921
785
1
http://purl.obolibrary.org/obo/MONDO_0011909
Charcot-Marie-tooth disease dominant intermediate d
'Charcot-Marie-tooth disease dominant intermediate d' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4359
'Charcot-Marie-tooth disease dominant intermediate d' EquivalentTo 'Charcot-Marie-tooth disease' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4359)
http://purl.obolibrary.org/obo/MONDO_0011912
autosomal recessive nonsyndromic deafness 37
'autosomal recessive nonsyndromic deafness 37' EquivalentTo 'autosomal recessive nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4646)
'autosomal recessive nonsyndromic deafness 37' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4646
http://purl.obolibrary.org/obo/MONDO_0011932
hypotrichosis 6
'hypotrichosis 6' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_147409
'hypotrichosis 6' EquivalentTo 'hypotrichosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_147409)
http://purl.obolibrary.org/obo/MONDO_0011938
atrial heart septal defect 2
'atrial heart septal defect 2' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2626
'atrial heart septal defect 2' EquivalentTo 'atrial heart septal defect' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2626)
http://purl.obolibrary.org/obo/MONDO_0011935
retinitis pigmentosa 30
'retinitis pigmentosa 30' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_25794)
'retinitis pigmentosa 30' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_25794
http://purl.obolibrary.org/obo/MONDO_0011947
HNP1
http://purl.obolibrary.org/obo/MESH_C563161 EquivalentTo 'HNP1'
http://purl.obolibrary.org/obo/MONDO_0011963
Joubert syndrome 2
'Joubert syndrome 2' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_51259
'Joubert syndrome 2' EquivalentTo 'Joubert syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_51259)
http://purl.obolibrary.org/obo/MONDO_0011974
retinitis pigmentosa 7
'retinitis pigmentosa 7' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6094
'retinitis pigmentosa 7' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5961
'retinitis pigmentosa 7' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5961) and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6094)
http://purl.obolibrary.org/obo/MONDO_0011987
cone-rod dystrophy 13
'cone-rod dystrophy 13' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_57096
'cone-rod dystrophy 13' EquivalentTo 'cone-rod dystrophy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_57096)
http://purl.obolibrary.org/obo/MONDO_0011994
autosomal dominant nonsyndromic deafness 41
'autosomal dominant nonsyndromic deafness 41' EquivalentTo 'autosomal dominant nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_22953)
'autosomal dominant nonsyndromic deafness 41' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_22953
http://purl.obolibrary.org/obo/MONDO_0011832
autosomal dominant nonsyndromic deafness 44
'autosomal dominant nonsyndromic deafness 44' EquivalentTo 'autosomal dominant nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_152137)
'autosomal dominant nonsyndromic deafness 44' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_152137
http://purl.obolibrary.org/obo/MONDO_0011839
Newfoundland cone-rod dystrophy
'Newfoundland cone-rod dystrophy' EquivalentTo 'cone-rod dystrophy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6017)
'Newfoundland cone-rod dystrophy' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6017
http://purl.obolibrary.org/obo/MONDO_0011843
hypertrophic cardiomyopathy 25
'hypertrophic cardiomyopathy 25' EquivalentTo 'hypertrophic cardiomyopathy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_8557)
'hypertrophic cardiomyopathy 25' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_8557
http://purl.obolibrary.org/obo/MONDO_0011865
COL4A1-related familial vascular leukoencephalopathy
http://purl.obolibrary.org/obo/MESH_C531642 EquivalentTo 'COL4A1-related familial vascular leukoencephalopathy'
http://purl.obolibrary.org/obo/MONDO_0021207
Crohn jejunitis
'Crohn jejunitis' SubClassOf 'inflammatory disease'
'Crohn jejunitis' SubClassOf 'Crohn disease'
'Crohn jejunitis' SubClassOf 'small bowel Crohn disease'
http://purl.obolibrary.org/obo/DOID_0050786
http://purl.obolibrary.org/obo/DOID_0050786 EquivalentTo 'anterior segment dysgenesis 3'
http://purl.obolibrary.org/obo/DOID_0050786 EquivalentTo 'anterior segment dysgenesis 4'
http://purl.obolibrary.org/obo/MONDO_0011708
autosomal dominant nonsyndromic deafness 36
'autosomal dominant nonsyndromic deafness 36' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_117531
'autosomal dominant nonsyndromic deafness 36' EquivalentTo 'autosomal dominant nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_117531)
http://purl.obolibrary.org/obo/MONDO_0011718
primary ciliary dyskinesia 2
'primary ciliary dyskinesia 2' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_352909
'primary ciliary dyskinesia 2' EquivalentTo 'primary ciliary dyskinesia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_352909)
http://purl.obolibrary.org/obo/MONDO_0011748
Usher syndrome type 1G
'Usher syndrome type 1G' EquivalentTo 'Usher syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_124590)
'Usher syndrome type 1G' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_124590
http://purl.obolibrary.org/obo/MONDO_0011767
autosomal recessive nonsyndromic deafness 31
'autosomal recessive nonsyndromic deafness 31' EquivalentTo 'autosomal recessive nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_25861)
'autosomal recessive nonsyndromic deafness 31' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_25861
http://purl.obolibrary.org/obo/MONDO_0011764
autosomal dominant Parkinson disease 8
'autosomal dominant Parkinson disease 8' SubClassOf 'hereditary late onset Parkinson disease'
'autosomal dominant Parkinson disease 8' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_120892
'autosomal dominant Parkinson disease 8' SubClassOf 'hereditary late onset Parkinson disease'
'autosomal dominant Parkinson disease 8' EquivalentTo 'Parkinson disease' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_120892)
http://purl.obolibrary.org/obo/MONDO_0011762
autosomal recessive nonsyndromic deafness 22
'autosomal recessive nonsyndromic deafness 22' EquivalentTo 'autosomal recessive nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_146183)
'autosomal recessive nonsyndromic deafness 22' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_146183
http://purl.obolibrary.org/obo/MONDO_0011774
autosomal recessive nonsyndromic deafness 30
'autosomal recessive nonsyndromic deafness 30' EquivalentTo 'autosomal recessive nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_53904)
'autosomal recessive nonsyndromic deafness 30' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_53904
http://purl.obolibrary.org/obo/MONDO_0021108
meningitis (disease)
'meningitis (disease)' SubClassOf 'central nervous system disease'
'meningitis (disease)' SubClassOf 'inflammatory disease'
'meningitis (disease)' SubClassOf 'encephalomyelitis'
http://purl.obolibrary.org/obo/MONDO_0021156
hypophysitis
'hypophysitis' SubClassOf 'inflammatory disease'
'hypophysitis' SubClassOf 'rare endocrine disease'
'hypophysitis' SubClassOf 'encephalitis'
http://purl.obolibrary.org/obo/MONDO_0011600
congenital myasthenic syndrome 4A
'congenital myasthenic syndrome 4A' EquivalentTo 'congenital myasthenic syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1145)
'congenital myasthenic syndrome 4A' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1145
http://purl.obolibrary.org/obo/MONDO_0011613
autosomal recessive early-onset Parkinson disease 6
'autosomal recessive early-onset Parkinson disease 6' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_65018
'autosomal recessive early-onset Parkinson disease 6' EquivalentTo 'Parkinson disease' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_65018)
http://purl.obolibrary.org/obo/MONDO_0011638
neuroferritinopathy
'neuroferritinopathy' SubClassOf 'inherited neurodegenerative disorder'
'neuroferritinopathy' SubClassOf 'metabolic disease with dementia'
http://purl.obolibrary.org/obo/MONDO_0011632
amyotrophic lateral sclerosis type 21
'amyotrophic lateral sclerosis type 21' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9782
'amyotrophic lateral sclerosis type 21' EquivalentTo 'amyotrophic lateral sclerosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9782)
http://purl.obolibrary.org/obo/MONDO_0011630
retinitis pigmentosa 28
'retinitis pigmentosa 28' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_84140)
'retinitis pigmentosa 28' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_84140
http://purl.obolibrary.org/obo/MONDO_0011658
autosomal recessive early-onset Parkinson disease 7
'autosomal recessive early-onset Parkinson disease 7' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_11315
'autosomal recessive early-onset Parkinson disease 7' EquivalentTo 'Parkinson disease' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_11315)
http://purl.obolibrary.org/obo/MONDO_0011660
autosomal dominant nonsyndromic deafness 22
'autosomal dominant nonsyndromic deafness 22' EquivalentTo 'autosomal dominant nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4646)
'autosomal dominant nonsyndromic deafness 22' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4646
http://purl.obolibrary.org/obo/MONDO_0011674
Charcot-Marie-tooth disease dominant intermediate b
'Charcot-Marie-tooth disease dominant intermediate b' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1785
'Charcot-Marie-tooth disease dominant intermediate b' EquivalentTo 'Charcot-Marie-tooth disease' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1785)
http://purl.obolibrary.org/obo/MONDO_0011680
autosomal recessive congenital ichthyosis 3
'autosomal recessive congenital ichthyosis 3' EquivalentTo 'autosomal recessive congenital ichthyosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_59344)
'autosomal recessive congenital ichthyosis 3' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_59344
http://purl.obolibrary.org/obo/MONDO_0021084
vision disorder
'vision disorder' EquivalentTo 'disease' and ('disease has location' some http://purl.obolibrary.org/obo/UBERON_0002104)
'vision disorder' SubClassOf 'sensory system disease'
'vision disorder' SubClassOf 'disease has location' some http://purl.obolibrary.org/obo/UBERON_0002104
'vision disorder' EquivalentTo http://purl.obolibrary.org/obo/SCTID_95677002
'vision disorder' EquivalentTo 'disease' and ('disease disrupts' some http://purl.obolibrary.org/obo/GO_0007601)
'vision disorder' SubClassOf http://purl.obolibrary.org/obo/MONDO_0024458
http://linkedlifedata.com/resource/umls/id/C0042790 EquivalentTo 'vision disorder'
http://purl.obolibrary.org/obo/GARD_0002482
http://purl.obolibrary.org/obo/GARD_0002482 EquivalentTo 'anterior segment dysgenesis 3'
http://purl.obolibrary.org/obo/GARD_0002482 EquivalentTo http://purl.obolibrary.org/obo/MONDO_0024456
http://purl.obolibrary.org/obo/MONDO_0011505
familial hypobetalipoproteinemia 2
'familial hypobetalipoproteinemia 2' EquivalentTo 'hypobetalipoproteinemia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_27329)
'familial hypobetalipoproteinemia 2' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_27329
http://purl.obolibrary.org/obo/MONDO_0011502
Wolfram syndrome 2
'Wolfram syndrome 2' EquivalentTo 'Wolfram syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_493856)
'Wolfram syndrome 2' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_493856
http://purl.obolibrary.org/obo/MONDO_0011519
autosomal dominant nonsyndromic deafness 23
'autosomal dominant nonsyndromic deafness 23' EquivalentTo 'autosomal dominant nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6495)
'autosomal dominant nonsyndromic deafness 23' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6495
http://purl.obolibrary.org/obo/MONDO_0011535
split hand-foot malformation 4
'split hand-foot malformation 4' EquivalentTo 'split hand-foot malformation' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_8626)
'split hand-foot malformation 4' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_8626
http://purl.obolibrary.org/obo/MONDO_0011532
hereditary spastic paraplegia 13
'hereditary spastic paraplegia 13' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3329
'hereditary spastic paraplegia 13' EquivalentTo 'hereditary spastic paraplegia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3329)
http://purl.obolibrary.org/obo/MONDO_0011549
hypotrichosis 1
'hypotrichosis 1' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_147495
'hypotrichosis 1' EquivalentTo 'hypotrichosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_147495)
http://purl.obolibrary.org/obo/MONDO_0011545
autosomal dominant nocturnal frontal lobe epilepsy 3
'autosomal dominant nocturnal frontal lobe epilepsy 3' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1141
'autosomal dominant nocturnal frontal lobe epilepsy 3' EquivalentTo 'autosomal dominant nocturnal frontal lobe epilepsy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1141)
http://purl.obolibrary.org/obo/MONDO_0011568
autosomal dominant nonsyndromic deafness 25
'autosomal dominant nonsyndromic deafness 25' EquivalentTo 'autosomal dominant nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_246213)
'autosomal dominant nonsyndromic deafness 25' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_246213
http://purl.obolibrary.org/obo/MONDO_0011562
autosomal dominant Parkinson disease 4
'autosomal dominant Parkinson disease 4' SubClassOf 'hereditary late onset Parkinson disease'
'autosomal dominant Parkinson disease 4' SubClassOf 'hereditary late onset Parkinson disease'
http://purl.obolibrary.org/obo/MONDO_0011599
birdshot chorioretinopathy
'birdshot chorioretinopathy' SubClassOf 'posterior uveitis'
http://purl.obolibrary.org/obo/MONDO_0011405
poikiloderma with neutropenia
'poikiloderma with neutropenia' SubClassOf 'disease has feature' some 'neutropenia'
http://purl.obolibrary.org/obo/MONDO_0011415
Leber congenital amaurosis 3
'Leber congenital amaurosis 3' EquivalentTo 'Leber congenital amaurosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_55812)
'Leber congenital amaurosis 3' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_55812
http://purl.obolibrary.org/obo/MONDO_0011425
dilated cardiomyopathy 1H
http://purl.obolibrary.org/obo/MESH_C536277 EquivalentTo 'dilated cardiomyopathy 1H'
http://purl.obolibrary.org/obo/MONDO_0011426
aceruloplasminemia
'aceruloplasminemia' SubClassOf 'inherited neurodegenerative disorder'
'aceruloplasminemia' SubClassOf 'metabolic disease with dementia'
'aceruloplasminemia' SubClassOf 'iron metabolism disease'
http://purl.obolibrary.org/obo/MONDO_0011436
autosomal recessive distal spinal muscular atrophy 1
'autosomal recessive distal spinal muscular atrophy 1' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3508
'autosomal recessive distal spinal muscular atrophy 1' EquivalentTo 'spinal muscular atrophy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3508)
http://purl.obolibrary.org/obo/MONDO_0011442
advanced sleep phase syndrome 1
'advanced sleep phase syndrome 1' EquivalentTo 'advanced sleep phase syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_8864)
'advanced sleep phase syndrome 1' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_8864
http://purl.obolibrary.org/obo/MONDO_0011445
hereditary spastic paraplegia 11
'hereditary spastic paraplegia 11' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_80208
'hereditary spastic paraplegia 11' EquivalentTo 'hereditary spastic paraplegia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_80208)
http://purl.obolibrary.org/obo/MONDO_0011458
Leber congenital amaurosis 4
'Leber congenital amaurosis 4' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_23746
'Leber congenital amaurosis 4' EquivalentTo 'Leber congenital amaurosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_23746)
http://purl.obolibrary.org/obo/MONDO_0011452
hypotrichosis 7
'hypotrichosis 7' EquivalentTo 'hypotrichosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_200879)
'hypotrichosis 7' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_200879
http://purl.obolibrary.org/obo/MONDO_0011474
progressive familial heart block type IB
'progressive familial heart block type IB' EquivalentTo 'progressive familial heart block' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_54795)
'progressive familial heart block type IB' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_54795
http://purl.obolibrary.org/obo/MONDO_0011473
Leber congenital amaurosis 5
'Leber congenital amaurosis 5' EquivalentTo 'Leber congenital amaurosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_167691)
'Leber congenital amaurosis 5' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_167691
http://purl.obolibrary.org/obo/MONDO_0011480
autosomal dominant nonsyndromic deafness 20
'autosomal dominant nonsyndromic deafness 20' EquivalentTo 'autosomal dominant nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_71)
'autosomal dominant nonsyndromic deafness 20' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_71
http://purl.obolibrary.org/obo/MONDO_0006728
discitis
'discitis' SubClassOf 'arthropathy'
'discitis' SubClassOf 'inflammatory disease'
'discitis' SubClassOf 'arthritis'
http://purl.obolibrary.org/obo/MONDO_0006769
gastroparesis (disease)
'gastroparesis (disease)' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002013
http://purl.obolibrary.org/obo/MONDO_0016142
qualitative or quantitative defects of beta-sarcoglycan
http://purl.obolibrary.org/obo/MESH_C535435 EquivalentTo 'qualitative or quantitative defects of beta-sarcoglycan'
http://purl.obolibrary.org/obo/MONDO_0006656
aortitis
'aortitis' SubClassOf 'inflammatory disease'
'aortitis' SubClassOf 'vasculitis'
http://purl.obolibrary.org/obo/MONDO_0006683
brachial plexus neuropathy
'brachial plexus neuropathy' SubClassOf 'peripheral neuropathy'
'brachial plexus neuropathy' SubClassOf http://purl.obolibrary.org/obo/MONDO_0024432
http://purl.obolibrary.org/obo/MONDO_0016003
ehrlichiosis
'ehrlichiosis' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002315
'ehrlichiosis' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0012735
http://purl.obolibrary.org/obo/DOID_0060766
http://purl.obolibrary.org/obo/DOID_0060766 EquivalentTo 'autosomal dominant Robinow syndrome 1'
http://purl.obolibrary.org/obo/DOID_0060766 EquivalentTo http://purl.obolibrary.org/obo/MONDO_0024455
http://purl.obolibrary.org/obo/MONDO_0006547
exanthem (disease)
'exanthem (disease)' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0000988
'exanthem (disease)' SubClassOf 'disease has feature' some 'exanthem (disease)'
http://purl.obolibrary.org/obo/MONDO_0006544
erythema infectiosum
'erythema infectiosum' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_1511900
http://purl.obolibrary.org/obo/GARD_0002751
http://purl.obolibrary.org/obo/GARD_0002751 EquivalentTo 'neurodegeneration with brain iron accumulation 2a'
http://purl.obolibrary.org/obo/GARD_0002751 EquivalentTo http://purl.obolibrary.org/obo/MONDO_0024457
http://purl.obolibrary.org/obo/OMIM_256600
'neurodegeneration with brain iron accumulation 2a' EquivalentTo http://purl.obolibrary.org/obo/OMIM_256600
http://purl.obolibrary.org/obo/MONDO_0024457 EquivalentTo http://purl.obolibrary.org/obo/OMIM_256600
http://purl.obolibrary.org/obo/MONDO_0006292
malignant mesothelioma (disease)
'malignant mesothelioma (disease)' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0030828
http://purl.obolibrary.org/obo/MONDO_0006005
Venezuelan equine encephalitis
'Venezuelan equine encephalitis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_11036
'Venezuelan equine encephalitis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_11036
http://purl.obolibrary.org/obo/MONDO_0006012
viral pneumonia
'viral pneumonia' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_10239
'viral pneumonia' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_10239
http://purl.obolibrary.org/obo/MONDO_0002251
hepatitis
'hepatitis' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002027
http://purl.obolibrary.org/obo/MONDO_0002269
gastroenteritis
'gastroenteritis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_194
'gastroenteritis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_142786
'gastroenteritis' SubClassOf 'disease has feature' some 'dysentery'
'gastroenteritis' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002013
'gastroenteritis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_10912
http://purl.obolibrary.org/obo/MONDO_0002282
West nile fever
'West nile fever' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_11082
'West nile fever' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_11082
http://purl.obolibrary.org/obo/MONDO_0002122
neuritis
'neuritis' SubClassOf 'inflammatory disease'
http://purl.obolibrary.org/obo/MONDO_0002138
allergic contact dermatitis of eyelid
'allergic contact dermatitis of eyelid' SubClassOf 'eye allergy'
http://purl.obolibrary.org/obo/MONDO_0016472
dracunculiasis
'dracunculiasis' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002013
'dracunculiasis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_318479
http://purl.obolibrary.org/obo/MONDO_0006950
retinal vasculitis
'retinal vasculitis' SubClassOf 'rare eye disease'
'retinal vasculitis' SubClassOf 'retinitis'
http://purl.obolibrary.org/obo/MONDO_0006823
Klinefelter syndrome
'Klinefelter syndrome' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0000027
http://purl.obolibrary.org/obo/MONDO_0006879
optic papillitis
'optic papillitis' SubClassOf 'retinopathy'
'optic papillitis' SubClassOf 'inflammatory disease'
'optic papillitis' SubClassOf 'retinitis'
http://purl.obolibrary.org/obo/MONDO_0012604
isolated microphthalmia 3
'isolated microphthalmia 3' EquivalentTo 'isolated microphthalmia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_30062)
'isolated microphthalmia 3' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_30062
http://purl.obolibrary.org/obo/MONDO_0012605
isolated microphthalmia 5
'isolated microphthalmia 5' EquivalentTo 'isolated microphthalmia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_83552)
'isolated microphthalmia 5' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_83552
http://purl.obolibrary.org/obo/MONDO_0012602
autosomal recessive nonsyndromic deafness 24
'autosomal recessive nonsyndromic deafness 24' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5962
'autosomal recessive nonsyndromic deafness 24' EquivalentTo 'autosomal recessive nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5962)
http://purl.obolibrary.org/obo/MONDO_0012610
inflammatory bowel disease 10
'inflammatory bowel disease 10' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_55054
'inflammatory bowel disease 10' EquivalentTo 'inflammatory bowel disease' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_55054)
http://purl.obolibrary.org/obo/MONDO_0012625
retinitis pigmentosa 37
'retinitis pigmentosa 37' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10002
'retinitis pigmentosa 37' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10002)
http://purl.obolibrary.org/obo/MONDO_0012654
atrial heart septal defect 4
'atrial heart septal defect 4' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_57057
'atrial heart septal defect 4' EquivalentTo 'atrial heart septal defect' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_57057)
http://purl.obolibrary.org/obo/MONDO_0012662
Usher syndrome type 2D
'Usher syndrome type 2D' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_25861
'Usher syndrome type 2D' EquivalentTo 'Usher syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_25861)
http://purl.obolibrary.org/obo/MONDO_0012670
autosomal recessive nonsyndromic deafness 63
'autosomal recessive nonsyndromic deafness 63' EquivalentTo 'autosomal recessive nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_220074)
'autosomal recessive nonsyndromic deafness 63' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_220074
http://purl.obolibrary.org/obo/MONDO_0012694
Joubert syndrome 7
'Joubert syndrome 7' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_23322
'Joubert syndrome 7' EquivalentTo 'Joubert syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_23322)
http://purl.obolibrary.org/obo/MONDO_0012698
Waardenburg syndrome type 2E
'Waardenburg syndrome type 2E' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6663
'Waardenburg syndrome type 2E' EquivalentTo 'Waardenburg syndrome type 2' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6663)
http://purl.obolibrary.org/obo/MONDO_0012517
atypical Gaucher disease due to saposin C deficiency
'atypical Gaucher disease due to saposin C deficiency' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5660
'atypical Gaucher disease due to saposin C deficiency' EquivalentTo 'Gaucher disease' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5660)
http://purl.obolibrary.org/obo/MONDO_0012528
hypogonadotropic hypogonadism 4 with or without anosmia
'hypogonadotropic hypogonadism 4 with or without anosmia' EquivalentTo 'hypogonadotropic hypogonadism' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_60675)
'hypogonadotropic hypogonadism 4 with or without anosmia' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_60675
http://purl.obolibrary.org/obo/MONDO_0012525
Leber congenital amaurosis 12
'Leber congenital amaurosis 12' EquivalentTo 'Leber congenital amaurosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_343035)
'Leber congenital amaurosis 12' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_343035
http://purl.obolibrary.org/obo/MONDO_0012523
retinitis pigmentosa 36
'retinitis pigmentosa 36' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_768206)
'retinitis pigmentosa 36' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_768206
http://purl.obolibrary.org/obo/MONDO_0012538
nemaline myopathy 7
'nemaline myopathy 7' EquivalentTo 'nemaline myopathy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1073)
'nemaline myopathy 7' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1073
http://purl.obolibrary.org/obo/MONDO_0012539
Joubert syndrome 6
'Joubert syndrome 6' EquivalentTo 'Joubert syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_91147)
'Joubert syndrome 6' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_91147
http://purl.obolibrary.org/obo/MONDO_0012536
osteogenesis imperfecta type 7
'osteogenesis imperfecta type 7' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10491
'osteogenesis imperfecta type 7' EquivalentTo 'osteogenesis imperfecta' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10491)
http://purl.obolibrary.org/obo/MONDO_0012531
xeroderma pigmentosum group B
'xeroderma pigmentosum group B' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2071
'xeroderma pigmentosum group B' EquivalentTo 'xeroderma pigmentosum' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2071)
http://purl.obolibrary.org/obo/MONDO_0012563
holoprosencephaly 9
'holoprosencephaly 9' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2736
'holoprosencephaly 9' EquivalentTo 'holoprosencephaly' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2736)
http://purl.obolibrary.org/obo/MONDO_0012562
holoprosencephaly 7
'holoprosencephaly 7' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5727
'holoprosencephaly 7' EquivalentTo 'holoprosencephaly' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5727)
http://purl.obolibrary.org/obo/MONDO_0012565
Fanconi anemia complementation group N
'Fanconi anemia complementation group N' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_79728
'Fanconi anemia complementation group N' EquivalentTo 'Fanconi anemia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_79728)
http://purl.obolibrary.org/obo/MONDO_0012571
primary ciliary dyskinesia 6
'primary ciliary dyskinesia 6' EquivalentTo 'primary ciliary dyskinesia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_51314)
'primary ciliary dyskinesia 6' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_51314
http://purl.obolibrary.org/obo/MONDO_0012581
osteogenesis imperfecta type 8
'osteogenesis imperfecta type 8' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_64175
'osteogenesis imperfecta type 8' EquivalentTo 'osteogenesis imperfecta' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_64175)
http://purl.obolibrary.org/obo/MONDO_0012592
osteogenesis imperfecta type 11
'osteogenesis imperfecta type 11' EquivalentTo 'osteogenesis imperfecta' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_60681)
'osteogenesis imperfecta type 11' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_60681
http://purl.obolibrary.org/obo/MONDO_0012399
complex cortical dysplasia with other brain malformations 7
'complex cortical dysplasia with other brain malformations 7' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_347733
'complex cortical dysplasia with other brain malformations 7' EquivalentTo 'complex cortical dysplasia with other brain malformations' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_347733)
http://purl.obolibrary.org/obo/MONDO_0012409
isolated microphthalmia 2
'isolated microphthalmia 2' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_338917
'isolated microphthalmia 2' EquivalentTo 'isolated microphthalmia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_338917)
http://purl.obolibrary.org/obo/MONDO_0012411
giant axonal neuropathy 2
'giant axonal neuropathy 2' EquivalentTo 'giant axonal neuropathy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_50717)
'giant axonal neuropathy 2' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_50717
http://purl.obolibrary.org/obo/MONDO_0012421
autosomal recessive nonsyndromic deafness 44
'autosomal recessive nonsyndromic deafness 44' EquivalentTo 'autosomal recessive nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_107)
'autosomal recessive nonsyndromic deafness 44' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_107
http://purl.obolibrary.org/obo/MONDO_0012432
Joubert syndrome 5
'Joubert syndrome 5' EquivalentTo 'Joubert syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_80184)
'Joubert syndrome 5' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_80184
http://purl.obolibrary.org/obo/MONDO_0012448
hereditary spastic paraplegia 33
'hereditary spastic paraplegia 33' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_118813
'hereditary spastic paraplegia 33' EquivalentTo 'hereditary spastic paraplegia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_118813)
http://purl.obolibrary.org/obo/MONDO_0012442
autosomal recessive nonsyndromic deafness 66
'autosomal recessive nonsyndromic deafness 66' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_51473
'autosomal recessive nonsyndromic deafness 66' EquivalentTo 'autosomal recessive nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_51473)
http://purl.obolibrary.org/obo/MONDO_0012445
autosomal recessive nonsyndromic deafness 59
'autosomal recessive nonsyndromic deafness 59' EquivalentTo 'autosomal recessive nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_494513)
'autosomal recessive nonsyndromic deafness 59' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_494513
http://purl.obolibrary.org/obo/MONDO_0012464
cone-rod dystrophy 10
'cone-rod dystrophy 10' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_64218
'cone-rod dystrophy 10' EquivalentTo 'cone-rod dystrophy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_64218)
http://purl.obolibrary.org/obo/MONDO_0012463
retinitis pigmentosa 35
'retinitis pigmentosa 35' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_64218
'retinitis pigmentosa 35' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_64218)
http://purl.obolibrary.org/obo/MONDO_0012460
autosomal recessive nonsyndromic deafness 67
'autosomal recessive nonsyndromic deafness 67' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_222662
'autosomal recessive nonsyndromic deafness 67' EquivalentTo 'autosomal recessive nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_222662)
http://purl.obolibrary.org/obo/MONDO_0012474
autosomal dominant nocturnal frontal lobe epilepsy 4
'autosomal dominant nocturnal frontal lobe epilepsy 4' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1135
'autosomal dominant nocturnal frontal lobe epilepsy 4' EquivalentTo 'autosomal dominant nocturnal frontal lobe epilepsy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1135)
http://purl.obolibrary.org/obo/MONDO_0012477
retinitis pigmentosa 33
'retinitis pigmentosa 33' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_23020)
'retinitis pigmentosa 33' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_23020
http://purl.obolibrary.org/obo/MONDO_0012485
autosomal recessive nonsyndromic deafness 68
'autosomal recessive nonsyndromic deafness 68' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9294
'autosomal recessive nonsyndromic deafness 68' EquivalentTo 'autosomal recessive nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9294)
http://purl.obolibrary.org/obo/MONDO_0012483
cone-rod dystrophy 11
'cone-rod dystrophy 11' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_84839
'cone-rod dystrophy 11' EquivalentTo 'cone-rod dystrophy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_84839)
http://purl.obolibrary.org/obo/MONDO_0012497
congenital stationary night blindness autosomal dominant 3
'congenital stationary night blindness autosomal dominant 3' SubClassOf 'autosomal dominant disease'
'congenital stationary night blindness autosomal dominant 3' SubClassOf 'hereditary retinal dystrophy'
'congenital stationary night blindness autosomal dominant 3' SubClassOf 'has modifier' some http://purl.obolibrary.org/obo/HP_0000006
'congenital stationary night blindness autosomal dominant 3' SubClassOf 'hereditary night blindness'
'congenital stationary night blindness autosomal dominant 3' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2779
'congenital stationary night blindness autosomal dominant 3' EquivalentTo 'congenital stationary night blindness' and ('has modifier' some http://purl.obolibrary.org/obo/HP_0000006) and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2779)
http://purl.obolibrary.org/obo/MONDO_0012498
congenital stationary night blindness autosomal dominant 1
'congenital stationary night blindness autosomal dominant 1' EquivalentTo 'congenital stationary night blindness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6010)
'congenital stationary night blindness autosomal dominant 1' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6010
http://purl.obolibrary.org/obo/MONDO_0012496
Koolen de Vries syndrome
'Koolen de Vries syndrome' SubClassOf 'rare genetic syndromic intellectual disability'
http://purl.obolibrary.org/obo/DOID_0070076 EquivalentTo 'Koolen de Vries syndrome'
http://purl.obolibrary.org/obo/MONDO_0012268
AIDS
'AIDS' SubClassOf 'disease has feature' some 'dysentery'
'AIDS' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_12721
http://purl.obolibrary.org/obo/MONDO_0012273
autosomal recessive nonsyndromic deafness 48
'autosomal recessive nonsyndromic deafness 48' EquivalentTo 'autosomal recessive nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10518)
'autosomal recessive nonsyndromic deafness 48' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10518
http://purl.obolibrary.org/obo/MONDO_0012293
autosomal recessive nonsyndromic deafness 23
'autosomal recessive nonsyndromic deafness 23' EquivalentTo 'autosomal recessive nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_65217)
'autosomal recessive nonsyndromic deafness 23' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_65217
http://purl.obolibrary.org/obo/MONDO_0012326
autosomal recessive nonsyndromic deafness 42
'autosomal recessive nonsyndromic deafness 42' EquivalentTo 'autosomal recessive nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_286676)
'autosomal recessive nonsyndromic deafness 42' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_286676
http://purl.obolibrary.org/obo/MONDO_0012333
autosomal recessive nonsyndromic deafness 53
'autosomal recessive nonsyndromic deafness 53' EquivalentTo 'autosomal recessive nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1302)
'autosomal recessive nonsyndromic deafness 53' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1302
http://purl.obolibrary.org/obo/MONDO_0012367
retinitis pigmentosa 31
'retinitis pigmentosa 31' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10210)
'retinitis pigmentosa 31' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10210
http://purl.obolibrary.org/obo/MONDO_0012144
Waardenburg syndrome type 2D
'Waardenburg syndrome type 2D' EquivalentTo 'Waardenburg syndrome type 2' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6591)
'Waardenburg syndrome type 2D' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6591
http://purl.obolibrary.org/obo/MONDO_0012157
congenital myasthenic syndrome 4C
'congenital myasthenic syndrome 4C' SubClassOf 'postsynaptic congenital myasthenic syndrome'
'congenital myasthenic syndrome 4C' EquivalentTo 'congenital myasthenic syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1145) and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2673)
'congenital myasthenic syndrome 4C' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1145
'congenital myasthenic syndrome 4C' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2673
'congenital myasthenic syndrome 4C' SubClassOf 'congenital myasthenic syndrome 4A'
http://purl.obolibrary.org/obo/MONDO_0012162
patterned macular dystrophy 2
'patterned macular dystrophy 2' EquivalentTo 'patterned macular dystrophy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1495)
'patterned macular dystrophy 2' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1495
http://purl.obolibrary.org/obo/MONDO_0012170
autosomal recessive nonsyndromic deafness 36
'autosomal recessive nonsyndromic deafness 36' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_83715
'autosomal recessive nonsyndromic deafness 36' EquivalentTo 'autosomal recessive nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_83715)
http://purl.obolibrary.org/obo/MONDO_0012199
posterior polymorphous corneal dystrophy 2
'posterior polymorphous corneal dystrophy 2' EquivalentTo 'posterior polymorphous corneal dystrophy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1296)
'posterior polymorphous corneal dystrophy 2' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1296
http://purl.obolibrary.org/obo/MONDO_0002840
eosinophilic gastritis
'eosinophilic gastritis' SubClassOf 'gastritis (disease)'
'eosinophilic gastritis' SubClassOf 'bacterial gastritis'
'eosinophilic gastritis' SubClassOf 'viral gastritis'
http://purl.obolibrary.org/obo/MONDO_0012200
posterior polymorphous corneal dystrophy 3
'posterior polymorphous corneal dystrophy 3' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6935
'posterior polymorphous corneal dystrophy 3' EquivalentTo 'posterior polymorphous corneal dystrophy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6935)
http://purl.obolibrary.org/obo/MONDO_0012220
Griscelli syndrome type 3
'Griscelli syndrome type 3' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_79083
'Griscelli syndrome type 3' EquivalentTo 'Griscelli syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_79083)
http://purl.obolibrary.org/obo/MONDO_0012239
nemaline myopathy 1
'nemaline myopathy 1' EquivalentTo 'nemaline myopathy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7170)
'nemaline myopathy 1' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7170
http://purl.obolibrary.org/obo/MONDO_0012237
nemaline myopathy 6
'nemaline myopathy 6' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_390594
'nemaline myopathy 6' EquivalentTo 'nemaline myopathy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_390594)
http://purl.obolibrary.org/obo/MONDO_0012240
nemaline myopathy 4
'nemaline myopathy 4' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7169
'nemaline myopathy 4' EquivalentTo 'nemaline myopathy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7169)
http://purl.obolibrary.org/obo/MONDO_0012024
retinitis pigmentosa 26
'retinitis pigmentosa 26' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_375298
'retinitis pigmentosa 26' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_375298)
http://purl.obolibrary.org/obo/MONDO_0012056
Leber congenital amaurosis 9
'Leber congenital amaurosis 9' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_64802
'Leber congenital amaurosis 9' EquivalentTo 'Leber congenital amaurosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_64802)
http://purl.obolibrary.org/obo/MONDO_0012060
autosomal recessive nonsyndromic deafness 35
'autosomal recessive nonsyndromic deafness 35' EquivalentTo 'autosomal recessive nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2103)
'autosomal recessive nonsyndromic deafness 35' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2103
http://purl.obolibrary.org/obo/MONDO_0012078
Joubert syndrome 3
'Joubert syndrome 3' EquivalentTo 'Joubert syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_54806)
'Joubert syndrome 3' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_54806
http://purl.obolibrary.org/obo/MONDO_0012088
primary ciliary dyskinesia 5
'primary ciliary dyskinesia 5' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_54768
'primary ciliary dyskinesia 5' EquivalentTo 'primary ciliary dyskinesia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_54768)
http://purl.obolibrary.org/obo/MONDO_0012083
autosomal dominant nonsyndromic deafness 28
'autosomal dominant nonsyndromic deafness 28' EquivalentTo 'autosomal dominant nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_79977)
'autosomal dominant nonsyndromic deafness 28' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_79977
http://purl.obolibrary.org/obo/MONDO_0012085
primary ciliary dyskinesia 3
'primary ciliary dyskinesia 3' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1767
'primary ciliary dyskinesia 3' EquivalentTo 'primary ciliary dyskinesia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1767)
http://purl.obolibrary.org/obo/MONDO_0002708
retinitis
'retinitis' SubClassOf 'inflammatory disease'
'retinitis' SubClassOf 'posterior uveitis'
http://purl.obolibrary.org/obo/MONDO_0012112
hypertrophic cardiomyopathy 10
'hypertrophic cardiomyopathy 10' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4633
'hypertrophic cardiomyopathy 10' EquivalentTo 'hypertrophic cardiomyopathy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4633)
http://purl.obolibrary.org/obo/MONDO_0012111
hypertrophic cardiomyopathy 8
'hypertrophic cardiomyopathy 8' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4634
'hypertrophic cardiomyopathy 8' EquivalentTo 'hypertrophic cardiomyopathy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4634)
http://purl.obolibrary.org/obo/MONDO_0012128
dextro-looped transposition of the great arteries 1
'dextro-looped transposition of the great arteries 1' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_23389
'dextro-looped transposition of the great arteries 1' EquivalentTo 'dextro-looped transposition of the great arteries' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_23389)
http://purl.obolibrary.org/obo/MONDO_0012125
hypomyelinating leukodystrophy 2
'hypomyelinating leukodystrophy 2' EquivalentTo 'leukodystrophy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_57165)
'hypomyelinating leukodystrophy 2' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_57165
http://purl.obolibrary.org/obo/MONDO_0002615
xanthomatosis (disease)
'xanthomatosis (disease)' SubClassOf 'disease has feature' some 'xanthoma (disease)'
'xanthomatosis (disease)' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0001114
http://purl.obolibrary.org/obo/MONDO_0002645
cerebritis
'cerebritis' SubClassOf 'brain disease'
'cerebritis' SubClassOf 'inflammatory disease'
'cerebritis' SubClassOf 'encephalitis'
http://purl.obolibrary.org/obo/MONDO_0002691
liver cancer
'liver cancer' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002027
http://purl.obolibrary.org/obo/MONDO_0012014
Charcot-Marie-tooth disease recessive intermediate a
'Charcot-Marie-tooth disease recessive intermediate a' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_54332
'Charcot-Marie-tooth disease recessive intermediate a' EquivalentTo 'Charcot-Marie-tooth disease' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_54332)
http://purl.obolibrary.org/obo/MONDO_0012012
Charcot-Marie-tooth disease dominant intermediate c
'Charcot-Marie-tooth disease dominant intermediate c' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_8565
'Charcot-Marie-tooth disease dominant intermediate c' EquivalentTo 'Charcot-Marie-tooth disease' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_8565)
http://purl.obolibrary.org/obo/OMIMPS_601419
'obsolete myopathy, myofibrillar' EquivalentTo http://purl.obolibrary.org/obo/OMIMPS_601419
'myofibrillar myopathy (disease)' EquivalentTo http://purl.obolibrary.org/obo/OMIMPS_601419
http://purl.obolibrary.org/obo/MONDO_0002521
multiple symmetrical lipomatosis
'multiple symmetrical lipomatosis' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C4392
'multiple symmetrical lipomatosis' EquivalentTo http://purl.obolibrary.org/obo/SCTID_238902007
http://purl.obolibrary.org/obo/DOID_3137 EquivalentTo 'multiple symmetrical lipomatosis'
'multiple symmetrical lipomatosis' SubClassOf 'multiple symmetric lipomatosis'
'multiple symmetrical lipomatosis' SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/MONDO_0002565
myelitis
'myelitis' SubClassOf 'inflammatory disease'
'myelitis' SubClassOf 'encephalomyelitis'
http://purl.obolibrary.org/obo/MONDO_0002572
aspiration pneumonitis
'aspiration pneumonitis' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002789
http://purl.obolibrary.org/obo/MONDO_0007223
brachydactyly type E1
'brachydactyly type E1' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3239
'brachydactyly type E1' EquivalentTo 'brachydactyly type E' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3239)
http://purl.obolibrary.org/obo/MONDO_0007220
brachydactyly type B1
'brachydactyly type B1' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4920
'brachydactyly type B1' EquivalentTo 'brachydactyly type B' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4920)
http://purl.obolibrary.org/obo/MONDO_0007256
hepatocellular carcinoma
'hepatocellular carcinoma' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002027
http://purl.obolibrary.org/obo/MONDO_0007266
hypertrophic cardiomyopathy 2
'hypertrophic cardiomyopathy 2' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7139
'hypertrophic cardiomyopathy 2' EquivalentTo 'hypertrophic cardiomyopathy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7139)
http://purl.obolibrary.org/obo/MONDO_0007267
hypertrophic cardiomyopathy 3
'hypertrophic cardiomyopathy 3' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7168
'hypertrophic cardiomyopathy 3' EquivalentTo 'hypertrophic cardiomyopathy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7168)
http://purl.obolibrary.org/obo/MONDO_0007294
central core myopathy
'central core myopathy' SubClassOf 'congenital structural myopathy'
http://purl.obolibrary.org/obo/DOID_0110735
http://purl.obolibrary.org/obo/DOID_0110735 EquivalentTo 'neurodegeneration with brain iron accumulation 2a'
http://purl.obolibrary.org/obo/DOID_0110735 EquivalentTo http://purl.obolibrary.org/obo/MONDO_0024457
http://purl.obolibrary.org/obo/MONDO_0007103
amyotrophic lateral sclerosis type 1
'amyotrophic lateral sclerosis type 1' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1639
'amyotrophic lateral sclerosis type 1' EquivalentTo 'amyotrophic lateral sclerosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1639) and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4744) and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5630) and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6647)
'amyotrophic lateral sclerosis type 1' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6647
'amyotrophic lateral sclerosis type 1' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4744
'amyotrophic lateral sclerosis type 1' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5630
http://purl.obolibrary.org/obo/MONDO_0007118
isolated anhidrosis with normal sweat glands
'isolated anhidrosis with normal sweat glands' EquivalentTo 'anhidrosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3709)
'isolated anhidrosis with normal sweat glands' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3709
http://purl.obolibrary.org/obo/MONDO_0007147
obstructive sleep apnea syndrome
http://linkedlifedata.com/resource/umls/id/C0520679 EquivalentTo 'obstructive sleep apnea syndrome'
http://purl.obolibrary.org/obo/MONDO_0007186
gastroesophageal reflux disease
'gastroesophageal reflux disease' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0012735
http://purl.obolibrary.org/obo/MONDO_0007021
wheat allergic disease
'wheat allergic disease' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_4564
http://purl.obolibrary.org/obo/MONDO_0007093
hypomaturation-hypoplastic amelogenesis imperfecta with taurodontism
'hypomaturation-hypoplastic amelogenesis imperfecta with taurodontism' EquivalentTo 'amelogenesis imperfecta' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1747)
'hypomaturation-hypoplastic amelogenesis imperfecta with taurodontism' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1747
http://purl.obolibrary.org/obo/MONDO_0007094
amelogenesis imperfecta type 1A
'amelogenesis imperfecta type 1A' EquivalentTo 'amelogenesis imperfecta' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3914)
'amelogenesis imperfecta type 1A' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3914
http://purl.obolibrary.org/obo/MONDO_0007092
amelogenesis imperfecta type 1B
'amelogenesis imperfecta type 1B' EquivalentTo 'amelogenesis imperfecta' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10117)
'amelogenesis imperfecta type 1B' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10117
http://purl.obolibrary.org/obo/DOID_3137
http://purl.obolibrary.org/obo/DOID_3137 EquivalentTo 'multiple symmetrical lipomatosis'
http://purl.obolibrary.org/obo/DOID_3137 EquivalentTo 'multiple symmetric lipomatosis'
http://purl.obolibrary.org/obo/MONDO_0012906
primary ciliary dyskinesia 9
'primary ciliary dyskinesia 9' EquivalentTo 'primary ciliary dyskinesia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_64446)
'primary ciliary dyskinesia 9' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_64446
http://purl.obolibrary.org/obo/MONDO_0012918
primary ciliary dyskinesia 10
'primary ciliary dyskinesia 10' EquivalentTo 'primary ciliary dyskinesia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_55172)
'primary ciliary dyskinesia 10' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_55172
http://purl.obolibrary.org/obo/MONDO_0012919
type 1 diabetes mellitus 20
'type 1 diabetes mellitus 20' EquivalentTo 'type 1 diabetes mellitus' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6927)
'type 1 diabetes mellitus 20' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6927
http://purl.obolibrary.org/obo/MONDO_0012921
type 1 diabetes mellitus 22
'type 1 diabetes mellitus 22' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1234
'type 1 diabetes mellitus 22' EquivalentTo 'type 1 diabetes mellitus' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1234)
http://purl.obolibrary.org/obo/MONDO_0012926
amelogenesis imperfecta hypomaturation type 2A2
'amelogenesis imperfecta hypomaturation type 2A2' EquivalentTo 'amelogenesis imperfecta' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9313)
'amelogenesis imperfecta hypomaturation type 2A2' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9313
http://purl.obolibrary.org/obo/MONDO_0012943
retinitis pigmentosa 46
'retinitis pigmentosa 46' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3420)
'retinitis pigmentosa 46' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3420
http://purl.obolibrary.org/obo/MONDO_0012941
inflammatory bowel disease 25
'inflammatory bowel disease 25' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3588
'inflammatory bowel disease 25' EquivalentTo 'inflammatory bowel disease' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3588)
http://purl.obolibrary.org/obo/MONDO_0012978
primary ciliary dyskinesia 11
'primary ciliary dyskinesia 11' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_345895
'primary ciliary dyskinesia 11' EquivalentTo 'primary ciliary dyskinesia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_345895)
http://purl.obolibrary.org/obo/MONDO_0012979
primary ciliary dyskinesia 12
'primary ciliary dyskinesia 12' EquivalentTo 'primary ciliary dyskinesia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_221421)
'primary ciliary dyskinesia 12' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_221421
http://purl.obolibrary.org/obo/MONDO_0012976
autosomal dominant nonsyndromic deafness 2B
'autosomal dominant nonsyndromic deafness 2B' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2707
'autosomal dominant nonsyndromic deafness 2B' EquivalentTo 'autosomal dominant nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2707)
http://purl.obolibrary.org/obo/MONDO_0012977
autosomal recessive nonsyndromic deafness 1B
'autosomal recessive nonsyndromic deafness 1B' EquivalentTo 'autosomal recessive nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10804)
'autosomal recessive nonsyndromic deafness 1B' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10804
http://purl.obolibrary.org/obo/MONDO_0012975
autosomal dominant nonsyndromic deafness 3B
'autosomal dominant nonsyndromic deafness 3B' EquivalentTo 'autosomal dominant nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10804)
'autosomal dominant nonsyndromic deafness 3B' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10804
http://purl.obolibrary.org/obo/MONDO_0012988
hypogonadotropic hypogonadism 6 with or without anosmia
'hypogonadotropic hypogonadism 6 with or without anosmia' EquivalentTo 'hypogonadotropic hypogonadism' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2253)
'hypogonadotropic hypogonadism 6 with or without anosmia' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2253
http://purl.obolibrary.org/obo/MONDO_0012981
hereditary spherocytosis type 4
'hereditary spherocytosis type 4' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6521
'hereditary spherocytosis type 4' EquivalentTo 'hereditary spherocytosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6521)
http://purl.obolibrary.org/obo/MONDO_0012985
hereditary spherocytosis type 5
'hereditary spherocytosis type 5' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2038
'hereditary spherocytosis type 5' EquivalentTo 'hereditary spherocytosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2038)
http://purl.obolibrary.org/obo/MONDO_0012983
cone-rod dystrophy 12
'cone-rod dystrophy 12' EquivalentTo 'cone-rod dystrophy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_8842)
'cone-rod dystrophy 12' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_8842
http://purl.obolibrary.org/obo/MONDO_0012990
Leber congenital amaurosis 13
'Leber congenital amaurosis 13' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_145226
'Leber congenital amaurosis 13' EquivalentTo 'Leber congenital amaurosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_145226)
http://purl.obolibrary.org/obo/MONDO_0012804
hypertrophic cardiomyopathy 12
'hypertrophic cardiomyopathy 12' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_8048
'hypertrophic cardiomyopathy 12' EquivalentTo 'hypertrophic cardiomyopathy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_8048)
http://purl.obolibrary.org/obo/MONDO_0012824
hypomyelinating leukodystrophy 4
'hypomyelinating leukodystrophy 4' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3329
'hypomyelinating leukodystrophy 4' EquivalentTo 'leukodystrophy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3329)
http://purl.obolibrary.org/obo/MONDO_0012831
inflammatory bowel disease 13
'inflammatory bowel disease 13' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5243
'inflammatory bowel disease 13' EquivalentTo 'inflammatory bowel disease' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5243)
http://purl.obolibrary.org/obo/MONDO_0012832
inflammatory bowel disease 14
'inflammatory bowel disease 14' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3663
'inflammatory bowel disease 14' EquivalentTo 'inflammatory bowel disease' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3663)
http://purl.obolibrary.org/obo/MONDO_0012847
autosomal recessive congenital ichthyosis 6
'autosomal recessive congenital ichthyosis 6' EquivalentTo 'autosomal recessive congenital ichthyosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_348938)
'autosomal recessive congenital ichthyosis 6' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_348938
http://purl.obolibrary.org/obo/MONDO_0012849
Joubert syndrome 9
'Joubert syndrome 9' EquivalentTo 'Joubert syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_57545)
'Joubert syndrome 9' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_57545
http://purl.obolibrary.org/obo/MONDO_0012840
inflammatory bowel disease 17
'inflammatory bowel disease 17' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_149233
'inflammatory bowel disease 17' EquivalentTo 'inflammatory bowel disease' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_149233)
http://purl.obolibrary.org/obo/MONDO_0012855
Joubert syndrome 8
'Joubert syndrome 8' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_200894
'Joubert syndrome 8' EquivalentTo 'Joubert syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_200894)
http://purl.obolibrary.org/obo/MONDO_0012850
hypophosphatemic nephrolithiasis/osteoporosis 1
'hypophosphatemic nephrolithiasis/osteoporosis 1' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002905
'hypophosphatemic nephrolithiasis/osteoporosis 1' SubClassOf 'disease has feature' some 'hyperphosphatemia (disease)'
http://purl.obolibrary.org/obo/MONDO_0012851
hypophosphatemic nephrolithiasis/osteoporosis 2
'hypophosphatemic nephrolithiasis/osteoporosis 2' SubClassOf 'disease has feature' some 'hyperphosphatemia (disease)'
'hypophosphatemic nephrolithiasis/osteoporosis 2' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002905
http://purl.obolibrary.org/obo/MONDO_0012880
hypogonadotropic hypogonadism 5 with or without anosmia
'hypogonadotropic hypogonadism 5 with or without anosmia' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_55636
'hypogonadotropic hypogonadism 5 with or without anosmia' EquivalentTo 'hypogonadotropic hypogonadism' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_55636)
http://purl.obolibrary.org/obo/MONDO_0012723
Leber congenital amaurosis 10
'Leber congenital amaurosis 10' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_80184
'Leber congenital amaurosis 10' EquivalentTo 'Leber congenital amaurosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_80184)
http://purl.obolibrary.org/obo/MONDO_0012728
Brugada syndrome 2
'Brugada syndrome 2' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_23171
'Brugada syndrome 2' EquivalentTo 'Brugada syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_23171)
http://purl.obolibrary.org/obo/MONDO_0012736
long QT syndrome 9
'long QT syndrome 9' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_859
'long QT syndrome 9' EquivalentTo 'long QT syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_859)
http://purl.obolibrary.org/obo/MONDO_0012737
long QT syndrome 10
'long QT syndrome 10' EquivalentTo 'long QT syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6330)
'long QT syndrome 10' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6330
http://purl.obolibrary.org/obo/MONDO_0012738
long QT syndrome 11
'long QT syndrome 11' EquivalentTo 'long QT syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10142)
'long QT syndrome 11' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10142
http://purl.obolibrary.org/obo/MONDO_0012748
primary ciliary dyskinesia 7
'primary ciliary dyskinesia 7' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_8701
'primary ciliary dyskinesia 7' EquivalentTo 'primary ciliary dyskinesia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_8701)
http://purl.obolibrary.org/obo/MONDO_0012743
Brugada syndrome 4
'Brugada syndrome 4' EquivalentTo 'Brugada syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_783)
'Brugada syndrome 4' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_783
http://purl.obolibrary.org/obo/MONDO_0012742
Brugada syndrome 3
'Brugada syndrome 3' EquivalentTo 'Brugada syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_775)
'Brugada syndrome 3' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_775
http://purl.obolibrary.org/obo/MONDO_0012762
catecholaminergic polymorphic ventricular tachycardia 2
'catecholaminergic polymorphic ventricular tachycardia 2' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_845
'catecholaminergic polymorphic ventricular tachycardia 2' EquivalentTo 'catecholaminergic polymorphic ventricular tachycardia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_845)
http://purl.obolibrary.org/obo/MONDO_0012799
hypertrophic cardiomyopathy 11
'hypertrophic cardiomyopathy 11' EquivalentTo 'hypertrophic cardiomyopathy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_70)
'hypertrophic cardiomyopathy 11' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_70
http://purl.obolibrary.org/obo/MONDO_0012796
retinitis pigmentosa 41
'retinitis pigmentosa 41' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_8842)
'retinitis pigmentosa 41' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_8842
http://purl.obolibrary.org/obo/MONDO_0007805
hypotrichosis 2
'hypotrichosis 2' EquivalentTo 'hypotrichosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1041)
'hypotrichosis 2' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1041
http://purl.obolibrary.org/obo/MONDO_0007801
hypoplasia of teeth roots
'hypoplasia of teeth roots' SubClassOf 'dentin dysplasia'
'hypoplasia of teeth roots' SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/MONDO_0007806
hypotrichosis 4
'hypotrichosis 4' EquivalentTo 'hypotrichosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_55806)
'hypotrichosis 4' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_55806
http://purl.obolibrary.org/obo/MONDO_0007844
hypogonadotropic hypogonadism 2 with or without anosmia
'hypogonadotropic hypogonadism 2 with or without anosmia' EquivalentTo 'hypogonadotropic hypogonadism' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2260)
'hypogonadotropic hypogonadism 2 with or without anosmia' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2260
http://purl.obolibrary.org/obo/MONDO_0017209
infectious posterior uveitis
'infectious posterior uveitis' SubClassOf 'infectious disease of the nervous system'
'infectious posterior uveitis' EquivalentTo 'infectious disease' and ('disease has inflammation site' some http://purl.obolibrary.org/obo/UBERON_0001776)
'infectious posterior uveitis' SubClassOf 'endophthalmitis'
'infectious posterior uveitis' SubClassOf 'disease has inflammation site' some http://purl.obolibrary.org/obo/UBERON_0001776
http://purl.obolibrary.org/obo/MONDO_0017210
infectious anterior uveitis
'infectious anterior uveitis' SubClassOf 'infectious disease of the nervous system'
'infectious anterior uveitis' SubClassOf 'endophthalmitis'
'infectious anterior uveitis' EquivalentTo 'infectious disease' and ('disease has inflammation site' some http://purl.obolibrary.org/obo/UBERON_0011892)
'infectious anterior uveitis' SubClassOf 'disease has inflammation site' some http://purl.obolibrary.org/obo/UBERON_0011892
http://purl.obolibrary.org/obo/MONDO_0017211
infectious panuveitis
'infectious panuveitis' SubClassOf 'infectious disease of the nervous system'
'infectious panuveitis' SubClassOf 'endophthalmitis'
http://purl.obolibrary.org/obo/MONDO_0007908
multiple symmetric lipomatosis
'multiple symmetric lipomatosis' EquivalentTo http://purl.obolibrary.org/obo/SCTID_63365006
'multiple symmetric lipomatosis' SubClassOf 'lipomatosis'
'multiple symmetric lipomatosis' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C4392
http://purl.obolibrary.org/obo/DOID_3137 EquivalentTo 'multiple symmetric lipomatosis'
'multiple symmetric lipomatosis' SubClassOf 'lipomatosis'
'multiple symmetric lipomatosis' EquivalentTo http://purl.obolibrary.org/obo/SCTID_238902007
http://purl.obolibrary.org/obo/MONDO_0007739
Huntington disease
'Huntington disease' SubClassOf 'disease has feature' some 'dementia'
http://purl.obolibrary.org/obo/MONDO_0007733
holoprosencephaly 3
'holoprosencephaly 3' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6469
'holoprosencephaly 3' EquivalentTo 'holoprosencephaly' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6469)
http://purl.obolibrary.org/obo/MONDO_0007794
hypogonadotropic hypogonadism 7 with or without anosmia
'hypogonadotropic hypogonadism 7 with or without anosmia' SubClassOf 'hypogonadotropic hypogonadism 17 with or without anosmia'
'hypogonadotropic hypogonadism 7 with or without anosmia' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_55717
'hypogonadotropic hypogonadism 7 with or without anosmia' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2798
'hypogonadotropic hypogonadism 7 with or without anosmia' SubClassOf 'hypogonadotropic hypogonadism 18 with or without anosmia'
'hypogonadotropic hypogonadism 7 with or without anosmia' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1848
'hypogonadotropic hypogonadism 7 with or without anosmia' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_285025
'hypogonadotropic hypogonadism 7 with or without anosmia' EquivalentTo 'hypogonadotropic hypogonadism' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10011) and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1848) and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_23767) and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2796) and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2798) and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_285025) and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_389549) and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_54756) and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_55703) and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_55717) and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_558) and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_81848) and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_8822) and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9723)
'hypogonadotropic hypogonadism 7 with or without anosmia' SubClassOf 'hypogonadotropic hypogonadism 20 with or without anosmia'
'hypogonadotropic hypogonadism 7 with or without anosmia' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_8822
'hypogonadotropic hypogonadism 7 with or without anosmia' SubClassOf 'hypogonadotropic hypogonadism 19 with or without anosmia'
'hypogonadotropic hypogonadism 7 with or without anosmia' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9723
'hypogonadotropic hypogonadism 7 with or without anosmia' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_55703
'hypogonadotropic hypogonadism 7 with or without anosmia' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10011
'hypogonadotropic hypogonadism 7 with or without anosmia' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2796
'hypogonadotropic hypogonadism 7 with or without anosmia' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_389549
'hypogonadotropic hypogonadism 7 with or without anosmia' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_54756
'hypogonadotropic hypogonadism 7 with or without anosmia' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_558
'hypogonadotropic hypogonadism 7 with or without anosmia' SubClassOf 'hypogonadotropic hypogonadism 22 with or without anosmia'
'hypogonadotropic hypogonadism 7 with or without anosmia' SubClassOf 'hypogonadotropic hypogonadism 14 with or without anosmia'
'hypogonadotropic hypogonadism 7 with or without anosmia' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_81848
'hypogonadotropic hypogonadism 7 with or without anosmia' SubClassOf 'hypogonadotropic hypogonadism 21 with or without anosmia'
'hypogonadotropic hypogonadism 7 with or without anosmia' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_23767
http://purl.obolibrary.org/obo/MONDO_0007791
familial hypocalciuric hypercalcemia 1
'familial hypocalciuric hypercalcemia 1' EquivalentTo 'familial hypocalciuric hypercalcemia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_846)
'familial hypocalciuric hypercalcemia 1' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_846
http://purl.obolibrary.org/obo/MONDO_0017137
onchocerciasis
'onchocerciasis' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0000618
'onchocerciasis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_6282
'onchocerciasis' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0000988
'onchocerciasis' SubClassOf 'disease has feature' some 'blindness'
'onchocerciasis' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0000618
'onchocerciasis' SubClassOf 'disease has feature' some 'exanthem (disease)'
http://purl.obolibrary.org/obo/MONDO_0007603
Felty syndrome
'Felty syndrome' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0001882
http://purl.obolibrary.org/obo/MONDO_0007656
Gerstmann-Straussler-Scheinker syndrome
http://purl.obolibrary.org/obo/MESH_C535800 EquivalentTo 'Gerstmann-Straussler-Scheinker syndrome'
http://purl.obolibrary.org/obo/MONDO_0007662
anterior segment dysgenesis 4
'anterior segment dysgenesis 4' SubClassOf 'anterior segment dysgenesis'
'anterior segment dysgenesis 4' EquivalentTo 'anterior segment dysgenesis 3' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5308)
'anterior segment dysgenesis 4' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5308
http://purl.obolibrary.org/obo/DOID_0050786 EquivalentTo 'anterior segment dysgenesis 4'
http://purl.obolibrary.org/obo/MONDO_0007538
hypocalcified amelogenesis imperfecta
'hypocalcified amelogenesis imperfecta' EquivalentTo 'amelogenesis imperfecta' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_286077)
'hypocalcified amelogenesis imperfecta' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_286077
http://purl.obolibrary.org/obo/MONDO_0007589
exudative vitreoretinopathy 1
http://purl.obolibrary.org/obo/MESH_C536382 EquivalentTo 'exudative vitreoretinopathy 1'
http://purl.obolibrary.org/obo/MONDO_0007424
autosomal dominant nonsyndromic deafness 1
'autosomal dominant nonsyndromic deafness 1' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1729
'autosomal dominant nonsyndromic deafness 1' EquivalentTo 'autosomal dominant nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1729)
http://purl.obolibrary.org/obo/MONDO_0007454
type 1 diabetes mellitus 2
'type 1 diabetes mellitus 2' EquivalentTo 'type 1 diabetes mellitus' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3630)
'type 1 diabetes mellitus 2' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3630
http://purl.obolibrary.org/obo/MONDO_0007349
familial cold autoinflammatory syndrome 1
'familial cold autoinflammatory syndrome 1' EquivalentTo 'familial cold autoinflammatory syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_114548)
'familial cold autoinflammatory syndrome 1' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_114548
http://purl.obolibrary.org/obo/MONDO_0007362
cone-rod dystrophy 2
'cone-rod dystrophy 2' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1406
'cone-rod dystrophy 2' EquivalentTo 'cone-rod dystrophy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1406)
http://purl.obolibrary.org/obo/MONDO_0007378
posterior polymorphous corneal dystrophy 1
'posterior polymorphous corneal dystrophy 1' EquivalentTo 'posterior polymorphous corneal dystrophy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_30813) and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_58495)
'posterior polymorphous corneal dystrophy 1' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_30813
'posterior polymorphous corneal dystrophy 1' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_58495
http://purl.obolibrary.org/obo/MONDO_0013002
cone-rod dystrophy 9
'cone-rod dystrophy 9' EquivalentTo 'cone-rod dystrophy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_8754)
'cone-rod dystrophy 9' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_8754
http://purl.obolibrary.org/obo/MONDO_0013015
Brugada syndrome 5
'Brugada syndrome 5' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6324
'Brugada syndrome 5' EquivalentTo 'Brugada syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6324)
http://purl.obolibrary.org/obo/MONDO_0013011
atrial heart septal defect 5
'atrial heart septal defect 5' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_70
'atrial heart septal defect 5' EquivalentTo 'atrial heart septal defect' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_70)
http://purl.obolibrary.org/obo/MONDO_0013048
hereditary spastic paraplegia 50
'hereditary spastic paraplegia 50' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9179
'hereditary spastic paraplegia 50' EquivalentTo 'hereditary spastic paraplegia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9179)
http://purl.obolibrary.org/obo/MONDO_0013052
retinitis pigmentosa 42
'retinitis pigmentosa 42' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_55975
'retinitis pigmentosa 42' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_55975)
http://purl.obolibrary.org/obo/MONDO_0013062
long QT syndrome 12
'long QT syndrome 12' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6640
'long QT syndrome 12' EquivalentTo 'long QT syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6640)
http://purl.obolibrary.org/obo/MONDO_0013060
autosomal recessive Parkinson disease 14
'autosomal recessive Parkinson disease 14' SubClassOf 'hereditary late onset Parkinson disease'
'autosomal recessive Parkinson disease 14' SubClassOf 'hereditary late onset Parkinson disease'
http://purl.obolibrary.org/obo/MONDO_0013081
lymphoproliferative syndrome 1
'lymphoproliferative syndrome 1' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3702
'lymphoproliferative syndrome 1' EquivalentTo 'lymphoproliferative syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3702)
http://purl.obolibrary.org/obo/MONDO_0003700
brachial plexus neoplasm
'brachial plexus neoplasm' SubClassOf 'brachial plexus neuropathy'
'brachial plexus neoplasm' SubClassOf 'central nervous system neoplasm'
http://purl.obolibrary.org/obo/MONDO_0017999
fatty acid hydroxylase-associated neurodegeneration
'fatty acid hydroxylase-associated neurodegeneration' SubClassOf 'metabolic disease with dementia'
http://purl.obolibrary.org/obo/MONDO_0017998
PLA2G6-associated neurodegeneration
'PLA2G6-associated neurodegeneration' SubClassOf 'metabolic disease with dementia'
'PLA2G6-associated neurodegeneration' SubClassOf 'neurodegeneration with brain iron accumulation'
'PLA2G6-associated neurodegeneration' SubClassOf 'rare dyslipidemia'
'PLA2G6-associated neurodegeneration' SubClassOf 'disorder of phospholipids, sphingolipids and fatty acids biosynthesis with central nervous system predominant involvement'
'PLA2G6-associated neurodegeneration' SubClassOf 'inherited neurodegenerative disorder'
'PLA2G6-associated neurodegeneration' SubClassOf 'neurodegeneration with brain iron accumulation'
'PLA2G6-associated neurodegeneration' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_8398
'PLA2G6-associated neurodegeneration' EquivalentTo 'neurodegeneration with brain iron accumulation' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_8398)
http://purl.obolibrary.org/obo/MONDO_0017874
Argentine hemorrhagic fever
'Argentine hemorrhagic fever' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0001882
'Argentine hemorrhagic fever' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0001882
'Argentine hemorrhagic fever' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002315
http://purl.obolibrary.org/obo/MONDO_0017882
Omsk hemorrhagic fever
'Omsk hemorrhagic fever' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_12542
'Omsk hemorrhagic fever' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_12542
http://purl.obolibrary.org/obo/MONDO_0017941
chikungunya
'chikungunya' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_37124
'chikungunya' SubClassOf 'disease has feature' some 'exanthem (disease)'
'chikungunya' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0000988
http://purl.obolibrary.org/obo/MONDO_0003100
nerve plexus neoplasm
'nerve plexus neoplasm' SubClassOf http://purl.obolibrary.org/obo/MONDO_0024432
http://purl.obolibrary.org/obo/MONDO_0017775
melioidosis
'melioidosis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_28450
'melioidosis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_28450
http://purl.obolibrary.org/obo/MONDO_0017809
parkinsonism due to ATP13A2 deficiency
'parkinsonism due to ATP13A2 deficiency' SubClassOf 'metabolic disease with dementia'
http://purl.obolibrary.org/obo/MONDO_0003014
rhinitis
'rhinitis' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002315
http://purl.obolibrary.org/obo/MONDO_0017572
tick-borne encephalitis
'tick-borne encephalitis' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002315
'tick-borne encephalitis' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002013
http://purl.obolibrary.org/obo/MONDO_0013906
amelogenesis imperfecta hypomaturation type 2A4
'amelogenesis imperfecta hypomaturation type 2A4' EquivalentTo 'amelogenesis imperfecta' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_152816)
'amelogenesis imperfecta hypomaturation type 2A4' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_152816
http://purl.obolibrary.org/obo/MONDO_0013913
hypogonadotropic hypogonadism 11 with or without anosmia
'hypogonadotropic hypogonadism 11 with or without anosmia' EquivalentTo 'hypogonadotropic hypogonadism' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6870)
'hypogonadotropic hypogonadism 11 with or without anosmia' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6870
http://purl.obolibrary.org/obo/MONDO_0013911
hypogonadotropic hypogonadism 9 with or without anosmia
'hypogonadotropic hypogonadism 9 with or without anosmia' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_26012
'hypogonadotropic hypogonadism 9 with or without anosmia' EquivalentTo 'hypogonadotropic hypogonadism' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_26012)
http://purl.obolibrary.org/obo/MONDO_0013912
hypogonadotropic hypogonadism 10 with or without anosmia
'hypogonadotropic hypogonadism 10 with or without anosmia' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6866
'hypogonadotropic hypogonadism 10 with or without anosmia' EquivalentTo 'hypogonadotropic hypogonadism' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6866)
http://purl.obolibrary.org/obo/MONDO_0013915
hypogonadotropic hypogonadism 13 with or without anosmia
'hypogonadotropic hypogonadism 13 with or without anosmia' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3814
'hypogonadotropic hypogonadism 13 with or without anosmia' EquivalentTo 'hypogonadotropic hypogonadism' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3814)
http://purl.obolibrary.org/obo/MONDO_0013910
hypogonadotropic hypogonadism 8 with or without anosmia
'hypogonadotropic hypogonadism 8 with or without anosmia' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_84634
'hypogonadotropic hypogonadism 8 with or without anosmia' EquivalentTo 'hypogonadotropic hypogonadism' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_84634)
http://purl.obolibrary.org/obo/MONDO_0013924
osteogenesis imperfecta type 13
'osteogenesis imperfecta type 13' EquivalentTo 'osteogenesis imperfecta' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_649)
'osteogenesis imperfecta type 13' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_649
http://purl.obolibrary.org/obo/MONDO_0013929
autosomal recessive nonsyndromic deafness 98
'autosomal recessive nonsyndromic deafness 98' EquivalentTo 'autosomal recessive nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_54084)
'autosomal recessive nonsyndromic deafness 98' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_54084
http://purl.obolibrary.org/obo/MONDO_0013926
hypogonadotropic hypogonadism 14 with or without anosmia
'hypogonadotropic hypogonadism 14 with or without anosmia' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_55717
'hypogonadotropic hypogonadism 14 with or without anosmia' EquivalentTo 'hypogonadotropic hypogonadism' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_55717)
http://purl.obolibrary.org/obo/MONDO_0013935
Usher syndrome type 1J
'Usher syndrome type 1J' EquivalentTo 'Usher syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10518)
'Usher syndrome type 1J' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10518
http://purl.obolibrary.org/obo/MONDO_0013946
hypogonadotropic hypogonadism 15 with or without anosmia
'hypogonadotropic hypogonadism 15 with or without anosmia' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9394
'hypogonadotropic hypogonadism 15 with or without anosmia' EquivalentTo 'hypogonadotropic hypogonadism' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9394)
http://purl.obolibrary.org/obo/MONDO_0013940
primary ciliary dyskinesia 18
'primary ciliary dyskinesia 18' EquivalentTo 'primary ciliary dyskinesia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_54919)
'primary ciliary dyskinesia 18' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_54919
http://purl.obolibrary.org/obo/MONDO_0013966
catecholaminergic polymorphic ventricular tachycardia 4
'catecholaminergic polymorphic ventricular tachycardia 4' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_801
'catecholaminergic polymorphic ventricular tachycardia 4' EquivalentTo 'catecholaminergic polymorphic ventricular tachycardia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_801)
http://purl.obolibrary.org/obo/MONDO_0013961
hypogonadotropic hypogonadism 16 with or without anosmia
'hypogonadotropic hypogonadism 16 with or without anosmia' EquivalentTo 'hypogonadotropic hypogonadism' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10371)
'hypogonadotropic hypogonadism 16 with or without anosmia' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10371
http://purl.obolibrary.org/obo/MONDO_0013963
autosomal recessive nonsyndromic deafness 93
'autosomal recessive nonsyndromic deafness 93' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_51475
'autosomal recessive nonsyndromic deafness 93' EquivalentTo 'autosomal recessive nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_51475)
http://purl.obolibrary.org/obo/MONDO_0013979
primary ciliary dyskinesia 19
'primary ciliary dyskinesia 19' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_23639
'primary ciliary dyskinesia 19' EquivalentTo 'primary ciliary dyskinesia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_23639)
http://purl.obolibrary.org/obo/MONDO_0013978
autosomal recessive nonsyndromic deafness 70
'autosomal recessive nonsyndromic deafness 70' EquivalentTo 'autosomal recessive nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_87178)
'autosomal recessive nonsyndromic deafness 70' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_87178
http://purl.obolibrary.org/obo/MONDO_0013984
autosomal recessive nonsyndromic deafness 84B
'autosomal recessive nonsyndromic deafness 84B' EquivalentTo 'autosomal recessive nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_283310)
'autosomal recessive nonsyndromic deafness 84B' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_283310
http://purl.obolibrary.org/obo/MONDO_0013985
autosomal recessive nonsyndromic deafness 18B
'autosomal recessive nonsyndromic deafness 18B' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_340990
'autosomal recessive nonsyndromic deafness 18B' EquivalentTo 'autosomal recessive nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_340990)
http://purl.obolibrary.org/obo/MONDO_0013994
Joubert syndrome 20
'Joubert syndrome 20' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_79583
'Joubert syndrome 20' EquivalentTo 'Joubert syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_79583)
http://purl.obolibrary.org/obo/MONDO_0013807
congenital stationary night blindness 1E
'congenital stationary night blindness 1E' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_440435
'congenital stationary night blindness 1E' EquivalentTo 'congenital stationary night blindness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_440435)
http://purl.obolibrary.org/obo/MONDO_0013825
congenital diarrhea 6
'congenital diarrhea 6' EquivalentTo 'congenital diarrhea' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2984)
'congenital diarrhea 6' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2984
http://purl.obolibrary.org/obo/MONDO_0013826
autosomal recessive nonsyndromic deafness 86
'autosomal recessive nonsyndromic deafness 86' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_57465
'autosomal recessive nonsyndromic deafness 86' EquivalentTo 'autosomal recessive nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_57465)
http://purl.obolibrary.org/obo/MONDO_0013823
autosomal dominant nonsyndromic deafness 4B
'autosomal dominant nonsyndromic deafness 4B' EquivalentTo 'autosomal dominant nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_388551)
'autosomal dominant nonsyndromic deafness 4B' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_388551
http://purl.obolibrary.org/obo/MONDO_0013824
Joubert syndrome 17
'Joubert syndrome 17' EquivalentTo 'Joubert syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_65250)
'Joubert syndrome 17' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_65250
http://purl.obolibrary.org/obo/MONDO_0013854
primary ciliary dyskinesia 17
'primary ciliary dyskinesia 17' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_388389
'primary ciliary dyskinesia 17' EquivalentTo 'primary ciliary dyskinesia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_388389)
http://purl.obolibrary.org/obo/MONDO_0013861
amyotrophic lateral sclerosis type 17
'amyotrophic lateral sclerosis type 17' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_25978
'amyotrophic lateral sclerosis type 17' EquivalentTo 'amyotrophic lateral sclerosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_25978)
http://purl.obolibrary.org/obo/MONDO_0013866
neuronal ceroid lipofuscinosis 11
'neuronal ceroid lipofuscinosis 11' EquivalentTo 'neuronal ceroid lipofuscinosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2896)
'neuronal ceroid lipofuscinosis 11' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2896
http://purl.obolibrary.org/obo/MONDO_0013875
3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome
'3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_84947
'3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome' EquivalentTo '3-methylglutaconic aciduria' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_84947)
http://purl.obolibrary.org/obo/MONDO_0013898
karyomegalic interstitial nephritis
'karyomegalic interstitial nephritis' EquivalentTo 'interstitial nephritis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_22909)
'karyomegalic interstitial nephritis' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_22909
http://purl.obolibrary.org/obo/MONDO_0013896
Joubert syndrome 18
'Joubert syndrome 18' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_26123
'Joubert syndrome 18' EquivalentTo 'Joubert syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_26123)
http://purl.obolibrary.org/obo/MONDO_0013891
amyotrophic lateral sclerosis type 18
'amyotrophic lateral sclerosis type 18' EquivalentTo 'amyotrophic lateral sclerosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5216)
'amyotrophic lateral sclerosis type 18' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5216
http://purl.obolibrary.org/obo/ENVO_00003030
http://purl.obolibrary.org/obo/ENVO_00003030 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/ENVO_00003030 SubClassOf http://purl.obolibrary.org/obo/ENVO_0010003
http://purl.obolibrary.org/obo/MONDO_0013715
amyotrophic lateral sclerosis type 16
'amyotrophic lateral sclerosis type 16' EquivalentTo 'amyotrophic lateral sclerosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10280)
'amyotrophic lateral sclerosis type 16' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10280
http://purl.obolibrary.org/obo/MONDO_0013722
hypomyelinating leukodystrophy 8 with or without oligodontia and-or hypogonadotropic hypogonadism
'hypomyelinating leukodystrophy 8 with or without oligodontia and-or hypogonadotropic hypogonadism' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_55703
'hypomyelinating leukodystrophy 8 with or without oligodontia and-or hypogonadotropic hypogonadism' EquivalentTo 'leukodystrophy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_55703)
'hypomyelinating leukodystrophy 8 with or without oligodontia and-or hypogonadotropic hypogonadism' SubClassOf 'leukodystrophy'
http://purl.obolibrary.org/obo/MONDO_0013745
Joubert syndrome 14
'Joubert syndrome 14' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_65062
'Joubert syndrome 14' EquivalentTo 'Joubert syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_65062)
http://purl.obolibrary.org/obo/MONDO_0013750
atrial heart septal defect 8
'atrial heart septal defect 8' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10370
'atrial heart septal defect 8' EquivalentTo 'atrial heart septal defect' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10370)
http://purl.obolibrary.org/obo/MONDO_0013753
Charcot-Marie-tooth disease axonal type 2P
'Charcot-Marie-tooth disease axonal type 2P' EquivalentTo 'Charcot-Marie-tooth disease' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_90678)
'Charcot-Marie-tooth disease axonal type 2P' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_90678
http://purl.obolibrary.org/obo/MONDO_0013763
Joubert syndrome 15
'Joubert syndrome 15' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_95681
'Joubert syndrome 15' EquivalentTo 'Joubert syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_95681)
http://purl.obolibrary.org/obo/MONDO_0013766
familial cold autoinflammatory syndrome 3
'familial cold autoinflammatory syndrome 3' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5336
'familial cold autoinflammatory syndrome 3' EquivalentTo 'familial cold autoinflammatory syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5336)
http://purl.obolibrary.org/obo/MONDO_0013764
Joubert syndrome 16
'Joubert syndrome 16' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_51524
'Joubert syndrome 16' EquivalentTo 'Joubert syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_51524)
http://purl.obolibrary.org/obo/MONDO_0013770
atrial heart septal defect 9
'atrial heart septal defect 9' EquivalentTo 'atrial heart septal defect' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2627)
'atrial heart septal defect 9' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2627
http://purl.obolibrary.org/obo/MONDO_0013788
Usher syndrome type 3B
'Usher syndrome type 3B' EquivalentTo 'Usher syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3035)
'Usher syndrome type 3B' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3035
http://purl.obolibrary.org/obo/MONDO_0013786
cone-rod dystrophy 16
'cone-rod dystrophy 16' EquivalentTo 'cone-rod dystrophy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_157657)
'cone-rod dystrophy 16' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_157657
http://purl.obolibrary.org/obo/MONDO_0013598
myostatin-related muscle hypertrophy
'myostatin-related muscle hypertrophy' SubClassOf 'disease has feature' some 'myostatin-related muscle hypertrophy'
http://purl.obolibrary.org/obo/MONDO_0013593
autosomal dominant nonsyndromic deafness 64
'autosomal dominant nonsyndromic deafness 64' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_56616
'autosomal dominant nonsyndromic deafness 64' EquivalentTo 'autosomal dominant nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_56616)
http://purl.obolibrary.org/obo/MONDO_0013606
Hermansky-Pudlak syndrome 9
'Hermansky-Pudlak syndrome 9' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_26258
'Hermansky-Pudlak syndrome 9' EquivalentTo 'Hermansky-Pudlak syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_26258)
http://purl.obolibrary.org/obo/MONDO_0013608
Joubert syndrome 13
'Joubert syndrome 13' EquivalentTo 'Joubert syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_79600)
'Joubert syndrome 13' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_79600
http://purl.obolibrary.org/obo/MONDO_0013613
Leber congenital amaurosis 16
'Leber congenital amaurosis 16' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3769
'Leber congenital amaurosis 16' EquivalentTo 'Leber congenital amaurosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3769)
http://purl.obolibrary.org/obo/MONDO_0013610
retinitis pigmentosa 61
'retinitis pigmentosa 61' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7401
'retinitis pigmentosa 61' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7401)
http://purl.obolibrary.org/obo/MONDO_0013611
retinitis pigmentosa 62
'retinitis pigmentosa 62' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4117)
'retinitis pigmentosa 62' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4117
http://purl.obolibrary.org/obo/MONDO_0013625
Parkinson disease 17
'Parkinson disease 17' SubClassOf 'hereditary late onset Parkinson disease'
'Parkinson disease 17' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_55737
'Parkinson disease 17' SubClassOf 'hereditary late onset Parkinson disease'
'Parkinson disease 17' EquivalentTo 'Parkinson disease' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_55737)
http://purl.obolibrary.org/obo/MONDO_0013620
congenital myasthenic syndrome 16
'congenital myasthenic syndrome 16' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6329
'congenital myasthenic syndrome 16' EquivalentTo 'congenital myasthenic syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6329)
http://purl.obolibrary.org/obo/MONDO_0013638
Warburg micro syndrome 3
'Warburg micro syndrome 3' EquivalentTo 'Warburg micro syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_22931)
'Warburg micro syndrome 3' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_22931
http://purl.obolibrary.org/obo/MONDO_0013641
Warburg micro syndrome 2
'Warburg micro syndrome 2' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_25782
'Warburg micro syndrome 2' EquivalentTo 'Warburg micro syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_25782)
http://purl.obolibrary.org/obo/MONDO_0013642
holoprosencephaly 11
'holoprosencephaly 11' EquivalentTo 'holoprosencephaly' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_50937)
'holoprosencephaly 11' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_50937
http://purl.obolibrary.org/obo/MONDO_0013644
Charcot-Marie-tooth disease axonal type 2O
'Charcot-Marie-tooth disease axonal type 2O' EquivalentTo 'Charcot-Marie-tooth disease' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1778)
'Charcot-Marie-tooth disease axonal type 2O' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1778
http://purl.obolibrary.org/obo/MONDO_0013679
sclerosteosis 2
'sclerosteosis 2' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4038
'sclerosteosis 2' EquivalentTo 'sclerosteosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4038)
http://purl.obolibrary.org/obo/MONDO_0013476
hypertrophic cardiomyopathy 19
'hypertrophic cardiomyopathy 19' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_125972
'hypertrophic cardiomyopathy 19' EquivalentTo 'hypertrophic cardiomyopathy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_125972)
http://purl.obolibrary.org/obo/MONDO_0013477
hypertrophic cardiomyopathy 20
'hypertrophic cardiomyopathy 20' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_91624
'hypertrophic cardiomyopathy 20' EquivalentTo 'hypertrophic cardiomyopathy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_91624)
http://purl.obolibrary.org/obo/MONDO_0013474
hypertrophic cardiomyopathy 17
'hypertrophic cardiomyopathy 17' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_57158
'hypertrophic cardiomyopathy 17' EquivalentTo 'hypertrophic cardiomyopathy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_57158)
http://purl.obolibrary.org/obo/MONDO_0013475
hypertrophic cardiomyopathy 18
'hypertrophic cardiomyopathy 18' EquivalentTo 'hypertrophic cardiomyopathy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5350)
'hypertrophic cardiomyopathy 18' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5350
http://purl.obolibrary.org/obo/MONDO_0013471
autosomal recessive nonsyndromic deafness 61
'autosomal recessive nonsyndromic deafness 61' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_375611
'autosomal recessive nonsyndromic deafness 61' EquivalentTo 'autosomal recessive nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_375611)
http://purl.obolibrary.org/obo/MONDO_0013489
autosomal recessive nonsyndromic deafness 89
'autosomal recessive nonsyndromic deafness 89' EquivalentTo 'autosomal recessive nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3735)
'autosomal recessive nonsyndromic deafness 89' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3735
http://purl.obolibrary.org/obo/MONDO_0013499
Fanconi anemia complementation group P
'Fanconi anemia complementation group P' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_84464
'Fanconi anemia complementation group P' EquivalentTo 'Fanconi anemia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_84464)
http://purl.obolibrary.org/obo/MONDO_0013495
autosomal recessive congenital ichthyosis 8
'autosomal recessive congenital ichthyosis 8' EquivalentTo 'autosomal recessive congenital ichthyosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_643418)
'autosomal recessive congenital ichthyosis 8' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_643418
http://purl.obolibrary.org/obo/MONDO_0013501
amyotrophic lateral sclerosis type 14
'amyotrophic lateral sclerosis type 14' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7415
'amyotrophic lateral sclerosis type 14' EquivalentTo 'amyotrophic lateral sclerosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7415)
http://purl.obolibrary.org/obo/MONDO_0013515
osteogenesis imperfecta type 6
'osteogenesis imperfecta type 6' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5176
'osteogenesis imperfecta type 6' EquivalentTo 'osteogenesis imperfecta' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5176)
http://purl.obolibrary.org/obo/MONDO_0013516
retinitis pigmentosa 60
'retinitis pigmentosa 60' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_24148)
'retinitis pigmentosa 60' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_24148
http://purl.obolibrary.org/obo/MONDO_0013514
hypotrichosis 3
'hypotrichosis 3' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_121391
'hypotrichosis 3' EquivalentTo 'hypotrichosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_121391)
http://purl.obolibrary.org/obo/MONDO_0013525
primary ciliary dyskinesia 16
'primary ciliary dyskinesia 16' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_83544
'primary ciliary dyskinesia 16' EquivalentTo 'primary ciliary dyskinesia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_83544)
http://purl.obolibrary.org/obo/MONDO_0013537
autosomal recessive nonsyndromic deafness 29
'autosomal recessive nonsyndromic deafness 29' EquivalentTo 'autosomal recessive nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_23562)
'autosomal recessive nonsyndromic deafness 29' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_23562
http://purl.obolibrary.org/obo/MONDO_0013541
complex cortical dysplasia with other brain malformations 1
'complex cortical dysplasia with other brain malformations 1' EquivalentTo 'complex cortical dysplasia with other brain malformations' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10381)
'complex cortical dysplasia with other brain malformations 1' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10381
http://purl.obolibrary.org/obo/MONDO_0013559
Hermansky-Pudlak syndrome 7
'Hermansky-Pudlak syndrome 7' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_84062
'Hermansky-Pudlak syndrome 7' EquivalentTo 'Hermansky-Pudlak syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_84062)
http://purl.obolibrary.org/obo/MONDO_0013553
immunodeficiency-centromeric instability-facial anomalies syndrome 2
'immunodeficiency-centromeric instability-facial anomalies syndrome 2' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9841
'immunodeficiency-centromeric instability-facial anomalies syndrome 2' EquivalentTo 'immunodeficiency-centromeric instability-facial anomalies syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9841)
http://purl.obolibrary.org/obo/MONDO_0013551
hereditary spastic paraplegia 47
'hereditary spastic paraplegia 47' EquivalentTo 'hereditary spastic paraplegia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10717)
'hereditary spastic paraplegia 47' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10717
http://purl.obolibrary.org/obo/MONDO_0013552
hereditary spastic paraplegia 52
'hereditary spastic paraplegia 52' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_11154
'hereditary spastic paraplegia 52' EquivalentTo 'hereditary spastic paraplegia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_11154)
http://purl.obolibrary.org/obo/MONDO_0013557
Hermansky-Pudlak syndrome 5
'Hermansky-Pudlak syndrome 5' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_11234
'Hermansky-Pudlak syndrome 5' EquivalentTo 'Hermansky-Pudlak syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_11234)
http://purl.obolibrary.org/obo/MONDO_0013558
Hermansky-Pudlak syndrome 6
'Hermansky-Pudlak syndrome 6' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_79803
'Hermansky-Pudlak syndrome 6' EquivalentTo 'Hermansky-Pudlak syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_79803)
http://purl.obolibrary.org/obo/MONDO_0013555
Hermansky-Pudlak syndrome 3
'Hermansky-Pudlak syndrome 3' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_84343
'Hermansky-Pudlak syndrome 3' EquivalentTo 'Hermansky-Pudlak syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_84343)
http://purl.obolibrary.org/obo/MONDO_0013556
Hermansky-Pudlak syndrome 4
'Hermansky-Pudlak syndrome 4' EquivalentTo 'Hermansky-Pudlak syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_89781)
'Hermansky-Pudlak syndrome 4' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_89781
http://purl.obolibrary.org/obo/MONDO_0013566
Fanconi anemia complementation group L
'Fanconi anemia complementation group L' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_55120
'Fanconi anemia complementation group L' EquivalentTo 'Fanconi anemia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_55120)
http://purl.obolibrary.org/obo/MONDO_0013567
atrial heart septal defect 3
'atrial heart septal defect 3' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4624
'atrial heart septal defect 3' EquivalentTo 'atrial heart septal defect' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4624)
http://purl.obolibrary.org/obo/MONDO_0013560
Hermansky-Pudlak syndrome 8
'Hermansky-Pudlak syndrome 8' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_388552
'Hermansky-Pudlak syndrome 8' EquivalentTo 'Hermansky-Pudlak syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_388552)
http://purl.obolibrary.org/obo/MONDO_0013589
focal segmental glomerulosclerosis 6
'focal segmental glomerulosclerosis 6' EquivalentTo 'focal segmental glomerulosclerosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4643)
'focal segmental glomerulosclerosis 6' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4643
http://purl.obolibrary.org/obo/MONDO_0013369
hypertrophic cardiomyopathy 7
'hypertrophic cardiomyopathy 7' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7137
'hypertrophic cardiomyopathy 7' EquivalentTo 'hypertrophic cardiomyopathy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7137)
http://purl.obolibrary.org/obo/MONDO_0013377
isolated microphthalmia 7
'isolated microphthalmia 7' EquivalentTo 'isolated microphthalmia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9573)
'isolated microphthalmia 7' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9573
http://purl.obolibrary.org/obo/MONDO_0013379
Noonan syndrome 7
'Noonan syndrome 7' EquivalentTo 'Noonan syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_673)
'Noonan syndrome 7' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_673
http://purl.obolibrary.org/obo/MONDO_0013370
long QT syndrome 6
'long QT syndrome 6' EquivalentTo 'long QT syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9992)
'long QT syndrome 6' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9992
http://purl.obolibrary.org/obo/MONDO_0013372
long QT syndrome 5
'long QT syndrome 5' EquivalentTo 'long QT syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3753)
'long QT syndrome 5' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3753
http://purl.obolibrary.org/obo/MONDO_0013386
autosomal recessive nonsyndromic deafness 74
'autosomal recessive nonsyndromic deafness 74' EquivalentTo 'autosomal recessive nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_253827)
'autosomal recessive nonsyndromic deafness 74' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_253827
http://purl.obolibrary.org/obo/MONDO_0013395
retinitis pigmentosa 4
'retinitis pigmentosa 4' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6010)
'retinitis pigmentosa 4' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6010
http://purl.obolibrary.org/obo/OMIM_601631
'anterior segment dysgenesis 3' EquivalentTo http://purl.obolibrary.org/obo/OMIM_601631
http://purl.obolibrary.org/obo/MONDO_0024456 EquivalentTo http://purl.obolibrary.org/obo/OMIM_601631
http://purl.obolibrary.org/obo/MONDO_0013407
retinitis pigmentosa 47
'retinitis pigmentosa 47' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6295)
'retinitis pigmentosa 47' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6295
http://purl.obolibrary.org/obo/MONDO_0013405
retinitis pigmentosa 49
'retinitis pigmentosa 49' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1259
'retinitis pigmentosa 49' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1259)
http://purl.obolibrary.org/obo/MONDO_0013401
hereditary spastic paraplegia 51
'hereditary spastic paraplegia 51' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_23431
'hereditary spastic paraplegia 51' EquivalentTo 'hereditary spastic paraplegia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_23431)
http://purl.obolibrary.org/obo/MONDO_0013402
retinitis pigmentosa 27
'retinitis pigmentosa 27' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4901
'retinitis pigmentosa 27' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4901)
http://purl.obolibrary.org/obo/MONDO_0013414
retinitis pigmentosa 44
'retinitis pigmentosa 44' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5995
'retinitis pigmentosa 44' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5995)
http://purl.obolibrary.org/obo/MONDO_0013412
hypertrophic cardiomyopathy 9
'hypertrophic cardiomyopathy 9' EquivalentTo 'hypertrophic cardiomyopathy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7273)
'hypertrophic cardiomyopathy 9' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7273
http://purl.obolibrary.org/obo/MONDO_0013413
retinitis pigmentosa 45
'retinitis pigmentosa 45' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1258)
'retinitis pigmentosa 45' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1258
http://purl.obolibrary.org/obo/MONDO_0013429
retinitis pigmentosa 40
'retinitis pigmentosa 40' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5158)
'retinitis pigmentosa 40' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5158
http://purl.obolibrary.org/obo/MONDO_0013425
retinitis pigmentosa 20
'retinitis pigmentosa 20' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6121
'retinitis pigmentosa 20' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6121)
http://purl.obolibrary.org/obo/MONDO_0013436
retinitis pigmentosa 39
'retinitis pigmentosa 39' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7399)
'retinitis pigmentosa 39' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7399
http://purl.obolibrary.org/obo/MONDO_0013437
retinitis pigmentosa 43
'retinitis pigmentosa 43' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5145)
'retinitis pigmentosa 43' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5145
http://purl.obolibrary.org/obo/MONDO_0013434
primary ciliary dyskinesia 14
'primary ciliary dyskinesia 14' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_339829
'primary ciliary dyskinesia 14' EquivalentTo 'primary ciliary dyskinesia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_339829)
http://purl.obolibrary.org/obo/MONDO_0013435
primary ciliary dyskinesia 15
'primary ciliary dyskinesia 15' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_55036
'primary ciliary dyskinesia 15' EquivalentTo 'primary ciliary dyskinesia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_55036)
http://purl.obolibrary.org/obo/MONDO_0013449
Leber congenital amaurosis 7
'Leber congenital amaurosis 7' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1406
'Leber congenital amaurosis 7' EquivalentTo 'Leber congenital amaurosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1406)
http://purl.obolibrary.org/obo/MONDO_0013447
retinitis pigmentosa 48
'retinitis pigmentosa 48' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2979)
'retinitis pigmentosa 48' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2979
http://purl.obolibrary.org/obo/MONDO_0013446
Leber congenital amaurosis 6
'Leber congenital amaurosis 6' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_57096
'Leber congenital amaurosis 6' EquivalentTo 'Leber congenital amaurosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_57096)
http://purl.obolibrary.org/obo/MONDO_0013454
Leber congenital amaurosis 11
'Leber congenital amaurosis 11' EquivalentTo 'Leber congenital amaurosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3614)
'Leber congenital amaurosis 11' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3614
http://purl.obolibrary.org/obo/MONDO_0013455
hypertrophic cardiomyopathy 16
'hypertrophic cardiomyopathy 16' EquivalentTo 'hypertrophic cardiomyopathy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_51778)
'hypertrophic cardiomyopathy 16' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_51778
http://purl.obolibrary.org/obo/MONDO_0013453
Leber congenital amaurosis 8
'Leber congenital amaurosis 8' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_23418
'Leber congenital amaurosis 8' EquivalentTo 'Leber congenital amaurosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_23418)
http://purl.obolibrary.org/obo/MONDO_0013459
osteogenesis imperfecta type 10
'osteogenesis imperfecta type 10' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_871
'osteogenesis imperfecta type 10' EquivalentTo 'osteogenesis imperfecta' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_871)
http://purl.obolibrary.org/obo/MONDO_0013457
Leber congenital amaurosis 15
'Leber congenital amaurosis 15' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7287
'Leber congenital amaurosis 15' EquivalentTo 'Leber congenital amaurosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7287)
http://purl.obolibrary.org/obo/MONDO_0013450
congenital stationary night blindness 1D
'congenital stationary night blindness 1D' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9187
'congenital stationary night blindness 1D' EquivalentTo 'congenital stationary night blindness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9187)
http://purl.obolibrary.org/obo/MONDO_0013465
achromatopsia 4
'achromatopsia 4' EquivalentTo 'achromatopsia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2780)
'achromatopsia 4' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2780
http://purl.obolibrary.org/obo/MONDO_0013463
dextro-looped transposition of the great arteries 3
'dextro-looped transposition of the great arteries 3' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2657
'dextro-looped transposition of the great arteries 3' EquivalentTo 'dextro-looped transposition of the great arteries' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2657)
http://purl.obolibrary.org/obo/MONDO_0013469
retinitis pigmentosa 38
'retinitis pigmentosa 38' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10461
'retinitis pigmentosa 38' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10461)
http://purl.obolibrary.org/obo/MONDO_0013468
retinitis pigmentosa 59
'retinitis pigmentosa 59' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_79947)
'retinitis pigmentosa 59' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_79947
http://purl.obolibrary.org/obo/MONDO_0013460
osteogenesis imperfecta type 12
'osteogenesis imperfecta type 12' EquivalentTo 'osteogenesis imperfecta' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_121340)
'osteogenesis imperfecta type 12' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_121340
http://purl.obolibrary.org/obo/MONDO_0013231
Leber congenital amaurosis 14
'Leber congenital amaurosis 14' EquivalentTo 'Leber congenital amaurosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9227)
'Leber congenital amaurosis 14' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9227
http://purl.obolibrary.org/obo/MONDO_0013244
brachydactyly type E2
'brachydactyly type E2' EquivalentTo 'brachydactyly type E' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5744)
'brachydactyly type E2' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5744
http://purl.obolibrary.org/obo/MONDO_0013249
autosomal recessive nonsyndromic deafness 84A
'autosomal recessive nonsyndromic deafness 84A' EquivalentTo 'autosomal recessive nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_374462)
'autosomal recessive nonsyndromic deafness 84A' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_374462
http://purl.obolibrary.org/obo/MONDO_0013248
Fanconi anemia complementation group O
'Fanconi anemia complementation group O' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5889
'Fanconi anemia complementation group O' EquivalentTo 'Fanconi anemia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5889)
http://purl.obolibrary.org/obo/MONDO_0013259
Oguchi disease-2
'Oguchi disease-2' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6011
'Oguchi disease-2' EquivalentTo 'Oguchi disease' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6011)
http://purl.obolibrary.org/obo/MONDO_0013269
autosomal recessive nonsyndromic deafness 91
'autosomal recessive nonsyndromic deafness 91' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5269
'autosomal recessive nonsyndromic deafness 91' EquivalentTo 'autosomal recessive nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5269)
http://purl.obolibrary.org/obo/MONDO_0013263
retinitis pigmentosa 54
'retinitis pigmentosa 54' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_388939
'retinitis pigmentosa 54' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_388939)
http://purl.obolibrary.org/obo/MONDO_0013264
amyotrophic lateral sclerosis type 12
'amyotrophic lateral sclerosis type 12' EquivalentTo 'amyotrophic lateral sclerosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10133)
'amyotrophic lateral sclerosis type 12' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10133
http://purl.obolibrary.org/obo/MONDO_0013279
long QT syndrome 13
'long QT syndrome 13' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3762
'long QT syndrome 13' EquivalentTo 'long QT syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3762)
http://purl.obolibrary.org/obo/MONDO_0013274
retinitis pigmentosa 51
'retinitis pigmentosa 51' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_123016)
'retinitis pigmentosa 51' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_123016
http://purl.obolibrary.org/obo/MONDO_0013293
isolated microphthalmia 6
'isolated microphthalmia 6' EquivalentTo 'isolated microphthalmia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_646960)
'isolated microphthalmia 6' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_646960
http://purl.obolibrary.org/obo/MONDO_0003912
malignant ciliary body melanoma
'malignant ciliary body melanoma' SubClassOf 'iris melanoma'
'malignant ciliary body melanoma' SubClassOf 'iris melanoma'
http://purl.obolibrary.org/obo/MONDO_0013312
retinitis pigmentosa 55
'retinitis pigmentosa 55' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_84100)
'retinitis pigmentosa 55' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_84100
http://purl.obolibrary.org/obo/MONDO_0013315
retinitis pigmentosa 57
'retinitis pigmentosa 57' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5148
'retinitis pigmentosa 57' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5148)
http://purl.obolibrary.org/obo/MONDO_0013314
retinitis pigmentosa 56
'retinitis pigmentosa 56' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_50939
'retinitis pigmentosa 56' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_50939)
http://purl.obolibrary.org/obo/MONDO_0013328
retinitis pigmentosa 58
'retinitis pigmentosa 58' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_130557)
'retinitis pigmentosa 58' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_130557
http://purl.obolibrary.org/obo/MONDO_0013338
Charcot-Marie-tooth disease recessive intermediate b
'Charcot-Marie-tooth disease recessive intermediate b' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3735
'Charcot-Marie-tooth disease recessive intermediate b' EquivalentTo 'Charcot-Marie-tooth disease' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3735)
http://purl.obolibrary.org/obo/MONDO_0013348
cone-rod dystrophy 15
'cone-rod dystrophy 15' EquivalentTo 'cone-rod dystrophy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_92211)
'cone-rod dystrophy 15' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_92211
http://purl.obolibrary.org/obo/MONDO_0013341
methylmalonic acidemia due to transcobalamin receptor defect
'methylmalonic acidemia due to transcobalamin receptor defect' EquivalentTo 'methylmalonic acidemia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_51293)
'methylmalonic acidemia due to transcobalamin receptor defect' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_51293
http://purl.obolibrary.org/obo/MONDO_0013119
autosomal recessive nonsyndromic deafness 77
'autosomal recessive nonsyndromic deafness 77' EquivalentTo 'autosomal recessive nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_125336)
'autosomal recessive nonsyndromic deafness 77' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_125336
http://purl.obolibrary.org/obo/MONDO_0013114
autosomal dominant nonsyndromic deafness 50
'autosomal dominant nonsyndromic deafness 50' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_407053
'autosomal dominant nonsyndromic deafness 50' EquivalentTo 'autosomal dominant nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_407053)
http://purl.obolibrary.org/obo/MESH_C535535
http://purl.obolibrary.org/obo/MESH_C535535 EquivalentTo 'anterior segment dysgenesis 3'
http://purl.obolibrary.org/obo/MESH_C535535 EquivalentTo http://purl.obolibrary.org/obo/MONDO_0024456
http://purl.obolibrary.org/obo/MONDO_0013123
atrial heart septal defect 6
'atrial heart septal defect 6' EquivalentTo 'atrial heart septal defect' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7092)
'atrial heart septal defect 6' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7092
http://purl.obolibrary.org/obo/MONDO_0013130
isolated microphthalmia 4
'isolated microphthalmia 4' EquivalentTo 'isolated microphthalmia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_392255)
'isolated microphthalmia 4' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_392255
http://purl.obolibrary.org/obo/MONDO_0013146
Brugada syndrome 7
'Brugada syndrome 7' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_55800
'Brugada syndrome 7' EquivalentTo 'Brugada syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_55800)
http://purl.obolibrary.org/obo/MONDO_0013145
Brugada syndrome 6
'Brugada syndrome 6' EquivalentTo 'Brugada syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10008)
'Brugada syndrome 6' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10008
http://purl.obolibrary.org/obo/MONDO_0013148
Brugada syndrome 8
'Brugada syndrome 8' EquivalentTo 'Brugada syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10021)
'Brugada syndrome 8' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10021
http://purl.obolibrary.org/obo/MONDO_0013141
autosomal dominant macrothrombocytopenia TUBB1-related
'autosomal dominant macrothrombocytopenia TUBB1-related' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_81027
'autosomal dominant macrothrombocytopenia TUBB1-related' EquivalentTo 'autosomal dominant macrothrombocytopenia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_81027)
http://purl.obolibrary.org/obo/MONDO_0013153
inflammatory bowel disease 28
'inflammatory bowel disease 28' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3587
'inflammatory bowel disease 28' EquivalentTo 'inflammatory bowel disease' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3587)
http://purl.obolibrary.org/obo/MONDO_0013177
congenital muscular dystrophy due to integrin alpha-7 deficiency
'congenital muscular dystrophy due to integrin alpha-7 deficiency' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3679
'congenital muscular dystrophy due to integrin alpha-7 deficiency' EquivalentTo 'congenital muscular dystrophy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3679)
http://purl.obolibrary.org/obo/MONDO_0013178
congenital muscular dystrophy due to LMNA mutation
'congenital muscular dystrophy due to LMNA mutation' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4000
'congenital muscular dystrophy due to LMNA mutation' EquivalentTo 'congenital muscular dystrophy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4000)
http://purl.obolibrary.org/obo/MONDO_0013175
retinitis pigmentosa 50
'retinitis pigmentosa 50' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7439)
'retinitis pigmentosa 50' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7439
http://purl.obolibrary.org/obo/MONDO_0013174
primary ciliary dyskinesia 13
'primary ciliary dyskinesia 13' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_123872
'primary ciliary dyskinesia 13' EquivalentTo 'primary ciliary dyskinesia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_123872)
http://purl.obolibrary.org/obo/MONDO_0013183
congenital stationary night blindness 1C
'congenital stationary night blindness 1C' EquivalentTo 'congenital stationary night blindness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4308)
'congenital stationary night blindness 1C' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4308
http://purl.obolibrary.org/obo/MONDO_0013181
amelogenesis imperfecta hypomaturation type 2A3
'amelogenesis imperfecta hypomaturation type 2A3' EquivalentTo 'amelogenesis imperfecta' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_256764)
'amelogenesis imperfecta hypomaturation type 2A3' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_256764
http://purl.obolibrary.org/obo/MONDO_0013191
focal segmental glomerulosclerosis 5
'focal segmental glomerulosclerosis 5' EquivalentTo 'focal segmental glomerulosclerosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_64423)
'focal segmental glomerulosclerosis 5' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_64423
http://purl.obolibrary.org/obo/MONDO_0013197
hypertrophic cardiomyopathy 14
'hypertrophic cardiomyopathy 14' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4624
'hypertrophic cardiomyopathy 14' EquivalentTo 'hypertrophic cardiomyopathy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4624)
http://purl.obolibrary.org/obo/MONDO_0013195
hypertrophic cardiomyopathy 13
'hypertrophic cardiomyopathy 13' EquivalentTo 'hypertrophic cardiomyopathy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7134)
'hypertrophic cardiomyopathy 13' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7134
http://purl.obolibrary.org/obo/OMIM_180700
'autosomal dominant Robinow syndrome 1' EquivalentTo http://purl.obolibrary.org/obo/OMIM_180700
http://purl.obolibrary.org/obo/MONDO_0024455 EquivalentTo http://purl.obolibrary.org/obo/OMIM_180700
http://purl.obolibrary.org/obo/MONDO_0013200
hypertrophic cardiomyopathy 15
'hypertrophic cardiomyopathy 15' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7414
'hypertrophic cardiomyopathy 15' EquivalentTo 'hypertrophic cardiomyopathy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7414)
http://purl.obolibrary.org/obo/MONDO_0013210
autosomal recessive nonsyndromic deafness 25
'autosomal recessive nonsyndromic deafness 25' EquivalentTo 'autosomal recessive nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_389207)
'autosomal recessive nonsyndromic deafness 25' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_389207
http://purl.obolibrary.org/obo/MONDO_0013215
autosomal recessive nonsyndromic deafness 79
'autosomal recessive nonsyndromic deafness 79' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_286262
'autosomal recessive nonsyndromic deafness 79' EquivalentTo 'autosomal recessive nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_286262)
http://purl.obolibrary.org/obo/MONDO_0013220
hemochromatosis type 2B
'hemochromatosis type 2B' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_57817
'hemochromatosis type 2B' EquivalentTo 'hemochromatosis type 2' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_57817)
http://purl.obolibrary.org/obo/MONDO_0008538
temporal arteritis
'temporal arteritis' SubClassOf 'inflammatory disease'
http://purl.obolibrary.org/obo/MONDO_0008437
hereditary spastic paraplegia 3A
'hereditary spastic paraplegia 3A' EquivalentTo 'hereditary spastic paraplegia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_51062)
'hereditary spastic paraplegia 3A' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_51062
http://purl.obolibrary.org/obo/MONDO_0008447
hereditary spherocytosis type 1
'hereditary spherocytosis type 1' EquivalentTo 'hereditary spherocytosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_286)
'hereditary spherocytosis type 1' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_286
http://purl.obolibrary.org/obo/MONDO_0008379
retinitis pigmentosa 10
'retinitis pigmentosa 10' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3614
'retinitis pigmentosa 10' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3614)
http://purl.obolibrary.org/obo/MONDO_0008378
retinitis pigmentosa 9
'retinitis pigmentosa 9' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6100
'retinitis pigmentosa 9' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6100)
http://purl.obolibrary.org/obo/MONDO_0008377
retinitis pigmentosa 1
'retinitis pigmentosa 1' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6101)
'retinitis pigmentosa 1' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6101
http://purl.obolibrary.org/obo/MONDO_0008389
autosomal dominant Robinow syndrome 1
http://purl.obolibrary.org/obo/DOID_0060766 EquivalentTo 'autosomal dominant Robinow syndrome 1'
'autosomal dominant Robinow syndrome 1' EquivalentTo http://purl.obolibrary.org/obo/OMIM_180700
http://purl.obolibrary.org/obo/NCIT_C4392
'multiple symmetrical lipomatosis' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C4392
'multiple symmetric lipomatosis' EquivalentTo http://purl.obolibrary.org/obo/NCIT_C4392
http://purl.obolibrary.org/obo/MONDO_0008204
patella aplasia, coxa vara, and tarsal synostosis
'patella aplasia, coxa vara, and tarsal synostosis' SubClassOf 'Coxopodopatellar syndrome'
'patella aplasia, coxa vara, and tarsal synostosis' SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/MONDO_0008200
autosomal dominant Parkinson disease 1
'autosomal dominant Parkinson disease 1' SubClassOf 'hereditary late onset Parkinson disease'
'autosomal dominant Parkinson disease 1' SubClassOf 'hereditary late onset Parkinson disease'
http://purl.obolibrary.org/obo/MONDO_0008210
patterned macular dystrophy 1
'patterned macular dystrophy 1' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5961
'patterned macular dystrophy 1' EquivalentTo 'patterned macular dystrophy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5961)
http://purl.obolibrary.org/obo/MONDO_0008029
Bethlem myopathy
'Bethlem myopathy' SubClassOf 'contracture'
http://purl.obolibrary.org/obo/MONDO_0008070
nemaline myopathy 3
http://purl.obolibrary.org/obo/MESH_C580202 EquivalentTo 'nemaline myopathy 3'
http://purl.obolibrary.org/obo/MONDO_0008087
hereditary neuropathy with liability to pressure palsies
http://purl.obolibrary.org/obo/MESH_C536965 EquivalentTo 'hereditary neuropathy with liability to pressure palsies'
http://purl.obolibrary.org/obo/MONDO_0008099
congenital stationary night blindness autosomal dominant 2
'congenital stationary night blindness autosomal dominant 2' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5158
'congenital stationary night blindness autosomal dominant 2' EquivalentTo 'congenital stationary night blindness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5158)
http://purl.obolibrary.org/obo/MONDO_0018756
euthyroid Graves orbitopathy
'euthyroid Graves orbitopathy' SubClassOf 'disease arises from feature' some 'Graves disease'
http://purl.obolibrary.org/obo/MONDO_0018642
NIK deficiency
'NIK deficiency' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0004313
'NIK deficiency' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9020
'NIK deficiency' SubClassOf 'disease caused by disruption of' some http://purl.obolibrary.org/obo/GO_0007249
'NIK deficiency' EquivalentTo 'non-severe combined immunodeficiency' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9020)
'NIK deficiency' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0010976
http://purl.obolibrary.org/obo/MONDO_0018656
tremor-ataxia-central hypomyelination syndrome
'tremor-ataxia-central hypomyelination syndrome' SubClassOf 'hypomyelinating leukodystrophy 7 with or without oligodontia and-or hypogonadotropic hypogonadism'
http://purl.obolibrary.org/obo/MONDO_0018655
hypomyelination-cerebellar atrophy-hypoplasia of the corpus callosum syndrome
'hypomyelination-cerebellar atrophy-hypoplasia of the corpus callosum syndrome' SubClassOf 'hypomyelinating leukodystrophy 7 with or without oligodontia and-or hypogonadotropic hypogonadism'
http://purl.obolibrary.org/obo/MONDO_0018661
Zika virus disease
'Zika virus disease' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0000509
'Zika virus disease' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_64320
'Zika virus disease' SubClassOf 'disease has feature' some 'conjunctivitis (disease)'
'Zika virus disease' SubClassOf 'Flaviviridae infectious disease'
'Zika virus disease' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002315
http://purl.obolibrary.org/obo/MONDO_0008903
lung cancer
'lung cancer' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0030828
'lung cancer' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0012735
http://purl.obolibrary.org/obo/MONDO_0008944
Joubert syndrome 1
'Joubert syndrome 1' EquivalentTo 'Joubert syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_56623)
'Joubert syndrome 1' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_56623
http://purl.obolibrary.org/obo/MONDO_0008962
Griscelli syndrome type 1
'Griscelli syndrome type 1' EquivalentTo 'Griscelli syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4644)
'Griscelli syndrome type 1' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4644
http://purl.obolibrary.org/obo/MONDO_0018307
neurodegeneration with brain iron accumulation
'neurodegeneration with brain iron accumulation' SubClassOf 'metabolic disease with dementia'
'neurodegeneration with brain iron accumulation' SubClassOf 'iron metabolism disease'
'neurodegeneration with brain iron accumulation' SubClassOf 'neuroaxonal dystrophy'
http://purl.obolibrary.org/obo/MESH_C538421 EquivalentTo 'neurodegeneration with brain iron accumulation'
'neurodegeneration with brain iron accumulation' SubClassOf 'inherited neurodegenerative disorder'
http://purl.obolibrary.org/obo/MONDO_0008854
Bardet-Biedl syndrome 1
'Bardet-Biedl syndrome 1' SubClassOf 'Bardet-Biedl syndrome'
'Bardet-Biedl syndrome 1' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_8195
'Bardet-Biedl syndrome 1' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_582
'Bardet-Biedl syndrome 1' EquivalentTo 'Bardet-Biedl syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10806) and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_582) and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_585) and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_79140) and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_8195) and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_84100) and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_91147)
'Bardet-Biedl syndrome 1' SubClassOf 'retinitis pigmentosa 55'
'Bardet-Biedl syndrome 1' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10806
'Bardet-Biedl syndrome 1' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_91147
'Bardet-Biedl syndrome 1' SubClassOf 'Bardet-Biedl syndrome 16'
'Bardet-Biedl syndrome 1' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_84100
'Bardet-Biedl syndrome 1' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_79140
'Bardet-Biedl syndrome 1' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_585
http://purl.obolibrary.org/obo/MONDO_0008871
microcephalic osteodysplastic primordial dwarfism type i
'microcephalic osteodysplastic primordial dwarfism type i' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_100151683
'microcephalic osteodysplastic primordial dwarfism type i' EquivalentTo 'microcephalic osteodysplastic primordial dwarfism' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_100151683)
http://purl.obolibrary.org/obo/MONDO_0008713
acrodermatitis enteropathica
'acrodermatitis enteropathica' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0000534
http://purl.obolibrary.org/obo/MONDO_0008748
Hermansky-Pudlak syndrome 1
'Hermansky-Pudlak syndrome 1' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3257
'Hermansky-Pudlak syndrome 1' EquivalentTo 'Hermansky-Pudlak syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3257)
http://purl.obolibrary.org/obo/MONDO_0008768
neuronal ceroid lipofuscinosis 4A
'neuronal ceroid lipofuscinosis 4A' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_54982
'neuronal ceroid lipofuscinosis 4A' EquivalentTo 'neuronal ceroid lipofuscinosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_54982)
http://purl.obolibrary.org/obo/MONDO_0008765
Leber congenital amaurosis 2
'Leber congenital amaurosis 2' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6121
'Leber congenital amaurosis 2' EquivalentTo 'Leber congenital amaurosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6121)
http://purl.obolibrary.org/obo/MONDO_0008764
Leber congenital amaurosis 1
'Leber congenital amaurosis 1' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3000
'Leber congenital amaurosis 1' EquivalentTo 'Leber congenital amaurosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3000)
http://purl.obolibrary.org/obo/MONDO_0008772
amelogenesis imperfecta type 2A1
'amelogenesis imperfecta type 2A1' EquivalentTo 'amelogenesis imperfecta' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9622)
'amelogenesis imperfecta type 2A1' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9622
http://linkedlifedata.com/resource/umls/id/C0751762
http://linkedlifedata.com/resource/umls/id/C0751762 EquivalentTo 'central sleep apnea syndrome'
http://linkedlifedata.com/resource/umls/id/C0751762 EquivalentTo 'primary central sleep apnea syndrome'
http://purl.obolibrary.org/obo/MONDO_0008647
hypertrophic cardiomyopathy 1
'hypertrophic cardiomyopathy 1' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_859
'hypertrophic cardiomyopathy 1' EquivalentTo 'hypertrophic cardiomyopathy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4624) and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4625) and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_85366) and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_859)
'hypertrophic cardiomyopathy 1' SubClassOf 'hypertrophic cardiomyopathy 14'
'hypertrophic cardiomyopathy 1' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_85366
'hypertrophic cardiomyopathy 1' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4625
'hypertrophic cardiomyopathy 1' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4624
http://purl.obolibrary.org/obo/MONDO_0008678
Williams syndrome
'Williams syndrome' SubClassOf 'disease has feature' some 'supravalvular aortic stenosis (disease)'
'Williams syndrome' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0004381
http://purl.obolibrary.org/obo/MONDO_0018076
tuberculosis
'tuberculosis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_1773
'tuberculosis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_1773
http://purl.obolibrary.org/obo/MONDO_0018077
tularemia
'tularemia' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_263
'tularemia' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_263
http://purl.obolibrary.org/obo/MONDO_0014323
retinitis pigmentosa 68
'retinitis pigmentosa 68' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_57709)
'retinitis pigmentosa 68' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_57709
http://purl.obolibrary.org/obo/MONDO_0014326
nemaline myopathy 9
'nemaline myopathy 9' EquivalentTo 'nemaline myopathy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10324)
'nemaline myopathy 9' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10324
http://purl.obolibrary.org/obo/MONDO_0014337
complex cortical dysplasia with other brain malformations 5
'complex cortical dysplasia with other brain malformations 5' EquivalentTo 'complex cortical dysplasia with other brain malformations' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7280)
'complex cortical dysplasia with other brain malformations 5' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7280
http://purl.obolibrary.org/obo/MONDO_0014345
retinitis pigmentosa 69
'retinitis pigmentosa 69' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_55857
'retinitis pigmentosa 69' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_55857)
http://purl.obolibrary.org/obo/MONDO_0014341
complex cortical dysplasia with other brain malformations 6
'complex cortical dysplasia with other brain malformations 6' EquivalentTo 'complex cortical dysplasia with other brain malformations' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_203068)
'complex cortical dysplasia with other brain malformations 6' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_203068
http://purl.obolibrary.org/obo/MONDO_0014352
abdominal obesity-metabolic syndrome 3
'abdominal obesity-metabolic syndrome 3' EquivalentTo 'metabolic syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9149)
'abdominal obesity-metabolic syndrome 3' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9149
http://purl.obolibrary.org/obo/MONDO_0014363
autosomal recessive nonsyndromic deafness 101
'autosomal recessive nonsyndromic deafness 101' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_643226
'autosomal recessive nonsyndromic deafness 101' EquivalentTo 'autosomal recessive nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_643226)
http://purl.obolibrary.org/obo/MONDO_0014378
primary ciliary dyskinesia 29
'primary ciliary dyskinesia 29' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10309
'primary ciliary dyskinesia 29' EquivalentTo 'primary ciliary dyskinesia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10309)
http://purl.obolibrary.org/obo/MONDO_0014375
congenital diarrhea 7 with exudative enteropathy
'congenital diarrhea 7 with exudative enteropathy' EquivalentTo 'congenital diarrhea' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_8694)
'congenital diarrhea 7 with exudative enteropathy' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_8694
http://purl.obolibrary.org/obo/MONDO_0014372
cone-rod dystrophy 19
'cone-rod dystrophy 19' EquivalentTo 'cone-rod dystrophy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_23093)
'cone-rod dystrophy 19' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_23093
http://purl.obolibrary.org/obo/MONDO_0014385
amelogenesis imperfecta hypomaturation type 2A5
'amelogenesis imperfecta hypomaturation type 2A5' EquivalentTo 'amelogenesis imperfecta' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_123041)
'amelogenesis imperfecta hypomaturation type 2A5' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_123041
http://purl.obolibrary.org/obo/MONDO_0014384
hypotrichosis 12
'hypotrichosis 12' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6144
'hypotrichosis 12' EquivalentTo 'hypotrichosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6144)
http://purl.obolibrary.org/obo/MONDO_0014390
hypotrichosis 13
'hypotrichosis 13' EquivalentTo 'hypotrichosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_112802)
'hypotrichosis 13' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_112802
http://purl.obolibrary.org/obo/MONDO_0014400
retinitis pigmentosa 70
'retinitis pigmentosa 70' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9128
'retinitis pigmentosa 70' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9128)
http://purl.obolibrary.org/obo/SCTID_238902007
'multiple symmetrical lipomatosis' EquivalentTo http://purl.obolibrary.org/obo/SCTID_238902007
'multiple symmetric lipomatosis' EquivalentTo http://purl.obolibrary.org/obo/SCTID_238902007
http://purl.obolibrary.org/obo/MONDO_0014428
autosomal recessive nonsyndromic deafness 102
'autosomal recessive nonsyndromic deafness 102' EquivalentTo 'autosomal recessive nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2059)
'autosomal recessive nonsyndromic deafness 102' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2059
http://purl.obolibrary.org/obo/MONDO_0014427
cone-rod dystrophy 20
'cone-rod dystrophy 20' EquivalentTo 'cone-rod dystrophy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_282809)
'cone-rod dystrophy 20' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_282809
http://purl.obolibrary.org/obo/MONDO_0014439
Bardet-Biedl syndrome 11
'Bardet-Biedl syndrome 11' EquivalentTo 'Bardet-Biedl syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_22954)
'Bardet-Biedl syndrome 11' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_22954
http://purl.obolibrary.org/obo/MONDO_0014432
Bardet-Biedl syndrome 2
'Bardet-Biedl syndrome 2' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_583
'Bardet-Biedl syndrome 2' EquivalentTo 'Bardet-Biedl syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_583)
'Bardet-Biedl syndrome 2' SubClassOf 'retinitis pigmentosa 74'
http://purl.obolibrary.org/obo/MONDO_0014438
Bardet-Biedl syndrome 10
'Bardet-Biedl syndrome 10' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_79738
'Bardet-Biedl syndrome 10' EquivalentTo 'Bardet-Biedl syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_79738)
http://purl.obolibrary.org/obo/MONDO_0014208
Charcot-Marie-tooth disease type 2R
'Charcot-Marie-tooth disease type 2R' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_23321
'Charcot-Marie-tooth disease type 2R' EquivalentTo 'Charcot-Marie-tooth disease type 2' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_23321)
http://purl.obolibrary.org/obo/MONDO_0014203
primary ciliary dyskinesia 25
'primary ciliary dyskinesia 25' EquivalentTo 'primary ciliary dyskinesia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_161582)
'primary ciliary dyskinesia 25' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_161582
http://purl.obolibrary.org/obo/MONDO_0014202
primary ciliary dyskinesia 24
'primary ciliary dyskinesia 24' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_89765
'primary ciliary dyskinesia 24' EquivalentTo 'primary ciliary dyskinesia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_89765)
http://purl.obolibrary.org/obo/MONDO_0014211
primary ciliary dyskinesia 26
'primary ciliary dyskinesia 26' EquivalentTo 'primary ciliary dyskinesia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_56683)
'primary ciliary dyskinesia 26' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_56683
http://purl.obolibrary.org/obo/MONDO_0014216
primary ciliary dyskinesia 28
'primary ciliary dyskinesia 28' EquivalentTo 'primary ciliary dyskinesia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6674)
'primary ciliary dyskinesia 28' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6674
http://purl.obolibrary.org/obo/MONDO_0014215
primary ciliary dyskinesia 27
'primary ciliary dyskinesia 27' EquivalentTo 'primary ciliary dyskinesia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_85478)
'primary ciliary dyskinesia 27' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_85478
http://purl.obolibrary.org/obo/MONDO_0014223
amyotrophic lateral sclerosis type 19
'amyotrophic lateral sclerosis type 19' EquivalentTo 'amyotrophic lateral sclerosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2066)
'amyotrophic lateral sclerosis type 19' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2066
http://purl.obolibrary.org/obo/MONDO_0014233
early-onset Parkinson disease 20
'early-onset Parkinson disease 20' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_8867
'early-onset Parkinson disease 20' EquivalentTo 'Parkinson disease' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_8867)
http://purl.obolibrary.org/obo/MONDO_0014237
autosomal recessive nonsyndromic deafness 76
'autosomal recessive nonsyndromic deafness 76' EquivalentTo 'autosomal recessive nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_163183)
'autosomal recessive nonsyndromic deafness 76' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_163183
http://purl.obolibrary.org/obo/MONDO_0014231
juvenile onset Parkinson disease 19A
'juvenile onset Parkinson disease 19A' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9829
'juvenile onset Parkinson disease 19A' EquivalentTo 'Parkinson disease' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9829)
http://purl.obolibrary.org/obo/MONDO_0014256
retinitis pigmentosa 67
'retinitis pigmentosa 67' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4751
'retinitis pigmentosa 67' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4751)
http://purl.obolibrary.org/obo/MONDO_0014252
familial hypobetalipoproteinemia 1
'familial hypobetalipoproteinemia 1' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_338
'familial hypobetalipoproteinemia 1' EquivalentTo 'hypobetalipoproteinemia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_338)
http://purl.obolibrary.org/obo/MONDO_0014288
Joubert syndrome 21
'Joubert syndrome 21' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_79848
'Joubert syndrome 21' EquivalentTo 'Joubert syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_79848)
http://purl.obolibrary.org/obo/MONDO_0014283
autosomal dominant nonsyndromic deafness 56
'autosomal dominant nonsyndromic deafness 56' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3371
'autosomal dominant nonsyndromic deafness 56' EquivalentTo 'autosomal dominant nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3371)
http://purl.obolibrary.org/obo/MONDO_0014297
Joubert syndrome 22
'Joubert syndrome 22' EquivalentTo 'Joubert syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5147)
'Joubert syndrome 22' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5147
http://purl.obolibrary.org/obo/MONDO_0014296
Warburg micro syndrome 4
'Warburg micro syndrome 4' EquivalentTo 'Warburg micro syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_128637)
'Warburg micro syndrome 4' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_128637
http://purl.obolibrary.org/obo/MONDO_0004967
acute lymphoblastic leukemia (disease)
'acute lymphoblastic leukemia (disease)' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002027
http://purl.obolibrary.org/obo/MONDO_0004985
bipolar disorder
'bipolar disorder' SubClassOf 'disease has feature' some 'recurrent hypersomnia'
http://purl.obolibrary.org/obo/MONDO_0004767
vesiculitis
'vesiculitis' SubClassOf 'testicular disease'
'vesiculitis' SubClassOf 'inflammatory disease'
'vesiculitis' SubClassOf 'orchitis (disease)'
http://purl.obolibrary.org/obo/MONDO_0004774
gonococcal iridocyclitis
'gonococcal iridocyclitis' SubClassOf 'gonorrhea'
'gonococcal iridocyclitis' SubClassOf 'iridocyclitis (disease)'
'gonococcal iridocyclitis' SubClassOf 'rare bacterial infectious disease'
'gonococcal iridocyclitis' SubClassOf 'infectious disease of the nervous system'
'gonococcal iridocyclitis' SubClassOf 'infectious anterior uveitis'
'gonococcal iridocyclitis' SubClassOf 'gonococcal endophthalmia'
http://purl.obolibrary.org/obo/MONDO_0014103
hypogonadotropic hypogonadism 18 with or without anosmia
'hypogonadotropic hypogonadism 18 with or without anosmia' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_54756
'hypogonadotropic hypogonadism 18 with or without anosmia' EquivalentTo 'hypogonadotropic hypogonadism' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_54756)
http://purl.obolibrary.org/obo/MONDO_0014102
hypogonadotropic hypogonadism 17 with or without anosmia
'hypogonadotropic hypogonadism 17 with or without anosmia' EquivalentTo 'hypogonadotropic hypogonadism' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_81848)
'hypogonadotropic hypogonadism 17 with or without anosmia' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_81848
http://purl.obolibrary.org/obo/MONDO_0014108
Fanconi anemia complementation group Q
'Fanconi anemia complementation group Q' EquivalentTo 'Fanconi anemia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2072)
'Fanconi anemia complementation group Q' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2072
http://purl.obolibrary.org/obo/MONDO_0014107
hypogonadotropic hypogonadism 21 with or without anosmia
'hypogonadotropic hypogonadism 21 with or without anosmia' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_23767
'hypogonadotropic hypogonadism 21 with or without anosmia' EquivalentTo 'hypogonadotropic hypogonadism' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_23767)
http://purl.obolibrary.org/obo/MONDO_0014106
hypogonadotropic hypogonadism 20 with or without anosmia
'hypogonadotropic hypogonadism 20 with or without anosmia' EquivalentTo 'hypogonadotropic hypogonadism' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_8822)
'hypogonadotropic hypogonadism 20 with or without anosmia' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_8822
http://purl.obolibrary.org/obo/MONDO_0014105
hypogonadotropic hypogonadism 19 with or without anosmia
'hypogonadotropic hypogonadism 19 with or without anosmia' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1848
'hypogonadotropic hypogonadism 19 with or without anosmia' EquivalentTo 'hypogonadotropic hypogonadism' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1848)
http://purl.obolibrary.org/obo/MONDO_0014100
dilated cardiomyopathy 1KK
'dilated cardiomyopathy 1KK' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_84665
'dilated cardiomyopathy 1KK' EquivalentTo 'dilated cardiomyopathy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_84665)
http://purl.obolibrary.org/obo/MONDO_0004796
infectious meningitis
'infectious meningitis' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002315
http://purl.obolibrary.org/obo/MONDO_0014116
complex cortical dysplasia with other brain malformations 2
'complex cortical dysplasia with other brain malformations 2' EquivalentTo 'complex cortical dysplasia with other brain malformations' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3800)
'complex cortical dysplasia with other brain malformations 2' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3800
http://purl.obolibrary.org/obo/MONDO_0014123
primary ciliary dyskinesia 21
'primary ciliary dyskinesia 21' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_92749
'primary ciliary dyskinesia 21' EquivalentTo 'primary ciliary dyskinesia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_92749)
http://purl.obolibrary.org/obo/MONDO_0014147
neuronal ceroid lipofuscinosis 13
'neuronal ceroid lipofuscinosis 13' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_8722
'neuronal ceroid lipofuscinosis 13' EquivalentTo 'neuronal ceroid lipofuscinosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_8722)
http://purl.obolibrary.org/obo/MONDO_0014145
Leber congenital amaurosis 17
'Leber congenital amaurosis 17' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_392255
'Leber congenital amaurosis 17' EquivalentTo 'Leber congenital amaurosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_392255)
http://purl.obolibrary.org/obo/MONDO_0014143
Noonan syndrome 8
'Noonan syndrome 8' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6016
'Noonan syndrome 8' EquivalentTo 'Noonan syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6016)
http://purl.obolibrary.org/obo/MONDO_0014154
Charcot-Marie-tooth disease recessive intermediate c
'Charcot-Marie-tooth disease recessive intermediate c' EquivalentTo 'Charcot-Marie-tooth disease' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_57449)
'Charcot-Marie-tooth disease recessive intermediate c' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_57449
http://purl.obolibrary.org/obo/MONDO_0014153
cone-rod dystrophy 18
'cone-rod dystrophy 18' EquivalentTo 'cone-rod dystrophy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9364)
'cone-rod dystrophy 18' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9364
http://purl.obolibrary.org/obo/ENVO_02000099
http://purl.obolibrary.org/obo/ENVO_02000099 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/ENVO_02000099 SubClassOf http://purl.obolibrary.org/obo/ENVO_00002008
http://purl.obolibrary.org/obo/MONDO_0014171
complex cortical dysplasia with other brain malformations 4
'complex cortical dysplasia with other brain malformations 4' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7283
'complex cortical dysplasia with other brain malformations 4' EquivalentTo 'complex cortical dysplasia with other brain malformations' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7283)
http://purl.obolibrary.org/obo/MONDO_0014170
complex cortical dysplasia with other brain malformations 3
'complex cortical dysplasia with other brain malformations 3' EquivalentTo 'complex cortical dysplasia with other brain malformations' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3796)
'complex cortical dysplasia with other brain malformations 3' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3796
http://purl.obolibrary.org/obo/MONDO_0014191
catecholaminergic polymorphic ventricular tachycardia 5
'catecholaminergic polymorphic ventricular tachycardia 5' EquivalentTo 'catecholaminergic polymorphic ventricular tachycardia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10345)
'catecholaminergic polymorphic ventricular tachycardia 5' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10345
http://purl.obolibrary.org/obo/MONDO_0014182
autosomal recessive nonsyndromic deafness 88
'autosomal recessive nonsyndromic deafness 88' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_84173
'autosomal recessive nonsyndromic deafness 88' EquivalentTo 'autosomal recessive nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_84173)
http://purl.obolibrary.org/obo/MONDO_0014181
amyotrophic lateral sclerosis type 20
'amyotrophic lateral sclerosis type 20' EquivalentTo 'amyotrophic lateral sclerosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3178)
'amyotrophic lateral sclerosis type 20' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3178
http://purl.obolibrary.org/obo/MONDO_0014186
retinitis pigmentosa with or without situs inversus
'retinitis pigmentosa with or without situs inversus' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_23568
'retinitis pigmentosa with or without situs inversus' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_23568)
http://purl.obolibrary.org/obo/MONDO_0014193
primary ciliary dyskinesia 23
'primary ciliary dyskinesia 23' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_55130
'primary ciliary dyskinesia 23' EquivalentTo 'primary ciliary dyskinesia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_55130)
http://purl.obolibrary.org/obo/MONDO_0014192
primary ciliary dyskinesia 22
'primary ciliary dyskinesia 22' EquivalentTo 'primary ciliary dyskinesia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_51364)
'primary ciliary dyskinesia 22' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_51364
http://purl.obolibrary.org/obo/MONDO_0004852
gonococcal keratitis
'gonococcal keratitis' SubClassOf 'rare eye disease'
'gonococcal keratitis' SubClassOf 'rare bacterial infectious disease'
'gonococcal keratitis' SubClassOf 'gonorrhea'
'gonococcal keratitis' SubClassOf 'infectious disease of the nervous system'
'gonococcal keratitis' SubClassOf 'gonococcal endophthalmia'
http://purl.obolibrary.org/obo/MONDO_0004652
bacterial pneumonia
'bacterial pneumonia' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_2
http://purl.obolibrary.org/obo/MONDO_0004651
smallpox
'smallpox' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_10255
'smallpox' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_10255
http://purl.obolibrary.org/obo/MONDO_0004668
fascioliasis
'fascioliasis' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0000988
'fascioliasis' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0001903
'fascioliasis' SubClassOf 'disease has feature' some 'anemia (disease)'
'fascioliasis' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002027
'fascioliasis' SubClassOf 'disease has feature' some 'exanthem (disease)'
'fascioliasis' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002013
http://purl.obolibrary.org/obo/MONDO_0014002
autosomal dominant nocturnal frontal lobe epilepsy 5
'autosomal dominant nocturnal frontal lobe epilepsy 5' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_57582
'autosomal dominant nocturnal frontal lobe epilepsy 5' EquivalentTo 'autosomal dominant nocturnal frontal lobe epilepsy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_57582)
http://purl.obolibrary.org/obo/MONDO_0014016
hereditary spastic paraplegia 49
'hereditary spastic paraplegia 49' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9895
'hereditary spastic paraplegia 49' EquivalentTo 'hereditary spastic paraplegia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9895)
http://purl.obolibrary.org/obo/MONDO_0014015
hereditary spastic paraplegia 56
'hereditary spastic paraplegia 56' EquivalentTo 'hereditary spastic paraplegia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_113612)
'hereditary spastic paraplegia 56' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_113612
http://purl.obolibrary.org/obo/MONDO_0014012
Charcot-Marie-tooth disease axonal type 2Q
'Charcot-Marie-tooth disease axonal type 2Q' EquivalentTo 'Charcot-Marie-tooth disease' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_55526)
'Charcot-Marie-tooth disease axonal type 2Q' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_55526
http://purl.obolibrary.org/obo/MONDO_0014011
autosomal recessive congenital ichthyosis 10
'autosomal recessive congenital ichthyosis 10' EquivalentTo 'autosomal recessive congenital ichthyosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_285848)
'autosomal recessive congenital ichthyosis 10' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_285848
http://purl.obolibrary.org/obo/MONDO_0014010
autosomal recessive congenital ichthyosis 9
'autosomal recessive congenital ichthyosis 9' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_204219
'autosomal recessive congenital ichthyosis 9' EquivalentTo 'autosomal recessive congenital ichthyosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_204219)
http://purl.obolibrary.org/obo/MONDO_0014027
hypotrichosis 11
'hypotrichosis 11' EquivalentTo 'hypotrichosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6635)
'hypotrichosis 11' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6635
http://purl.obolibrary.org/obo/MONDO_0014026
congenital stationary night blindness 1F
'congenital stationary night blindness 1F' EquivalentTo 'congenital stationary night blindness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_345193)
'congenital stationary night blindness 1F' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_345193
http://purl.obolibrary.org/obo/MONDO_0014029
osteogenesis imperfecta type 14
'osteogenesis imperfecta type 14' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_55151
'osteogenesis imperfecta type 14' EquivalentTo 'osteogenesis imperfecta' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_55151)
http://purl.obolibrary.org/obo/MONDO_0014030
primary ciliary dyskinesia 20
'primary ciliary dyskinesia 20' EquivalentTo 'primary ciliary dyskinesia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_93233)
'primary ciliary dyskinesia 20' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_93233
http://purl.obolibrary.org/obo/MONDO_0014032
brachydactyly type A1C
'brachydactyly type A1C' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_8200
'brachydactyly type A1C' EquivalentTo 'brachydactyly type A1' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_8200)
http://purl.obolibrary.org/obo/MONDO_0014052
congenital myasthenic syndrome 8
'congenital myasthenic syndrome 8' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_375790
'congenital myasthenic syndrome 8' EquivalentTo 'congenital myasthenic syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_375790)
http://purl.obolibrary.org/obo/MONDO_0014050
isolated microphthalmia 8
'isolated microphthalmia 8' EquivalentTo 'isolated microphthalmia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_220)
'isolated microphthalmia 8' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_220
http://purl.obolibrary.org/obo/MONDO_0014054
lymphoproliferative syndrome 2
'lymphoproliferative syndrome 2' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_939
'lymphoproliferative syndrome 2' EquivalentTo 'lymphoproliferative syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_939)
http://purl.obolibrary.org/obo/MONDO_0014088
advanced sleep phase syndrome 2
'advanced sleep phase syndrome 2' EquivalentTo 'advanced sleep phase syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1453)
'advanced sleep phase syndrome 2' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1453
http://purl.obolibrary.org/obo/MONDO_0014086
osteogenesis imperfecta type 15
'osteogenesis imperfecta type 15' EquivalentTo 'osteogenesis imperfecta' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7471)
'osteogenesis imperfecta type 15' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7471
http://purl.obolibrary.org/obo/MONDO_0014093
retinitis pigmentosa 66
'retinitis pigmentosa 66' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5949)
'retinitis pigmentosa 66' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5949
http://purl.obolibrary.org/obo/MONDO_0004731
central sleep apnea syndrome
http://linkedlifedata.com/resource/umls/id/C0751762 EquivalentTo 'central sleep apnea syndrome'
http://linkedlifedata.com/resource/umls/id/C3887547 EquivalentTo 'central sleep apnea syndrome'
http://purl.obolibrary.org/obo/MONDO_0004551
Meckel diverticulitis
'Meckel diverticulitis' SubClassOf 'gastroenteritis'
http://purl.obolibrary.org/obo/MONDO_0004588
night blindness
'night blindness' SubClassOf 'retinopathy'
http://purl.obolibrary.org/obo/MONDO_0004592
impetigo
'impetigo' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_1314
'impetigo' SubClassOf 'staphylococcus aureus infection'
'impetigo' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_1280
'impetigo' SubClassOf 'streptococcal infection'
http://purl.obolibrary.org/obo/MONDO_0004619
measles
'measles' SubClassOf 'disease has feature' some 'dysentery'
'measles' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0012735
http://purl.obolibrary.org/obo/MONDO_0004625
phlebitis
'phlebitis' SubClassOf 'inflammatory disease'
'phlebitis' SubClassOf 'vasculitis'
http://purl.obolibrary.org/obo/MONDO_0004628
gastroduodenitis
'gastroduodenitis' SubClassOf 'gastritis (disease)'
'gastroduodenitis' SubClassOf 'gastroenteritis'
'gastroduodenitis' SubClassOf 'viral gastritis'
'gastroduodenitis' SubClassOf 'bacterial gastritis'
http://purl.obolibrary.org/obo/MONDO_0004627
duodenitis
'duodenitis' SubClassOf 'inflammatory disease'
'duodenitis' SubClassOf 'gastroenteritis'
http://purl.obolibrary.org/obo/MONDO_0004466
neuronitis
'neuronitis' SubClassOf 'inflammatory disease'
http://purl.obolibrary.org/obo/MONDO_0004492
mediastinitis
'mediastinitis' SubClassOf 'inflammatory disease'
http://purl.obolibrary.org/obo/MONDO_0018943
myofibrillar myopathy (disease)
'myofibrillar myopathy (disease)' SubClassOf 'myopathy'
'myofibrillar myopathy (disease)' SubClassOf 'congenital structural myopathy'
'myofibrillar myopathy (disease)' EquivalentTo http://purl.obolibrary.org/obo/OMIMPS_601419
http://purl.obolibrary.org/obo/MONDO_0018800
Kallmann syndrome
'Kallmann syndrome' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0000939
'Kallmann syndrome' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0000789
http://purl.obolibrary.org/obo/MONDO_0018852
achromatopsia
'achromatopsia' SubClassOf 'disease has feature' some 'amblyopia (disease)'
'achromatopsia' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0000646
http://purl.obolibrary.org/obo/MONDO_0004235
diverticulitis
'diverticulitis' SubClassOf 'disease has feature' some 'dysentery'
'diverticulitis' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002019
'diverticulitis' SubClassOf 'disease has feature' some 'constipation disorder'
'diverticulitis' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002027
http://purl.obolibrary.org/obo/MONDO_0018874
acute myeloid leukemia
'acute myeloid leukemia' SubClassOf 'disease has feature' some 'anemia (disease)'
'acute myeloid leukemia' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0001903
http://purl.obolibrary.org/obo/MONDO_0004247
peptic ulcer disease
'peptic ulcer disease' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002249
http://purl.obolibrary.org/obo/MONDO_0018882
vasculitis
'vasculitis' SubClassOf 'inflammatory disease'
http://purl.obolibrary.org/obo/MONDO_0004277
gonorrhea
'gonorrhea' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_485
'gonorrhea' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_485
http://purl.obolibrary.org/obo/MONDO_0010016
sclerosteosis 1
'sclerosteosis 1' EquivalentTo 'sclerosteosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_50964)
'sclerosteosis 1' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_50964
http://purl.obolibrary.org/obo/MONDO_0010030
Sjogren syndrome
'Sjogren syndrome' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0001097
http://purl.obolibrary.org/obo/MONDO_0010043
hereditary spastic paraplegia 17
'hereditary spastic paraplegia 17' EquivalentTo 'hereditary spastic paraplegia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_26580)
'hereditary spastic paraplegia 17' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_26580
http://purl.obolibrary.org/obo/MONDO_0010053
hereditary spherocytosis type 3
'hereditary spherocytosis type 3' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6708
'hereditary spherocytosis type 3' EquivalentTo 'hereditary spherocytosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6708)
http://purl.obolibrary.org/obo/MONDO_0009073
Ritscher-Schinzel syndrome 1
'Ritscher-Schinzel syndrome 1' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9897
'Ritscher-Schinzel syndrome 1' EquivalentTo 'Ritscher-Schinzel syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9897)
http://purl.obolibrary.org/obo/MONDO_0000598
aphasia
'aphasia' SubClassOf 'disease has feature' some 'mutism (disease)'
'aphasia' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002300
http://purl.obolibrary.org/obo/MONDO_0000410
funisitis
'funisitis' SubClassOf 'inflammatory disease'
http://purl.obolibrary.org/obo/MONDO_0000432
lymphoplasmacytic lymphoma
'lymphoplasmacytic lymphoma' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0005508
'lymphoplasmacytic lymphoma' SubClassOf 'disease has feature' some 'lymphoplasmacytic lymphoma'
http://purl.obolibrary.org/obo/MONDO_0000463
urofacial syndrome
'urofacial syndrome' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0000011
'urofacial syndrome' SubClassOf 'disease has feature' some 'neurogenic bladder (disease)'
http://purl.obolibrary.org/obo/MONDO_0000290
primary amebic meningoencephalitis
'primary amebic meningoencephalitis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_5763
'primary amebic meningoencephalitis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_5763
http://purl.obolibrary.org/obo/MONDO_0024278
proctocolitis
'proctocolitis' SubClassOf 'gastroenteritis'
http://purl.obolibrary.org/obo/MONDO_0014909
primary ciliary dyskinesia 34
'primary ciliary dyskinesia 34' EquivalentTo 'primary ciliary dyskinesia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_374407)
'primary ciliary dyskinesia 34' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_374407
http://purl.obolibrary.org/obo/MONDO_0014910
primary ciliary dyskinesia 35
'primary ciliary dyskinesia 35' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_83538
'primary ciliary dyskinesia 35' EquivalentTo 'primary ciliary dyskinesia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_83538)
http://purl.obolibrary.org/obo/MONDO_0014928
Joubert syndrome 28
'Joubert syndrome 28' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_54903
'Joubert syndrome 28' EquivalentTo 'Joubert syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_54903)
http://purl.obolibrary.org/obo/MONDO_0014927
Joubert syndrome 27
'Joubert syndrome 27' EquivalentTo 'Joubert syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_27077)
'Joubert syndrome 27' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_27077
http://purl.obolibrary.org/obo/MONDO_0014920
patterned macular dystrophy 3
'patterned macular dystrophy 3' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7867
'patterned macular dystrophy 3' EquivalentTo 'patterned macular dystrophy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7867)
http://purl.obolibrary.org/obo/MONDO_0014939
congenital myasthenic syndrome 20
'congenital myasthenic syndrome 20' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_60482
'congenital myasthenic syndrome 20' EquivalentTo 'congenital myasthenic syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_60482)
http://purl.obolibrary.org/obo/MONDO_0000330
endemic typhus
'endemic typhus' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_785
'endemic typhus' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_785
http://purl.obolibrary.org/obo/MONDO_0000337
exanthema subitum
'exanthema subitum' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_10368
'exanthema subitum' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_10368
http://purl.obolibrary.org/obo/MONDO_0000342
O'nyong'nyong fever
'O'nyong'nyong fever' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_11027
'O'nyong'nyong fever' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0000988
'O'nyong'nyong fever' SubClassOf 'disease has feature' some 'exanthem (disease)'
http://purl.obolibrary.org/obo/MONDO_0014983
congenital myasthenic syndrome 21
'congenital myasthenic syndrome 21' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6572
'congenital myasthenic syndrome 21' EquivalentTo 'congenital myasthenic syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6572)
http://purl.obolibrary.org/obo/MONDO_0014987
Fanconi anemia complementation group U
'Fanconi anemia complementation group U' EquivalentTo 'Fanconi anemia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7516)
'Fanconi anemia complementation group U' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7516
http://purl.obolibrary.org/obo/MONDO_0014986
Fanconi anemia complementation group r
'Fanconi anemia complementation group r' EquivalentTo 'Fanconi anemia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5888)
'Fanconi anemia complementation group r' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5888
http://purl.obolibrary.org/obo/MONDO_0014985
Fanconi anemia complementation group v
'Fanconi anemia complementation group v' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10459
'Fanconi anemia complementation group v' EquivalentTo 'Fanconi anemia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10459)
http://purl.obolibrary.org/obo/MONDO_0024356
primary central sleep apnea syndrome
http://linkedlifedata.com/resource/umls/id/C0751762 EquivalentTo 'primary central sleep apnea syndrome'
http://purl.obolibrary.org/obo/MONDO_0024358
mixed sleep apnea
'mixed sleep apnea' SubClassOf 'central sleep apnea syndrome'
'mixed sleep apnea' SubClassOf 'obstructive sleep apnea syndrome'
'mixed sleep apnea' SubClassOf 'central sleep apnea syndrome'
'mixed sleep apnea' SubClassOf 'obstructive sleep apnea syndrome'
http://purl.obolibrary.org/obo/MONDO_0014814
advanced sleep phase syndrome 3
'advanced sleep phase syndrome 3' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_8863
'advanced sleep phase syndrome 3' EquivalentTo 'advanced sleep phase syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_8863)
http://purl.obolibrary.org/obo/MONDO_0014813
hypomyelinating leukodystrophy 13
'hypomyelinating leukodystrophy 13' EquivalentTo 'leukodystrophy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_51501)
'hypomyelinating leukodystrophy 13' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_51501
http://purl.obolibrary.org/obo/MONDO_0014819
autosomal dominant Robinow syndrome 3
'autosomal dominant Robinow syndrome 3' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1857
'autosomal dominant Robinow syndrome 3' EquivalentTo 'Robinow syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1857)
http://purl.obolibrary.org/obo/MONDO_0014829
immunodeficiency-centromeric instability-facial anomalies syndrome 4
'immunodeficiency-centromeric instability-facial anomalies syndrome 4' EquivalentTo 'immunodeficiency-centromeric instability-facial anomalies syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3070)
'immunodeficiency-centromeric instability-facial anomalies syndrome 4' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3070
http://purl.obolibrary.org/obo/MONDO_0014828
immunodeficiency-centromeric instability-facial anomalies syndrome 3
'immunodeficiency-centromeric instability-facial anomalies syndrome 3' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_83879
'immunodeficiency-centromeric instability-facial anomalies syndrome 3' EquivalentTo 'immunodeficiency-centromeric instability-facial anomalies syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_83879)
http://purl.obolibrary.org/obo/MONDO_0014836
Charcot-Marie-tooth disease axonal type 2CC
'Charcot-Marie-tooth disease axonal type 2CC' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4744
'Charcot-Marie-tooth disease axonal type 2CC' EquivalentTo 'Charcot-Marie-tooth disease' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4744)
http://purl.obolibrary.org/obo/MONDO_0014849
autosomal recessive nonsyndromic deafness 105
'autosomal recessive nonsyndromic deafness 105' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_8556
'autosomal recessive nonsyndromic deafness 105' EquivalentTo 'autosomal recessive nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_8556)
http://purl.obolibrary.org/obo/MONDO_0014854
autosomal dominant nonsyndromic deafness 66
'autosomal dominant nonsyndromic deafness 66' EquivalentTo 'autosomal dominant nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_8763)
'autosomal dominant nonsyndromic deafness 66' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_8763
http://purl.obolibrary.org/obo/MONDO_0014853
autosomal dominant nonsyndromic deafness 70
'autosomal dominant nonsyndromic deafness 70' EquivalentTo 'autosomal dominant nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4171)
'autosomal dominant nonsyndromic deafness 70' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4171
http://purl.obolibrary.org/obo/MONDO_0014866
Charcot-Marie-tooth disease axonal type 2T
'Charcot-Marie-tooth disease axonal type 2T' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4311
'Charcot-Marie-tooth disease axonal type 2T' EquivalentTo 'Charcot-Marie-tooth disease' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3300) and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4311)
'Charcot-Marie-tooth disease axonal type 2T' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3300
http://purl.obolibrary.org/obo/MONDO_0014872
congenital stationary night blindness 1H
'congenital stationary night blindness 1H' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2784
'congenital stationary night blindness 1H' EquivalentTo 'congenital stationary night blindness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2784)
http://purl.obolibrary.org/obo/MONDO_0014871
retinitis pigmentosa 75
'retinitis pigmentosa 75' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_60509)
'retinitis pigmentosa 75' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_60509
http://purl.obolibrary.org/obo/MONDO_0000245
tinea imbricata
'tinea imbricata' EquivalentTo 'infectious disease' and ('realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_63419)
http://purl.obolibrary.org/obo/MONDO_0014883
hypertrophic cardiomyopathy 26
'hypertrophic cardiomyopathy 26' EquivalentTo 'hypertrophic cardiomyopathy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2318)
'hypertrophic cardiomyopathy 26' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2318
http://purl.obolibrary.org/obo/MONDO_0014882
hereditary spastic paraplegia 77
'hereditary spastic paraplegia 77' EquivalentTo 'hereditary spastic paraplegia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10667)
'hereditary spastic paraplegia 77' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10667
http://purl.obolibrary.org/obo/MONDO_0000252
inflammatory diarrhea
'inflammatory diarrhea' SubClassOf 'intestinal disease'
'inflammatory diarrhea' SubClassOf 'gastroenteritis'
http://purl.obolibrary.org/obo/MONDO_0000261
adenoiditis
'adenoiditis' SubClassOf 'nasopharyngeal disease'
'adenoiditis' SubClassOf 'nasopharyngitis'
http://purl.obolibrary.org/obo/MONDO_0014687
retinitis pigmentosa 73
'retinitis pigmentosa 73' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_138050
'retinitis pigmentosa 73' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_138050)
http://purl.obolibrary.org/obo/MONDO_0014693
Noonan syndrome 10
'Noonan syndrome 10' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_8216
'Noonan syndrome 10' EquivalentTo 'Noonan syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_8216)
http://purl.obolibrary.org/obo/MONDO_0014692
retinitis pigmentosa 74
'retinitis pigmentosa 74' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_583
'retinitis pigmentosa 74' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_583)
http://purl.obolibrary.org/obo/MONDO_0014691
Noonan syndrome 9
'Noonan syndrome 9' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6655
'Noonan syndrome 9' EquivalentTo 'Noonan syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6655)
http://purl.obolibrary.org/obo/MONDO_0000071
obsolete myopathy, myofibrillar
'obsolete myopathy, myofibrillar' EquivalentTo http://purl.obolibrary.org/obo/OMIMPS_601419
http://purl.obolibrary.org/obo/MONDO_0014711
autosomal dominant Charcot-Marie-Tooth disease type 2W
'autosomal dominant Charcot-Marie-Tooth disease type 2W' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3035
'autosomal dominant Charcot-Marie-Tooth disease type 2W' EquivalentTo 'Charcot-Marie-tooth disease type 2' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3035)
http://purl.obolibrary.org/obo/MONDO_0014726
Charcot-Marie-tooth disease axonal type 2X
'Charcot-Marie-tooth disease axonal type 2X' EquivalentTo 'Charcot-Marie-tooth disease' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_80208)
'Charcot-Marie-tooth disease axonal type 2X' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_80208
http://purl.obolibrary.org/obo/MONDO_0014729
hereditary spastic paraplegia 75
'hereditary spastic paraplegia 75' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4099
'hereditary spastic paraplegia 75' EquivalentTo 'hereditary spastic paraplegia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4099)
http://purl.obolibrary.org/obo/MONDO_0014724
Joubert syndrome 24
'Joubert syndrome 24' EquivalentTo 'Joubert syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_79867)
'Joubert syndrome 24' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_79867
http://purl.obolibrary.org/obo/MONDO_0014739
autosomal recessive nonsyndromic deafness 97
'autosomal recessive nonsyndromic deafness 97' EquivalentTo 'autosomal recessive nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4233)
'autosomal recessive nonsyndromic deafness 97' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4233
http://purl.obolibrary.org/obo/MONDO_0014738
autosomal dominant nonsyndromic deafness 69
'autosomal dominant nonsyndromic deafness 69' EquivalentTo 'autosomal dominant nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4254)
'autosomal dominant nonsyndromic deafness 69' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4254
http://purl.obolibrary.org/obo/MONDO_0014736
Charcot-Marie-tooth disease axonal type 2Z
'Charcot-Marie-tooth disease axonal type 2Z' EquivalentTo 'Charcot-Marie-tooth disease' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_22880)
'Charcot-Marie-tooth disease axonal type 2Z' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_22880
http://purl.obolibrary.org/obo/MONDO_0014735
Charcot-Marie-tooth disease type 2Y
'Charcot-Marie-tooth disease type 2Y' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7415
'Charcot-Marie-tooth disease type 2Y' EquivalentTo 'Charcot-Marie-tooth disease type 2' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7415)
http://purl.obolibrary.org/obo/MONDO_0014732
hypomyelinating leukodystrophy 12
'hypomyelinating leukodystrophy 12' EquivalentTo 'leukodystrophy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_55823)
'hypomyelinating leukodystrophy 12' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_55823
http://purl.obolibrary.org/obo/MONDO_0014740
autosomal dominant nonsyndromic deafness 68
'autosomal dominant nonsyndromic deafness 68' EquivalentTo 'autosomal dominant nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9455)
'autosomal dominant nonsyndromic deafness 68' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9455
http://purl.obolibrary.org/obo/MONDO_0014745
congenital myasthenic syndrome 19
'congenital myasthenic syndrome 19' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1305
'congenital myasthenic syndrome 19' EquivalentTo 'congenital myasthenic syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1305)
http://purl.obolibrary.org/obo/MONDO_0014743
rhizomelic chondrodysplasia punctata type 5
'rhizomelic chondrodysplasia punctata type 5' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5830
'rhizomelic chondrodysplasia punctata type 5' EquivalentTo 'rhizomelic chondrodysplasia punctata' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5830)
http://purl.obolibrary.org/obo/MONDO_0014750
primary ciliary dyskinesia 33
'primary ciliary dyskinesia 33' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2622
'primary ciliary dyskinesia 33' EquivalentTo 'primary ciliary dyskinesia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2622)
http://purl.obolibrary.org/obo/MONDO_0014768
CADASIL 2
'CADASIL 2' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5654
'CADASIL 2' EquivalentTo 'CADASIL' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5654)
http://purl.obolibrary.org/obo/MONDO_0000128
giant axonal neuropathy
http://purl.obolibrary.org/obo/MESH_D056768 EquivalentTo 'giant axonal neuropathy'
http://purl.obolibrary.org/obo/MONDO_0014771
Joubert syndrome 26
'Joubert syndrome 26' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_23247
'Joubert syndrome 26' EquivalentTo 'Joubert syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_23247)
http://purl.obolibrary.org/obo/MONDO_0014770
Joubert syndrome 25
'Joubert syndrome 25' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9731
'Joubert syndrome 25' EquivalentTo 'Joubert syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9731)
http://purl.obolibrary.org/obo/MONDO_0014788
autosomal recessive limb-girdle muscular dystrophy type 2W
'autosomal recessive limb-girdle muscular dystrophy type 2W' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_55679
'autosomal recessive limb-girdle muscular dystrophy type 2W' EquivalentTo 'autosomal recessive limb-girdle muscular dystrophy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_55679)
http://purl.obolibrary.org/obo/MONDO_0014782
autosomal recessive limb-girdle muscular dystrophy type 2X
'autosomal recessive limb-girdle muscular dystrophy type 2X' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_11149
'autosomal recessive limb-girdle muscular dystrophy type 2X' EquivalentTo 'autosomal recessive limb-girdle muscular dystrophy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_11149)
http://purl.obolibrary.org/obo/MONDO_0014798
brachydactyly type A1D
'brachydactyly type A1D' EquivalentTo 'brachydactyly type A1' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_658)
'brachydactyly type A1D' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_658
http://purl.obolibrary.org/obo/MONDO_0014564
congenital bile acid synthesis defect 5
'congenital bile acid synthesis defect 5' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5825
'congenital bile acid synthesis defect 5' EquivalentTo 'congenital bile acid synthesis defect' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5825)
http://purl.obolibrary.org/obo/MONDO_0014561
3-methylglutaconic aciduria with cataracts, neurologic involvement and neutropenia
'3-methylglutaconic aciduria with cataracts, neurologic involvement and neutropenia' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_81570
'3-methylglutaconic aciduria with cataracts, neurologic involvement and neutropenia' EquivalentTo '3-methylglutaconic aciduria' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_81570)
http://purl.obolibrary.org/obo/MONDO_0014560
amelogenesis imperfecta type 1F
'amelogenesis imperfecta type 1F' EquivalentTo 'amelogenesis imperfecta' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_258)
'amelogenesis imperfecta type 1F' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_258
http://purl.obolibrary.org/obo/MONDO_0014578
congenital myasthenic syndrome 17
'congenital myasthenic syndrome 17' EquivalentTo 'congenital myasthenic syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4038)
'congenital myasthenic syndrome 17' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4038
http://purl.obolibrary.org/obo/MONDO_0014588
congenital myasthenic syndrome 11
'congenital myasthenic syndrome 11' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5913
'congenital myasthenic syndrome 11' EquivalentTo 'congenital myasthenic syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5913)
http://purl.obolibrary.org/obo/MONDO_0014587
congenital myasthenic syndrome 9
'congenital myasthenic syndrome 9' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4593
'congenital myasthenic syndrome 9' EquivalentTo 'congenital myasthenic syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4593)
http://purl.obolibrary.org/obo/MONDO_0014591
autosomal dominant Robinow syndrome 2
'autosomal dominant Robinow syndrome 2' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1855
'autosomal dominant Robinow syndrome 2' EquivalentTo 'autosomal dominant Robinow syndrome 1' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1855)
http://purl.obolibrary.org/obo/MONDO_0014590
congenital myasthenic syndrome 18
'congenital myasthenic syndrome 18' EquivalentTo 'congenital myasthenic syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6616)
'congenital myasthenic syndrome 18' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6616
http://purl.obolibrary.org/obo/MONDO_0014594
autosomal dominant nonsyndromic deafness 67
'autosomal dominant nonsyndromic deafness 67' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9885
'autosomal dominant nonsyndromic deafness 67' EquivalentTo 'autosomal dominant nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9885)
http://purl.obolibrary.org/obo/MONDO_0014592
microcephaly and chorioretinopathy 3
'microcephaly and chorioretinopathy 3' EquivalentTo 'microcephaly and chorioretinopathy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_27229)
'microcephaly and chorioretinopathy 3' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_27229
http://purl.obolibrary.org/obo/MONDO_0014603
autosomal dominant nonsyndromic deafness 40
'autosomal dominant nonsyndromic deafness 40' EquivalentTo 'autosomal dominant nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1428)
'autosomal dominant nonsyndromic deafness 40' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1428
http://purl.obolibrary.org/obo/MONDO_0014618
retinitis pigmentosa 71
'retinitis pigmentosa 71' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_26160)
'retinitis pigmentosa 71' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_26160
http://purl.obolibrary.org/obo/MONDO_0014614
congenital stationary night blindness 1G
'congenital stationary night blindness 1G' SubClassOf 'hereditary night blindness'
'congenital stationary night blindness 1G' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2779
'congenital stationary night blindness 1G' SubClassOf 'has modifier' some http://purl.obolibrary.org/obo/HP_0000007
'congenital stationary night blindness 1G' SubClassOf 'hereditary retinal dystrophy'
'congenital stationary night blindness 1G' EquivalentTo 'congenital stationary night blindness' and ('has modifier' some http://purl.obolibrary.org/obo/HP_0000007) and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2779)
'congenital stationary night blindness 1G' SubClassOf 'autosomal recessive disease'
http://purl.obolibrary.org/obo/MONDO_0014621
Brugada syndrome 9
'Brugada syndrome 9' EquivalentTo 'Brugada syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3752)
'Brugada syndrome 9' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3752
http://purl.obolibrary.org/obo/MONDO_0014638
Fanconi anemia complementation group T
'Fanconi anemia complementation group T' EquivalentTo 'Fanconi anemia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_29089)
'Fanconi anemia complementation group T' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_29089
http://purl.obolibrary.org/obo/MONDO_0014632
hypomyelinating leukodystrophy 10
'hypomyelinating leukodystrophy 10' EquivalentTo 'leukodystrophy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_29920)
'hypomyelinating leukodystrophy 10' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_29920
http://purl.obolibrary.org/obo/MONDO_0014644
hereditary spastic paraplegia 74
'hereditary spastic paraplegia 74' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_200205
'hereditary spastic paraplegia 74' EquivalentTo 'hereditary spastic paraplegia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_200205)
http://purl.obolibrary.org/obo/MONDO_0014653
retinitis pigmentosa 72
'retinitis pigmentosa 72' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_79797
'retinitis pigmentosa 72' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_79797)
http://purl.obolibrary.org/obo/MONDO_0014651
acrofacial dysostosis Cincinnati type
'acrofacial dysostosis Cincinnati type' EquivalentTo 'acrofacial dysostosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_25885)
'acrofacial dysostosis Cincinnati type' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_25885
http://purl.obolibrary.org/obo/MONDO_0014657
primary ciliary dyskinesia 32
'primary ciliary dyskinesia 32' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_83861
'primary ciliary dyskinesia 32' EquivalentTo 'primary ciliary dyskinesia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_83861)
http://purl.obolibrary.org/obo/MONDO_0014665
Charcot-Marie-tooth disease axonal type 2V
'Charcot-Marie-tooth disease axonal type 2V' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4669
'Charcot-Marie-tooth disease axonal type 2V' EquivalentTo 'Charcot-Marie-tooth disease' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4669)
http://purl.obolibrary.org/obo/MONDO_0014664
Joubert syndrome 23
'Joubert syndrome 23' EquivalentTo 'Joubert syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9786)
'Joubert syndrome 23' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9786
http://purl.obolibrary.org/obo/MONDO_0014666
hypomyelinating leukodystrophy 11
'hypomyelinating leukodystrophy 11' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9533
'hypomyelinating leukodystrophy 11' SubClassOf 'leukodystrophy'
'hypomyelinating leukodystrophy 11' EquivalentTo 'leukodystrophy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9533)
http://purl.obolibrary.org/obo/MONDO_0014675
autosomal recessive nonsyndromic deafness 104
'autosomal recessive nonsyndromic deafness 104' EquivalentTo 'autosomal recessive nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9750)
'autosomal recessive nonsyndromic deafness 104' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9750
http://purl.obolibrary.org/obo/MONDO_0014677
achromatopsia 7
'achromatopsia 7' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_22926
'achromatopsia 7' EquivalentTo 'achromatopsia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_22926)
http://purl.obolibrary.org/obo/MONDO_0014672
osteogenesis imperfecta type 17
'osteogenesis imperfecta type 17' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6678
'osteogenesis imperfecta type 17' EquivalentTo 'osteogenesis imperfecta' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6678)
http://purl.obolibrary.org/obo/MONDO_0014445
Bardet-Biedl syndrome 17
'Bardet-Biedl syndrome 17' EquivalentTo 'Bardet-Biedl syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_54585)
'Bardet-Biedl syndrome 17' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_54585
http://purl.obolibrary.org/obo/MONDO_0014444
Bardet-Biedl syndrome 16
'Bardet-Biedl syndrome 16' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10806
'Bardet-Biedl syndrome 16' EquivalentTo 'Bardet-Biedl syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10806)
http://purl.obolibrary.org/obo/MONDO_0014443
Bardet-Biedl syndrome 15
'Bardet-Biedl syndrome 15' EquivalentTo 'Bardet-Biedl syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_51057)
'Bardet-Biedl syndrome 15' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_51057
http://purl.obolibrary.org/obo/MONDO_0014442
Bardet-Biedl syndrome 14
'Bardet-Biedl syndrome 14' EquivalentTo 'Bardet-Biedl syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_80184) and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_91147)
'Bardet-Biedl syndrome 14' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_91147
'Bardet-Biedl syndrome 14' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_80184
http://purl.obolibrary.org/obo/MONDO_0014447
Bardet-Biedl syndrome 19
'Bardet-Biedl syndrome 19' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_11020
'Bardet-Biedl syndrome 19' EquivalentTo 'Bardet-Biedl syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_11020)
http://purl.obolibrary.org/obo/MONDO_0014446
Bardet-Biedl syndrome 18
'Bardet-Biedl syndrome 18' EquivalentTo 'Bardet-Biedl syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_92482)
'Bardet-Biedl syndrome 18' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_92482
http://purl.obolibrary.org/obo/MONDO_0014441
Bardet-Biedl syndrome 13
'Bardet-Biedl syndrome 13' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_54903
'Bardet-Biedl syndrome 13' EquivalentTo 'Bardet-Biedl syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_54903)
http://purl.obolibrary.org/obo/MONDO_0014440
Bardet-Biedl syndrome 12
'Bardet-Biedl syndrome 12' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_166379
'Bardet-Biedl syndrome 12' EquivalentTo 'Bardet-Biedl syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_166379)
http://purl.obolibrary.org/obo/MONDO_0014451
focal segmental glomerulosclerosis 7
'focal segmental glomerulosclerosis 7' EquivalentTo 'focal segmental glomerulosclerosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5076)
'focal segmental glomerulosclerosis 7' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5076
http://purl.obolibrary.org/obo/MONDO_0014467
Charcot-Marie-tooth disease recessive intermediate d
'Charcot-Marie-tooth disease recessive intermediate d' EquivalentTo 'Charcot-Marie-tooth disease' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1337)
'Charcot-Marie-tooth disease recessive intermediate d' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1337
http://purl.obolibrary.org/obo/MONDO_0014465
primary ciliary dyskinesia 30
'primary ciliary dyskinesia 30' EquivalentTo 'primary ciliary dyskinesia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_115948)
'primary ciliary dyskinesia 30' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_115948
http://purl.obolibrary.org/obo/MONDO_0014469
autosomal recessive nonsyndromic deafness 103
'autosomal recessive nonsyndromic deafness 103' EquivalentTo 'autosomal recessive nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_53405)
'autosomal recessive nonsyndromic deafness 103' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_53405
http://purl.obolibrary.org/obo/MONDO_0014468
congenital myasthenic syndrome 7
'congenital myasthenic syndrome 7' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_127833
'congenital myasthenic syndrome 7' EquivalentTo 'congenital myasthenic syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_127833)
http://purl.obolibrary.org/obo/MONDO_0014462
focal segmental glomerulosclerosis 8
'focal segmental glomerulosclerosis 8' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_54443
'focal segmental glomerulosclerosis 8' EquivalentTo 'focal segmental glomerulosclerosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_54443)
http://purl.obolibrary.org/obo/MONDO_0014461
hypogonadotropic hypogonadism 22 with or without anosmia
'hypogonadotropic hypogonadism 22 with or without anosmia' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_389549
'hypogonadotropic hypogonadism 22 with or without anosmia' EquivalentTo 'hypogonadotropic hypogonadism' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_389549)
http://purl.obolibrary.org/obo/MONDO_0014470
autosomal dominant nonsyndromic deafness 65
'autosomal dominant nonsyndromic deafness 65' EquivalentTo 'autosomal dominant nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_57465)
'autosomal dominant nonsyndromic deafness 65' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_57465
http://purl.obolibrary.org/obo/MONDO_0014474
autosomal recessive limb-girdle muscular dystrophy type 2U
'autosomal recessive limb-girdle muscular dystrophy type 2U' EquivalentTo 'autosomal recessive limb-girdle muscular dystrophy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_729920)
'autosomal recessive limb-girdle muscular dystrophy type 2U' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_729920
http://purl.obolibrary.org/obo/MONDO_0014498
familial cold autoinflammatory syndrome 4
'familial cold autoinflammatory syndrome 4' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_58484
'familial cold autoinflammatory syndrome 4' EquivalentTo 'familial cold autoinflammatory syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_58484)
http://purl.obolibrary.org/obo/MONDO_0014506
hypomyelinating leukodystrophy 9
'hypomyelinating leukodystrophy 9' EquivalentTo 'leukodystrophy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5917)
'hypomyelinating leukodystrophy 9' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5917
http://purl.obolibrary.org/obo/MONDO_0014516
microcephaly and chorioretinopathy 2
'microcephaly and chorioretinopathy 2' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10733
'microcephaly and chorioretinopathy 2' EquivalentTo 'microcephaly and chorioretinopathy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10733)
http://purl.obolibrary.org/obo/MONDO_0014511
Charcot-Marie-tooth disease axonal type 2S
'Charcot-Marie-tooth disease axonal type 2S' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3508
'Charcot-Marie-tooth disease axonal type 2S' EquivalentTo 'Charcot-Marie-tooth disease' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3508)
http://purl.obolibrary.org/obo/MONDO_0014513
nemaline myopathy 10
'nemaline myopathy 10' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_56203
'nemaline myopathy 10' EquivalentTo 'nemaline myopathy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_56203)
http://purl.obolibrary.org/obo/MONDO_0014539
focal segmental glomerulosclerosis 9
'focal segmental glomerulosclerosis 9' EquivalentTo 'focal segmental glomerulosclerosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_286204)
'focal segmental glomerulosclerosis 9' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_286204
http://purl.obolibrary.org/obo/MONDO_0014542
congenital myasthenic syndrome 15
'congenital myasthenic syndrome 15' EquivalentTo 'congenital myasthenic syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_199857)
'congenital myasthenic syndrome 15' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_199857
http://purl.obolibrary.org/obo/MONDO_0014548
long QT syndrome 14
'long QT syndrome 14' EquivalentTo 'long QT syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_801)
'long QT syndrome 14' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_801
http://purl.obolibrary.org/obo/MONDO_0014540
amelogenesis imperfecta type 1H
'amelogenesis imperfecta type 1H' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3694
'amelogenesis imperfecta type 1H' EquivalentTo 'amelogenesis imperfecta' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3694)
http://purl.obolibrary.org/obo/MONDO_0014550
long QT syndrome 15
'long QT syndrome 15' EquivalentTo 'long QT syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_805)
'long QT syndrome 15' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_805
http://purl.obolibrary.org/obo/MONDO_0009805
osteogenesis imperfecta type 9
'osteogenesis imperfecta type 9' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5479
'osteogenesis imperfecta type 9' EquivalentTo 'osteogenesis imperfecta' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5479)
http://purl.obolibrary.org/obo/MONDO_0010807
autosomal recessive nonsyndromic deafness 2
'autosomal recessive nonsyndromic deafness 2' EquivalentTo 'autosomal recessive nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4647)
'autosomal recessive nonsyndromic deafness 2' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4647
http://purl.obolibrary.org/obo/MONDO_0010806
retinitis pigmentosa 13
'retinitis pigmentosa 13' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10594)
'retinitis pigmentosa 13' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10594
http://purl.obolibrary.org/obo/MONDO_0010818
retinitis pigmentosa 12
'retinitis pigmentosa 12' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_23418
'retinitis pigmentosa 12' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_23418)
http://purl.obolibrary.org/obo/MONDO_0010817
autosomal dominant nonsyndromic deafness 2A
'autosomal dominant nonsyndromic deafness 2A' EquivalentTo 'autosomal dominant nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9132)
'autosomal dominant nonsyndromic deafness 2A' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9132
http://purl.obolibrary.org/obo/MONDO_0010828
retinitis pigmentosa 11
'retinitis pigmentosa 11' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_26121
'retinitis pigmentosa 11' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_26121)
http://purl.obolibrary.org/obo/MONDO_0009831
malignant pancreatic neoplasm
'malignant pancreatic neoplasm' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0001735
'malignant pancreatic neoplasm' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002027
'malignant pancreatic neoplasm' SubClassOf 'disease has feature' some 'acute pancreatitis'
http://purl.obolibrary.org/obo/MONDO_0010823
rhizomelic chondrodysplasia punctata type 3
'rhizomelic chondrodysplasia punctata type 3' EquivalentTo 'rhizomelic chondrodysplasia punctata' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_8540)
'rhizomelic chondrodysplasia punctata type 3' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_8540
http://purl.obolibrary.org/obo/MONDO_0010822
Warburg micro syndrome 1
'Warburg micro syndrome 1' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_22930
'Warburg micro syndrome 1' EquivalentTo 'Warburg micro syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_22930)
http://purl.obolibrary.org/obo/MONDO_0010827
retinitis pigmentosa 14
'retinitis pigmentosa 14' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7287
'retinitis pigmentosa 14' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7287)
http://purl.obolibrary.org/obo/MONDO_0010830
neuronal ceroid lipofuscinosis 8
'neuronal ceroid lipofuscinosis 8' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2055
'neuronal ceroid lipofuscinosis 8' EquivalentTo 'neuronal ceroid lipofuscinosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2055)
http://purl.obolibrary.org/obo/MONDO_0009867
lethal congenital glycogen storage disease of heart
'lethal congenital glycogen storage disease of heart' EquivalentTo 'glycogen storage disease' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_51422)
'lethal congenital glycogen storage disease of heart' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_51422
'lethal congenital glycogen storage disease of heart' SubClassOf 'hypertrophic cardiomyopathy 6'
http://purl.obolibrary.org/obo/MONDO_0009875
achromatopsia 3
'achromatopsia 3' EquivalentTo 'achromatopsia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_54714)
'achromatopsia 3' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_54714
http://purl.obolibrary.org/obo/MONDO_0010860
autosomal recessive nonsyndromic deafness 3
'autosomal recessive nonsyndromic deafness 3' EquivalentTo 'autosomal recessive nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_51168)
'autosomal recessive nonsyndromic deafness 3' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_51168
http://purl.obolibrary.org/obo/MONDO_0010863
type 1 diabetes mellitus 5
'type 1 diabetes mellitus 5' EquivalentTo 'type 1 diabetes mellitus' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_387082)
'type 1 diabetes mellitus 5' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_387082
http://purl.obolibrary.org/obo/MONDO_0019209
Japanese encephalitis
'Japanese encephalitis' SubClassOf 'encephalomyelitis'
'Japanese encephalitis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_11072
'Japanese encephalitis' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002013
'Japanese encephalitis' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002315
'Japanese encephalitis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_11072
http://purl.obolibrary.org/obo/MONDO_0010899
autosomal dominant nocturnal frontal lobe epilepsy 1
'autosomal dominant nocturnal frontal lobe epilepsy 1' EquivalentTo 'autosomal dominant nocturnal frontal lobe epilepsy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1137)
'autosomal dominant nocturnal frontal lobe epilepsy 1' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1137
http://purl.obolibrary.org/obo/MONDO_0009739
neurodegeneration with brain iron accumulation 2a
http://purl.obolibrary.org/obo/GARD_0002751 EquivalentTo 'neurodegeneration with brain iron accumulation 2a'
'neurodegeneration with brain iron accumulation 2a' EquivalentTo http://purl.obolibrary.org/obo/OMIM_256600
'neurodegeneration with brain iron accumulation 2a' SubClassOf 'neuroaxonal dystrophy'
http://purl.obolibrary.org/obo/DOID_0110735 EquivalentTo 'neurodegeneration with brain iron accumulation 2a'
http://purl.obolibrary.org/obo/MONDO_0010723
retinitis pigmentosa 2
'retinitis pigmentosa 2' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6102
'retinitis pigmentosa 2' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6102)
http://purl.obolibrary.org/obo/MONDO_0009747
Navajo neurohepatopathy
http://purl.obolibrary.org/obo/MESH_C538344 EquivalentTo 'Navajo neurohepatopathy'
http://purl.obolibrary.org/obo/MONDO_0009758
congenital stationary night blindness 1B
'congenital stationary night blindness 1B' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2916
'congenital stationary night blindness 1B' EquivalentTo 'congenital stationary night blindness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2916)
http://purl.obolibrary.org/obo/MONDO_0009775
Oguchi disease-1
'Oguchi disease-1' EquivalentTo 'Oguchi disease' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6295)
'Oguchi disease-1' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6295
http://purl.obolibrary.org/obo/MONDO_0009770
3MC syndrome 1
'3MC syndrome 1' EquivalentTo '3MC syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5648)
'3MC syndrome 1' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5648
http://purl.obolibrary.org/obo/MONDO_0019173
rabies
'rabies' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_11292
'rabies' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_11292
http://purl.obolibrary.org/obo/MONDO_0019177
odontoleukodystrophy
'odontoleukodystrophy' SubClassOf 'hypomyelinating leukodystrophy 7 with or without oligodontia and-or hypogonadotropic hypogonadism'
'odontoleukodystrophy' SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/MONDO_0019186
Q fever
'Q fever' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_777
'Q fever' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002013
'Q fever' SubClassOf 'disease has feature' some 'dysentery'
'Q fever' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_777
'Q fever' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002315
'Q fever' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002027
http://purl.obolibrary.org/obo/MONDO_0009670
lethal congenital contracture syndrome 1
'lethal congenital contracture syndrome 1' EquivalentTo 'lethal congenital contracture syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2733)
'lethal congenital contracture syndrome 1' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2733
http://purl.obolibrary.org/obo/MONDO_0009690
congenital myasthenic syndrome 10
'congenital myasthenic syndrome 10' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_285489
'congenital myasthenic syndrome 10' EquivalentTo 'congenital myasthenic syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_285489)
http://purl.obolibrary.org/obo/MONDO_0010684
X-linked myopathy with excessive autophagy
http://purl.obolibrary.org/obo/MESH_C536522 EquivalentTo 'X-linked myopathy with excessive autophagy'
http://purl.obolibrary.org/obo/MONDO_0010690
congenital stationary night blindness 1A
'congenital stationary night blindness 1A' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_60506
'congenital stationary night blindness 1A' EquivalentTo 'congenital stationary night blindness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_60506)
http://purl.obolibrary.org/obo/MONDO_0019095
plague
'plague' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_632
'plague' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002315
'plague' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002013
http://purl.obolibrary.org/obo/MONDO_0020066
Ehlers-Danlos syndrome
'Ehlers-Danlos syndrome' EquivalentTo http://purl.obolibrary.org/obo/OMIMPS_130000
http://purl.obolibrary.org/obo/MONDO_0010521
amelogenesis imperfecta type 1E
'amelogenesis imperfecta type 1E' EquivalentTo 'amelogenesis imperfecta' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_265)
'amelogenesis imperfecta type 1E' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_265
http://purl.obolibrary.org/obo/MONDO_0009554
3MC syndrome 3
'3MC syndrome 3' EquivalentTo '3MC syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10584)
'3MC syndrome 3' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10584
http://purl.obolibrary.org/obo/MONDO_0010542
dilated cardiomyopathy 3B
http://purl.obolibrary.org/obo/MESH_C580047 EquivalentTo 'dilated cardiomyopathy 3B'
'dilated cardiomyopathy 3B' EquivalentTo 'dilated cardiomyopathy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1756)
'dilated cardiomyopathy 3B' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1756
http://purl.obolibrary.org/obo/MONDO_0010564
red-green color blindness
'red-green color blindness' SubClassOf 'rare genetic eye disease'
'red-green color blindness' SubClassOf 'genetic nervous system disorder'
http://purl.obolibrary.org/obo/MONDO_0010565
red color blindness
'red color blindness' SubClassOf 'rare genetic eye disease'
http://purl.obolibrary.org/obo/MONDO_0009406
hypertrichotic osteochondrodysplasia Cantu type
'hypertrichotic osteochondrodysplasia Cantu type' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0000998
'hypertrichotic osteochondrodysplasia Cantu type' SubClassOf 'disease has feature' some 'hypertrichosis (disease)'
http://purl.obolibrary.org/obo/MONDO_0009419
Woodhouse-Sakati syndrome
'Woodhouse-Sakati syndrome' SubClassOf 'inherited neurodegenerative disorder'
'Woodhouse-Sakati syndrome' SubClassOf 'metabolic disease with dementia'
http://purl.obolibrary.org/obo/MONDO_0009441
autosomal recessive congenital ichthyosis 1
'autosomal recessive congenital ichthyosis 1' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7051
'autosomal recessive congenital ichthyosis 1' EquivalentTo 'autosomal recessive congenital ichthyosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7051)
http://purl.obolibrary.org/obo/MONDO_0010431
Joubert syndrome 10
'Joubert syndrome 10' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_8481
'Joubert syndrome 10' EquivalentTo 'Joubert syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_8481)
http://purl.obolibrary.org/obo/MONDO_0009454
immunodeficiency-centromeric instability-facial anomalies syndrome 1
'immunodeficiency-centromeric instability-facial anomalies syndrome 1' EquivalentTo 'immunodeficiency-centromeric instability-facial anomalies syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1789)
'immunodeficiency-centromeric instability-facial anomalies syndrome 1' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1789
http://purl.obolibrary.org/obo/MONDO_0010459
amyotrophic lateral sclerosis type 15
'amyotrophic lateral sclerosis type 15' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_29978
'amyotrophic lateral sclerosis type 15' EquivalentTo 'amyotrophic lateral sclerosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_29978)
http://purl.obolibrary.org/obo/MONDO_0009482
hypogonadotropic hypogonadism 3 with or without anosmia
'hypogonadotropic hypogonadism 3 with or without anosmia' EquivalentTo 'hypogonadotropic hypogonadism' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_128674)
'hypogonadotropic hypogonadism 3 with or without anosmia' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_128674
http://purl.obolibrary.org/obo/MONDO_0009484
primary ciliary dyskinesia 1
'primary ciliary dyskinesia 1' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_27019
'primary ciliary dyskinesia 1' EquivalentTo 'primary ciliary dyskinesia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_27019)
http://purl.obolibrary.org/obo/MONDO_0010499
Ritscher-Schinzel syndrome 2
'Ritscher-Schinzel syndrome 2' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_28952
'Ritscher-Schinzel syndrome 2' EquivalentTo 'Ritscher-Schinzel syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_28952)
http://purl.obolibrary.org/obo/MONDO_0000916
intestinal infectious disease
'intestinal infectious disease' SubClassOf 'infectious disease'
'intestinal infectious disease' SubClassOf 'intestinal disease'
'intestinal infectious disease' SubClassOf 'viral infectious disease'
'intestinal infectious disease' SubClassOf 'gastroenteritis'
'intestinal infectious disease' SubClassOf 'bacterial infectious disease'
http://purl.obolibrary.org/obo/MONDO_0000913
hereditary spherocytosis type 2
'hereditary spherocytosis type 2' EquivalentTo 'hereditary spherocytosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6710)
'hereditary spherocytosis type 2' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6710
http://purl.obolibrary.org/obo/MONDO_0000958
neuroretinitis
'neuroretinitis' SubClassOf 'rare peripheral neuropathy'
http://purl.obolibrary.org/obo/MONDO_0009319
pantothenate kinase-associated neurodegeneration
'pantothenate kinase-associated neurodegeneration' SubClassOf 'metabolic disease with dementia'
'pantothenate kinase-associated neurodegeneration' SubClassOf 'inherited neurodegenerative disorder'
http://purl.obolibrary.org/obo/MONDO_0000989
mumps
'mumps' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_11161
'mumps' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_11161
http://purl.obolibrary.org/obo/MONDO_0010320
retinitis pigmentosa 23
'retinitis pigmentosa 23' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_8481
'retinitis pigmentosa 23' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_8481)
http://purl.obolibrary.org/obo/SCTID_63365006
'multiple symmetric lipomatosis' EquivalentTo http://purl.obolibrary.org/obo/SCTID_63365006
http://purl.obolibrary.org/obo/MONDO_0000827
salmonellosis
'salmonellosis' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002013
'salmonellosis' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002027
'salmonellosis' SubClassOf 'disease has feature' some 'dysentery'
http://purl.obolibrary.org/obo/MONDO_0009215
Fanconi anemia complementation group a
'Fanconi anemia complementation group a' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2175
'Fanconi anemia complementation group a' EquivalentTo 'Fanconi anemia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2175)
http://purl.obolibrary.org/obo/MONDO_0010206
hypotrichosis 8
'hypotrichosis 8' EquivalentTo 'hypotrichosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10161)
'hypotrichosis 8' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10161
http://purl.obolibrary.org/obo/MONDO_0010216
xeroderma pigmentosum group G
'xeroderma pigmentosum group G' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2073
'xeroderma pigmentosum group G' EquivalentTo 'xeroderma pigmentosum' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2073)
http://purl.obolibrary.org/obo/MONDO_0010215
xeroderma pigmentosum group F
'xeroderma pigmentosum group F' EquivalentTo 'xeroderma pigmentosum' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2072)
'xeroderma pigmentosum group F' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2072
http://purl.obolibrary.org/obo/MONDO_0009223
hypogonadotropic hypogonadism 23 with or without anosmia
'hypogonadotropic hypogonadism 23 with or without anosmia' EquivalentTo 'hypogonadotropic hypogonadism' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3972)
'hypogonadotropic hypogonadism 23 with or without anosmia' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3972
http://purl.obolibrary.org/obo/MONDO_0010210
xeroderma pigmentosum group A
'xeroderma pigmentosum group A' EquivalentTo 'xeroderma pigmentosum' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7507)
'xeroderma pigmentosum group A' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7507
http://purl.obolibrary.org/obo/MONDO_0010212
xeroderma pigmentosum group D
'xeroderma pigmentosum group D' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2068
'xeroderma pigmentosum group D' EquivalentTo 'xeroderma pigmentosum' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2068)
http://purl.obolibrary.org/obo/MONDO_0009239
hypogonadotropic hypogonadism 24 without anosmia
'hypogonadotropic hypogonadism 24 without anosmia' EquivalentTo 'hypogonadotropic hypogonadism' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2488)
'hypogonadotropic hypogonadism 24 without anosmia' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2488
http://purl.obolibrary.org/obo/MONDO_0010227
retinitis pigmentosa 3
'retinitis pigmentosa 3' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6103)
'retinitis pigmentosa 3' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6103
http://purl.obolibrary.org/obo/MONDO_0010241
congenital stationary night blindness 2A
'congenital stationary night blindness 2A' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_778
'congenital stationary night blindness 2A' EquivalentTo 'congenital stationary night blindness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_778)
http://purl.obolibrary.org/obo/MONDO_0010298
Lesch-Nyhan syndrome
'Lesch-Nyhan syndrome' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0100716
http://purl.obolibrary.org/obo/MONDO_0000709
Crohn ileitis
'Crohn ileitis' SubClassOf 'inflammatory disease'
'Crohn ileitis' SubClassOf 'Crohn disease'
'Crohn ileitis' SubClassOf 'small bowel Crohn disease'
http://purl.obolibrary.org/obo/MONDO_0000705
clostridium difficile colitis
'clostridium difficile colitis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_1496
'clostridium difficile colitis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_1496
http://purl.obolibrary.org/obo/MONDO_0000710
gastroduodenal Crohn disease
'gastroduodenal Crohn disease' SubClassOf 'gastritis (disease)'
'gastroduodenal Crohn disease' SubClassOf 'Crohn disease'
'gastroduodenal Crohn disease' SubClassOf 'bacterial gastritis'
'gastroduodenal Crohn disease' SubClassOf 'viral gastritis'
'gastroduodenal Crohn disease' SubClassOf 'small bowel Crohn disease'
http://purl.obolibrary.org/obo/MONDO_0000727
scapuloperoneal myopathy
'scapuloperoneal myopathy' SubClassOf 'muscular dystrophy'
http://purl.obolibrary.org/obo/MESH_C536624 EquivalentTo 'scapuloperoneal myopathy'
'scapuloperoneal myopathy' SubClassOf 'Emery-Dreifuss muscular dystrophy'
http://purl.obolibrary.org/obo/MONDO_0000758
bacillary angiomatosis
'bacillary angiomatosis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_38323
http://purl.obolibrary.org/obo/MONDO_0009101
Wolfram syndrome 1
'Wolfram syndrome 1' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7466
'Wolfram syndrome 1' EquivalentTo 'Wolfram syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7466)
http://purl.obolibrary.org/obo/MONDO_0009112
rhizomelic chondrodysplasia punctata type 2
'rhizomelic chondrodysplasia punctata type 2' EquivalentTo 'rhizomelic chondrodysplasia punctata' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_8443)
'rhizomelic chondrodysplasia punctata type 2' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_8443
http://purl.obolibrary.org/obo/MONDO_0009157
split hand-foot malformation 6
'split hand-foot malformation 6' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7480
'split hand-foot malformation 6' EquivalentTo 'split hand-foot malformation' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7480)
http://purl.obolibrary.org/obo/MONDO_0010169
Usher syndrome type 2A
'Usher syndrome type 2A' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7399
'Usher syndrome type 2A' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_79955
'Usher syndrome type 2A' EquivalentTo 'Usher syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7399) and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_79955)
'Usher syndrome type 2A' SubClassOf 'retinitis pigmentosa 39'
http://purl.obolibrary.org/obo/MONDO_0010170
Usher syndrome type 3A
'Usher syndrome type 3A' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7401
'Usher syndrome type 3A' EquivalentTo 'Usher syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7401)
'Usher syndrome type 3A' SubClassOf 'retinitis pigmentosa 61'
http://purl.obolibrary.org/obo/MONDO_0010198
Wernicke-Korsakoff syndrome
'Wernicke-Korsakoff syndrome' SubClassOf 'inborn errors of metabolism'
'Wernicke-Korsakoff syndrome' SubClassOf 'alcohol amnestic disorder'
http://purl.obolibrary.org/obo/MESH_C538669 EquivalentTo 'Wernicke-Korsakoff syndrome'
http://purl.obolibrary.org/obo/MONDO_0005404
myalgic encephalomeyelitis/Chronic fatigue syndrome
'myalgic encephalomeyelitis/Chronic fatigue syndrome' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002315
http://purl.obolibrary.org/obo/MONDO_0005459
human african trypanosomiasis
'human african trypanosomiasis' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002315
'human african trypanosomiasis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_5691
'human african trypanosomiasis' SubClassOf 'disease has feature' some 'anemia (disease)'
'human african trypanosomiasis' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0001903
http://purl.obolibrary.org/obo/MONDO_0005316
bacterial vaginosis
'bacterial vaginosis' SubClassOf 'bacterial infectious disease'
'bacterial vaginosis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_2702
'bacterial vaginosis' SubClassOf 'bifidobacteriales infectious disease'
http://purl.obolibrary.org/obo/MONDO_0019956
encephalitis
'encephalitis' SubClassOf 'inflammatory disease'
'encephalitis' SubClassOf 'encephalomyelitis'
http://purl.obolibrary.org/obo/MONDO_0019960
VIPoma
'VIPoma' SubClassOf 'disease has feature' some 'pancreatic cholera'
http://purl.obolibrary.org/obo/MONDO_0005344
hepatitis B
'hepatitis B' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_10407
'hepatitis B' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_10407
http://purl.obolibrary.org/obo/MONDO_0005393
gout
'gout' SubClassOf 'disease has feature' some 'hydrarthrosis'
http://purl.obolibrary.org/obo/MONDO_0005231
hepatitis C
'hepatitis C' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_11103
'hepatitis C' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_11103
http://purl.obolibrary.org/obo/MONDO_0005249
pneumonia
'pneumonia' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0012735
'pneumonia' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002789
http://purl.obolibrary.org/obo/MONDO_0005250
placental villitis
'placental villitis' SubClassOf 'inflammatory disease'
http://purl.obolibrary.org/obo/MONDO_0005277
migraine disorder
'migraine disorder' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002013
http://purl.obolibrary.org/obo/MONDO_0005291
brain aneurysm
'brain aneurysm' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002013
'brain aneurysm' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0009830
http://purl.obolibrary.org/obo/MONDO_0005108
viral infectious disease
'viral infectious disease' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_10239
'viral infectious disease' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_10239
http://purl.obolibrary.org/obo/MONDO_0005113
bacterial infectious disease
'bacterial infectious disease' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_2
'bacterial infectious disease' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_2
http://purl.obolibrary.org/obo/MONDO_0005124
leprosy
'leprosy' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_1769
'leprosy' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_1769
'leprosy' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_480418
http://purl.obolibrary.org/obo/MONDO_0005136
malaria
'malaria' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_5820
'malaria' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0001903
'malaria' SubClassOf 'disease has feature' some 'anemia (disease)'
http://purl.obolibrary.org/obo/MONDO_0019632
lyme disease
'lyme disease' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_139
'lyme disease' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_139
'lyme disease' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002315
'lyme disease' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0011675
http://purl.obolibrary.org/obo/MONDO_0005011
Crohn disease
'Crohn disease' SubClassOf 'disease has feature' some 'gingivitis'
'Crohn disease' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0000230
'Crohn disease' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0011107
'Crohn disease' SubClassOf 'disease has feature' some 'dysentery'
'Crohn disease' SubClassOf 'disease has feature' some 'constipation disorder'
'Crohn disease' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002019
'Crohn disease' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002027
http://purl.obolibrary.org/obo/MONDO_0005059
leukemia (disease)
'leukemia (disease)' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002321
http://purl.obolibrary.org/obo/MONDO_0005077
whooping cough
'whooping cough' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_520
'whooping cough' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_520
http://purl.obolibrary.org/obo/MONDO_0005091
severe acute respiratory syndrome
'severe acute respiratory syndrome' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0012735
'severe acute respiratory syndrome' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002315
'severe acute respiratory syndrome' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_694009
http://purl.obolibrary.org/obo/MONDO_0019508
van der Woude syndrome
'van der Woude syndrome' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0000175
'van der Woude syndrome' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0100267
http://purl.obolibrary.org/obo/MONDO_0019505
hypomyelination-hypogonadotropic hypogonadism-hypodontia syndrome
'hypomyelination-hypogonadotropic hypogonadism-hypodontia syndrome' SubClassOf 'hypomyelinating leukodystrophy 7 with or without oligodontia and-or hypogonadotropic hypogonadism'
http://purl.obolibrary.org/obo/MONDO_0019516
exudative vitreoretinopathy
http://purl.obolibrary.org/obo/MESH_C580083 EquivalentTo 'exudative vitreoretinopathy'
http://purl.obolibrary.org/obo/MONDO_0020502
yellow fever
'yellow fever' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_11089
'yellow fever' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002013
'yellow fever' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_11089
'yellow fever' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002315
http://purl.obolibrary.org/obo/MONDO_0019496
neuroendocrine tumor
'neuroendocrine tumor' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002027
'neuroendocrine tumor' SubClassOf 'disease has feature' some 'dysentery'
http://purl.obolibrary.org/obo/MONDO_0009927
3MC syndrome 2
'3MC syndrome 2' EquivalentTo '3MC syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_78989)
'3MC syndrome 2' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_78989
http://purl.obolibrary.org/obo/MONDO_0010915
autosomal dominant nonsyndromic deafness 4A
'autosomal dominant nonsyndromic deafness 4A' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_79784
'autosomal dominant nonsyndromic deafness 4A' EquivalentTo 'autosomal dominant nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_79784)
http://purl.obolibrary.org/obo/MONDO_0010926
familial hypocalciuric hypercalcemia 3
'familial hypocalciuric hypercalcemia 3' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1175
'familial hypocalciuric hypercalcemia 3' EquivalentTo 'familial hypocalciuric hypercalcemia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1175)
http://purl.obolibrary.org/obo/MONDO_0010933
autosomal recessive nonsyndromic deafness 4
'autosomal recessive nonsyndromic deafness 4' EquivalentTo 'autosomal recessive nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2299) and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3766) and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5172)
'autosomal recessive nonsyndromic deafness 4' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3766
'autosomal recessive nonsyndromic deafness 4' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2299
'autosomal recessive nonsyndromic deafness 4' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5172
http://purl.obolibrary.org/obo/MONDO_0010946
hypertrophic cardiomyopathy 6
'hypertrophic cardiomyopathy 6' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_51422
'hypertrophic cardiomyopathy 6' EquivalentTo 'hypertrophic cardiomyopathy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_51422)
http://purl.obolibrary.org/obo/MONDO_0010945
retinitis pigmentosa 17
'retinitis pigmentosa 17' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_762)
'retinitis pigmentosa 17' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_762
http://purl.obolibrary.org/obo/MONDO_0010953
Fanconi anemia complementation group E
'Fanconi anemia complementation group E' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2178
'Fanconi anemia complementation group E' EquivalentTo 'Fanconi anemia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2178)
http://purl.obolibrary.org/obo/MONDO_0009960
inflammatory bowel disease 1
'inflammatory bowel disease 1' EquivalentTo 'inflammatory bowel disease' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3569) and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_64127)
'inflammatory bowel disease 1' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_64127
'inflammatory bowel disease 1' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3569
http://purl.obolibrary.org/obo/MONDO_0010963
autosomal dominant nonsyndromic deafness 6
'autosomal dominant nonsyndromic deafness 6' EquivalentTo 'autosomal dominant nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7466)
'autosomal dominant nonsyndromic deafness 6' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7466
http://purl.obolibrary.org/obo/MONDO_0010965
autosomal recessive nonsyndromic deafness 6
'autosomal recessive nonsyndromic deafness 6' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_259236
'autosomal recessive nonsyndromic deafness 6' EquivalentTo 'autosomal recessive nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_259236)
http://purl.obolibrary.org/obo/MONDO_0010967
autosomal recessive nonsyndromic deafness 7
'autosomal recessive nonsyndromic deafness 7' EquivalentTo 'autosomal recessive nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_117531)
'autosomal recessive nonsyndromic deafness 7' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_117531
http://purl.obolibrary.org/obo/MONDO_0010979
Timothy syndrome
'Timothy syndrome' SubClassOf 'disease has feature' some 'ventricular fibrillation (disease)'
'Timothy syndrome' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0001663
'Timothy syndrome' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0001279
'Timothy syndrome' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0001649
'Timothy syndrome' SubClassOf 'disease has feature' some 'heart conduction disease'
http://purl.obolibrary.org/obo/MONDO_0010973
autosomal dominant nonsyndromic deafness 5
'autosomal dominant nonsyndromic deafness 5' EquivalentTo 'autosomal dominant nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1687)
'autosomal dominant nonsyndromic deafness 5' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1687
http://purl.obolibrary.org/obo/MONDO_0010986
autosomal recessive nonsyndromic deafness 9
'autosomal recessive nonsyndromic deafness 9' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9381
'autosomal recessive nonsyndromic deafness 9' EquivalentTo 'autosomal recessive nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9381)
http://purl.obolibrary.org/obo/MONDO_0010995
Charcot-Marie-tooth disease type 1C
'Charcot-Marie-tooth disease type 1C' EquivalentTo 'Charcot-Marie-tooth disease type 1' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9516)
'Charcot-Marie-tooth disease type 1C' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9516
http://purl.obolibrary.org/obo/MONDO_0019345
shigellosis
'shigellosis' SubClassOf 'disease has feature' some 'dysentery'
'shigellosis' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002027
'shigellosis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_620
http://purl.obolibrary.org/obo/MONDO_0019355
adult-onset Still disease
'adult-onset Still disease' SubClassOf 'disease has feature' some 'hemophagocytic syndrome'
'adult-onset Still disease' SubClassOf 'disease has feature' some 'pharyngitis'
http://purl.obolibrary.org/obo/MONDO_0019362
epidemic typhus
'epidemic typhus' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_782
'epidemic typhus' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_782
http://purl.obolibrary.org/obo/MONDO_0019380
western equine encephalitis
'western equine encephalitis' SubClassOf 'encephalomyelitis'
http://purl.obolibrary.org/obo/MONDO_0019383
acute disseminated encephalomyelitis
'acute disseminated encephalomyelitis' SubClassOf 'encephalomyelitis'
http://purl.obolibrary.org/obo/MONDO_0001112
bubonic plague
'bubonic plague' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_632
http://purl.obolibrary.org/obo/MONDO_0015766
cholera
'cholera' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002013
'cholera' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_666
'cholera' SubClassOf 'disease has feature' some 'dysentery'
http://purl.obolibrary.org/obo/MONDO_0015636
dirofilariasis
'dirofilariasis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_6287
'dirofilariasis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_6286
'dirofilariasis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_31241
http://purl.obolibrary.org/obo/MONDO_0015474
cryptosporidiosis
'cryptosporidiosis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_5807
'cryptosporidiosis' SubClassOf 'disease has feature' some 'dysentery'
http://purl.obolibrary.org/obo/MONDO_0005976
syphilis
'syphilis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_160
http://purl.obolibrary.org/obo/MONDO_0005978
theileriasis
'theileriasis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_5873
http://purl.obolibrary.org/obo/MONDO_0005974
strongyloidiasis
'strongyloidiasis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_6248
http://purl.obolibrary.org/obo/MONDO_0005988
toxocariasis
'toxocariasis' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0000618
'toxocariasis' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0012735
'toxocariasis' SubClassOf 'disease has feature' some 'blindness'
'toxocariasis' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002315
'toxocariasis' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002027
http://purl.obolibrary.org/obo/MONDO_0005989
toxoplasmosis
'toxoplasmosis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_5811
'toxoplasmosis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_5811
'toxoplasmosis' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002383
http://purl.obolibrary.org/obo/MONDO_0005996
trichuriasis
'trichuriasis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_36087
'trichuriasis' SubClassOf 'disease has feature' some 'hypochromic anemia (disease)'
'trichuriasis' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002027
'trichuriasis' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0001880
'trichuriasis' SubClassOf 'disease has feature' some 'dysentery'
'trichuriasis' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0001931
'trichuriasis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_36087
http://purl.obolibrary.org/obo/MONDO_0005992
trichinosis
'trichinosis' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0001880
'trichinosis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_6333
'trichinosis' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002027
'trichinosis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_6334
http://purl.obolibrary.org/obo/MONDO_0005885
optic neuritis
'optic neuritis' SubClassOf 'encephalomyelitis'
http://purl.obolibrary.org/obo/MONDO_0015254
schistosomiasis
'schistosomiasis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_6181
http://purl.obolibrary.org/obo/MONDO_0015260
diphyllobothriasis
'diphyllobothriasis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_372083
'diphyllobothriasis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_60516
'diphyllobothriasis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_28844
'diphyllobothriasis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_28845
http://purl.obolibrary.org/obo/MONDO_0015288
herpes simplex virus keratitis
'herpes simplex virus keratitis' SubClassOf 'infectious disease of the nervous system'
'herpes simplex virus keratitis' SubClassOf 'rare inflammatory eye disease'
'herpes simplex virus keratitis' SubClassOf 'endophthalmitis'
http://purl.obolibrary.org/obo/MONDO_0005901
pasteurellosis
'pasteurellosis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_747
'pasteurellosis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_745
'pasteurellosis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_747
http://purl.obolibrary.org/obo/MONDO_0005952
scarlet fever
'scarlet fever' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0000988
'scarlet fever' SubClassOf 'disease has feature' some 'exanthem (disease)'
'scarlet fever' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_1314
'scarlet fever' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002013
'scarlet fever' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002027
http://purl.obolibrary.org/obo/MONDO_0005961
sinusitis
'sinusitis' SubClassOf 'inflammatory disease'
http://purl.obolibrary.org/obo/MONDO_0005969
st. Louis encephalitis
'st. Louis encephalitis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_11080
'st. Louis encephalitis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_11080
http://purl.obolibrary.org/obo/MONDO_0005737
Ebola hemorrhagic fever
'Ebola hemorrhagic fever' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002013
'Ebola hemorrhagic fever' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002315
'Ebola hemorrhagic fever' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0000509
'Ebola hemorrhagic fever' SubClassOf 'disease has feature' some 'dysentery'
'Ebola hemorrhagic fever' SubClassOf 'disease has feature' some 'conjunctivitis (disease)'
http://purl.obolibrary.org/obo/MONDO_0005738
echinococcosis
'echinococcosis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_6210
'echinococcosis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_6209
http://purl.obolibrary.org/obo/MONDO_0005746
enterobiasis
'enterobiasis' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002027
'enterobiasis' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002019
'enterobiasis' SubClassOf 'disease has feature' some 'constipation disorder'
http://purl.obolibrary.org/obo/MONDO_0005753
epiglottitis
'epiglottitis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_727
http://purl.obolibrary.org/obo/MONDO_0005761
filarial elephantiasis
'filarial elephantiasis' SubClassOf 'disease has feature' some 'elephantiasis'
http://purl.obolibrary.org/obo/MONDO_0005777
granuloma inguinale
'granuloma inguinale' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_39824
'granuloma inguinale' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_39824
http://purl.obolibrary.org/obo/MONDO_0005800
hordeolum
'hordeolum' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_1280
http://purl.obolibrary.org/obo/MONDO_0005802
hymenolepiasis
'hymenolepiasis' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002013
'hymenolepiasis' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002027
'hymenolepiasis' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002315
'hymenolepiasis' SubClassOf 'disease has feature' some 'anemia (disease)'
'hymenolepiasis' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0001903
http://purl.obolibrary.org/obo/MONDO_0005808
inclusion conjunctivitis
'inclusion conjunctivitis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_813
http://purl.obolibrary.org/obo/MONDO_0005812
influenza
'influenza' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002315
'influenza' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_11308
http://purl.obolibrary.org/obo/MONDO_0005810
infectious mononucleosis
'infectious mononucleosis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_10376
http://purl.obolibrary.org/obo/MONDO_0005824
Legionnaires' disease
'Legionnaires' disease' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002315
'Legionnaires' disease' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_446
'Legionnaires' disease' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0012735
http://purl.obolibrary.org/obo/MONDO_0005829
louping ill
'louping ill' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_11086
'louping ill' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_11086
http://purl.obolibrary.org/obo/MONDO_0005834
lymphogranuloma venereum
'lymphogranuloma venereum' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_813
'lymphogranuloma venereum' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_471472
http://purl.obolibrary.org/obo/MONDO_0005832
lymphangitis
'lymphangitis' SubClassOf 'inflammatory disease'
'lymphangitis' SubClassOf 'vascular disease'
'lymphangitis' SubClassOf 'rare bacterial infectious disease'
'lymphangitis' SubClassOf 'streptococcal infection'
'lymphangitis' SubClassOf 'vasculitis'
'lymphangitis' SubClassOf 'rare immune disease'
'lymphangitis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_1314
http://purl.obolibrary.org/obo/MONDO_0005619
typhoid fever
'typhoid fever' SubClassOf 'primary bacterial infectious disease'
'typhoid fever' SubClassOf 'disease has feature' some 'intestinal perforation'
'typhoid fever' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_28901
'typhoid fever' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0000988
'typhoid fever' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002315
'typhoid fever' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002019
'typhoid fever' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002239
'typhoid fever' SubClassOf 'salmonellosis'
'typhoid fever' SubClassOf 'disease has feature' some 'exanthem (disease)'
'typhoid fever' SubClassOf 'disease has feature' some 'constipation disorder'
http://purl.obolibrary.org/obo/MONDO_0005631
actinomycosis
'actinomycosis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_1654
'actinomycosis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_1654
'actinomycosis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_1659
http://purl.obolibrary.org/obo/MONDO_0005649
appendicitis
'appendicitis' SubClassOf 'inflammatory disease'
'appendicitis' SubClassOf 'gastroenteritis'
'appendicitis' SubClassOf 'diverticulitis of colon'
'appendicitis' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002013
'appendicitis' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002027
http://purl.obolibrary.org/obo/MONDO_0005644
amebiasis
'amebiasis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_5759
http://purl.obolibrary.org/obo/MONDO_0005654
ascariasis
'ascariasis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_6252
http://purl.obolibrary.org/obo/MONDO_0005664
bartonellosis
'bartonellosis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_773
http://purl.obolibrary.org/obo/MONDO_0005661
babesiosis
'babesiosis' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002013
'babesiosis' SubClassOf 'disease has feature' some 'major depressive disorder'
'babesiosis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_5864
'babesiosis' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002315
http://purl.obolibrary.org/obo/MONDO_0005662
balantidiasis
'balantidiasis' SubClassOf 'disease has feature' some 'dysentery'
'balantidiasis' EquivalentTo 'infectious disease' and ('realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_71584)
'balantidiasis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_71584
'balantidiasis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_71585
'balantidiasis' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002027
http://purl.obolibrary.org/obo/MONDO_0005677
boutonneuse fever
'boutonneuse fever' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_781
http://purl.obolibrary.org/obo/MONDO_0005688
campylobacteriosis
'campylobacteriosis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_197
'campylobacteriosis' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002315
'campylobacteriosis' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002027
'campylobacteriosis' SubClassOf 'disease has feature' some 'dysentery'
'campylobacteriosis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_197
http://purl.obolibrary.org/obo/MONDO_0005683
brucellosis
'brucellosis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_234
http://purl.obolibrary.org/obo/MONDO_0005692
cat-scratch disease
'cat-scratch disease' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_38323
'cat-scratch disease' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_38323
http://purl.obolibrary.org/obo/MONDO_0015015
congenital bile acid synthesis defect 6
'congenital bile acid synthesis defect 6' EquivalentTo 'congenital bile acid synthesis defect' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_8309)
'congenital bile acid synthesis defect 6' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_8309
http://purl.obolibrary.org/obo/MONDO_0015023
nemaline myopathy 11
'nemaline myopathy 11' EquivalentTo 'nemaline myopathy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_84665)
'nemaline myopathy 11' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_84665
http://purl.obolibrary.org/obo/MONDO_0015091
autosomal dominant spastic paraplegia type 9
'autosomal dominant spastic paraplegia type 9' EquivalentTo 'autosomal dominant complex spastic paraplegia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5832)
'autosomal dominant spastic paraplegia type 9' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5832
http://purl.obolibrary.org/obo/MONDO_0005701
chlamydia trachomatis infectious disease
'chlamydia trachomatis infectious disease' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_813
'chlamydia trachomatis infectious disease' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_813
'chlamydia trachomatis infectious disease' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_272561
http://purl.obolibrary.org/obo/MONDO_0005700
chickenpox
'chickenpox' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002315
'chickenpox' SubClassOf 'disease has feature' some 'exanthem (disease)'
'chickenpox' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_10335
'chickenpox' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0000988
http://purl.obolibrary.org/obo/MONDO_0005709
common cold
'common cold' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0012735
http://purl.obolibrary.org/obo/MONDO_0005708
Colorado tick fever
'Colorado tick fever' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_46839
'Colorado tick fever' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_46839
http://purl.obolibrary.org/obo/MONDO_0005717
contagious pustular dermatitis
'contagious pustular dermatitis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_10258
'contagious pustular dermatitis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_10258
http://purl.obolibrary.org/obo/MONDO_0005724
cryptococcosis
'cryptococcosis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_552467
'cryptococcosis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_5207
http://purl.obolibrary.org/obo/MONDO_0005722
croup
'croup' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0012735
http://purl.obolibrary.org/obo/MONDO_0005504
diphtheria
'diphtheria' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_1717
http://purl.obolibrary.org/obo/MONDO_0005502
dengue disease
'dengue disease' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_12637
'dengue disease' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002315
'dengue disease' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002013
http://purl.obolibrary.org/obo/MONDO_0005526
tetanus
'tetanus' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_1513
'tetanus' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_1513
http://purl.obolibrary.org/obo/MONDO_0005537
perianal Crohn disease
'perianal Crohn disease' SubClassOf 'inflammatory disease'
'perianal Crohn disease' SubClassOf 'gastroenteritis'
http://purl.obolibrary.org/obo/MONDO_0005539
small bowel Crohn disease
'small bowel Crohn disease' SubClassOf 'inflammatory disease'
'small bowel Crohn disease' SubClassOf 'gastroenteritis'
http://purl.obolibrary.org/obo/MONDO_0005538
proctitis
'proctitis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_485
http://purl.obolibrary.org/obo/MONDO_0005533
distal colitis
'distal colitis' SubClassOf 'inflammatory disease'
'distal colitis' SubClassOf 'gastroenteritis'
http://purl.obolibrary.org/obo/MONDO_0005609
herpes zoster
'herpes zoster' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_10335
http://purl.obolibrary.org/obo/MONDO_0001941
blindness
'blindness' SubClassOf 'retinopathy'
'blindness' EquivalentTo http://purl.obolibrary.org/obo/SCTID_105597003
'blindness' EquivalentTo 'vision disorder' and ('disease has major feature' some http://purl.obolibrary.org/obo/HP_0000618)
'blindness' SubClassOf 'disease has major feature' some http://purl.obolibrary.org/obo/HP_0000618
http://purl.obolibrary.org/obo/ICD10_H54 EquivalentTo 'blindness'
'blindness' SubClassOf 'vision disorder'
http://purl.obolibrary.org/obo/MONDO_0001979
dumping syndrome
'dumping syndrome' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0001943
http://purl.obolibrary.org/obo/MONDO_0011303
focal segmental glomerulosclerosis 1
'focal segmental glomerulosclerosis 1' EquivalentTo 'focal segmental glomerulosclerosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_81)
'focal segmental glomerulosclerosis 1' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_81
http://purl.obolibrary.org/obo/MONDO_0011339
hereditary spastic paraplegia 8
'hereditary spastic paraplegia 8' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9897
'hereditary spastic paraplegia 8' EquivalentTo 'hereditary spastic paraplegia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9897)
http://purl.obolibrary.org/obo/MONDO_0011351
autosomal recessive nonsyndromic deafness 21
'autosomal recessive nonsyndromic deafness 21' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7007
'autosomal recessive nonsyndromic deafness 21' EquivalentTo 'autosomal recessive nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7007)
http://purl.obolibrary.org/obo/MONDO_0011355
cone-rod dystrophy 7
'cone-rod dystrophy 7' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_22999
'cone-rod dystrophy 7' EquivalentTo 'cone-rod dystrophy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_22999)
http://purl.obolibrary.org/obo/MONDO_0011350
autosomal dominant nonsyndromic deafness 17
'autosomal dominant nonsyndromic deafness 17' EquivalentTo 'autosomal dominant nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4627)
'autosomal dominant nonsyndromic deafness 17' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4627
http://purl.obolibrary.org/obo/MONDO_0011364
autosomal recessive nonsyndromic deafness 16
'autosomal recessive nonsyndromic deafness 16' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_161497
'autosomal recessive nonsyndromic deafness 16' EquivalentTo 'autosomal recessive nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_161497)
http://purl.obolibrary.org/obo/MONDO_0011397
autosomal dominant cerebellar ataxia, deafness and narcolepsy
'autosomal dominant cerebellar ataxia, deafness and narcolepsy' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0030050
http://purl.obolibrary.org/obo/MONDO_0011390
focal segmental glomerulosclerosis 2
'focal segmental glomerulosclerosis 2' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7225
'focal segmental glomerulosclerosis 2' EquivalentTo 'focal segmental glomerulosclerosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7225)
http://purl.obolibrary.org/obo/MONDO_0011192
autosomal recessive nonsyndromic deafness 18A
'autosomal recessive nonsyndromic deafness 18A' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10083
'autosomal recessive nonsyndromic deafness 18A' EquivalentTo 'autosomal recessive nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_10083)
http://purl.obolibrary.org/obo/MONDO_0001829
lumbosacral plexus lesion
'lumbosacral plexus lesion' SubClassOf 'peripheral nervous system disease'
'lumbosacral plexus lesion' SubClassOf http://purl.obolibrary.org/obo/MONDO_0024432
http://purl.obolibrary.org/obo/MONDO_0001835
facial paralysis
'facial paralysis' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0000297
http://purl.obolibrary.org/obo/MONDO_0011216
hemochromatosis type 2A
'hemochromatosis type 2A' EquivalentTo 'hemochromatosis type 2' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_148738)
'hemochromatosis type 2A' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_148738
http://purl.obolibrary.org/obo/MONDO_0011226
autosomal dominant nonsyndromic deafness 15
'autosomal dominant nonsyndromic deafness 15' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5459
'autosomal dominant nonsyndromic deafness 15' EquivalentTo 'autosomal dominant nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_5459)
http://purl.obolibrary.org/obo/MONDO_0011233
Axenfeld-Rieger syndrome type 3
'Axenfeld-Rieger syndrome type 3' SubClassOf http://purl.obolibrary.org/obo/MONDO_0024456
'Axenfeld-Rieger syndrome type 3' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2296
'Axenfeld-Rieger syndrome type 3' EquivalentTo 'Axenfeld-Rieger syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2296)
http://purl.obolibrary.org/obo/MONDO_0011272
retinitis pigmentosa 25
'retinitis pigmentosa 25' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_346007)
'retinitis pigmentosa 25' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_346007
http://purl.obolibrary.org/obo/MONDO_0011058
autosomal dominant nonsyndromic deafness 9
'autosomal dominant nonsyndromic deafness 9' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1690
'autosomal dominant nonsyndromic deafness 9' EquivalentTo 'autosomal dominant nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1690)
http://purl.obolibrary.org/obo/MONDO_0011068
type 1 diabetes mellitus 12
'type 1 diabetes mellitus 12' EquivalentTo 'type 1 diabetes mellitus' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1493)
'type 1 diabetes mellitus 12' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1493
http://purl.obolibrary.org/obo/MONDO_0011067
autosomal recessive nonsyndromic deafness 12
'autosomal recessive nonsyndromic deafness 12' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_64072
'autosomal recessive nonsyndromic deafness 12' EquivalentTo 'autosomal recessive nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_491) and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_64072)
'autosomal recessive nonsyndromic deafness 12' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_491
http://purl.obolibrary.org/obo/MONDO_0011075
retinitis pigmentosa 18
'retinitis pigmentosa 18' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9129)
'retinitis pigmentosa 18' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_9129
http://purl.obolibrary.org/obo/MONDO_0011088
congenital myasthenic syndrome 1A
'congenital myasthenic syndrome 1A' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1134
'congenital myasthenic syndrome 1A' EquivalentTo 'congenital myasthenic syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1134)
http://purl.obolibrary.org/obo/MONDO_0001714
bejel
'bejel' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_160
http://purl.obolibrary.org/obo/MONDO_0011103
autosomal dominant nonsyndromic deafness 3A
'autosomal dominant nonsyndromic deafness 3A' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2706
'autosomal dominant nonsyndromic deafness 3A' EquivalentTo 'autosomal dominant nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2706)
http://purl.obolibrary.org/obo/MONDO_0011102
autosomal dominant nonsyndromic deafness 12
'autosomal dominant nonsyndromic deafness 12' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7007
'autosomal dominant nonsyndromic deafness 12' EquivalentTo 'autosomal dominant nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7007)
http://purl.obolibrary.org/obo/MONDO_0001797
chancroid
'chancroid' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_730
'chancroid' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_730
http://purl.obolibrary.org/obo/MONDO_0011119
anterior segment dysgenesis 3
http://purl.obolibrary.org/obo/DOID_0050786 EquivalentTo 'anterior segment dysgenesis 3'
'anterior segment dysgenesis 3' EquivalentTo http://purl.obolibrary.org/obo/OMIM_601631
http://purl.obolibrary.org/obo/MESH_C535535 EquivalentTo 'anterior segment dysgenesis 3'
'anterior segment dysgenesis 3' SubClassOf 'autosomal dominant disease'
http://purl.obolibrary.org/obo/GARD_0002482 EquivalentTo 'anterior segment dysgenesis 3'
'anterior segment dysgenesis 3' SubClassOf 'anterior segment dysgenesis'
http://purl.obolibrary.org/obo/MONDO_0011137
retinitis pigmentosa 19
'retinitis pigmentosa 19' EquivalentTo 'retinitis pigmentosa' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_24)
'retinitis pigmentosa 19' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_24
http://purl.obolibrary.org/obo/MONDO_0011143
cone-rod dystrophy 6
'cone-rod dystrophy 6' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3000
'cone-rod dystrophy 6' EquivalentTo 'cone-rod dystrophy' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3000)
http://purl.obolibrary.org/obo/MONDO_0011159
autosomal dominant nonsyndromic deafness 13
'autosomal dominant nonsyndromic deafness 13' EquivalentTo 'autosomal dominant nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1302)
'autosomal dominant nonsyndromic deafness 13' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_1302
http://purl.obolibrary.org/obo/MONDO_0011168
type 1 diabetes mellitus 10
'type 1 diabetes mellitus 10' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3559
'type 1 diabetes mellitus 10' EquivalentTo 'type 1 diabetes mellitus' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_3559)
http://purl.obolibrary.org/obo/MONDO_0011160
autosomal recessive nonsyndromic deafness 15
'autosomal recessive nonsyndromic deafness 15' EquivalentTo 'autosomal recessive nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_126326)
'autosomal recessive nonsyndromic deafness 15' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_126326
http://purl.obolibrary.org/obo/MONDO_0001650
acute cystitis (disease)
'acute cystitis (disease)' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0002027
http://purl.obolibrary.org/obo/MONDO_0011001
Brugada syndrome 1
'Brugada syndrome 1' EquivalentTo 'Brugada syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6331)
'Brugada syndrome 1' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_6331
http://purl.obolibrary.org/obo/MONDO_0011013
autosomal dominant hypocalcemia 1
'autosomal dominant hypocalcemia 1' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_846
'autosomal dominant hypocalcemia 1' EquivalentTo 'autosomal dominant hypocalcemia' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_846)
http://purl.obolibrary.org/obo/MONDO_0011026
autosomal recessive congenital ichthyosis 4A
'autosomal recessive congenital ichthyosis 4A' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_26154
'autosomal recessive congenital ichthyosis 4A' EquivalentTo 'autosomal recessive congenital ichthyosis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_26154)
http://purl.obolibrary.org/obo/MONDO_0011032
autosomal dominant nonsyndromic deafness 11
'autosomal dominant nonsyndromic deafness 11' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4647
'autosomal dominant nonsyndromic deafness 11' EquivalentTo 'autosomal dominant nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_4647)
http://purl.obolibrary.org/obo/MONDO_0011031
autosomal dominant nonsyndromic deafness 10
'autosomal dominant nonsyndromic deafness 10' EquivalentTo 'autosomal dominant nonsyndromic deafness' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2070)
'autosomal dominant nonsyndromic deafness 10' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2070
http://purl.obolibrary.org/obo/MONDO_0001517
dysentery
'dysentery' SubClassOf 'gastroenteritis'
http://purl.obolibrary.org/obo/MONDO_0001543
lesion of sciatic nerve
'lesion of sciatic nerve' SubClassOf http://purl.obolibrary.org/obo/MONDO_0024432
http://purl.obolibrary.org/obo/MONDO_0001424
sarcoid meningitis
'sarcoid meningitis' SubClassOf 'infectious posterior uveitis'
http://purl.obolibrary.org/obo/MONDO_0001444
Chagas disease
'Chagas disease' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_5693
'Chagas disease' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_5693
'Chagas disease' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_70999
http://purl.obolibrary.org/obo/MONDO_0001263
histoplasmosis retinitis
'histoplasmosis retinitis' SubClassOf 'rare eye disease'
'histoplasmosis retinitis' SubClassOf 'infectious disease of the nervous system'
'histoplasmosis retinitis' SubClassOf 'endophthalmitis'
http://purl.obolibrary.org/obo/MONDO_0001277
cerebral arteritis
'cerebral arteritis' SubClassOf 'inflammatory disease'
'cerebral arteritis' SubClassOf 'central nervous system vasculitis'
http://purl.obolibrary.org/obo/MONDO_0001280
choroiditis
'choroiditis' SubClassOf 'uveitis (disease)'
'choroiditis' SubClassOf 'posterior uveitis'
http://purl.obolibrary.org/obo/MONDO_0001307
corneal abscess
'corneal abscess' SubClassOf 'rare eye disease'
'corneal abscess' SubClassOf 'infectious disease of the nervous system'
'corneal abscess' SubClassOf 'endophthalmitis'
http://purl.obolibrary.org/obo/MONDO_0001324
hyperandrogenism
'hyperandrogenism' SubClassOf 'disease has feature' some 'acne (disease)'
'hyperandrogenism' SubClassOf 'disease has feature' some http://purl.obolibrary.org/obo/HP_0001061
http://purl.obolibrary.org/obo/MONDO_0001154
Siberian tick typhus
'Siberian tick typhus' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_35793
'Siberian tick typhus' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_35793
http://purl.obolibrary.org/obo/MONDO_0015805
intestinal botulism
'intestinal botulism' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_1491
http://purl.obolibrary.org/obo/MONDO_0015804
infant botulism
'infant botulism' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_1491
http://purl.obolibrary.org/obo/MONDO_0015803
wound botulism
'wound botulism' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_1491
http://purl.obolibrary.org/obo/MONDO_0001217
pseudomembranous conjunctivitis
'pseudomembranous conjunctivitis' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_1717
http://purl.obolibrary.org/obo/MONDO_0001246
typhus
'typhus' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_780
'typhus' SubClassOf 'realized in response to stimulus' some http://purl.obolibrary.org/obo/NCBITaxon_780
http://purl.obolibrary.org/obo/NCBIGene_4171
http://purl.obolibrary.org/obo/NCBIGene_4171 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_85366
http://purl.obolibrary.org/obo/NCBIGene_85366 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/HP_0004381
http://purl.obolibrary.org/obo/HP_0004381 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_4117
http://purl.obolibrary.org/obo/NCBIGene_4117 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_152137
http://purl.obolibrary.org/obo/NCBIGene_152137 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_4311
http://purl.obolibrary.org/obo/NCBIGene_4311 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_4308
http://purl.obolibrary.org/obo/NCBIGene_4308 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_4254
http://purl.obolibrary.org/obo/NCBIGene_4254 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_4233
http://purl.obolibrary.org/obo/NCBIGene_4233 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBITaxon_7524
http://purl.obolibrary.org/obo/NCBITaxon_7524 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_33342
http://purl.obolibrary.org/obo/NCBIGene_4359
http://purl.obolibrary.org/obo/NCBIGene_4359 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_343035
http://purl.obolibrary.org/obo/NCBIGene_343035 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/PATO_0000048
http://purl.obolibrary.org/obo/PATO_0000048 SubClassOf http://purl.obolibrary.org/obo/PATO_0001546
http://purl.obolibrary.org/obo/NCBITaxon_135623
http://purl.obolibrary.org/obo/NCBITaxon_135623 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_1236
http://purl.obolibrary.org/obo/NCBIGene_85478
http://purl.obolibrary.org/obo/NCBIGene_85478 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBITaxon_33084
http://purl.obolibrary.org/obo/NCBITaxon_33084 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_555406
http://purl.obolibrary.org/obo/NCBIGene_259236
http://purl.obolibrary.org/obo/NCBIGene_259236 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_347733
http://purl.obolibrary.org/obo/NCBIGene_347733 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_166379
http://purl.obolibrary.org/obo/NCBIGene_166379 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_117531
http://purl.obolibrary.org/obo/NCBIGene_117531 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_4038
http://purl.obolibrary.org/obo/NCBIGene_4038 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_4000
http://purl.obolibrary.org/obo/NCBIGene_4000 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_4099
http://purl.obolibrary.org/obo/NCBIGene_4099 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBITaxon_37124
http://purl.obolibrary.org/obo/NCBITaxon_37124 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_177875
http://purl.obolibrary.org/obo/HP_0000011
http://purl.obolibrary.org/obo/HP_0000011 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/HP_0000027
http://purl.obolibrary.org/obo/HP_0000027 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_8540
http://purl.obolibrary.org/obo/NCBIGene_8540 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_8565
http://purl.obolibrary.org/obo/NCBIGene_8565 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_8557
http://purl.obolibrary.org/obo/NCBIGene_8557 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_8556
http://purl.obolibrary.org/obo/NCBIGene_8556 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_768206
http://purl.obolibrary.org/obo/NCBIGene_768206 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_8701
http://purl.obolibrary.org/obo/NCBIGene_8701 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/DOID_0070076
http://purl.obolibrary.org/obo/DOID_0070076 EquivalentTo 'Koolen de Vries syndrome'
http://purl.obolibrary.org/obo/NCBIGene_8626
http://purl.obolibrary.org/obo/NCBIGene_8626 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_8694
http://purl.obolibrary.org/obo/NCBIGene_8694 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/HP_0000230
http://purl.obolibrary.org/obo/HP_0000230 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_8822
http://purl.obolibrary.org/obo/NCBIGene_8822 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/HP_0000297
http://purl.obolibrary.org/obo/HP_0000297 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_8763
http://purl.obolibrary.org/obo/NCBIGene_8763 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_8754
http://purl.obolibrary.org/obo/NCBIGene_8754 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_8722
http://purl.obolibrary.org/obo/NCBIGene_8722 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBITaxon_27994
http://purl.obolibrary.org/obo/NCBITaxon_27994 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_5863
http://purl.obolibrary.org/obo/HP_0000175
http://purl.obolibrary.org/obo/HP_0000175 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_8863
http://purl.obolibrary.org/obo/NCBIGene_8863 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_8864
http://purl.obolibrary.org/obo/NCBIGene_8864 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_8867
http://purl.obolibrary.org/obo/NCBIGene_8867 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_8842
http://purl.obolibrary.org/obo/NCBIGene_8842 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_95681
http://purl.obolibrary.org/obo/NCBIGene_95681 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_81027
http://purl.obolibrary.org/obo/NCBIGene_81027 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_8195
http://purl.obolibrary.org/obo/NCBIGene_8195 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_22999
http://purl.obolibrary.org/obo/NCBIGene_22999 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBITaxon_27479
http://purl.obolibrary.org/obo/NCBITaxon_27479 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_33356
http://purl.obolibrary.org/obo/NCBIGene_22880
http://purl.obolibrary.org/obo/NCBIGene_22880 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_56203
http://purl.obolibrary.org/obo/NCBIGene_56203 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/ENVO_0010003
http://purl.obolibrary.org/obo/ENVO_0010003 SubClassOf http://purl.obolibrary.org/obo/ENVO_0010001
http://purl.obolibrary.org/obo/ENVO_0010001
http://purl.obolibrary.org/obo/ENVO_0010001 SubClassOf http://purl.obolibrary.org/obo/ENVO_00010483
http://purl.obolibrary.org/obo/NCBIGene_494513
http://purl.obolibrary.org/obo/NCBIGene_494513 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_22953
http://purl.obolibrary.org/obo/NCBIGene_22953 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_22954
http://purl.obolibrary.org/obo/NCBIGene_22954 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_22931
http://purl.obolibrary.org/obo/NCBIGene_22931 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_22930
http://purl.obolibrary.org/obo/NCBIGene_22930 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_8216
http://purl.obolibrary.org/obo/NCBIGene_8216 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_22926
http://purl.obolibrary.org/obo/NCBIGene_22926 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_8200
http://purl.obolibrary.org/obo/NCBIGene_8200 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_22909
http://purl.obolibrary.org/obo/NCBIGene_22909 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/HP_0000646
http://purl.obolibrary.org/obo/HP_0000646 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_81570
http://purl.obolibrary.org/obo/NCBIGene_81570 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_8398
http://purl.obolibrary.org/obo/NCBIGene_8398 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/PATO_0000386
http://purl.obolibrary.org/obo/PATO_0000386 SubClassOf http://purl.obolibrary.org/obo/PATO_0000048
http://purl.obolibrary.org/obo/PATO_0000386 SubClassOf http://purl.obolibrary.org/obo/PATO_0002305
http://purl.obolibrary.org/obo/NCBITaxon_552467
http://purl.obolibrary.org/obo/NCBITaxon_552467 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_1884637
http://purl.obolibrary.org/obo/NCBIGene_8309
http://purl.obolibrary.org/obo/NCBIGene_8309 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_56616
http://purl.obolibrary.org/obo/NCBIGene_56616 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/HP_0000534
http://purl.obolibrary.org/obo/HP_0000534 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_8481
http://purl.obolibrary.org/obo/NCBIGene_8481 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_8443
http://purl.obolibrary.org/obo/NCBIGene_8443 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_55526
http://purl.obolibrary.org/obo/NCBIGene_55526 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/HP_0000789
http://purl.obolibrary.org/obo/HP_0000789 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_558
http://purl.obolibrary.org/obo/NCBIGene_558 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_582
http://purl.obolibrary.org/obo/NCBIGene_582 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_583
http://purl.obolibrary.org/obo/NCBIGene_583 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_585
http://purl.obolibrary.org/obo/NCBIGene_585 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_491
http://purl.obolibrary.org/obo/NCBIGene_491 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/MESH_C538344
http://purl.obolibrary.org/obo/MESH_C538344 EquivalentTo 'Navajo neurohepatopathy'
http://purl.obolibrary.org/obo/NCBIGene_65062
http://purl.obolibrary.org/obo/NCBIGene_65062 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_673
http://purl.obolibrary.org/obo/NCBIGene_673 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_649
http://purl.obolibrary.org/obo/NCBIGene_649 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_55679
http://purl.obolibrary.org/obo/NCBIGene_55679 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_658
http://purl.obolibrary.org/obo/NCBIGene_658 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_65018
http://purl.obolibrary.org/obo/NCBIGene_65018 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_55703
http://purl.obolibrary.org/obo/NCBIGene_55703 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_55717
http://purl.obolibrary.org/obo/NCBIGene_55717 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_55737
http://purl.obolibrary.org/obo/NCBIGene_55737 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_79728
http://purl.obolibrary.org/obo/NCBIGene_79728 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_123872
http://purl.obolibrary.org/obo/NCBIGene_123872 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_79583
http://purl.obolibrary.org/obo/NCBIGene_79583 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/HP_0000998
http://purl.obolibrary.org/obo/HP_0000998 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_8048
http://purl.obolibrary.org/obo/NCBIGene_8048 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_783
http://purl.obolibrary.org/obo/NCBIGene_783 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/MESH_C563161
http://purl.obolibrary.org/obo/MESH_C563161 EquivalentTo 'HNP1'
http://purl.obolibrary.org/obo/NCBIGene_762
http://purl.obolibrary.org/obo/NCBIGene_762 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_778
http://purl.obolibrary.org/obo/NCBIGene_778 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_775
http://purl.obolibrary.org/obo/NCBIGene_775 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_55636
http://purl.obolibrary.org/obo/NCBIGene_55636 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_79600
http://purl.obolibrary.org/obo/NCBIGene_79600 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/HP_0000939
http://purl.obolibrary.org/obo/HP_0000939 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_79867
http://purl.obolibrary.org/obo/NCBIGene_79867 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_65217
http://purl.obolibrary.org/obo/NCBIGene_65217 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_65250
http://purl.obolibrary.org/obo/NCBIGene_65250 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_55975
http://purl.obolibrary.org/obo/NCBIGene_55975 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_79947
http://purl.obolibrary.org/obo/NCBIGene_79947 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_79955
http://purl.obolibrary.org/obo/NCBIGene_79955 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/MESH_C538669
http://purl.obolibrary.org/obo/MESH_C538669 EquivalentTo 'Wernicke-Korsakoff syndrome'
http://purl.obolibrary.org/obo/NCBIGene_79738
http://purl.obolibrary.org/obo/NCBIGene_79738 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_107
http://purl.obolibrary.org/obo/NCBIGene_107 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_79784
http://purl.obolibrary.org/obo/NCBIGene_79784 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_79797
http://purl.obolibrary.org/obo/NCBIGene_79797 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_55812
http://purl.obolibrary.org/obo/NCBIGene_55812 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_55823
http://purl.obolibrary.org/obo/NCBIGene_55823 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_79803
http://purl.obolibrary.org/obo/NCBIGene_79803 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_55857
http://purl.obolibrary.org/obo/NCBIGene_55857 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_79848
http://purl.obolibrary.org/obo/NCBIGene_79848 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_55806
http://purl.obolibrary.org/obo/NCBIGene_55806 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_55800
http://purl.obolibrary.org/obo/NCBIGene_55800 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_220
http://purl.obolibrary.org/obo/NCBIGene_220 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_147495
http://purl.obolibrary.org/obo/NCBIGene_147495 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/HP_0009830
http://purl.obolibrary.org/obo/HP_0009830 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_147409
http://purl.obolibrary.org/obo/NCBIGene_147409 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/MESH_C538421
http://purl.obolibrary.org/obo/MESH_C538421 EquivalentTo 'neurodegeneration with brain iron accumulation'
http://purl.obolibrary.org/obo/NCBIGene_387082
http://purl.obolibrary.org/obo/NCBIGene_387082 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_79977
http://purl.obolibrary.org/obo/NCBIGene_79977 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_338
http://purl.obolibrary.org/obo/NCBIGene_338 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_265
http://purl.obolibrary.org/obo/NCBIGene_265 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_258
http://purl.obolibrary.org/obo/NCBIGene_258 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_286
http://purl.obolibrary.org/obo/NCBIGene_286 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_3762
http://purl.obolibrary.org/obo/NCBIGene_3762 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_3766
http://purl.obolibrary.org/obo/NCBIGene_3766 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_3769
http://purl.obolibrary.org/obo/NCBIGene_3769 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_3752
http://purl.obolibrary.org/obo/NCBIGene_3752 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_3753
http://purl.obolibrary.org/obo/NCBIGene_3753 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_3735
http://purl.obolibrary.org/obo/NCBIGene_3735 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBITaxon_1314886
http://purl.obolibrary.org/obo/NCBITaxon_1314886 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_71583
http://purl.obolibrary.org/obo/NCBIGene_3702
http://purl.obolibrary.org/obo/NCBIGene_3702 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_3709
http://purl.obolibrary.org/obo/NCBIGene_3709 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_51057
http://purl.obolibrary.org/obo/NCBIGene_51057 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_90678
http://purl.obolibrary.org/obo/NCBIGene_90678 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_51062
http://purl.obolibrary.org/obo/NCBIGene_51062 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_3796
http://purl.obolibrary.org/obo/NCBIGene_3796 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_26123
http://purl.obolibrary.org/obo/NCBIGene_26123 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_26121
http://purl.obolibrary.org/obo/NCBIGene_26121 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_89765
http://purl.obolibrary.org/obo/NCBIGene_89765 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_51168
http://purl.obolibrary.org/obo/NCBIGene_51168 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_26160
http://purl.obolibrary.org/obo/NCBIGene_26160 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_26154
http://purl.obolibrary.org/obo/NCBIGene_26154 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_26012
http://purl.obolibrary.org/obo/NCBIGene_26012 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_3814
http://purl.obolibrary.org/obo/NCBIGene_3814 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_3800
http://purl.obolibrary.org/obo/NCBIGene_3800 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/HP_0010976
http://purl.obolibrary.org/obo/HP_0010976 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/PATO_0015022
http://purl.obolibrary.org/obo/PATO_0015022 SubClassOf http://purl.obolibrary.org/obo/PATO_0002305
http://purl.obolibrary.org/obo/PATO_0015022 SubClassOf http://purl.obolibrary.org/obo/PATO_0015021
http://purl.obolibrary.org/obo/PATO_0015021
http://purl.obolibrary.org/obo/PATO_0015021 SubClassOf http://purl.obolibrary.org/obo/PATO_0001018
http://purl.obolibrary.org/obo/HP_0030050
http://purl.obolibrary.org/obo/HP_0030050 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_3972
http://purl.obolibrary.org/obo/NCBIGene_3972 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_123016
http://purl.obolibrary.org/obo/NCBIGene_123016 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_51293
http://purl.obolibrary.org/obo/NCBIGene_51293 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_123041
http://purl.obolibrary.org/obo/NCBIGene_123041 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBITaxon_33833
http://purl.obolibrary.org/obo/NCBITaxon_33833 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_163343
http://purl.obolibrary.org/obo/NCBIGene_51364
http://purl.obolibrary.org/obo/NCBIGene_51364 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_3914
http://purl.obolibrary.org/obo/NCBIGene_3914 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_51314
http://purl.obolibrary.org/obo/NCBIGene_51314 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_113612
http://purl.obolibrary.org/obo/NCBIGene_113612 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_89781
http://purl.obolibrary.org/obo/NCBIGene_89781 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_221421
http://purl.obolibrary.org/obo/NCBIGene_221421 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_26258
http://purl.obolibrary.org/obo/NCBIGene_26258 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_51259
http://purl.obolibrary.org/obo/NCBIGene_51259 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_3371
http://purl.obolibrary.org/obo/NCBIGene_3371 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_3329
http://purl.obolibrary.org/obo/NCBIGene_3329 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_3300
http://purl.obolibrary.org/obo/NCBIGene_3300 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_26580
http://purl.obolibrary.org/obo/NCBIGene_26580 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_51501
http://purl.obolibrary.org/obo/NCBIGene_51501 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_51524
http://purl.obolibrary.org/obo/NCBIGene_51524 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_729920
http://purl.obolibrary.org/obo/NCBIGene_729920 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_392255
http://purl.obolibrary.org/obo/NCBIGene_392255 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_3420
http://purl.obolibrary.org/obo/NCBIGene_3420 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_51475
http://purl.obolibrary.org/obo/NCBIGene_51475 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_51473
http://purl.obolibrary.org/obo/NCBIGene_51473 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_51422
http://purl.obolibrary.org/obo/NCBIGene_51422 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_646960
http://purl.obolibrary.org/obo/NCBIGene_646960 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/GO_0043122
http://purl.obolibrary.org/obo/GO_0043122 SubClassOf http://purl.obolibrary.org/obo/GO_1902531
http://purl.obolibrary.org/obo/GO_0043123
http://purl.obolibrary.org/obo/GO_0043123 SubClassOf http://purl.obolibrary.org/obo/GO_1902533
http://purl.obolibrary.org/obo/GO_0043123 SubClassOf http://purl.obolibrary.org/obo/GO_0043122
http://purl.obolibrary.org/obo/GO_0043124
http://purl.obolibrary.org/obo/GO_0043124 SubClassOf http://purl.obolibrary.org/obo/GO_1902532
http://purl.obolibrary.org/obo/GO_0043124 SubClassOf http://purl.obolibrary.org/obo/GO_0043122
http://purl.obolibrary.org/obo/NCBIGene_3508
http://purl.obolibrary.org/obo/NCBIGene_3508 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_152816
http://purl.obolibrary.org/obo/NCBIGene_152816 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/HP_0005508
http://purl.obolibrary.org/obo/HP_0005508 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_3587
http://purl.obolibrary.org/obo/NCBIGene_3587 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_3588
http://purl.obolibrary.org/obo/NCBIGene_3588 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_3569
http://purl.obolibrary.org/obo/NCBIGene_3569 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_3559
http://purl.obolibrary.org/obo/NCBIGene_3559 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBITaxon_33356
http://purl.obolibrary.org/obo/NCBITaxon_33356 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_33354
http://purl.obolibrary.org/obo/NCBITaxon_33354
http://purl.obolibrary.org/obo/NCBITaxon_33354 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_33351
http://purl.obolibrary.org/obo/NCBITaxon_33351
http://purl.obolibrary.org/obo/NCBITaxon_33351 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_33349
http://purl.obolibrary.org/obo/NCBITaxon_33349
http://purl.obolibrary.org/obo/NCBITaxon_33349 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_33347
http://purl.obolibrary.org/obo/NCBITaxon_33347
http://purl.obolibrary.org/obo/NCBITaxon_33347 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_33345
http://purl.obolibrary.org/obo/NCBITaxon_33345
http://purl.obolibrary.org/obo/NCBITaxon_33345 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_33343
http://purl.obolibrary.org/obo/NCBITaxon_33343
http://purl.obolibrary.org/obo/NCBITaxon_33343 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_7524
http://purl.obolibrary.org/obo/NCBIGene_127833
http://purl.obolibrary.org/obo/NCBIGene_127833 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_51778
http://purl.obolibrary.org/obo/NCBIGene_51778 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_3630
http://purl.obolibrary.org/obo/NCBIGene_3630 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_3614
http://purl.obolibrary.org/obo/NCBIGene_3614 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_3694
http://purl.obolibrary.org/obo/NCBIGene_3694 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_3679
http://purl.obolibrary.org/obo/NCBIGene_3679 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_3663
http://purl.obolibrary.org/obo/NCBIGene_3663 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_23020
http://purl.obolibrary.org/obo/NCBIGene_23020 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBITaxon_6334
http://purl.obolibrary.org/obo/NCBITaxon_6334 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_6333
http://purl.obolibrary.org/obo/NCBIGene_23093
http://purl.obolibrary.org/obo/NCBIGene_23093 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBITaxon_6332
http://purl.obolibrary.org/obo/NCBITaxon_6332 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_6329
http://purl.obolibrary.org/obo/NCBITaxon_6333
http://purl.obolibrary.org/obo/NCBITaxon_6333 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_6332
http://purl.obolibrary.org/obo/NCBIGene_5479
http://purl.obolibrary.org/obo/NCBIGene_5479 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_5459
http://purl.obolibrary.org/obo/NCBIGene_5459 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_5660
http://purl.obolibrary.org/obo/NCBIGene_5660 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_5654
http://purl.obolibrary.org/obo/NCBIGene_5654 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBITaxon_6295
http://purl.obolibrary.org/obo/NCBITaxon_6295 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_6274
http://purl.obolibrary.org/obo/NCBITaxon_6296
http://purl.obolibrary.org/obo/NCBITaxon_6296 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_6295
http://purl.obolibrary.org/obo/NCBITaxon_6281
http://purl.obolibrary.org/obo/NCBITaxon_6281 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_6296
http://purl.obolibrary.org/obo/NCBIGene_5648
http://purl.obolibrary.org/obo/NCBIGene_5648 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBITaxon_6286
http://purl.obolibrary.org/obo/NCBITaxon_6286 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_6296
http://purl.obolibrary.org/obo/NCBITaxon_6287
http://purl.obolibrary.org/obo/NCBITaxon_6287 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_6286
http://purl.obolibrary.org/obo/NCBITaxon_6282
http://purl.obolibrary.org/obo/NCBITaxon_6282 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_6281
http://purl.obolibrary.org/obo/NCBIGene_5630
http://purl.obolibrary.org/obo/NCBIGene_5630 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBITaxon_6210
http://purl.obolibrary.org/obo/NCBITaxon_6210 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_6209
http://purl.obolibrary.org/obo/NCBITaxon_6209
http://purl.obolibrary.org/obo/NCBITaxon_6209 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_6208
http://purl.obolibrary.org/obo/NCBITaxon_6251
http://purl.obolibrary.org/obo/NCBITaxon_6251 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_6250
http://purl.obolibrary.org/obo/NCBITaxon_6252
http://purl.obolibrary.org/obo/NCBITaxon_6252 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_6251
http://linkedlifedata.com/resource/umls/id/C0520679
http://linkedlifedata.com/resource/umls/id/C0520679 EquivalentTo 'obstructive sleep apnea syndrome'
http://purl.obolibrary.org/obo/NCBITaxon_6248
http://purl.obolibrary.org/obo/NCBITaxon_6248 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_6247
http://purl.obolibrary.org/obo/NCBITaxon_6246
http://purl.obolibrary.org/obo/NCBITaxon_6246 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_55746
http://purl.obolibrary.org/obo/NCBITaxon_12721
http://purl.obolibrary.org/obo/NCBITaxon_12721 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_693660
http://purl.obolibrary.org/obo/NCBITaxon_6247
http://purl.obolibrary.org/obo/NCBITaxon_6247 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_6246
http://purl.obolibrary.org/obo/MESH_C535800
http://purl.obolibrary.org/obo/MESH_C535800 EquivalentTo 'Gerstmann-Straussler-Scheinker syndrome'
http://purl.obolibrary.org/obo/NCBIGene_23247
http://purl.obolibrary.org/obo/NCBIGene_23247 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_5744
http://purl.obolibrary.org/obo/NCBIGene_5744 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_5727
http://purl.obolibrary.org/obo/NCBIGene_5727 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_5830
http://purl.obolibrary.org/obo/NCBIGene_5830 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_5832
http://purl.obolibrary.org/obo/NCBIGene_5832 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_5825
http://purl.obolibrary.org/obo/NCBIGene_5825 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/HP_0030828
http://purl.obolibrary.org/obo/HP_0030828 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_5888
http://purl.obolibrary.org/obo/NCBIGene_5888 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_5889
http://purl.obolibrary.org/obo/NCBIGene_5889 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_23171
http://purl.obolibrary.org/obo/NCBIGene_23171 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_23418
http://purl.obolibrary.org/obo/NCBIGene_23418 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/MESH_C580202
http://purl.obolibrary.org/obo/MESH_C580202 EquivalentTo 'nemaline myopathy 3'
http://purl.obolibrary.org/obo/NCBIGene_23431
http://purl.obolibrary.org/obo/NCBIGene_23431 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_5076
http://purl.obolibrary.org/obo/NCBIGene_5076 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_24
http://purl.obolibrary.org/obo/NCBIGene_24 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_23389
http://purl.obolibrary.org/obo/NCBIGene_23389 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_70
http://purl.obolibrary.org/obo/NCBIGene_70 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_71
http://purl.obolibrary.org/obo/NCBIGene_71 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_81
http://purl.obolibrary.org/obo/NCBIGene_81 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_23321
http://purl.obolibrary.org/obo/NCBIGene_23321 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_23322
http://purl.obolibrary.org/obo/NCBIGene_23322 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_5158
http://purl.obolibrary.org/obo/NCBIGene_5158 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_5145
http://purl.obolibrary.org/obo/NCBIGene_5145 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_5147
http://purl.obolibrary.org/obo/NCBIGene_5147 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_5148
http://purl.obolibrary.org/obo/NCBIGene_5148 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_5172
http://purl.obolibrary.org/obo/NCBIGene_5172 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_5176
http://purl.obolibrary.org/obo/NCBIGene_5176 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_23639
http://purl.obolibrary.org/obo/NCBIGene_23639 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBITaxon_6181
http://purl.obolibrary.org/obo/NCBITaxon_6181 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_31245
http://purl.obolibrary.org/obo/NCBITaxon_6180
http://purl.obolibrary.org/obo/NCBITaxon_6180 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_6179
http://purl.obolibrary.org/obo/NCBIGene_5308
http://purl.obolibrary.org/obo/NCBIGene_5308 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_200205
http://purl.obolibrary.org/obo/NCBIGene_200205 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/HP_0001114
http://purl.obolibrary.org/obo/HP_0001114 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/HP_0001097
http://purl.obolibrary.org/obo/HP_0001097 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_5269
http://purl.obolibrary.org/obo/NCBIGene_5269 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_5243
http://purl.obolibrary.org/obo/NCBIGene_5243 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/HP_0001061
http://purl.obolibrary.org/obo/HP_0001061 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_5216
http://purl.obolibrary.org/obo/NCBIGene_5216 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_57057
http://purl.obolibrary.org/obo/NCBIGene_57057 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_57096
http://purl.obolibrary.org/obo/NCBIGene_57096 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBITaxon_689832
http://purl.obolibrary.org/obo/NCBITaxon_689832 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_10880
http://purl.obolibrary.org/obo/NCBIGene_23568
http://purl.obolibrary.org/obo/NCBIGene_23568 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_23562
http://purl.obolibrary.org/obo/NCBIGene_23562 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_493856
http://purl.obolibrary.org/obo/NCBIGene_493856 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_5350
http://purl.obolibrary.org/obo/NCBIGene_5350 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_5336
http://purl.obolibrary.org/obo/NCBIGene_5336 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/MESH_C580083
http://purl.obolibrary.org/obo/MESH_C580083 EquivalentTo 'exudative vitreoretinopathy'
http://purl.obolibrary.org/obo/NCBITaxon_1897064
http://purl.obolibrary.org/obo/NCBITaxon_1897064 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_5206
http://purl.obolibrary.org/obo/MESH_C580047
http://purl.obolibrary.org/obo/MESH_C580047 EquivalentTo 'dilated cardiomyopathy 3B'
http://purl.obolibrary.org/obo/SCTID_128127008
'disease of visual system' EquivalentTo http://purl.obolibrary.org/obo/SCTID_128127008
http://purl.obolibrary.org/obo/NCBIGene_346007
http://purl.obolibrary.org/obo/NCBIGene_346007 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_9841
http://purl.obolibrary.org/obo/NCBIGene_9841 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_9829
http://purl.obolibrary.org/obo/NCBIGene_9829 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/MESH_C531642
http://purl.obolibrary.org/obo/MESH_C531642 EquivalentTo 'COL4A1-related familial vascular leukoencephalopathy'
http://purl.obolibrary.org/obo/NCBIGene_253827
http://purl.obolibrary.org/obo/NCBIGene_253827 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_9895
http://purl.obolibrary.org/obo/NCBIGene_9895 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_9897
http://purl.obolibrary.org/obo/NCBIGene_9897 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_9885
http://purl.obolibrary.org/obo/NCBIGene_9885 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_23767
http://purl.obolibrary.org/obo/NCBIGene_23767 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_23746
http://purl.obolibrary.org/obo/NCBIGene_23746 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/HP_0001279
http://purl.obolibrary.org/obo/HP_0001279 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_9992
http://purl.obolibrary.org/obo/NCBIGene_9992 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_57158
http://purl.obolibrary.org/obo/NCBIGene_57158 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_57165
http://purl.obolibrary.org/obo/NCBIGene_57165 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_57449
http://purl.obolibrary.org/obo/NCBIGene_57449 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_57465
http://purl.obolibrary.org/obo/NCBIGene_57465 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBITaxon_372083
http://purl.obolibrary.org/obo/NCBITaxon_372083 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_28844
http://purl.obolibrary.org/obo/NCBIGene_801
http://purl.obolibrary.org/obo/NCBIGene_801 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/HP_0011107
http://purl.obolibrary.org/obo/HP_0011107 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_805
http://purl.obolibrary.org/obo/NCBIGene_805 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBITaxon_480418
http://purl.obolibrary.org/obo/NCBITaxon_480418 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_1763
http://purl.obolibrary.org/obo/HP_0001735
http://purl.obolibrary.org/obo/HP_0001735 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_871
http://purl.obolibrary.org/obo/NCBIGene_871 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_845
http://purl.obolibrary.org/obo/NCBIGene_845 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_846
http://purl.obolibrary.org/obo/NCBIGene_846 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_859
http://purl.obolibrary.org/obo/NCBIGene_859 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_375790
http://purl.obolibrary.org/obo/NCBIGene_375790 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_57709
http://purl.obolibrary.org/obo/NCBIGene_57709 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_9455
http://purl.obolibrary.org/obo/NCBIGene_9455 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/HP_0001663
http://purl.obolibrary.org/obo/HP_0001663 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_939
http://purl.obolibrary.org/obo/NCBIGene_939 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_57582
http://purl.obolibrary.org/obo/NCBIGene_57582 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBITaxon_1511900
http://purl.obolibrary.org/obo/NCBITaxon_1511900 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_40121
http://purl.obolibrary.org/obo/NCBIGene_57545
http://purl.obolibrary.org/obo/NCBIGene_57545 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_9516
http://purl.obolibrary.org/obo/NCBIGene_9516 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_375611
http://purl.obolibrary.org/obo/NCBIGene_375611 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_9573
http://purl.obolibrary.org/obo/NCBIGene_9573 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_9533
http://purl.obolibrary.org/obo/NCBIGene_9533 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/SCTID_95677002
'vision disorder' EquivalentTo http://purl.obolibrary.org/obo/SCTID_95677002
http://purl.obolibrary.org/obo/NCBIGene_92211
http://purl.obolibrary.org/obo/NCBIGene_92211 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_9622
http://purl.obolibrary.org/obo/NCBIGene_9622 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/HP_0001931
http://purl.obolibrary.org/obo/HP_0001931 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_9750
http://purl.obolibrary.org/obo/NCBIGene_9750 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_9731
http://purl.obolibrary.org/obo/NCBIGene_9731 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_9723
http://purl.obolibrary.org/obo/NCBIGene_9723 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_57817
http://purl.obolibrary.org/obo/NCBIGene_57817 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_9782
http://purl.obolibrary.org/obo/NCBIGene_9782 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_9786
http://purl.obolibrary.org/obo/NCBIGene_9786 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_9020
http://purl.obolibrary.org/obo/NCBIGene_9020 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_91147
http://purl.obolibrary.org/obo/NCBIGene_91147 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBITaxon_431838
http://purl.obolibrary.org/obo/NCBITaxon_431838 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_5878
http://purl.obolibrary.org/obo/NCBITaxon_142786
http://purl.obolibrary.org/obo/NCBITaxon_142786 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_11974
http://purl.obolibrary.org/obo/UBERON_0034986
http://purl.obolibrary.org/obo/UBERON_0034986 SubClassOf http://purl.obolibrary.org/obo/UBERON_0001815
http://purl.obolibrary.org/obo/NCBIGene_9187
http://purl.obolibrary.org/obo/NCBIGene_9187 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_9179
http://purl.obolibrary.org/obo/NCBIGene_9179 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_9149
http://purl.obolibrary.org/obo/NCBIGene_9149 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_9132
http://purl.obolibrary.org/obo/NCBIGene_9132 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_9129
http://purl.obolibrary.org/obo/NCBIGene_9129 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_9128
http://purl.obolibrary.org/obo/NCBIGene_9128 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_56623
http://purl.obolibrary.org/obo/NCBIGene_56623 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBITaxon_2701
http://purl.obolibrary.org/obo/NCBITaxon_2701 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_31953
http://purl.obolibrary.org/obo/NCBITaxon_2702
http://purl.obolibrary.org/obo/NCBITaxon_2702 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_2701
http://purl.obolibrary.org/obo/NCBIGene_56683
http://purl.obolibrary.org/obo/NCBIGene_56683 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_9294
http://purl.obolibrary.org/obo/NCBIGene_9294 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_352909
http://purl.obolibrary.org/obo/NCBIGene_352909 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_9227
http://purl.obolibrary.org/obo/NCBIGene_9227 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_9394
http://purl.obolibrary.org/obo/NCBIGene_9394 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_9381
http://purl.obolibrary.org/obo/NCBIGene_9381 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_9364
http://purl.obolibrary.org/obo/NCBIGene_9364 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_81848
http://purl.obolibrary.org/obo/NCBIGene_81848 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_9313
http://purl.obolibrary.org/obo/NCBIGene_9313 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_161582
http://purl.obolibrary.org/obo/NCBIGene_161582 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_27077
http://purl.obolibrary.org/obo/NCBIGene_27077 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_27019
http://purl.obolibrary.org/obo/NCBIGene_27019 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_146183
http://purl.obolibrary.org/obo/NCBIGene_146183 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_27229
http://purl.obolibrary.org/obo/NCBIGene_27229 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_91624
http://purl.obolibrary.org/obo/NCBIGene_91624 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_112802
http://purl.obolibrary.org/obo/NCBIGene_112802 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_220074
http://purl.obolibrary.org/obo/NCBIGene_220074 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_199857
http://purl.obolibrary.org/obo/NCBIGene_199857 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_27329
http://purl.obolibrary.org/obo/NCBIGene_27329 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBITaxon_1648030
http://purl.obolibrary.org/obo/NCBITaxon_1648030 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_147389
http://purl.obolibrary.org/obo/NCBITaxon_1648038
http://purl.obolibrary.org/obo/NCBITaxon_1648038 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_147368
http://purl.obolibrary.org/obo/NCBITaxon_318477
http://purl.obolibrary.org/obo/NCBITaxon_318477 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_55872
http://purl.obolibrary.org/obo/NCBITaxon_318478
http://purl.obolibrary.org/obo/NCBITaxon_318478 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_318477
http://purl.obolibrary.org/obo/NCBITaxon_318479
http://purl.obolibrary.org/obo/NCBITaxon_318479 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_318478
http://purl.obolibrary.org/obo/NCBIGene_161497
http://purl.obolibrary.org/obo/NCBIGene_161497 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBITaxon_32594
http://purl.obolibrary.org/obo/NCBITaxon_32594 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_5863
http://purl.obolibrary.org/obo/NCBIGene_4624
http://purl.obolibrary.org/obo/NCBIGene_4624 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_4625
http://purl.obolibrary.org/obo/NCBIGene_4625 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_4627
http://purl.obolibrary.org/obo/NCBIGene_4627 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_200894
http://purl.obolibrary.org/obo/NCBIGene_200894 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_4669
http://purl.obolibrary.org/obo/NCBIGene_4669 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_126326
http://purl.obolibrary.org/obo/NCBIGene_126326 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_200879
http://purl.obolibrary.org/obo/NCBIGene_200879 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_4643
http://purl.obolibrary.org/obo/NCBIGene_4643 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_4644
http://purl.obolibrary.org/obo/NCBIGene_4644 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_4646
http://purl.obolibrary.org/obo/NCBIGene_4646 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_4647
http://purl.obolibrary.org/obo/NCBIGene_4647 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_4633
http://purl.obolibrary.org/obo/NCBIGene_4633 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_4634
http://purl.obolibrary.org/obo/NCBIGene_4634 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_4593
http://purl.obolibrary.org/obo/NCBIGene_4593 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_4744
http://purl.obolibrary.org/obo/NCBIGene_4744 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_4751
http://purl.obolibrary.org/obo/NCBIGene_4751 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBITaxon_71583
http://purl.obolibrary.org/obo/NCBITaxon_71583 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_33833
http://purl.obolibrary.org/obo/NCBITaxon_71584
http://purl.obolibrary.org/obo/NCBITaxon_71584 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_71583
http://purl.obolibrary.org/obo/NCBITaxon_71585
http://purl.obolibrary.org/obo/NCBITaxon_71585 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_1314886
http://purl.obolibrary.org/obo/MESH_C535435
http://purl.obolibrary.org/obo/MESH_C535435 EquivalentTo 'qualitative or quantitative defects of beta-sarcoglycan'
http://purl.obolibrary.org/obo/NCBITaxon_147389
http://purl.obolibrary.org/obo/NCBITaxon_147389 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_1648038
http://purl.obolibrary.org/obo/NCBIGene_4920
http://purl.obolibrary.org/obo/NCBIGene_4920 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_440435
http://purl.obolibrary.org/obo/NCBIGene_440435 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_4901
http://purl.obolibrary.org/obo/NCBIGene_4901 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_283310
http://purl.obolibrary.org/obo/NCBIGene_283310 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_286676
http://purl.obolibrary.org/obo/NCBIGene_286676 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_6870
http://purl.obolibrary.org/obo/NCBIGene_6870 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_6866
http://purl.obolibrary.org/obo/NCBIGene_6866 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/GO_0007249
http://purl.obolibrary.org/obo/GO_0007249 SubClassOf http://purl.obolibrary.org/obo/GO_0035556
http://purl.obolibrary.org/obo/NCBIGene_6927
http://purl.obolibrary.org/obo/NCBIGene_6927 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_6935
http://purl.obolibrary.org/obo/NCBIGene_6935 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/HP_0002013
http://purl.obolibrary.org/obo/HP_0002013 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBITaxon_60516
http://purl.obolibrary.org/obo/NCBITaxon_60516 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_28844
http://purl.obolibrary.org/obo/NCBITaxon_5234
http://purl.obolibrary.org/obo/NCBITaxon_5234 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_155616
http://purl.obolibrary.org/obo/NCBITaxon_5206
http://purl.obolibrary.org/obo/NCBITaxon_5206 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_1884633
http://purl.obolibrary.org/obo/NCBITaxon_5207
http://purl.obolibrary.org/obo/NCBITaxon_5207 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_1897064
http://purl.obolibrary.org/obo/HP_0100267
http://purl.obolibrary.org/obo/HP_0100267 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_10117
http://purl.obolibrary.org/obo/NCBIGene_10117 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_286204
http://purl.obolibrary.org/obo/NCBIGene_286204 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_345193
http://purl.obolibrary.org/obo/NCBIGene_345193 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_10161
http://purl.obolibrary.org/obo/NCBIGene_10161 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_10142
http://purl.obolibrary.org/obo/NCBIGene_10142 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_286262
http://purl.obolibrary.org/obo/NCBIGene_286262 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_10133
http://purl.obolibrary.org/obo/NCBIGene_10133 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/HP_0100716
http://purl.obolibrary.org/obo/HP_0100716 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_6330
http://purl.obolibrary.org/obo/NCBIGene_6330 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_6331
http://purl.obolibrary.org/obo/NCBIGene_6331 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_6324
http://purl.obolibrary.org/obo/NCBIGene_6324 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_6329
http://purl.obolibrary.org/obo/NCBIGene_6329 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBITaxon_471472
http://purl.obolibrary.org/obo/NCBITaxon_471472 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_813
http://purl.obolibrary.org/obo/NCBITaxon_35082
http://purl.obolibrary.org/obo/NCBITaxon_35082 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_423054
http://purl.obolibrary.org/obo/NCBIGene_130557
http://purl.obolibrary.org/obo/NCBIGene_130557 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_6521
http://purl.obolibrary.org/obo/NCBIGene_6521 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_10083
http://purl.obolibrary.org/obo/NCBIGene_10083 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/MESH_D056768
http://purl.obolibrary.org/obo/MESH_D056768 EquivalentTo 'giant axonal neuropathy'
http://purl.obolibrary.org/obo/NCBIGene_10021
http://purl.obolibrary.org/obo/NCBIGene_10021 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_10008
http://purl.obolibrary.org/obo/NCBIGene_10008 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_10002
http://purl.obolibrary.org/obo/NCBIGene_10002 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_10011
http://purl.obolibrary.org/obo/NCBIGene_10011 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_6469
http://purl.obolibrary.org/obo/NCBIGene_6469 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/HP_0002019
http://purl.obolibrary.org/obo/HP_0002019 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/HP_0002027
http://purl.obolibrary.org/obo/HP_0002027 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBITaxon_11027
http://purl.obolibrary.org/obo/NCBITaxon_11027 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_177875
http://purl.obolibrary.org/obo/NCBIGene_6495
http://purl.obolibrary.org/obo/NCBIGene_6495 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_10345
http://purl.obolibrary.org/obo/NCBIGene_10345 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_10324
http://purl.obolibrary.org/obo/NCBIGene_10324 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_10309
http://purl.obolibrary.org/obo/NCBIGene_10309 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_6640
http://purl.obolibrary.org/obo/NCBIGene_6640 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_6647
http://purl.obolibrary.org/obo/NCBIGene_6647 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_6635
http://purl.obolibrary.org/obo/NCBIGene_6635 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_6616
http://purl.obolibrary.org/obo/NCBIGene_6616 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_10381
http://purl.obolibrary.org/obo/NCBIGene_10381 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_10371
http://purl.obolibrary.org/obo/NCBIGene_10371 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_10370
http://purl.obolibrary.org/obo/NCBIGene_10370 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_6591
http://purl.obolibrary.org/obo/NCBIGene_6591 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_6572
http://purl.obolibrary.org/obo/NCBIGene_6572 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/HP_0002383
http://purl.obolibrary.org/obo/HP_0002383 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_10210
http://purl.obolibrary.org/obo/NCBIGene_10210 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/HP_0002300
http://purl.obolibrary.org/obo/HP_0002300 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_10280
http://purl.obolibrary.org/obo/NCBIGene_10280 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_6710
http://purl.obolibrary.org/obo/NCBIGene_6710 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_6708
http://purl.obolibrary.org/obo/NCBIGene_6708 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_6674
http://purl.obolibrary.org/obo/NCBIGene_6674 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_6678
http://purl.obolibrary.org/obo/NCBIGene_6678 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_6663
http://purl.obolibrary.org/obo/NCBIGene_6663 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_6655
http://purl.obolibrary.org/obo/NCBIGene_6655 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_10584
http://purl.obolibrary.org/obo/NCBIGene_10584 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_10594
http://purl.obolibrary.org/obo/NCBIGene_10594 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBITaxon_5988
http://purl.obolibrary.org/obo/NCBITaxon_5988 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_431838
http://purl.obolibrary.org/obo/NCBIGene_83538
http://purl.obolibrary.org/obo/NCBIGene_83538 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_83544
http://purl.obolibrary.org/obo/NCBIGene_83544 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBITaxon_39700
http://purl.obolibrary.org/obo/NCBITaxon_39700 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_5690
http://purl.obolibrary.org/obo/NCBIGene_83552
http://purl.obolibrary.org/obo/NCBIGene_83552 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBITaxon_5878
http://purl.obolibrary.org/obo/NCBITaxon_5878 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_33630
http://purl.obolibrary.org/obo/NCBITaxon_5873
http://purl.obolibrary.org/obo/NCBITaxon_5873 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_27994
http://purl.obolibrary.org/obo/NCBIGene_10461
http://purl.obolibrary.org/obo/NCBIGene_10461 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBITaxon_5807
http://purl.obolibrary.org/obo/NCBITaxon_5807 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_5806
http://purl.obolibrary.org/obo/NCBITaxon_5806
http://purl.obolibrary.org/obo/NCBITaxon_5806 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_35082
http://purl.obolibrary.org/obo/NCBIGene_10459
http://purl.obolibrary.org/obo/NCBIGene_10459 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBITaxon_5864
http://purl.obolibrary.org/obo/NCBITaxon_5864 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_32594
http://purl.obolibrary.org/obo/NCBITaxon_5863
http://purl.obolibrary.org/obo/NCBITaxon_5863 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_422676
http://purl.obolibrary.org/obo/NCBIGene_6094
http://purl.obolibrary.org/obo/NCBIGene_6094 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_10491
http://purl.obolibrary.org/obo/NCBIGene_10491 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_58484
http://purl.obolibrary.org/obo/NCBIGene_58484 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_10518
http://purl.obolibrary.org/obo/NCBIGene_10518 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_58495
http://purl.obolibrary.org/obo/NCBIGene_58495 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBITaxon_5758
http://purl.obolibrary.org/obo/NCBITaxon_5758 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_33084
http://purl.obolibrary.org/obo/NCBITaxon_5759
http://purl.obolibrary.org/obo/NCBITaxon_5759 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_5758
http://purl.obolibrary.org/obo/NCBIGene_6011
http://purl.obolibrary.org/obo/NCBIGene_6011 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_6010
http://purl.obolibrary.org/obo/NCBIGene_6010 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_6017
http://purl.obolibrary.org/obo/NCBIGene_6017 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_6016
http://purl.obolibrary.org/obo/NCBIGene_6016 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_83715
http://purl.obolibrary.org/obo/NCBIGene_83715 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_286077
http://purl.obolibrary.org/obo/NCBIGene_286077 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_120892
http://purl.obolibrary.org/obo/NCBIGene_120892 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_6121
http://purl.obolibrary.org/obo/NCBIGene_6121 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_6101
http://purl.obolibrary.org/obo/NCBIGene_6101 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_6100
http://purl.obolibrary.org/obo/NCBIGene_6100 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_6103
http://purl.obolibrary.org/obo/NCBIGene_6103 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_6102
http://purl.obolibrary.org/obo/NCBIGene_6102 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_6144
http://purl.obolibrary.org/obo/NCBIGene_6144 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_10806
http://purl.obolibrary.org/obo/NCBIGene_10806 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_10804
http://purl.obolibrary.org/obo/NCBIGene_10804 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_10667
http://purl.obolibrary.org/obo/NCBIGene_10667 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_6295
http://purl.obolibrary.org/obo/NCBIGene_6295 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_10733
http://purl.obolibrary.org/obo/NCBIGene_10733 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_10717
http://purl.obolibrary.org/obo/NCBIGene_10717 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_203068
http://purl.obolibrary.org/obo/NCBIGene_203068 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBITaxon_1884633
http://purl.obolibrary.org/obo/NCBITaxon_1884633 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_5234
http://purl.obolibrary.org/obo/NCBITaxon_1884637
http://purl.obolibrary.org/obo/NCBITaxon_1884637 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_5206
http://purl.obolibrary.org/obo/NCBIGene_374462
http://purl.obolibrary.org/obo/NCBIGene_374462 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_374407
http://purl.obolibrary.org/obo/NCBIGene_374407 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_83861
http://purl.obolibrary.org/obo/NCBIGene_83861 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_83879
http://purl.obolibrary.org/obo/NCBIGene_83879 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_388939
http://purl.obolibrary.org/obo/NCBIGene_388939 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_93233
http://purl.obolibrary.org/obo/NCBIGene_93233 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBITaxon_118882
http://purl.obolibrary.org/obo/NCBITaxon_118882 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_356
http://purl.obolibrary.org/obo/NCBITaxon_5691
http://purl.obolibrary.org/obo/NCBITaxon_5691 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_39700
http://purl.obolibrary.org/obo/NCBITaxon_55872
http://purl.obolibrary.org/obo/NCBITaxon_55872 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_6274
http://purl.obolibrary.org/obo/NCBIGene_92482
http://purl.obolibrary.org/obo/NCBIGene_92482 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/SCTID_105597003
'blindness (disorder)' EquivalentTo http://purl.obolibrary.org/obo/SCTID_105597003
http://purl.obolibrary.org/obo/HP_0012735
http://purl.obolibrary.org/obo/HP_0012735 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_375298
http://purl.obolibrary.org/obo/NCBIGene_375298 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBITaxon_1717
http://purl.obolibrary.org/obo/NCBITaxon_1717 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_1716
http://purl.obolibrary.org/obo/NCBITaxon_1716
http://purl.obolibrary.org/obo/NCBITaxon_1716 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_1653
http://purl.obolibrary.org/obo/ENVO_02000091
http://purl.obolibrary.org/obo/ENVO_02000091 SubClassOf http://purl.obolibrary.org/obo/ENVO_00002016
http://purl.obolibrary.org/obo/NCBIGene_145226
http://purl.obolibrary.org/obo/NCBIGene_145226 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_204219
http://purl.obolibrary.org/obo/NCBIGene_204219 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBITaxon_1653
http://purl.obolibrary.org/obo/NCBITaxon_1653 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_85007
http://purl.obolibrary.org/obo/NCBITaxon_1659
http://purl.obolibrary.org/obo/NCBITaxon_1659 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_1654
http://purl.obolibrary.org/obo/NCBIGene_121391
http://purl.obolibrary.org/obo/NCBIGene_121391 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/GO_0051092
http://purl.obolibrary.org/obo/GO_0051092 SubClassOf http://purl.obolibrary.org/obo/GO_0051091
http://purl.obolibrary.org/obo/NCBIGene_121340
http://purl.obolibrary.org/obo/NCBIGene_121340 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_390594
http://purl.obolibrary.org/obo/NCBIGene_390594 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_389549
http://purl.obolibrary.org/obo/NCBIGene_389549 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBITaxon_70999
http://purl.obolibrary.org/obo/NCBITaxon_70999 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_27479
http://purl.obolibrary.org/obo/NCBIGene_1687
http://purl.obolibrary.org/obo/NCBIGene_1687 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_1690
http://purl.obolibrary.org/obo/NCBIGene_1690 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_92749
http://purl.obolibrary.org/obo/NCBIGene_92749 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_125972
http://purl.obolibrary.org/obo/NCBIGene_125972 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_1639
http://purl.obolibrary.org/obo/NCBIGene_1639 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBITaxon_1314
http://purl.obolibrary.org/obo/NCBITaxon_1314 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_1301
http://purl.obolibrary.org/obo/NCBIGene_1789
http://purl.obolibrary.org/obo/NCBIGene_1789 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_1785
http://purl.obolibrary.org/obo/NCBIGene_1785 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_1767
http://purl.obolibrary.org/obo/NCBIGene_1767 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_1778
http://purl.obolibrary.org/obo/NCBIGene_1778 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_1747
http://purl.obolibrary.org/obo/NCBIGene_1747 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_1756
http://purl.obolibrary.org/obo/NCBIGene_1756 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_1729
http://purl.obolibrary.org/obo/NCBIGene_1729 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBITaxon_662
http://purl.obolibrary.org/obo/NCBITaxon_662 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_641
http://purl.obolibrary.org/obo/NCBITaxon_666
http://purl.obolibrary.org/obo/NCBITaxon_666 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_662
http://purl.obolibrary.org/obo/NCBITaxon_641
http://purl.obolibrary.org/obo/NCBITaxon_641 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_135623
http://purl.obolibrary.org/obo/NCBIGene_282809
http://purl.obolibrary.org/obo/NCBIGene_282809 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBITaxon_55746
http://purl.obolibrary.org/obo/NCBITaxon_55746 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_6236
http://purl.obolibrary.org/obo/NCBIGene_53405
http://purl.obolibrary.org/obo/NCBIGene_53405 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBITaxon_163343
http://purl.obolibrary.org/obo/NCBITaxon_163343 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_5988
http://purl.obolibrary.org/obo/NCBIGene_1848
http://purl.obolibrary.org/obo/NCBIGene_1848 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_1857
http://purl.obolibrary.org/obo/NCBIGene_1857 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_1855
http://purl.obolibrary.org/obo/NCBIGene_1855 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/MESH_C536522
http://purl.obolibrary.org/obo/MESH_C536522 EquivalentTo 'X-linked myopathy with excessive autophagy'
http://purl.obolibrary.org/obo/NCBIGene_1175
http://purl.obolibrary.org/obo/NCBIGene_1175 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_1145
http://purl.obolibrary.org/obo/NCBIGene_1145 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_1141
http://purl.obolibrary.org/obo/NCBIGene_1141 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_1137
http://purl.obolibrary.org/obo/NCBIGene_1137 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_1135
http://purl.obolibrary.org/obo/NCBIGene_1135 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_1134
http://purl.obolibrary.org/obo/NCBIGene_1134 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/MESH_C536624
http://purl.obolibrary.org/obo/MESH_C536624 EquivalentTo 'scapuloperoneal myopathy'
http://purl.obolibrary.org/obo/NCBIGene_1234
http://purl.obolibrary.org/obo/NCBIGene_1234 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/ENVO_00002016
http://purl.obolibrary.org/obo/ENVO_00002016 SubClassOf http://purl.obolibrary.org/obo/ENVO_00001995
http://purl.obolibrary.org/obo/NCBIGene_1296
http://purl.obolibrary.org/obo/NCBIGene_1296 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_1259
http://purl.obolibrary.org/obo/NCBIGene_1259 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_1258
http://purl.obolibrary.org/obo/NCBIGene_1258 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_1337
http://purl.obolibrary.org/obo/NCBIGene_1337 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_1305
http://purl.obolibrary.org/obo/NCBIGene_1305 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_1302
http://purl.obolibrary.org/obo/NCBIGene_1302 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_53904
http://purl.obolibrary.org/obo/NCBIGene_53904 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_28952
http://purl.obolibrary.org/obo/NCBIGene_28952 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBITaxon_1224679
http://purl.obolibrary.org/obo/NCBITaxon_1224679 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_6200
http://purl.obolibrary.org/obo/MESH_C536277
http://purl.obolibrary.org/obo/MESH_C536277 EquivalentTo 'dilated cardiomyopathy 1H'
http://purl.obolibrary.org/obo/NCBITaxon_234
http://purl.obolibrary.org/obo/NCBITaxon_234 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_118882
http://purl.obolibrary.org/obo/MONDO_0024432
nerve plexus disease
'nerve plexus disease' SubClassOf 'peripheral neuropathy'
'nerve plexus disease' SubClassOf 'disease has location' some http://purl.obolibrary.org/obo/UBERON_0001810
'nerve plexus disease' EquivalentTo http://purl.obolibrary.org/obo/SCTID_2231001
'nerve plexus disease' EquivalentTo 'disease' and ('disease has location' some http://purl.obolibrary.org/obo/UBERON_0001810)
http://purl.obolibrary.org/obo/MONDO_0024455
autosomal dominant Robinow syndrome 1
http://purl.obolibrary.org/obo/DOID_0060766 EquivalentTo 'autosomal dominant Robinow syndrome 1'
'autosomal dominant Robinow syndrome 1' EquivalentTo http://purl.obolibrary.org/obo/OMIM_180700
'autosomal dominant Robinow syndrome 1' EquivalentTo 'autosomal dominant Robinow syndrome' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7474)
'autosomal dominant Robinow syndrome 1' SubClassOf 'autosomal dominant Robinow syndrome'
'autosomal dominant Robinow syndrome 1' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_7474
http://purl.obolibrary.org/obo/MONDO_0024454
sacral nerve plexus disease
'sacral nerve plexus disease' SubClassOf 'nerve plexus disease'
'sacral nerve plexus disease' SubClassOf 'disease has location' some http://purl.obolibrary.org/obo/UBERON_0034986
http://purl.obolibrary.org/obo/MESH_C537224 EquivalentTo 'sacral nerve plexus disease'
'sacral nerve plexus disease' EquivalentTo 'disease' and ('disease has location' some http://purl.obolibrary.org/obo/UBERON_0034986)
http://purl.obolibrary.org/obo/MONDO_0024457
neurodegeneration with brain iron accumulation 2A
http://purl.obolibrary.org/obo/GARD_0002751 EquivalentTo 'neurodegeneration with brain iron accumulation 2A'
'neurodegeneration with brain iron accumulation 2A' EquivalentTo http://purl.obolibrary.org/obo/OMIM_256600
http://purl.obolibrary.org/obo/DOID_0110735 EquivalentTo 'neurodegeneration with brain iron accumulation 2A'
'neurodegeneration with brain iron accumulation 2A' SubClassOf 'neurodegeneration with brain iron accumulation'
http://purl.obolibrary.org/obo/MONDO_0024456
anterior segment dysgenesis 3
'anterior segment dysgenesis 3' EquivalentTo 'iridogoniodysgenesis' and ('disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2296)
'anterior segment dysgenesis 3' EquivalentTo http://purl.obolibrary.org/obo/OMIM_601631
'anterior segment dysgenesis 3' SubClassOf 'iris disease'
'anterior segment dysgenesis 3' SubClassOf 'disease has basis in dysfunction of' some http://purl.obolibrary.org/obo/NCBIGene_2296
http://purl.obolibrary.org/obo/MESH_C535535 EquivalentTo 'anterior segment dysgenesis 3'
http://purl.obolibrary.org/obo/GARD_0002482 EquivalentTo 'anterior segment dysgenesis 3'
'anterior segment dysgenesis 3' SubClassOf 'anterior segment dysgenesis'
'anterior segment dysgenesis 3' SubClassOf 'iridogoniodysgenesis'
http://purl.obolibrary.org/obo/MONDO_0024458
disease of visual system
'disease of visual system' SubClassOf 'sensory system disease'
'disease of visual system' SubClassOf 'disease has location' some http://purl.obolibrary.org/obo/UBERON_0002104
'disease of visual system' EquivalentTo http://purl.obolibrary.org/obo/SCTID_128127008
'disease of visual system' EquivalentTo 'disease' and ('disease has location' some http://purl.obolibrary.org/obo/UBERON_0002104)
http://purl.obolibrary.org/obo/NCBIGene_1453
http://purl.obolibrary.org/obo/NCBIGene_1453 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_1428
http://purl.obolibrary.org/obo/NCBIGene_1428 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_1406
http://purl.obolibrary.org/obo/NCBIGene_1406 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_87178
http://purl.obolibrary.org/obo/NCBIGene_87178 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_1495
http://purl.obolibrary.org/obo/NCBIGene_1495 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_1493
http://purl.obolibrary.org/obo/NCBIGene_1493 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBITaxon_160
http://purl.obolibrary.org/obo/NCBITaxon_160 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_157
http://purl.obolibrary.org/obo/NCBITaxon_31245
http://purl.obolibrary.org/obo/NCBITaxon_31245 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_31244
http://purl.obolibrary.org/obo/NCBITaxon_31244
http://purl.obolibrary.org/obo/NCBITaxon_31244 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_6180
http://purl.obolibrary.org/obo/NCBITaxon_31241
http://purl.obolibrary.org/obo/NCBITaxon_31241 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_6286
http://purl.obolibrary.org/obo/NCBIGene_389207
http://purl.obolibrary.org/obo/NCBIGene_389207 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/MESH_C536382
http://purl.obolibrary.org/obo/MESH_C536382 EquivalentTo 'exudative vitreoretinopathy 1'
http://purl.obolibrary.org/obo/NCBIGene_5949
http://purl.obolibrary.org/obo/NCBIGene_5949 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/MESH_C536965
http://purl.obolibrary.org/obo/MESH_C536965 EquivalentTo 'hereditary neuropathy with liability to pressure palsies'
http://purl.obolibrary.org/obo/NCBIGene_5913
http://purl.obolibrary.org/obo/NCBIGene_5913 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_5917
http://purl.obolibrary.org/obo/NCBIGene_5917 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_5995
http://purl.obolibrary.org/obo/NCBIGene_5995 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_5962
http://purl.obolibrary.org/obo/NCBIGene_5962 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_5961
http://purl.obolibrary.org/obo/NCBIGene_5961 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_345895
http://purl.obolibrary.org/obo/NCBIGene_345895 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBITaxon_11974
http://purl.obolibrary.org/obo/NCBITaxon_11974 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_35278
http://purl.obolibrary.org/obo/NCBIGene_149233
http://purl.obolibrary.org/obo/NCBIGene_149233 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_24148
http://purl.obolibrary.org/obo/NCBIGene_24148 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_1073
http://purl.obolibrary.org/obo/NCBIGene_1073 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_1041
http://purl.obolibrary.org/obo/NCBIGene_1041 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_125336
http://purl.obolibrary.org/obo/NCBIGene_125336 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_115948
http://purl.obolibrary.org/obo/NCBIGene_115948 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_11020
http://purl.obolibrary.org/obo/NCBIGene_11020 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_84062
http://purl.obolibrary.org/obo/NCBIGene_84062 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_128674
http://purl.obolibrary.org/obo/NCBIGene_128674 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_138050
http://purl.obolibrary.org/obo/NCBIGene_138050 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_3000
http://purl.obolibrary.org/obo/NCBIGene_3000 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_128637
http://purl.obolibrary.org/obo/NCBIGene_128637 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_25885
http://purl.obolibrary.org/obo/NCBIGene_25885 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_11234
http://purl.obolibrary.org/obo/NCBIGene_11234 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_25861
http://purl.obolibrary.org/obo/NCBIGene_25861 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_3070
http://purl.obolibrary.org/obo/NCBIGene_3070 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_100151683
http://purl.obolibrary.org/obo/NCBIGene_100151683 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_3035
http://purl.obolibrary.org/obo/NCBIGene_3035 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_50717
http://purl.obolibrary.org/obo/NCBIGene_50717 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_11154
http://purl.obolibrary.org/obo/NCBIGene_11154 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_25794
http://purl.obolibrary.org/obo/NCBIGene_25794 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_3257
http://purl.obolibrary.org/obo/NCBIGene_3257 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_25782
http://purl.obolibrary.org/obo/NCBIGene_25782 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_285489
http://purl.obolibrary.org/obo/NCBIGene_285489 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_3239
http://purl.obolibrary.org/obo/NCBIGene_3239 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_11149
http://purl.obolibrary.org/obo/NCBIGene_11149 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_84140
http://purl.obolibrary.org/obo/NCBIGene_84140 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_3178
http://purl.obolibrary.org/obo/NCBIGene_3178 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_84173
http://purl.obolibrary.org/obo/NCBIGene_84173 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_84100
http://purl.obolibrary.org/obo/NCBIGene_84100 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_163183
http://purl.obolibrary.org/obo/NCBIGene_163183 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_167691
http://purl.obolibrary.org/obo/NCBIGene_167691 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_84464
http://purl.obolibrary.org/obo/NCBIGene_84464 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_60482
http://purl.obolibrary.org/obo/NCBIGene_60482 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_11315
http://purl.obolibrary.org/obo/NCBIGene_11315 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_50939
http://purl.obolibrary.org/obo/NCBIGene_50939 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_50937
http://purl.obolibrary.org/obo/NCBIGene_50937 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_118813
http://purl.obolibrary.org/obo/NCBIGene_118813 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_50964
http://purl.obolibrary.org/obo/NCBIGene_50964 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_348938
http://purl.obolibrary.org/obo/NCBIGene_348938 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_25978
http://purl.obolibrary.org/obo/NCBIGene_25978 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_59344
http://purl.obolibrary.org/obo/NCBIGene_59344 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_84343
http://purl.obolibrary.org/obo/NCBIGene_84343 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_84634
http://purl.obolibrary.org/obo/NCBIGene_84634 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_60675
http://purl.obolibrary.org/obo/NCBIGene_60675 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_7867
http://purl.obolibrary.org/obo/NCBIGene_7867 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_84665
http://purl.obolibrary.org/obo/NCBIGene_84665 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_60681
http://purl.obolibrary.org/obo/NCBIGene_60681 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_60506
http://purl.obolibrary.org/obo/NCBIGene_60506 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_60509
http://purl.obolibrary.org/obo/NCBIGene_60509 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_285025
http://purl.obolibrary.org/obo/NCBIGene_285025 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/ICD10_H54
http://purl.obolibrary.org/obo/ICD10_H54 EquivalentTo 'blindness (disorder)'
http://linkedlifedata.com/resource/umls/id/C0042790
http://linkedlifedata.com/resource/umls/id/C0042790 EquivalentTo 'vision disorder'
http://purl.obolibrary.org/obo/NCBITaxon_555406
http://purl.obolibrary.org/obo/NCBITaxon_555406 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_554915
http://purl.obolibrary.org/obo/NCBIGene_84839
http://purl.obolibrary.org/obo/NCBIGene_84839 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_7280
http://purl.obolibrary.org/obo/NCBIGene_7280 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_7283
http://purl.obolibrary.org/obo/NCBIGene_7283 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBITaxon_4564
http://purl.obolibrary.org/obo/NCBITaxon_4564 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_1648030
http://purl.obolibrary.org/obo/NCBIGene_7287
http://purl.obolibrary.org/obo/NCBIGene_7287 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_7273
http://purl.obolibrary.org/obo/NCBIGene_7273 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_7225
http://purl.obolibrary.org/obo/NCBIGene_7225 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_7399
http://purl.obolibrary.org/obo/NCBIGene_7399 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_7439
http://purl.obolibrary.org/obo/NCBIGene_7439 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_7414
http://purl.obolibrary.org/obo/NCBIGene_7414 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_7415
http://purl.obolibrary.org/obo/NCBIGene_7415 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_7401
http://purl.obolibrary.org/obo/NCBIGene_7401 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_7480
http://purl.obolibrary.org/obo/NCBIGene_7480 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_7471
http://purl.obolibrary.org/obo/NCBIGene_7471 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_7474
http://purl.obolibrary.org/obo/NCBIGene_7474 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_7466
http://purl.obolibrary.org/obo/NCBIGene_7466 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_84947
http://purl.obolibrary.org/obo/NCBIGene_84947 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_7516
http://purl.obolibrary.org/obo/NCBIGene_7516 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_7507
http://purl.obolibrary.org/obo/NCBIGene_7507 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_55036
http://purl.obolibrary.org/obo/NCBIGene_55036 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_55054
http://purl.obolibrary.org/obo/NCBIGene_55054 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/ENVO_00001995
http://purl.obolibrary.org/obo/ENVO_00001995 SubClassOf http://purl.obolibrary.org/obo/ENVO_01000814
http://purl.obolibrary.org/obo/NCBIGene_79083
http://purl.obolibrary.org/obo/NCBIGene_79083 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_80208
http://purl.obolibrary.org/obo/NCBIGene_80208 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_7092
http://purl.obolibrary.org/obo/NCBIGene_7092 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_157657
http://purl.obolibrary.org/obo/NCBIGene_157657 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_7051
http://purl.obolibrary.org/obo/NCBIGene_7051 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBITaxon_28845
http://purl.obolibrary.org/obo/NCBITaxon_28845 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_28844
http://purl.obolibrary.org/obo/NCBITaxon_28844
http://purl.obolibrary.org/obo/NCBITaxon_28844 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_28843
http://purl.obolibrary.org/obo/NCBITaxon_28843
http://purl.obolibrary.org/obo/NCBITaxon_28843 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_1224679
http://purl.obolibrary.org/obo/NCBIGene_7007
http://purl.obolibrary.org/obo/NCBIGene_7007 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_338917
http://purl.obolibrary.org/obo/NCBIGene_338917 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_55130
http://purl.obolibrary.org/obo/NCBIGene_55130 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_55151
http://purl.obolibrary.org/obo/NCBIGene_55151 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_55172
http://purl.obolibrary.org/obo/NCBIGene_55172 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_79140
http://purl.obolibrary.org/obo/NCBIGene_79140 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_55120
http://purl.obolibrary.org/obo/NCBIGene_55120 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_407053
http://purl.obolibrary.org/obo/NCBIGene_407053 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_7170
http://purl.obolibrary.org/obo/NCBIGene_7170 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_80184
http://purl.obolibrary.org/obo/NCBIGene_80184 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_7168
http://purl.obolibrary.org/obo/NCBIGene_7168 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_7169
http://purl.obolibrary.org/obo/NCBIGene_7169 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_7134
http://purl.obolibrary.org/obo/NCBIGene_7134 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_7137
http://purl.obolibrary.org/obo/NCBIGene_7137 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_7139
http://purl.obolibrary.org/obo/NCBIGene_7139 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBITaxon_28901
http://purl.obolibrary.org/obo/NCBITaxon_28901 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_590
http://purl.obolibrary.org/obo/NCBIGene_29089
http://purl.obolibrary.org/obo/NCBIGene_29089 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_30062
http://purl.obolibrary.org/obo/NCBIGene_30062 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_54084
http://purl.obolibrary.org/obo/NCBIGene_54084 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_256764
http://purl.obolibrary.org/obo/NCBIGene_256764 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_388551
http://purl.obolibrary.org/obo/NCBIGene_388551 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_388552
http://purl.obolibrary.org/obo/NCBIGene_388552 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBITaxon_40121
http://purl.obolibrary.org/obo/NCBITaxon_40121 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_40119
http://purl.obolibrary.org/obo/NCBIGene_54332
http://purl.obolibrary.org/obo/NCBIGene_54332 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_340990
http://purl.obolibrary.org/obo/NCBIGene_340990 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_339829
http://purl.obolibrary.org/obo/NCBIGene_339829 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_2896
http://purl.obolibrary.org/obo/NCBIGene_2896 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_124590
http://purl.obolibrary.org/obo/NCBIGene_124590 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_54585
http://purl.obolibrary.org/obo/NCBIGene_54585 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_2979
http://purl.obolibrary.org/obo/NCBIGene_2979 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_2984
http://purl.obolibrary.org/obo/NCBIGene_2984 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_54443
http://purl.obolibrary.org/obo/NCBIGene_54443 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_2916
http://purl.obolibrary.org/obo/NCBIGene_2916 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBITaxon_272561
http://purl.obolibrary.org/obo/NCBITaxon_272561 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_813
http://linkedlifedata.com/resource/umls/id/C3887547
http://linkedlifedata.com/resource/umls/id/C3887547 EquivalentTo 'central sleep apnea syndrome'
http://purl.obolibrary.org/obo/NCBIGene_64127
http://purl.obolibrary.org/obo/NCBIGene_64127 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_64175
http://purl.obolibrary.org/obo/NCBIGene_64175 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_148738
http://purl.obolibrary.org/obo/NCBIGene_148738 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_64218
http://purl.obolibrary.org/obo/NCBIGene_64218 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_30813
http://purl.obolibrary.org/obo/NCBIGene_30813 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_54806
http://purl.obolibrary.org/obo/NCBIGene_54806 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_388389
http://purl.obolibrary.org/obo/NCBIGene_388389 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_64072
http://purl.obolibrary.org/obo/NCBIGene_64072 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_54756
http://purl.obolibrary.org/obo/NCBIGene_54756 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_54768
http://purl.obolibrary.org/obo/NCBIGene_54768 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_54795
http://purl.obolibrary.org/obo/NCBIGene_54795 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/MESH_C537224
http://purl.obolibrary.org/obo/MESH_C537224 EquivalentTo 'sacral nerve plexus disease'
http://purl.obolibrary.org/obo/NCBIGene_54714
http://purl.obolibrary.org/obo/NCBIGene_54714 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBITaxon_10912
http://purl.obolibrary.org/obo/NCBITaxon_10912 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_689832
http://purl.obolibrary.org/obo/NCBIGene_2488
http://purl.obolibrary.org/obo/NCBIGene_2488 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_222662
http://purl.obolibrary.org/obo/NCBIGene_222662 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_64423
http://purl.obolibrary.org/obo/NCBIGene_64423 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_64446
http://purl.obolibrary.org/obo/NCBIGene_64446 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_29920
http://purl.obolibrary.org/obo/NCBIGene_29920 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_54982
http://purl.obolibrary.org/obo/NCBIGene_54982 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_29978
http://purl.obolibrary.org/obo/NCBIGene_29978 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBITaxon_693660
http://purl.obolibrary.org/obo/NCBITaxon_693660 SubClassOf http://purl.obolibrary.org/obo/NCBITaxon_11652
http://purl.obolibrary.org/obo/NCBIGene_78989
http://purl.obolibrary.org/obo/NCBIGene_78989 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_54903
http://purl.obolibrary.org/obo/NCBIGene_54903 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_54919
http://purl.obolibrary.org/obo/NCBIGene_54919 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_2673
http://purl.obolibrary.org/obo/NCBIGene_2673 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_2657
http://purl.obolibrary.org/obo/NCBIGene_2657 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_643418
http://purl.obolibrary.org/obo/NCBIGene_643418 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_2627
http://purl.obolibrary.org/obo/NCBIGene_2627 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_2626
http://purl.obolibrary.org/obo/NCBIGene_2626 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_2622
http://purl.obolibrary.org/obo/NCBIGene_2622 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_2798
http://purl.obolibrary.org/obo/NCBIGene_2798 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_2796
http://purl.obolibrary.org/obo/NCBIGene_2796 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_2779
http://purl.obolibrary.org/obo/NCBIGene_2779 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_2784
http://purl.obolibrary.org/obo/NCBIGene_2784 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_2780
http://purl.obolibrary.org/obo/NCBIGene_2780 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_2736
http://purl.obolibrary.org/obo/NCBIGene_2736 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_2733
http://purl.obolibrary.org/obo/NCBIGene_2733 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_2707
http://purl.obolibrary.org/obo/NCBIGene_2707 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_2706
http://purl.obolibrary.org/obo/NCBIGene_2706 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_643226
http://purl.obolibrary.org/obo/NCBIGene_643226 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_2038
http://purl.obolibrary.org/obo/NCBIGene_2038 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_246213
http://purl.obolibrary.org/obo/NCBIGene_246213 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_64802
http://purl.obolibrary.org/obo/NCBIGene_64802 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_285848
http://purl.obolibrary.org/obo/NCBIGene_285848 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_2103
http://purl.obolibrary.org/obo/NCBIGene_2103 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_2073
http://purl.obolibrary.org/obo/NCBIGene_2073 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_2072
http://purl.obolibrary.org/obo/NCBIGene_2072 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_2071
http://purl.obolibrary.org/obo/NCBIGene_2071 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_2070
http://purl.obolibrary.org/obo/NCBIGene_2070 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_2059
http://purl.obolibrary.org/obo/NCBIGene_2059 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_2055
http://purl.obolibrary.org/obo/NCBIGene_2055 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_2068
http://purl.obolibrary.org/obo/NCBIGene_2068 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_2066
http://purl.obolibrary.org/obo/NCBIGene_2066 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_114548
http://purl.obolibrary.org/obo/NCBIGene_114548 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_2253
http://purl.obolibrary.org/obo/NCBIGene_2253 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_2260
http://purl.obolibrary.org/obo/NCBIGene_2260 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/SCTID_2231001
'nerve plexus disease' EquivalentTo http://purl.obolibrary.org/obo/SCTID_2231001
http://purl.obolibrary.org/obo/NCBIGene_2178
http://purl.obolibrary.org/obo/NCBIGene_2178 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_2175
http://purl.obolibrary.org/obo/NCBIGene_2175 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_2318
http://purl.obolibrary.org/obo/NCBIGene_2318 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_2299
http://purl.obolibrary.org/obo/NCBIGene_2299 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/NCBIGene_2296
http://purl.obolibrary.org/obo/NCBIGene_2296 SubClassOf http://www.w3.org/2002/07/owl#Thing
http://purl.obolibrary.org/obo/OMIMPS_130000
'Ehlers-Danlos syndrome' EquivalentTo http://purl.obolibrary.org/obo/OMIMPS_130000
http://purl.obolibrary.org/obo/SCTID_63365006
'multiple symmetric lipomatosis' EquivalentTo http://purl.obolibrary.org/obo/SCTID_63365006