.orpha.net/ORDO/Orphanet_369950
14979||2252||X-linked intellectual disability due to GRIA3 anomalies||http://www.orpha.net/ORDO/Orphanet_364028
14980||4266||Combined oxidative phosphorylation defect type 17||http://www.orpha.net/ORDO/Orphanet_369913
14981||13689||optic primordium||http://www.ebi.ac.uk/efo/EFO_0003541
14982||10652||obsolete_response to antidepressant||http://www.ebi.ac.uk/efo/EFO_0004675
14983||13689||pectoral fin musculature||http://www.ebi.ac.uk/efo/EFO_0003540
14984||10652||obsolete_response to diruetic||http://www.ebi.ac.uk/efo/EFO_0004676
14985||13689||statoacoustic (VIII) ganglion||http://www.ebi.ac.uk/efo/EFO_0003543
14986||10652||obsolete_response to lapatinib||http://www.ebi.ac.uk/efo/EFO_0004673
14987||13689||prootic||http://www.ebi.ac.uk/efo/EFO_0003542
14988||770||GM09585||http://purl.obolibrary.org/obo/CLO_0011391
14989||15538||data set||http://purl.obolibrary.org/obo/IAO_0000100
14990||770||GM09583||http://purl.obolibrary.org/obo/CLO_0011394
14991||10652||obsolete_response to gemcitabine||http://www.ebi.ac.uk/efo/EFO_0004672
14992||15538||image||http://purl.obolibrary.org/obo/IAO_0000101
14993||14970||beta-amyloid 1-42 measurement||http://www.ebi.ac.uk/efo/EFO_0004670
14994||13689||caudal tuberculum||http://www.ebi.ac.uk/efo/EFO_0003549
14995||13689||epihyal||http://www.ebi.ac.uk/efo/EFO_0003548
14997||13689||valvula cerebelli||http://www.ebi.ac.uk/efo/EFO_0003545
14996||10652||obsolete_response to glucocorticoid||http://www.ebi.ac.uk/efo/EFO_0004679
14998||13689||torus semicircularis||http://www.ebi.ac.uk/efo/EFO_0003544
15000||13689||quadrate||http://www.ebi.ac.uk/efo/EFO_0003547
14999||10652||obsolete_response to anticonvulsant||http://www.ebi.ac.uk/efo/EFO_0004677
15001||13689||vertical myoseptum||http://www.ebi.ac.uk/efo/EFO_0003546
15002||10652||obsolete_response to statin||http://www.ebi.ac.uk/efo/EFO_0004678
15003||11455||Dent disease type 2||http://www.orpha.net/ORDO/Orphanet_93623
15004||11455||Dent disease type 1||http://www.orpha.net/ORDO/Orphanet_93622
15005||1316||Orofaciodigital syndrome type 14||http://www.orpha.net/ORDO/Orphanet_369902
15006||13689||paraventricular organ||http://www.ebi.ac.uk/efo/EFO_0003532
15007||13689||trunk musculature||http://www.ebi.ac.uk/efo/EFO_0003531
15008||9429||processed genotype data file||http://www.ebi.ac.uk/efo/EFO_0004663
15010||15011||binding site identification design||http://www.ebi.ac.uk/efo/EFO_0004664
15009||13689||anguloarticular||http://www.ebi.ac.uk/efo/EFO_0003530
15011||14922||biomolecular annotation design||http://www.ebi.ac.uk/efo/EFO_0004665
15013||11037||Congenital reticular ichthyosiform erythroderma||http://www.orpha.net/ORDO/Orphanet_281190
15012||10652||obsolete_response to flurouracil||http://www.ebi.ac.uk/efo/EFO_0004661
15014||2672||presumptive mesoderm||http://purl.obolibrary.org/obo/UBERON_0006603
15015||10652||obsolete_otolith organ||http://www.ebi.ac.uk/efo/EFO_0003539
15016||13689||posttemporal||http://www.ebi.ac.uk/efo/EFO_0003538
15017||13689||marginal blastomere||http://www.ebi.ac.uk/efo/EFO_0003537
15019||15020||cellular modification design||http://www.ebi.ac.uk/efo/EFO_0004666
15018||10652||obsolete_hyoid muscle||http://www.ebi.ac.uk/efo/EFO_0003536
15020||14922||biological variation design||http://www.ebi.ac.uk/efo/EFO_0004667
15021||13689||periventricular grey zone||http://www.ebi.ac.uk/efo/EFO_0003535
15024||15026||array specific design||http://www.ebi.ac.uk/efo/EFO_0004668
15023||13689||dorsal telencephalon||http://www.ebi.ac.uk/efo/EFO_0003534
15022||2672||presumptive enteric nervous system||http://purl.obolibrary.org/obo/UBERON_0006600
15026||14922||methodological variation design||http://www.ebi.ac.uk/efo/EFO_0004669
15027||13689||caudal tuberal nucleus||http://www.ebi.ac.uk/efo/EFO_0003533
15025||2672||presumptive ectoderm||http://purl.obolibrary.org/obo/UBERON_0006601
15028||8375||Autosomal recessive cutis laxa type 2B||http://www.orpha.net/ORDO/Orphanet_357064
15029||2413||PYCR1-related De Barsy syndrome||http://www.orpha.net/ORDO/Orphanet_293633
15030||1826||Rosa hybrid cultivar||http://purl.obolibrary.org/obo/NCBITaxon_128735
15031||4259||response to TNF antagonist||http://www.ebi.ac.uk/efo/EFO_0004653
15032||13689||torus lateralis||http://www.ebi.ac.uk/efo/EFO_0003521
15033||13689||medial octavolateralis nucleus||http://www.ebi.ac.uk/efo/EFO_0003520
15034||13689||E-YSL||http://www.ebi.ac.uk/efo/EFO_0003523
15035||13689||ventral telencephalon||http://www.ebi.ac.uk/efo/EFO_0003522
15037||10652||obsolete_response to methylphenidate||http://www.ebi.ac.uk/efo/EFO_0004655
15036||10652||obsolete_olfactory region||http://www.ebi.ac.uk/efo/EFO_0003525
15038||13689||cephalic musculature||http://www.ebi.ac.uk/efo/EFO_0003524
15039||13689||pterosphenoid||http://www.ebi.ac.uk/efo/EFO_0003527
15040||10652||obsolete_heart tube||http://www.ebi.ac.uk/efo/EFO_0003526
15041||13689||anterior lateral line nerve||http://www.ebi.ac.uk/efo/EFO_0003529
15042||13689||retroarticular||http://www.ebi.ac.uk/efo/EFO_0003528
15043||13689||subopercle||http://www.ebi.ac.uk/efo/EFO_0003519
15044||2252||Blepharophimosis-intellectual disability syndrome||http://www.orpha.net/ORDO/Orphanet_293642
15045||12461||Genetic polycythemia||http://www.orpha.net/ORDO/Orphanet_250165
15046||15081||Autosomal recessive cutis laxa type 2, classic type||http://www.orpha.net/ORDO/Orphanet_357074
15047||1022||Monodelphis domestica||http://purl.obolibrary.org/obo/NCBITaxon_13616
15048||14970||haptoglobin measurement||http://www.ebi.ac.uk/efo/EFO_0004640
15049||13689||lateral ethmoid||http://www.ebi.ac.uk/efo/EFO_0003510
15050||14970||white matter integrity||http://www.ebi.ac.uk/efo/EFO_0004641
15051||14970||cortisol secretion measurement||http://www.ebi.ac.uk/efo/EFO_0004642
15052||10652||obsolete_coronory artery calcification||http://www.ebi.ac.uk/efo/EFO_0004643
15054||14970||TPE interval measurement||http://www.ebi.ac.uk/efo/EFO_0004644
15053||13689||opercle||http://www.ebi.ac.uk/efo/EFO_0003514
15056||4259||response to vaccine||http://www.ebi.ac.uk/efo/EFO_0004645
15055||10652||obsolete_neuromast||http://www.ebi.ac.uk/efo/EFO_0003513
15057||13689||metapterygoid||http://www.ebi.ac.uk/efo/EFO_0003512
15058||13689||mandibular muscle||http://www.ebi.ac.uk/efo/EFO_0003511
15059||12747||response to platinum based chemotherapy||http://www.ebi.ac.uk/efo/EFO_0004647
15060||13689||hair cell posterior macula||http://www.ebi.ac.uk/efo/EFO_0003518
15061||13689||preopercle||http://www.ebi.ac.uk/efo/EFO_0003517
15062||13689||pectoral fin cartilage||http://www.ebi.ac.uk/efo/EFO_0003516
15063||10652||obsolete_paraxial mesoderm||http://www.ebi.ac.uk/efo/EFO_0003515
15064||843||Infantile epileptic-dyskinetic encephalopathy||http://www.orpha.net/ORDO/Orphanet_364063
15065||13689||granular eminence||http://www.ebi.ac.uk/efo/EFO_0003509
15066||10652||obsolete_dentary||http://www.ebi.ac.uk/efo/EFO_0003508
15067||4706||Amyotrophic lateral sclerosis type 4||http://www.orpha.net/ORDO/Orphanet_357043
15068||13689||branchial muscle||http://www.ebi.ac.uk/efo/EFO_0003504
15069||10652||obsolete_bulbus arteriosus||http://www.ebi.ac.uk/efo/EFO_0003505
15070||13689||posterior lateral line nerve||http://www.ebi.ac.uk/efo/EFO_0003506
15072||9288||motor neuron||http://purl.obolibrary.org/obo/CL_0000100
15071||10652||obsolete_cleithrum||http://www.ebi.ac.uk/efo/EFO_0003507
15074||9288||sensory neuron||http://purl.obolibrary.org/obo/CL_0000101
15073||10652||obsolete_rhombomere 8||http://www.ebi.ac.uk/efo/EFO_0003500
15075||13689||tectal ventricle||http://www.ebi.ac.uk/efo/EFO_0003501
15076||13689||ventral mesenchyme||http://www.ebi.ac.uk/efo/EFO_0003502
15077||13689||basibranchial||http://www.ebi.ac.uk/efo/EFO_0003503
15078||2997||Autosomal dominant Charcot-Marie-Tooth disease type 2Q||http://www.orpha.net/ORDO/Orphanet_329258
15079||15044||Blepharophimosis-intellectual disability syndrome due to UBE3B deficiency||http://www.orpha.net/ORDO/Orphanet_329255
15080||2252||Spondylocostal dysostosis - hypospadias - intellectual disability||http://www.orpha.net/ORDO/Orphanet_329252
15081||7358||Autosomal recessive cutis laxa type 2A||http://www.orpha.net/ORDO/Orphanet_357058
15083||9621||X-linked endothelial corneal dystrophy||http://www.orpha.net/ORDO/Orphanet_293621
15082||9965||Severe early-childhood-onset retinal dystrophy||http://www.orpha.net/ORDO/Orphanet_364055
15084||1022||Rana pirica||http://purl.obolibrary.org/obo/NCBITaxon_79017
15085||14172||somatic nervous system||http://purl.obolibrary.org/obo/CL_0000111
15086||1022||Rana chensinensis||http://purl.obolibrary.org/obo/NCBITaxon_79015
15087||772||endothelial cell||http://purl.obolibrary.org/obo/CL_0000115
15088||772||columnar neuron||http://purl.obolibrary.org/obo/CL_0000112
15089||10876||Severe early-onset obesity-insulin resistance syndrome due to SH2B1 deficiency||http://www.orpha.net/ORDO/Orphanet_329249
15090||3866||Congenital chronic diarrhea with protein-losing enteropathy||http://www.orpha.net/ORDO/Orphanet_329242
15091||10078||Cystinuria type B||http://www.orpha.net/ORDO/Orphanet_93613
15092||11809||Hematological disorder with renal involvement||http://www.orpha.net/ORDO/Orphanet_93614
15093||6310||Hemoglobin H disease||http://www.orpha.net/ORDO/Orphanet_93616
15095||2593||Distal renal tubular acidosis with anemia||http://www.orpha.net/ORDO/Orphanet_93610
15094||4803||Familial retinoblastoma||http://www.orpha.net/ORDO/Orphanet_357027
15097||7675||Beta-propeller protein-associated neurodegeneration||http://www.orpha.net/ORDO/Orphanet_329284
15096||10078||Cystinuria type A||http://www.orpha.net/ORDO/Orphanet_93612
15098||10907||Exfoliative ichthyosis||http://www.orpha.net/ORDO/Orphanet_289586
15099||770||AG09877||http://purl.obolibrary.org/obo/CLO_0021943
15100||772||oligodendrocyte||http://purl.obolibrary.org/obo/CL_0000128
15101||772||astrocyte||http://purl.obolibrary.org/obo/CL_0000127
15102||772||microglial cell||http://purl.obolibrary.org/obo/CL_0000129
15103||772||glial cell||http://purl.obolibrary.org/obo/CL_0000125
15104||3068||gambling behaviour||http://www.ebi.ac.uk/efo/EFO_0004699
15105||12541||Myalgia||http://purl.obolibrary.org/obo/HP_0003326
15106||15195||factor XI measurement||http://www.ebi.ac.uk/efo/EFO_0004694
15107||5502||Mycobacterium bovis BCG str. Pasteur 1173P2||http://purl.obolibrary.org/obo/NCBITaxon_410289
15108||10652||obsolete_fetal hemoglobin measurement||http://www.ebi.ac.uk/efo/EFO_0004693
15109||10652||obsolete_Catecholaminergic polymorphic ventricular tachycardia||http://www.ebi.ac.uk/efo/EFO_0004692
15110||10652||obsolete_Brugada syndrome||http://www.ebi.ac.uk/efo/EFO_0004691
15111||1391||insomnia||http://www.ebi.ac.uk/efo/EFO_0004698
15112||14970||estradiol measurement||http://www.ebi.ac.uk/efo/EFO_0004697
15113||14970||sex hormone globulin binding measurement||http://www.ebi.ac.uk/efo/EFO_0004696
15114||14970||intraocular pressure measurement||http://www.ebi.ac.uk/efo/EFO_0004695
15115||10550||Antenatal Bartter syndrome||http://www.orpha.net/ORDO/Orphanet_93604
15116||10550||Classic Bartter syndrome||http://www.orpha.net/ORDO/Orphanet_93605
15117||6882||Xanthinuria type II||http://www.orpha.net/ORDO/Orphanet_93602
15118||8102||Primary hyperoxaluria type 3||http://www.orpha.net/ORDO/Orphanet_93600
15119||6882||Xanthinuria type I||http://www.orpha.net/ORDO/Orphanet_93601
15120||10652||obsolete_short QT syndrome||http://www.ebi.ac.uk/efo/EFO_0004690
15121||4987||Fatal multiple mitochondrial dysfunction syndrome||http://www.orpha.net/ORDO/Orphanet_289573
15122||6434||Unilateral retinoblastoma||http://www.orpha.net/ORDO/Orphanet_357034
15123||2593||Autosomal dominant distal renal tubular acidosis||http://www.orpha.net/ORDO/Orphanet_93608
15124||4810||Nephrogenic syndrome of inappropriate antidiuresis||http://www.orpha.net/ORDO/Orphanet_93606
15127||3787||Autosomal recessive proximal renal tubular acidosis||http://www.orpha.net/ORDO/Orphanet_93607
15126||772||chondrocyte||http://purl.obolibrary.org/obo/CL_0000138
15125||9621||Congenital hereditary endothelial dystrophy type II||http://www.orpha.net/ORDO/Orphanet_293603
15129||772||fat cell||http://purl.obolibrary.org/obo/CL_0000136
15128||10652||obsolete_Jervell and Lange-Nielsen syndrome||http://www.ebi.ac.uk/efo/EFO_0004689
15130||10652||obsolete_long QT syndrome||http://www.ebi.ac.uk/efo/EFO_0004688
15131||10652||obsolete_response to lithium||http://www.ebi.ac.uk/efo/EFO_0004681
15132||10652||obsolete_response to interferon beta||http://www.ebi.ac.uk/efo/EFO_0004680
15133||15504||wet macular degeneration||http://www.ebi.ac.uk/efo/EFO_0004683
15134||14970||QT interval||http://www.ebi.ac.uk/efo/EFO_0004682
15135||8700||hip geometry||http://www.ebi.ac.uk/efo/EFO_0004685
15136||14970||tumor necrosis factor-alpha measurement||http://www.ebi.ac.uk/efo/EFO_0004684
15137||10652||obsolete_inherited arrhythmia||http://www.ebi.ac.uk/efo/EFO_0004687
15138||1016||non-compaction cardiomyopathy||http://www.ebi.ac.uk/efo/EFO_0004686
15139||2672||blood||http://purl.obolibrary.org/obo/UBERON_0000178
15140||2672||excreta||http://purl.obolibrary.org/obo/UBERON_0000174
15141||5502||Geobacillus sp. E263||http://purl.obolibrary.org/obo/NCBITaxon_391290
15142||1022||Austrofundulus limnaeus||http://purl.obolibrary.org/obo/NCBITaxon_52670
15143||772||melanocyte||http://purl.obolibrary.org/obo/CL_0000148
15144||5502||Bordetella sp.||http://purl.obolibrary.org/obo/NCBITaxon_28081
15145||1022||Rhizoctonia solani||http://purl.obolibrary.org/obo/NCBITaxon_456999
15146||1022||Bubalus bubalis||http://purl.obolibrary.org/obo/NCBITaxon_89462
15147||1022||Locusta migratoria||http://purl.obolibrary.org/obo/NCBITaxon_7004
15148||772||secretory cell||http://purl.obolibrary.org/obo/CL_0000151
15149||770||AG09699||http://purl.obolibrary.org/obo/CLO_0021913
15150||15148||parietal cell||http://purl.obolibrary.org/obo/CL_0000162
15151||2672||theca cell layer||http://purl.obolibrary.org/obo/UBERON_0000155
15152||3134||pelvic fin||http://purl.obolibrary.org/obo/UBERON_0000152
15153||7464||ribonucleoside monophosphate metabolic process||http://purl.obolibrary.org/obo/GO_0009161
15154||3454||nucleoside biosynthetic process||http://purl.obolibrary.org/obo/GO_0009163
15155||14719||beta cell||http://purl.obolibrary.org/obo/CL_0000168
15156||5502||Staphylococcus aureus subsp. aureus N315||http://purl.obolibrary.org/obo/NCBITaxon_158879
15158||772||neuroendocrine cell||http://purl.obolibrary.org/obo/CL_0000165
15157||5502||Staphylococcus aureus subsp. aureus Mu50||http://purl.obolibrary.org/obo/NCBITaxon_158878
15159||1015||Thrombophlebitis||http://purl.obolibrary.org/obo/HP_0004418
15160||15159||Recurrent thrombophlebitis||http://purl.obolibrary.org/obo/HP_0004419
15161||1022||Solenopsis invicta||http://purl.obolibrary.org/obo/NCBITaxon_13686
15162||5502||Sphingomonas paucimobilis||http://purl.obolibrary.org/obo/NCBITaxon_13689
15163||7466||ribonucleoside monophosphate biosynthetic process||http://purl.obolibrary.org/obo/GO_0009156
15165||772||alpha cell||http://purl.obolibrary.org/obo/CL_0000171
15164||10652||obsolete_middle lateral line neuromast||http://www.ebi.ac.uk/efo/EFO_0003592
15167||13999||Congenital intestinal disease due to an enzymatic defect||http://www.orpha.net/ORDO/Orphanet_104006
15166||13689||neural crest midbrain||http://www.ebi.ac.uk/efo/EFO_0003591
15170||13999||Congenital intestinal transport defect||http://www.orpha.net/ORDO/Orphanet_104003
15168||2672||mouth||http://purl.obolibrary.org/obo/UBERON_0000165
15169||10652||obsolete_pectoral fin skeleton||http://www.ebi.ac.uk/efo/EFO_0003594
15171||13999||Intestinal disease due to vitamin absorption anomaly||http://www.orpha.net/ORDO/Orphanet_104004
15172||13689||posterior lateral line neuromast||http://www.ebi.ac.uk/efo/EFO_0003593
15174||13999||Congenital intestinal motility disorder||http://www.orpha.net/ORDO/Orphanet_104009
15173||5502||Bacillus weihenstephanensis||http://purl.obolibrary.org/obo/NCBITaxon_86662
15175||10652||obsolete_rhombomere 3||http://www.ebi.ac.uk/efo/EFO_0003596
15176||10652||obsolete_posterior lateral line||http://www.ebi.ac.uk/efo/EFO_0003595
15177||13999||Congenital enteropathy involving intestinal mucosa development||http://www.orpha.net/ORDO/Orphanet_104007
15178||13689||slow muscle cell somite 1||http://www.ebi.ac.uk/efo/EFO_0003598
15179||10652||obsolete_rhombomere 7||http://www.ebi.ac.uk/efo/EFO_0003597
15181||13689||slow muscle cell somite 4||http://www.ebi.ac.uk/efo/EFO_0003599
15180||772||Leydig cell||http://purl.obolibrary.org/obo/CL_0000178
15183||2672||intestine||http://purl.obolibrary.org/obo/UBERON_0000160
15182||5502||Ralstonia syzygii||http://purl.obolibrary.org/obo/NCBITaxon_28097
15184||1415||Autosomal recessive limb-girdle muscular dystrophy type 2Q||http://www.orpha.net/ORDO/Orphanet_254361
15185||4706||Genetic neurodegenerative disease with dementia||http://www.orpha.net/ORDO/Orphanet_276058
15186||1022||Schistocerca gregaria||http://purl.obolibrary.org/obo/NCBITaxon_7010
15187||7459||purine ribonucleoside monophosphate biosynthetic process||http://purl.obolibrary.org/obo/GO_0009168
15188||7463||purine ribonucleoside monophosphate metabolic process||http://purl.obolibrary.org/obo/GO_0009167
15190||2482||nucleotide biosynthetic process||http://purl.obolibrary.org/obo/GO_0009165
15189||5502||Streptococcus suis 05ZYH33||http://purl.obolibrary.org/obo/NCBITaxon_391295
15191||772||muscle cell||http://purl.obolibrary.org/obo/CL_0000187
15192||15195||protein S measurement||http://www.ebi.ac.uk/efo/EFO_0004637
15193||14970||phospholipid measurement||http://www.ebi.ac.uk/efo/EFO_0004639
15194||5502||Collimonas fungivorans||http://purl.obolibrary.org/obo/NCBITaxon_158899
15195||14970||coagulation factor measurement||http://www.ebi.ac.uk/efo/EFO_0004634
15196||15195||protein C measurement||http://www.ebi.ac.uk/efo/EFO_0004633
15197||13689||floor plate rhombomere 4||http://www.ebi.ac.uk/efo/EFO_0003588
15199||14970||leptin receptor measurement||http://www.ebi.ac.uk/efo/EFO_0004635
15198||13689||floor plate rhombomere 7||http://www.ebi.ac.uk/efo/EFO_0003589
15200||15195||factor VIII measurement||http://www.ebi.ac.uk/efo/EFO_0004630
15201||13689||floor plate rhombomere 3||http://www.ebi.ac.uk/efo/EFO_0003586
15202||13689||floor plate rhombomere 6||http://www.ebi.ac.uk/efo/EFO_0003587
15204||14970||nevus count||http://www.ebi.ac.uk/efo/EFO_0004632
15203||13689||floor plate rhombomere 1||http://www.ebi.ac.uk/efo/EFO_0003584
15206||14970||vitamin D measurement||http://www.ebi.ac.uk/efo/EFO_0004631
15205||13689||floor plate neural rod||http://www.ebi.ac.uk/efo/EFO_0003585
15207||13689||somite 12||http://www.ebi.ac.uk/efo/EFO_0003582
15208||13689||somite 4||http://www.ebi.ac.uk/efo/EFO_0003583
15209||10652||obsolete_rhombomere 5||http://www.ebi.ac.uk/efo/EFO_0003580
15211||13689||slow muscle cell somite 14||http://www.ebi.ac.uk/efo/EFO_0003581
15210||2672||midbrain tectum||http://purl.obolibrary.org/obo/UBERON_0002314
15212||772||hepatocyte||http://purl.obolibrary.org/obo/CL_0000182
15213||10652||obsolete_lateral mesenchyme derived from mesoderm||http://www.ebi.ac.uk/efo/EFO_0003590
15214||15185||Genetic frontotemporal degeneration with dementia||http://www.orpha.net/ORDO/Orphanet_276061
15215||4052||Bile acid CoA ligase deficiency and defective amidation||http://www.orpha.net/ORDO/Orphanet_276066
15216||15195||von Willebrand factor measurement||http://www.ebi.ac.uk/efo/EFO_0004629
15217||14970||insulin like growth factor measurement||http://www.ebi.ac.uk/efo/EFO_0004628
15218||14970||IGF-1 measurement||http://www.ebi.ac.uk/efo/EFO_0004627
15220||14970||IGFBP-3 measurement||http://www.ebi.ac.uk/efo/EFO_0004626
15219||1022||Acyrthosiphon pisum||http://purl.obolibrary.org/obo/NCBITaxon_7029
15222||14970||progranulin measurement||http://www.ebi.ac.uk/efo/EFO_0004625
15221||13689||nucleus of the medial longitudinal fasciculus medulla oblongata||http://www.ebi.ac.uk/efo/EFO_0003577
15223||14970||prostate specific antigen measurement||http://www.ebi.ac.uk/efo/EFO_0004624
15224||13689||primary neuron hindbrain||http://www.ebi.ac.uk/efo/EFO_0003578
15225||15195||fibrinogen measurement||http://www.ebi.ac.uk/efo/EFO_0004623
15226||10652||obsolete_rhombomere 2||http://www.ebi.ac.uk/efo/EFO_0003579
15227||14970||sphingolipid measurement||http://www.ebi.ac.uk/efo/EFO_0004622
15229||13712||vitamin B6 measurement||http://www.ebi.ac.uk/efo/EFO_0004621
15228||13689||neural crest diencephalon||http://www.ebi.ac.uk/efo/EFO_0003573
15230||13712||vitamin B12 measurement||http://www.ebi.ac.uk/efo/EFO_0004620
15232||13689||neural crest telencephalon||http://www.ebi.ac.uk/efo/EFO_0003574
15231||5502||Lactobacillus curvatus||http://purl.obolibrary.org/obo/NCBITaxon_28038
15234||13689||infraorbital lateral line neuromast||http://www.ebi.ac.uk/efo/EFO_0003575
15233||5502||Streptococcus mitis||http://purl.obolibrary.org/obo/NCBITaxon_28037
15235||13689||opercular lateral line neuromast||http://www.ebi.ac.uk/efo/EFO_0003576
15238||15191||smooth muscle cell||http://purl.obolibrary.org/obo/CL_0000192
15236||770||ND03432||http://purl.obolibrary.org/obo/CLO_0012496
15237||5502||Staphylococcus lugdunensis||http://purl.obolibrary.org/obo/NCBITaxon_28035
15239||13689||floor plate rhombomere 8||http://www.ebi.ac.uk/efo/EFO_0003570
15240||13689||spinal cord interneuron||http://www.ebi.ac.uk/efo/EFO_0003571
15241||10652||obsolete_mesenchyme derived from head neural crest||http://www.ebi.ac.uk/efo/EFO_0003572
15242||8190||4-phenylbutyric acid||http://purl.obolibrary.org/obo/CHEBI_41500
15243||1022||Bemisia tabaci||http://purl.obolibrary.org/obo/NCBITaxon_7038
15244||14970||high density lipoprotein cholesterol measurement||http://www.ebi.ac.uk/efo/EFO_0004612
15245||13689||floor plate rhombomere 2||http://www.ebi.ac.uk/efo/EFO_0003568
15246||14970||low density lipoprotein cholesterol measurement||http://www.ebi.ac.uk/efo/EFO_0004611
15247||13689||floor plate rhombomere 5||http://www.ebi.ac.uk/efo/EFO_0003569
15248||14970||apolipoprotein A 1 measurement||http://www.ebi.ac.uk/efo/EFO_0004614
15249||13689||somite 3||http://www.ebi.ac.uk/efo/EFO_0003566
15251||13689||basal plate midbrain region||http://www.ebi.ac.uk/efo/EFO_0003567
15250||10652||obsolete_triglyceride measurement||http://www.ebi.ac.uk/efo/EFO_0004613
15252||14655||osteoarthritis of the knee||http://www.ebi.ac.uk/efo/EFO_0004616
15253||14970||apolipoprotein B measurement||http://www.ebi.ac.uk/efo/EFO_0004615
15254||14970||vitamin K measurement||http://www.ebi.ac.uk/efo/EFO_0004618
15255||14970||cystatin C measurement||http://www.ebi.ac.uk/efo/EFO_0004617
15256||13689||symplectic||http://www.ebi.ac.uk/efo/EFO_0003560
15258||13689||tangential nucleus||http://www.ebi.ac.uk/efo/EFO_0003561
15257||4786||Genetic obesity||http://www.orpha.net/ORDO/Orphanet_77828
15259||13689||somite 14||http://www.ebi.ac.uk/efo/EFO_0003564
15260||13689||somite 2||http://www.ebi.ac.uk/efo/EFO_0003565
15262||13689||telencephalic ventricle||http://www.ebi.ac.uk/efo/EFO_0003562
15261||1391||acute lung injury||http://www.ebi.ac.uk/efo/EFO_0004610
15263||13689||I-YSL||http://www.ebi.ac.uk/efo/EFO_0003563
15264||7512||ribonucleoside triphosphate metabolic process||http://purl.obolibrary.org/obo/GO_0009199
15265||15195||factor VII measurement||http://www.ebi.ac.uk/efo/EFO_0004619
15266||1022||Polysphondylium pallidum||http://purl.obolibrary.org/obo/NCBITaxon_13642
15268||14989||metatranscriptomic data||http://www.ebi.ac.uk/efo/EFO_0004603
15267||13689||horizontal myoseptum||http://www.ebi.ac.uk/efo/EFO_0003555
15269||14989||metagenomic data||http://www.ebi.ac.uk/efo/EFO_0004602
15270||13689||hyomandibula||http://www.ebi.ac.uk/efo/EFO_0003556
15271||14989||transcriptomic data||http://www.ebi.ac.uk/efo/EFO_0004601
15273||13689||interopercle||http://www.ebi.ac.uk/efo/EFO_0003557
15272||10994||gemfibrozil||http://purl.obolibrary.org/obo/CHEBI_5296
15275||14989||genomic data||http://www.ebi.ac.uk/efo/EFO_0004600
15274||10652||obsolete_segmental intercostal artery||http://www.ebi.ac.uk/efo/EFO_0003558
15279||13689||hair cell anterior macula||http://www.ebi.ac.uk/efo/EFO_0003559
15277||1979||chronic bronchitis||http://purl.obolibrary.org/obo/HP_0004469
15278||1022||Pantherophis obsoletus||http://purl.obolibrary.org/obo/NCBITaxon_39099
15276||1391||duodenal ulcer||http://www.ebi.ac.uk/efo/EFO_0004607
15280||2162||gallbladder neoplasm||http://www.ebi.ac.uk/efo/EFO_0004606
15281||14989||viral RNA data||http://www.ebi.ac.uk/efo/EFO_0004605
15282||14989||synthetic DNA data||http://www.ebi.ac.uk/efo/EFO_0004604
15283||10994||labetalol||http://purl.obolibrary.org/obo/CHEBI_6343
15284||13689||descending octaval nucleus||http://www.ebi.ac.uk/efo/EFO_0003550
15285||10652||obsolete_dorsal fin musculature||http://www.ebi.ac.uk/efo/EFO_0003551
15286||13689||ectopterygoid||http://www.ebi.ac.uk/efo/EFO_0003552
15287||13689||entopterygoid||http://www.ebi.ac.uk/efo/EFO_0003553
15288||10652||obsolete_gill filament||http://www.ebi.ac.uk/efo/EFO_0003554
15289||1732||Rare genetic odontologic disease||http://www.orpha.net/ORDO/Orphanet_77830
15290||13999||Primary short bowel syndrome||http://www.orpha.net/ORDO/Orphanet_365563
15291||1391||cystic fibrosis associated meconium ileum||http://www.ebi.ac.uk/efo/EFO_0004608
15292||2004||treatment refractory schizophrenia||http://www.ebi.ac.uk/efo/EFO_0004609
15293||10118||CD56-positive, CD161-positive immature natural killer cell||http://purl.obolibrary.org/obo/CL_0002338
15294||4609||dehydroepiandrosterone sulfate||http://purl.obolibrary.org/obo/CHEBI_16814
15295||15608||LP.03 three leaves visible stage||http://purl.obolibrary.org/obo/PO_0007106
15296||8190||1-naphthylacetic acid||http://purl.obolibrary.org/obo/CHEBI_32918
15297||1319||methionine||http://purl.obolibrary.org/obo/CHEBI_16811
15298||770||osteosarcoma cell line||http://purl.obolibrary.org/obo/BTO_0000407
15300||11433||prostate gland||http://purl.obolibrary.org/obo/UBERON_0002367
15299||4194||Mammary-digital-nail syndrome||http://www.orpha.net/ORDO/Orphanet_238744
15302||15306||rosette growth stage||http://purl.obolibrary.org/obo/PO_0007113
15301||2672||meninx||http://purl.obolibrary.org/obo/UBERON_0002360
15303||15608||LP.11 eleven leaves visible stage||http://purl.obolibrary.org/obo/PO_0007116
15304||15608||LP.04 four leaves visible stage||http://purl.obolibrary.org/obo/PO_0007115
15305||772||preadipocyte||http://purl.obolibrary.org/obo/CL_0002334
15306||9746||1 main shoot growth stage||http://purl.obolibrary.org/obo/PO_0007112
15307||14614||mammary epithelial cell||http://purl.obolibrary.org/obo/CL_0002327
15308||15608||LP.16 sixteen leaves visible stage||http://purl.obolibrary.org/obo/PO_0007119
15309||4629||Hereditary arterial and articular multiple calcification syndrome||http://www.orpha.net/ORDO/Orphanet_289601
15310||10994||ciglitazone||http://purl.obolibrary.org/obo/CHEBI_64227
15311||10994||gibberellin A4||http://purl.obolibrary.org/obo/CHEBI_32902
15312||2672||myocardium||http://purl.obolibrary.org/obo/UBERON_0002349
15313||2672||peritoneum||http://purl.obolibrary.org/obo/UBERON_0002358
15314||2672||axilla||http://purl.obolibrary.org/obo/UBERON_0009472
15317||2672||perineum||http://purl.obolibrary.org/obo/UBERON_0002356
15315||1414||Autosomal dominant limb-girdle muscular dystrophy type 1H||http://www.orpha.net/ORDO/Orphanet_238755
15316||9753||megacolon||http://purl.obolibrary.org/obo/HP_0002251
15318||3980||Saccharomyces cerevisiae S288c||http://purl.obolibrary.org/obo/NCBITaxon_559292
15319||2672||pelvis||http://purl.obolibrary.org/obo/UBERON_0002355
15320||2672||atrioventricular node||http://purl.obolibrary.org/obo/UBERON_0002352
15321||1022||Chlorocebus sabaeus||http://purl.obolibrary.org/obo/NCBITaxon_60711
15322||14537||embryonic stem cell||http://purl.obolibrary.org/obo/CL_0002322
15323||772||embryonic cell||http://purl.obolibrary.org/obo/CL_0002321
15324||15608||LP.06 six leaves visible stage||http://purl.obolibrary.org/obo/PO_0007123
15325||6079||4q21 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_238750
15326||15608||LP.19 nineteen leaves visible stage||http://purl.obolibrary.org/obo/PO_0007120
15327||7502||purine ribonucleoside triphosphate biosynthetic process||http://purl.obolibrary.org/obo/GO_0009206
15328||7503||purine ribonucleoside triphosphate metabolic process||http://purl.obolibrary.org/obo/GO_0009205
15329||770||GM13811||http://purl.obolibrary.org/obo/CLO_0033628
15330||7511||ribonucleoside triphosphate biosynthetic process||http://purl.obolibrary.org/obo/GO_0009201
15331||772||progenitor cell of endocrine pancreas||http://purl.obolibrary.org/obo/CL_0002351
15332||2672||descending thoracic aorta||http://purl.obolibrary.org/obo/UBERON_0002345
15333||4732||Familial congenital mirror movements||http://www.orpha.net/ORDO/Orphanet_238722
15334||9343||fetal derived definitive erythrocyte||http://purl.obolibrary.org/obo/CL_0002357
15335||13362||primitive reticulocyte||http://purl.obolibrary.org/obo/CL_0002356
15336||15339||placental hematopoietic stem cell||http://purl.obolibrary.org/obo/CL_0002359
15337||13362||pyrenocyte||http://purl.obolibrary.org/obo/CL_0002358
15338||772||fetal liver hematopoietic progenitor cell||http://purl.obolibrary.org/obo/CL_0002353
15339||14543||gestational hematopoietic stem cell||http://purl.obolibrary.org/obo/CL_0002352
15340||13362||primitive red blood cell||http://purl.obolibrary.org/obo/CL_0002355
15341||15339||yolk sac hematopoietic stem cell||http://purl.obolibrary.org/obo/CL_0002354
15342||13342||CD27-high, CD11b-low natural killer cell||http://purl.obolibrary.org/obo/CL_0002349
15343||1319||S-adenosyl-L-methionine||http://purl.obolibrary.org/obo/CHEBI_15414
15344||3072||pulmonary trunk||http://purl.obolibrary.org/obo/UBERON_0002333
15345||2672||umbilical cord||http://purl.obolibrary.org/obo/UBERON_0002331
15346||2672||corpus callosum||http://purl.obolibrary.org/obo/UBERON_0002336
15349||15608||LP.09 nine leaves visible||http://purl.obolibrary.org/obo/PO_0007101
15347||13342||CD27-low, CD11b-high natural killer cell||http://purl.obolibrary.org/obo/CL_0002348
15348||2391||Unclassified intestinal pseudoobstruction||http://www.orpha.net/ORDO/Orphanet_104078
15350||13342||CD27-high, CD11b-high natural killer cell||http://purl.obolibrary.org/obo/CL_0002347
15351||10118||Dx5-negative, NK1.1-positive immature natural killer cell||http://purl.obolibrary.org/obo/CL_0002346
15353||2391||Myopathic intestinal pseudoobstruction||http://www.orpha.net/ORDO/Orphanet_104077
15352||10118||CD27-low, CD11b-low immature natural killer cell||http://purl.obolibrary.org/obo/CL_0002345
15354||4260||gastrointestinal hemorrhage||http://purl.obolibrary.org/obo/HP_0002239
15355||10118||CD56-negative, CD161-positive immature natural killer cell||http://purl.obolibrary.org/obo/CL_0002344
15356||15608||LP.15 fifteen leaves visible stage||http://purl.obolibrary.org/obo/PO_0007104
15357||10110||decidual natural killer cell||http://purl.obolibrary.org/obo/CL_0002343
15360||15608||LP.10 ten leaves visible stage||http://purl.obolibrary.org/obo/PO_0007103
15358||15087||circulating endothelial cell||http://purl.obolibrary.org/obo/CL_0002342
15359||772||prostate gland cancer cell||http://purl.obolibrary.org/obo/BTO_0001130
15361||6897||Isolated congenital megalocornea||http://www.orpha.net/ORDO/Orphanet_91489
15362||10994||glutathione||http://purl.obolibrary.org/obo/CHEBI_16856
15363||1732||Rare genetic tumor||http://www.orpha.net/ORDO/Orphanet_68336
15364||1732||Chromosomal anomaly||http://www.orpha.net/ORDO/Orphanet_68335
15365||5126||Rare hemorrhagic disorder due to a constitutional coagulation factors defect||http://www.orpha.net/ORDO/Orphanet_68334
15366||770||AG11513||http://purl.obolibrary.org/obo/CLO_0022604
15367||10994||6-propyl-2-thiouracil||http://purl.obolibrary.org/obo/CHEBI_8502
15368||8628||signaling receptor activity||http://purl.obolibrary.org/obo/GO_0038023
15369||13390||immature Vgamma2-positive fetal thymocyte||http://purl.obolibrary.org/obo/CL_0002378
15370||10652||obsolete_pulmonary artery||http://www.ebi.ac.uk/efo/EFO_0001399
15371||10652||obsolete_axilla||http://www.ebi.ac.uk/efo/EFO_0001395
15372||10652||obsolete_femur||http://www.ebi.ac.uk/efo/EFO_0001396
15373||3432||inguinal region||http://www.ebi.ac.uk/efo/EFO_0001397
15374||10652||obsolete_humerus||http://www.ebi.ac.uk/efo/EFO_0001398
15376||9665||Rieger anomaly||http://www.orpha.net/ORDO/Orphanet_91483
15375||10652||obsolete_somatosensory cortex||http://www.ebi.ac.uk/efo/EFO_0001391
15378||772||somatic cell||http://purl.obolibrary.org/obo/CL_0002371
15377||10652||obsolete_subthalamic nucleus||http://www.ebi.ac.uk/efo/EFO_0001392
15379||2672||synovial membrane||http://www.ebi.ac.uk/efo/EFO_0001393
15380||10652||obsolete_pons||http://www.ebi.ac.uk/efo/EFO_0001394
15381||9697||Familial congenital palsy of trochlear nerve||http://www.orpha.net/ORDO/Orphanet_91498
15382||4646||ribonucleotide metabolic process||http://purl.obolibrary.org/obo/GO_0009259
15383||1732||Rare genetic skin disease||http://www.orpha.net/ORDO/Orphanet_68346
15384||10994||formaldehyde||http://purl.obolibrary.org/obo/CHEBI_16842
15385||772||medullary thymic epithelial cell||http://purl.obolibrary.org/obo/CL_0002365
15386||2672||bile duct||http://purl.obolibrary.org/obo/UBERON_0002394
15387||2151||nucleus accumbens shell||http://www.ebi.ac.uk/efo/EFO_0002459
15388||772||keratocyte||http://purl.obolibrary.org/obo/CL_0002363
15391||13999||Metabolic disease with intestinal involvement||http://www.orpha.net/ORDO/Orphanet_104013
15390||2672||lymph||http://purl.obolibrary.org/obo/UBERON_0002391
15389||1819||hippocampus CA3||http://www.ebi.ac.uk/efo/EFO_0002456
15392||1819||hippocampus CA2||http://www.ebi.ac.uk/efo/EFO_0002455
15393||2151||nucleus accumbens core||http://www.ebi.ac.uk/efo/EFO_0002458
15395||14614||respiratory epithelial cell||http://purl.obolibrary.org/obo/CL_0002368
15394||1819||hippocampus CA4||http://www.ebi.ac.uk/efo/EFO_0002457
15396||5958||Non-syndromic congenital cataract||http://www.orpha.net/ORDO/Orphanet_91492
15398||15087||HUVEC cell||http://www.ebi.ac.uk/efo/EFO_0002451
15397||6897||Congenital ectropion uveae||http://www.orpha.net/ORDO/Orphanet_91491
15399||1819||hippocampus CA1||http://www.ebi.ac.uk/efo/EFO_0002454
15400||6897||Isolated congenital sclerocornea||http://www.orpha.net/ORDO/Orphanet_91490
15401||13362||primitive erythroid progenitor||http://purl.obolibrary.org/obo/CL_0002361
15402||9719||Snowflake vitreoretinal degeneration||http://www.orpha.net/ORDO/Orphanet_91496
15403||9654||Persistent hyperplastic primary vitreous||http://www.orpha.net/ORDO/Orphanet_91495
15404||5300||Macular coloboma - cleft palate - hallux valgus||http://www.orpha.net/ORDO/Orphanet_91494
15405||15339||AGM hematopoietic stem cell||http://purl.obolibrary.org/obo/CL_0002360
15406||6051||ribonucleotide biosynthetic process||http://purl.obolibrary.org/obo/GO_0009260
15407||10765||Homozygous 2p21 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_369886
15408||10994||metergoline||http://purl.obolibrary.org/obo/CHEBI_64216
15409||10994||2,3-dimethoxynaphthalene-1,4-dione||http://purl.obolibrary.org/obo/CHEBI_64215
15410||15407||2p21 microdeletion syndrome without cystinuria||http://www.orpha.net/ORDO/Orphanet_369881
15411||1682||neoplasm of immature B and T cells||http://www.ebi.ac.uk/efo/EFO_0002425
15412||7629||Glaucoma secondary to spherophakia/ectopia lentis and megalocornea||http://www.orpha.net/ORDO/Orphanet_238763
15413||15417||fibroma||http://www.ebi.ac.uk/efo/EFO_0002424
15414||96||multiple myeloma||http://www.ebi.ac.uk/efo/EFO_0001378
15415||15417||osteoma||http://www.ebi.ac.uk/efo/EFO_0002423
15416||1391||endocrine system disease||http://www.ebi.ac.uk/efo/EFO_0001379
15417||2162||benign neoplasm||http://www.ebi.ac.uk/efo/EFO_0002422
15418||10994||naproxen||http://purl.obolibrary.org/obo/CHEBI_7476
15420||5805||polycythemia vera||http://www.ebi.ac.uk/efo/EFO_0002429
15419||10167||CD14-low, CD16-positive monocyte||http://purl.obolibrary.org/obo/CL_0002396
15423||15429||CD14-positive, CD16-positive monocyte||http://purl.obolibrary.org/obo/CL_0002397
15422||15424||chronic myeloproliferative disorder||http://www.ebi.ac.uk/efo/EFO_0002428
15421||11680||pectoralis major||http://purl.obolibrary.org/obo/UBERON_0002381
15425||15429||Gr1-positive, CD43-positive monocyte||http://purl.obolibrary.org/obo/CL_0002398
15424||1682||myeloid neoplasm||http://www.ebi.ac.uk/efo/EFO_0002427
15426||1682||neoplasm of mature T-cells or NK-cells||http://www.ebi.ac.uk/efo/EFO_0002426
15427||8236||CD1c-positive myeloid dendritic cell||http://purl.obolibrary.org/obo/CL_0002399
15428||10994||cantharidin||http://purl.obolibrary.org/obo/CHEBI_64213
15429||9247||intermediate monocyte||http://purl.obolibrary.org/obo/CL_0002393
15430||10652||obsolete_intervertebral disc||http://www.ebi.ac.uk/efo/EFO_0001370
15431||10994||8-bromo-3 ,5 -cyclic AMP||http://purl.obolibrary.org/obo/CHEBI_64211
15434||5849||1q44 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_238769
15432||8236||CD141-positive myeloid dendritic cell||http://purl.obolibrary.org/obo/CL_0002394
15433||10652||obsolete_vertebra||http://www.ebi.ac.uk/efo/EFO_0001371
15437||15490||neonate||http://www.ebi.ac.uk/efo/EFO_0001372
15435||10994||sulindac sulfone||http://purl.obolibrary.org/obo/CHEBI_64212
15436||10176||Gr1-high classical monocyte||http://purl.obolibrary.org/obo/CL_0002395
15438||10652||obsolete_precentral gyrus||http://www.ebi.ac.uk/efo/EFO_0001373
15440||10994||4- {[(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalen-2-yl)carbonyl]amino }benzoic acid||http://purl.obolibrary.org/obo/CHEBI_64210
15439||2252||Ptosis - syndactyly - learning difficulties||http://www.orpha.net/ORDO/Orphanet_238766
15441||2002||synovial sarcoma||http://www.ebi.ac.uk/efo/EFO_0001376
15442||618||gastrula stage||http://purl.obolibrary.org/obo/UBERON_0000109
15443||10994||(2Z,3Z)-bis {amino[(2-aminophenyl)sulfanyl]methylidene }butanedinitrile||http://purl.obolibrary.org/obo/CHEBI_64208
15444||8775||Mitochondrial DNA depletion syndrome, encephalomyopathic form with variable craniofacial anomalies||http://www.orpha.net/ORDO/Orphanet_369897
15445||10652||obsolete_corpus callosum||http://www.ebi.ac.uk/efo/EFO_0001390
15446||5502||Enterococcus faecalis OG1RF||http://purl.obolibrary.org/obo/NCBITaxon_474186
15447||10994||spiramide||http://purl.obolibrary.org/obo/CHEBI_64207
15448||618||cleavage stage||http://purl.obolibrary.org/obo/UBERON_0000107
15449||2672||blastula stage||http://purl.obolibrary.org/obo/UBERON_0000108
15450||8190||bromochloroacetic acid||http://purl.obolibrary.org/obo/CHEBI_64206
15451||762||Early infantile epileptic encephalopathy without suppression burst||http://www.orpha.net/ORDO/Orphanet_369894
15452||2252||Cardiac anomalies-developmental delay-facial dysmorphism syndrome||http://www.orpha.net/ORDO/Orphanet_369891
15453||772||cumulus-oocyte complex||http://www.ebi.ac.uk/efo/EFO_0002433
15454||10652||obsolete_laryngopharynx||http://www.ebi.ac.uk/efo/EFO_0001388
15455||10652||obsolete_lacrimal gland||http://www.ebi.ac.uk/efo/EFO_0001389
15456||15457||palatine tonsil||http://purl.obolibrary.org/obo/UBERON_0002373
15457||2672||tonsil||http://purl.obolibrary.org/obo/UBERON_0002372
15458||2672||bone marrow||http://purl.obolibrary.org/obo/UBERON_0002371
15460||11433||thymus||http://purl.obolibrary.org/obo/UBERON_0002370
15461||10994||nandrolone||http://purl.obolibrary.org/obo/CHEBI_7466
15459||772||mesophyll cell||http://www.ebi.ac.uk/efo/EFO_0002439
15462||5295||puberty||http://www.ebi.ac.uk/efo/EFO_0001382
15464||2672||muscle of head||http://purl.obolibrary.org/obo/UBERON_0002376
15463||618||juvenile stage||http://purl.obolibrary.org/obo/UBERON_0000112
15465||10652||obsolete_postcentral gyrus||http://www.ebi.ac.uk/efo/EFO_0001383
15466||15416||hypopituitarism||http://www.ebi.ac.uk/efo/EFO_0001380
15467||6733||methiothepin maleate||http://purl.obolibrary.org/obo/CHEBI_64202
15469||10652||obsolete_Peyer s patch||http://www.ebi.ac.uk/efo/EFO_0001381
15468||10926||metacarpal bone||http://purl.obolibrary.org/obo/UBERON_0002374
15470||15422||primary myelofibrosis||http://www.ebi.ac.uk/efo/EFO_0002430
15471||10652||obsolete_uvula||http://www.ebi.ac.uk/efo/EFO_0001386
15472||10652||obsolete_submandibular gland||http://www.ebi.ac.uk/efo/EFO_0001387
15473||12798||platelet activation||http://purl.obolibrary.org/obo/GO_0030168
15474||10652||obsolete_prefrontal cortex||http://www.ebi.ac.uk/efo/EFO_0001384
15475||1002||tumour of cranial and spinal nerves||http://www.ebi.ac.uk/efo/EFO_0002431
15476||10652||obsolete_tibialis anterior muscle||http://www.ebi.ac.uk/efo/EFO_0001385
15477||3349||SALK_037727||http://www.ebi.ac.uk/efo/EFO_0001354
15478||14235||Lewis||http://www.ebi.ac.uk/efo/EFO_0001353
15479||14235||Sprague Dawley||http://www.ebi.ac.uk/efo/EFO_0001352
15480||14235||WKY||http://www.ebi.ac.uk/efo/EFO_0001351
15481||14235||Dahl salt-sensitive||http://www.ebi.ac.uk/efo/EFO_0001350
15482||1687||Inverse Klippel-Tr naunay syndrome||http://www.orpha.net/ORDO/Orphanet_329324
15483||5287||Mitochondrial disease||http://www.orpha.net/ORDO/Orphanet_68380
15484||10994||wortmannin||http://purl.obolibrary.org/obo/CHEBI_52289
15486||1902||Autosomal recessive frontotemporal pachygyria||http://www.orpha.net/ORDO/Orphanet_329329
15485||1398||type I diabetes mellitus||http://www.ebi.ac.uk/efo/EFO_0001359
15487||2102||post-traumatic stress disorder||http://www.ebi.ac.uk/efo/EFO_0001358
15488||3||sporadic amyotrophic lateral sclerosis||http://www.ebi.ac.uk/efo/EFO_0001357
15489||3||familial amyotrophic lateral sclerosis||http://www.ebi.ac.uk/efo/EFO_0001356
15490||618||infant||http://www.ebi.ac.uk/efo/EFO_0001355
15491||7248||Congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome||http://www.orpha.net/ORDO/Orphanet_369861
15492||10994||D-mannitol||http://purl.obolibrary.org/obo/CHEBI_16899
15493||2672||lower epidermis||http://purl.obolibrary.org/obo/BTO_0000488
15494||15571||Peroxisomal disease||http://www.orpha.net/ORDO/Orphanet_68373
15495||5488||Autosomal recessive intermediate Charcot-Marie-Tooth disease type C||http://www.orpha.net/ORDO/Orphanet_369867
15496||15044||Blepharophimosis-intellectual disability syndrome, MKB type||http://www.orpha.net/ORDO/Orphanet_293707
15497||4204||acute hypotension||http://www.ebi.ac.uk/efo/EFO_0002497
15498||3502||inner ear structure||http://www.ebi.ac.uk/efo/EFO_0001363
15499||5892||natural killer cell activation||http://purl.obolibrary.org/obo/GO_0030101
15502||2252||Microcephaly-cerebellar hypoplasia-cardiac conduction defect syndrome||http://www.orpha.net/ORDO/Orphanet_329332
15501||1790||aggressive insulitis||http://www.ebi.ac.uk/efo/EFO_0002498
15500||10652||obsolete_pulmonary arterial hypertension||http://www.ebi.ac.uk/efo/EFO_0001362
15504||12161||age-related macular degeneration||http://www.ebi.ac.uk/efo/EFO_0001365
15503||10652||accelerated neurological senescence||http://www.ebi.ac.uk/efo/EFO_0002495
15506||3502||organ of corti||http://www.ebi.ac.uk/efo/EFO_0001364
15505||2866||actinic keratosis||http://www.ebi.ac.uk/efo/EFO_0002496
15507||5700||Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy||http://www.orpha.net/ORDO/Orphanet_329336
15508||1015||pulmonary hypertension||http://www.ebi.ac.uk/efo/EFO_0001361
15509||1398||type II diabetes mellitus||http://www.ebi.ac.uk/efo/EFO_0001360
15510||11852||glycosylation||http://purl.obolibrary.org/obo/GO_0070085
15511||618||embryo stage||http://www.ebi.ac.uk/efo/EFO_0001367
15512||3043||dentate gyrus||http://www.ebi.ac.uk/efo/EFO_0001366
15514||2672||vertebral column structure||http://www.ebi.ac.uk/efo/EFO_0001369
15513||31||anaplastic astrocytoma||http://www.ebi.ac.uk/efo/EFO_0002499
15515||10652||obsolete_intercostal muscle||http://www.ebi.ac.uk/efo/EFO_0001368
15516||10907||Acral self-healing collodion baby||http://www.orpha.net/ORDO/Orphanet_281127
15517||2252||19p13.13 microdeletion syndrome||http://www.orpha.net/ORDO/Orphanet_357001
15518||10907||Self-healing collodion baby||http://www.orpha.net/ORDO/Orphanet_281122
15519||4621||Rare constitutional medullar aplasia||http://www.orpha.net/ORDO/Orphanet_68383
15520||6028||Atypical hemolytic-uremic syndrome with DGKE deficiency||http://www.orpha.net/ORDO/Orphanet_357008
15521||10876||Obesity due to SIM1 deficiency||http://www.orpha.net/ORDO/Orphanet_369873
15522||9918||Neurometabolic disease||http://www.orpha.net/ORDO/Orphanet_68385
15523||5502||Azoarcus sp.||http://purl.obolibrary.org/obo/NCBITaxon_29544
15524||8193||N-methylformamide||http://purl.obolibrary.org/obo/CHEBI_7438
15525||2063||hypertrophy||http://www.ebi.ac.uk/efo/EFO_0002460
15526||1391||skeletal system disease||http://www.ebi.ac.uk/efo/EFO_0002461
15527||2672||foetal structure||http://www.ebi.ac.uk/efo/EFO_0002462
15528||1471||129S1/SvImJ||http://www.ebi.ac.uk/efo/EFO_0001332
15531||3057||transport vesicle||http://purl.obolibrary.org/obo/GO_0030133
15530||1471||129P1/ReJ||http://www.ebi.ac.uk/efo/EFO_0001331
15529||10652||obsolete_geniculate nucleus||http://www.ebi.ac.uk/efo/EFO_0002463
15534||15531||ER to Golgi transport vesicle||http://purl.obolibrary.org/obo/GO_0030134
15532||10652||obsolete_hair follicle||http://www.ebi.ac.uk/efo/EFO_0002464
15533||10652||obsolete_C57BL/6J||http://www.ebi.ac.uk/efo/EFO_0001330
15536||3057||coated vesicle||http://purl.obolibrary.org/obo/GO_0030135
15535||10652||obsolete_inferior colliculus||http://www.ebi.ac.uk/efo/EFO_0002465
15537||13587||CBA/CaJ||http://www.ebi.ac.uk/efo/EFO_0001336
15538||7111||information entity||http://purl.obolibrary.org/obo/IAO_0000030
15539||10652||obsolete_middle temporal gyrus||http://www.ebi.ac.uk/efo/EFO_0002466
15540||3043||motor cortex||http://www.ebi.ac.uk/efo/EFO_0002467
15541||10652||obsolete_behavioural disease||http://www.ebi.ac.uk/efo/EFO_0001335
15542||10652||obsolete_oculomotor nucleus||http://www.ebi.ac.uk/efo/EFO_0002468
15543||10652||obsolete_ileum||http://www.ebi.ac.uk/efo/EFO_0001334
15545||3043||paraventricular nucleus||http://www.ebi.ac.uk/efo/EFO_0002469
15544||10652||obsolete_jejunum||http://www.ebi.ac.uk/efo/EFO_0001333
15546||13587||CB6F1||http://www.ebi.ac.uk/efo/EFO_0001339
15547||13587||TBP-71Q-16||http://www.ebi.ac.uk/efo/EFO_0001338
15548||14730||BDC2.5/NOD||http://www.ebi.ac.uk/efo/EFO_0001337
15549||9918||Leukodystrophy||http://www.orpha.net/ORDO/Orphanet_68356
15550||1415||Autosomal recessive limb-girdle muscular dystrophy type 2S||http://www.orpha.net/ORDO/Orphanet_369840
15551||4139||Intellectual disability-hyperkinetic movement-truncal ataxia syndrome||http://www.orpha.net/ORDO/Orphanet_369847
15552||3043||posterior cingulate cortex||http://www.ebi.ac.uk/efo/EFO_0002471
15553||3043||somatomotor cortex||http://www.ebi.ac.uk/efo/EFO_0002472
15554||3043||periaqueductal gray||http://www.ebi.ac.uk/efo/EFO_0002470
15555||13587||TBP-105Q||http://www.ebi.ac.uk/efo/EFO_0001341
15556||10652||obsolete_suprachiasmatic nucleus||http://www.ebi.ac.uk/efo/EFO_0002475
15557||13587||B6C3F1||http://www.ebi.ac.uk/efo/EFO_0001340
15558||10652||obsolete_supraoptic nucleus||http://www.ebi.ac.uk/efo/EFO_0002476
15560||14235||Wistar-Furth||http://www.ebi.ac.uk/efo/EFO_0001343
15559||2670||stamen abscission zone||http://www.ebi.ac.uk/efo/EFO_0002473
15562||14235||Wistar||http://www.ebi.ac.uk/efo/EFO_0001342
15561||10652||obsolete_superior colliculus||http://www.ebi.ac.uk/efo/EFO_0002474
15563||14235||Wistar-Kyoto||http://www.ebi.ac.uk/efo/EFO_0001345
15565||14235||Copenhagen||http://www.ebi.ac.uk/efo/EFO_0001344
15564||3249||extracellular vesicular exosome||http://purl.obolibrary.org/obo/GO_0070062
15566||14235||Syracuse Low Avoidance||http://www.ebi.ac.uk/efo/EFO_0001347
15567||14235||Syracuse High Avoidance||http://www.ebi.ac.uk/efo/EFO_0001346
15568||14235||Dahl salt-resistant||http://www.ebi.ac.uk/efo/EFO_0001349
15569||14235||Okamoto-Aoki||http://www.ebi.ac.uk/efo/EFO_0001348
15570||11037||Keratinopathic ichthyosis||http://www.orpha.net/ORDO/Orphanet_281103
15571||1732||Inborn errors of metabolism||http://www.orpha.net/ORDO/Orphanet_68367
15572||15571||Lysosomal disease||http://www.orpha.net/ORDO/Orphanet_68366
15573||8896||Recurrent infections-myelofibrosis-nephromegaly syndrome||http://www.orpha.net/ORDO/Orphanet_369852
15574||5129||Hemoglobinopathy||http://www.orpha.net/ORDO/Orphanet_68364
15575||15577||segmentation 5-9 somites||http://www.ebi.ac.uk/efo/EFO_0001317
15576||15577||segmentation 10-13 somites||http://www.ebi.ac.uk/efo/EFO_0001318
15577||618||segmentation stage||http://www.ebi.ac.uk/efo/EFO_0001315
15578||15577||segmentation 1-4 somites||http://www.ebi.ac.uk/efo/EFO_0001316
15579||7526||pharyngula prim-25||http://www.ebi.ac.uk/efo/EFO_0001313
15580||7526||pharyngula prim-5||http://www.ebi.ac.uk/efo/EFO_0001314
15581||7526||pharyngula high-pec||http://www.ebi.ac.uk/efo/EFO_0001311
15583||15538||data format specification||http://purl.obolibrary.org/obo/IAO_0000098
15582||7526||pharyngula prim-15||http://www.ebi.ac.uk/efo/EFO_0001312
15584||10652||obsolete_pharyngula stage||http://www.ebi.ac.uk/efo/EFO_0001310
15585||8191||mercury dichloride||http://purl.obolibrary.org/obo/CHEBI_31823
15586||15577||segmentation 14-19 somites||http://www.ebi.ac.uk/efo/EFO_0001319
15587||3349||SALK_049497||http://www.ebi.ac.uk/efo/EFO_0001326
15588||13587||A/J||http://www.ebi.ac.uk/efo/EFO_0001327
15589||13587||B6.Cg-Tg(SOD1-G93A)1Gur/J||http://www.ebi.ac.uk/efo/EFO_0001328
15590||13587||C3H/HeJ||http://www.ebi.ac.uk/efo/EFO_0001329
15591||618||fertilized egg stage||http://www.ebi.ac.uk/efo/EFO_0001322
15592||618||fetus||http://www.ebi.ac.uk/efo/EFO_0001323
15593||2672||tarsal region||http://purl.obolibrary.org/obo/UBERON_0004454
15594||10652||obsolete_Drosophila melanogaster strain||http://www.ebi.ac.uk/efo/EFO_0001324
15595||13786||Canton S||http://www.ebi.ac.uk/efo/EFO_0001325
15596||15577||segmentation 20-25 somites||http://www.ebi.ac.uk/efo/EFO_0001320
15597||15577||segmentation 26  somites||http://www.ebi.ac.uk/efo/EFO_0001321
15598||2252||Intellectual disability-seizures-hypotonia-ophthalmologic-skeletal anomalies syndrome||http://www.orpha.net/ORDO/Orphanet_369837
15599||13689||neural rod||http://purl.obolibrary.org/obo/UBERON_0005068
15600||9934||Congenital ptosis||http://www.orpha.net/ORDO/Orphanet_91411
15601||9934||Marcus-Gunn syndrome||http://www.orpha.net/ORDO/Orphanet_91412
15602||9934||Congenital Horner syndrome||http://www.orpha.net/ORDO/Orphanet_91413
15603||1022||Enchytraeus albidus||http://purl.obolibrary.org/obo/NCBITaxon_6390
15604||9986||Familial capillary hemangioma||http://www.orpha.net/ORDO/Orphanet_91415
15605||9603||Isolated congenital alacrima||http://www.orpha.net/ORDO/Orphanet_91416
15606||1022||Eisenia fetida||http://purl.obolibrary.org/obo/NCBITaxon_6396
15608||15306||leaf production stage||http://purl.obolibrary.org/obo/PO_0007133
15607||770||GM07348||http://purl.obolibrary.org/obo/CLO_0016951
15609||9746||seedling development stage||http://purl.obolibrary.org/obo/PO_0007131
15610||1125||biofilm||http://purl.obolibrary.org/obo/BTO_0002690
15611||4254||Fatty acid hydroxylase-associated neurodegeneration||http://www.orpha.net/ORDO/Orphanet_329308
15612||4254||PLA2G6-associated neurodegeneration||http://www.orpha.net/ORDO/Orphanet_329303
15613||1826||Funaria hygrometrica||http://purl.obolibrary.org/obo/NCBITaxon_29583
15614||15570||Annular epidermolytic ichthyosis||http://www.orpha.net/ORDO/Orphanet_281139
15615||772||neural cell||http://purl.obolibrary.org/obo/CL_0002319
15616||14556||periperhal blood mesothelial cell||http://purl.obolibrary.org/obo/CL_0002318
15617||772||erythroleukemia cell||http://purl.obolibrary.org/obo/BTO_0000426
15618||10652||obsolete_juvenile stage||http://www.ebi.ac.uk/efo/EFO_0001300
15620||15463||juvenile days 30-44||http://www.ebi.ac.uk/efo/EFO_0001301
15619||10994||sunitinib||http://purl.obolibrary.org/obo/CHEBI_38940
15622||15463||juvenile days 45-89||http://www.ebi.ac.uk/efo/EFO_0001302
15621||13543||Drosophila sechellia x Drosophila simulans||http://purl.obolibrary.org/obo/NCBITaxon_380737
15623||10652||obsolete_larval stage||http://www.ebi.ac.uk/efo/EFO_0001303
15624||14544||larval day 4||http://www.ebi.ac.uk/efo/EFO_0001304
15625||14544||larval day 5||http://www.ebi.ac.uk/efo/EFO_0001305
15626||1694||Hereditary thrombocytosis with transverse limb defect||http://www.orpha.net/ORDO/Orphanet_329319
15627||14544||larval day 6||http://www.ebi.ac.uk/efo/EFO_0001306
15628||14544||larval day 14-20||http://www.ebi.ac.uk/efo/EFO_0001307
15629||8780||Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency||http://www.orpha.net/ORDO/Orphanet_329314
15630||1826||Ceratopteris thalictroides||http://purl.obolibrary.org/obo/NCBITaxon_29596
15631||14544||larval day 7-13||http://www.ebi.ac.uk/efo/EFO_0001309
15632||14544||larval day 21-29||http://www.ebi.ac.uk/efo/EFO_0001308
