Human Phenotype Ontology 
Grandparent Node:
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Abnormal bleeding (HP:0001892)help
Grandparent Node:
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Abnormality of blood circulation (HP:0011028)help
Parent Node:
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Abnormal eye physiology (HP:0012373)help
Parent Node:
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Internal hemorrhage (HP:0011029)help
..Starting node
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Hemorrhage of the eye (HP:0011885)help
Term ID: 11885
Name: Hemorrhage of the eye
Synonym: Bleeding from the eye; Haemorrhage of the eye
Definition: Bleeding from vessels of the various tissues of the eye.
Comments:
Reference: HP:0011885
Genes and Diseases:
 
       Child Nodes:
........expandRetinal hemorrhage (HP:0000573) help
................... HP:0025243 Subretinal hemorrhage
................... HP:0025244 Subretinal pigment epithelium hemorrhage
................... HP:0025574 Macular hemmorhage
................... HP:0031611 Sub-inner limiting membrane hemorrhage
................... HP:0031805 Intraretinal hemorrhage
........expandVitreous hemorrhage (HP:0007902) help
........expandHyphema (HP:0011886) help
........expandChoroid hemorrhage (HP:0011887) help
........expandSubconjunctival hemorrhage (HP:0011896) help

 Sister Nodes: 
..expandAntepartum hemorrhage (HP:0025328) help
..expandGastrointestinal hemorrhage (HP:0002239) help
..expandIntracranial hemorrhage (HP:0002170) help
..expandJoint hemorrhage (HP:0005261) help
..expandMuscle hemorrhage (HP:0040242) help
..expandPulmonary hemorrhage (HP:0040223) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011885HP:0011885Hemorrhage of the eye0ABCC6 CL E G H36857ORPHA:51608Generalized arterial calcification of infancy415
HP:0011885HP:0011885Hemorrhage of the eye0ABCC6 CL E G H36857ORPHA:758Pseudoxanthoma elasticum415
HP:0011885HP:0011885Hemorrhage of the eye0ABCC6 CL E G H36857OMIM:177850Pseudoxanthoma elasticum, forme fruste415
HP:0011885HP:0011885Hemorrhage of the eye0ABCC6 CL E G H36857OMIM:264800PSEUDOXANTHOMA ELASTICUM; PXE415
HP:0011885HP:0011885Hemorrhage of the eye0APOE CL E G H348613OMIM:603075Macular degeneration, age-related, 139
HP:0011885HP:0011885Hemorrhage of the eye0ARPC1B CL E G H10095704OMIM:617718Platelet abnormalities with eosinophilia and immune-mediated inflammatory disease
HP:0011885HP:0011885Hemorrhage of the eye0ATOH7 CL E G H22020213907ORPHA:91495Persistent hyperplastic primary vitreous4
HP:0011885HP:0011885Hemorrhage of the eye0ATOH7 CL E G H22020213907OMIM:221900Persistent hyperplastic primary vitreous, autosomal recessive4
HP:0011885HP:0011885Hemorrhage of the eye0ATP6V0A2 CL E G H2354518481ORPHA:357074Autosomal recessive cutis laxa type 2, classic type140
HP:0011885HP:0011885Hemorrhage of the eye0ATP6V1A CL E G H523851ORPHA:357074Autosomal recessive cutis laxa type 2, classic type3
HP:0011885HP:0011885Hemorrhage of the eye0ATP6V1E1 CL E G H529857ORPHA:357074Autosomal recessive cutis laxa type 2, classic type2
HP:0011885HP:0011885Hemorrhage of the eye0BAP1 CL E G H8314950ORPHA:39044Uveal melanoma184
HP:0011885HP:0011885Hemorrhage of the eye0BEST1 CL E G H743912703OMIM:193220VITREORETINOCHOROIDOPATHY182
HP:0011885HP:0011885Hemorrhage of the eye0CAPN5 CL E G H7261482OMIM:193235Vitreoretinopathy, neovascular inflammatory6
HP:0011885HP:0011885Hemorrhage of the eye0CFH CL E G H30754883ORPHA:75376Familial drusen86
HP:0011885HP:0011885Hemorrhage of the eye0CFHR1 CL E G H30784888OMIM:603075Macular degeneration, age-related, 1
HP:0011885HP:0011885Hemorrhage of the eye0CFHR3 CL E G H1087816980OMIM:603075Macular degeneration, age-related, 1
HP:0011885HP:0011885Hemorrhage of the eye0CFI CL E G H34265394ORPHA:75376Familial drusen57
HP:0011885HP:0011885Hemorrhage of the eye0COL4A1 CL E G H12822202OMIM:611773Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps193
HP:0011885HP:0011885Hemorrhage of the eye0COL4A1 CL E G H12822202OMIM:175780Brain small vessel disease 1 with or without ocular anomalies193
HP:0011885HP:0011885Hemorrhage of the eye0COL4A1 CL E G H12822202OMIM:180000Retinal arteries, tortuosity of193
HP:0011885HP:0011885Hemorrhage of the eye0CTNNB1 CL E G H14992514ORPHA:891Familial exudative vitreoretinopathy88
HP:0011885HP:0011885Hemorrhage of the eye0CYSLTR2 CL E G H5710518274ORPHA:39044Uveal melanoma1
HP:0011885HP:0011885Hemorrhage of the eye0DNM2 CL E G H17852974OMIM:615368Lethal congenital contracture syndrome 5167
HP:0011885HP:0011885Hemorrhage of the eye0DST CL E G H6671090OMIM:614653Neuropathy, hereditary sensory and autonomic, type VI108
HP:0011885HP:0011885Hemorrhage of the eye0EFEMP1 CL E G H22023218ORPHA:75376Familial drusen54
HP:0011885HP:0011885Hemorrhage of the eye0ENPP1 CL E G H51673356ORPHA:51608Generalized arterial calcification of infancy151
HP:0011885HP:0011885Hemorrhage of the eye0ENPP1 CL E G H51673356ORPHA:758Pseudoxanthoma elasticum151
HP:0011885HP:0011885Hemorrhage of the eye0ERCC6 CL E G H20743438ORPHA:90324Cockayne syndrome type 3199
HP:0011885HP:0011885Hemorrhage of the eye0ERCC8 CL E G H11613439ORPHA:90324Cockayne syndrome type 355
HP:0011885HP:0011885Hemorrhage of the eye0FZD4 CL E G H83224042OMIM:133780Exudative vitreoretinopathy 1109
HP:0011885HP:0011885Hemorrhage of the eye0FZD4 CL E G H83224042ORPHA:891Familial exudative vitreoretinopathy109
HP:0011885HP:0011885Hemorrhage of the eye0FZD4 CL E G H83224042ORPHA:91495Persistent hyperplastic primary vitreous109
HP:0011885HP:0011885Hemorrhage of the eye0FZD4 CL E G H83224042ORPHA:90050Retinopathy of prematurity109
HP:0011885HP:0011885Hemorrhage of the eye0GCDH CL E G H26394189ORPHA:25Glutaryl-CoA dehydrogenase deficiency115
HP:0011885HP:0011885Hemorrhage of the eye0GNA11 CL E G H27674379ORPHA:39044Uveal melanoma16
HP:0011885HP:0011885Hemorrhage of the eye0GNAQ CL E G H27764390ORPHA:39044Uveal melanoma7
HP:0011885HP:0011885Hemorrhage of the eye0HMCN1 CL E G H8387219194OMIM:603075Macular degeneration, age-related, 1262
HP:0011885HP:0011885Hemorrhage of the eye0IFNG CL E G H34585438ORPHA:88Idiopathic aplastic anemia23
HP:0011885HP:0011885Hemorrhage of the eye0IKBKG CL E G H85175961ORPHA:464Incontinentia pigmenti52
HP:0011885HP:0011885Hemorrhage of the eye0IKBKG CL E G H85175961OMIM:308300Incontinentia pigmenti52
HP:0011885HP:0011885Hemorrhage of the eye0LAMB2 CL E G H39136487OMIM:609049Pierson syndrome92
HP:0011885HP:0011885Hemorrhage of the eye0LRP5 CL E G H40416697OMIM:133780Exudative vitreoretinopathy 1125
HP:0011885HP:0011885Hemorrhage of the eye0LRP5 CL E G H40416697OMIM:601813Exudative vitreoretinopathy 4125
HP:0011885HP:0011885Hemorrhage of the eye0LRP5 CL E G H40416697ORPHA:891Familial exudative vitreoretinopathy125
HP:0011885HP:0011885Hemorrhage of the eye0LRP5 CL E G H40416697ORPHA:90050Retinopathy of prematurity125
HP:0011885HP:0011885Hemorrhage of the eye0MYD88 CL E G H46157562ORPHA:33226Waldenström macroglobulinemia9
HP:0011885HP:0011885Hemorrhage of the eye0NDP CL E G H46937678ORPHA:891Familial exudative vitreoretinopathy39
HP:0011885HP:0011885Hemorrhage of the eye0NDP CL E G H46937678ORPHA:91495Persistent hyperplastic primary vitreous39
HP:0011885HP:0011885Hemorrhage of the eye0NDP CL E G H46937678ORPHA:90050Retinopathy of prematurity39
HP:0011885HP:0011885Hemorrhage of the eye0PRF1 CL E G H55519360ORPHA:88Idiopathic aplastic anemia58
HP:0011885HP:0011885Hemorrhage of the eye0PROC CL E G H56249451OMIM:612304Thrombophilia due to protein C deficiency, autosomal recessive65
HP:0011885HP:0011885Hemorrhage of the eye0RANBP2 CL E G H59039848ORPHA:88619Familial acute necrotizing encephalopathy57
HP:0011885HP:0011885Hemorrhage of the eye0RB1 CL E G H59259884OMIM:180200RETINOBLASTOMA365
HP:0011885HP:0011885Hemorrhage of the eye0RS1 CL E G H624710457OMIM:312700Retinoschisis 1, X-linked, juvenile148
HP:0011885HP:0011885Hemorrhage of the eye0SBDS CL E G H5111919440ORPHA:88Idiopathic aplastic anemia26
HP:0011885HP:0011885Hemorrhage of the eye0SF3B1 CL E G H2345110768ORPHA:39044Uveal melanoma19
HP:0011885HP:0011885Hemorrhage of the eye0TERC CL E G H701211727ORPHA:88Idiopathic aplastic anemia48
HP:0011885HP:0011885Hemorrhage of the eye0TERT CL E G H701511730ORPHA:88Idiopathic aplastic anemia238
HP:0011885HP:0011885Hemorrhage of the eye0TREX1 CL E G H1127712269OMIM:192315Vasculopathy, retinal, with cerebral leukodystrophy56
HP:0011885HP:0011885Hemorrhage of the eye0TSPAN12 CL E G H2355421641ORPHA:891Familial exudative vitreoretinopathy39
HP:0011885HP:0011885Hemorrhage of the eye0XYLT1 CL E G H6413115516OMIM:264800PSEUDOXANTHOMA ELASTICUM; PXE14
HP:0011885HP:0011885Hemorrhage of the eye0XYLT2 CL E G H6413215517OMIM:264800PSEUDOXANTHOMA ELASTICUM; PXE5
HP:0011885HP:0011885Hemorrhage of the eye0ZEB2 CL E G H983914881ORPHA:261552Mowat-Wilson syndrome due to a ZEB2 point mutation362
HP:0011885HP:0011885Hemorrhage of the eye0ZNF408 CL E G H7979720041ORPHA:891Familial exudative vitreoretinopathy14
HP:0011885HP:0000573Retinal hemorrhage1ABCC6 CL E G H36857ORPHA:51608Generalized arterial calcification of infancyHP:0040284 - Very rare415
HP:0011885HP:0000573Retinal hemorrhage1ABCC6 CL E G H36857ORPHA:758Pseudoxanthoma elasticumHP:0040281 - Very frequent415
HP:0011885HP:0000573Retinal hemorrhage1ABCC6 CL E G H36857OMIM:177850Pseudoxanthoma elasticum, forme fruste.415
HP:0011885HP:0000573Retinal hemorrhage1ABCC6 CL E G H36857OMIM:264800PSEUDOXANTHOMA ELASTICUM; PXE415
HP:0011885HP:0000573Retinal hemorrhage1APOE CL E G H348613OMIM:603075Macular degeneration, age-related, 139
HP:0011885HP:0011896Subconjunctival hemorrhage1ARPC1B CL E G H10095704OMIM:617718Platelet abnormalities with eosinophilia and immune-mediated inflammatory disease
HP:0011885HP:0011886Hyphema1ATOH7 CL E G H22020213907OMIM:221900Persistent hyperplastic primary vitreous, autosomal recessive.4
HP:0011885HP:0000573Retinal hemorrhage1ATP6V0A2 CL E G H2354518481ORPHA:357074Autosomal recessive cutis laxa type 2, classic type140
HP:0011885HP:0000573Retinal hemorrhage1ATP6V1A CL E G H523851ORPHA:357074Autosomal recessive cutis laxa type 2, classic type3
HP:0011885HP:0000573Retinal hemorrhage1ATP6V1E1 CL E G H529857ORPHA:357074Autosomal recessive cutis laxa type 2, classic type2
HP:0011885HP:0007902Vitreous hemorrhage1BAP1 CL E G H8314950ORPHA:39044Uveal melanomaHP:0040283 - Occasional184
HP:0011885HP:0007902Vitreous hemorrhage1BEST1 CL E G H743912703OMIM:193220VITREORETINOCHOROIDOPATHY.182
HP:0011885HP:0007902Vitreous hemorrhage1CAPN5 CL E G H7261482OMIM:193235Vitreoretinopathy, neovascular inflammatory.6
HP:0011885HP:0000573Retinal hemorrhage1CFH CL E G H30754883ORPHA:75376Familial drusen86
HP:0011885HP:0000573Retinal hemorrhage1CFHR1 CL E G H30784888OMIM:603075Macular degeneration, age-related, 1
HP:0011885HP:0000573Retinal hemorrhage1CFHR3 CL E G H1087816980OMIM:603075Macular degeneration, age-related, 1
HP:0011885HP:0000573Retinal hemorrhage1CFI CL E G H34265394ORPHA:75376Familial drusen57
HP:0011885HP:0000573Retinal hemorrhage1COL4A1 CL E G H12822202OMIM:611773Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps.193
HP:0011885HP:0000573Retinal hemorrhage1COL4A1 CL E G H12822202OMIM:175780Brain small vessel disease 1 with or without ocular anomalies193
HP:0011885HP:0000573Retinal hemorrhage1COL4A1 CL E G H12822202OMIM:180000Retinal arteries, tortuosity of.193
HP:0011885HP:0007902Vitreous hemorrhage1CTNNB1 CL E G H14992514ORPHA:891Familial exudative vitreoretinopathyHP:0040283 - Occasional88
HP:0011885HP:0007902Vitreous hemorrhage1CYSLTR2 CL E G H5710518274ORPHA:39044Uveal melanomaHP:0040283 - Occasional1
HP:0011885HP:0000573Retinal hemorrhage1DNM2 CL E G H17852974OMIM:615368Lethal congenital contracture syndrome 5.167
HP:0011885HP:0000573Retinal hemorrhage1DST CL E G H6671090OMIM:614653Neuropathy, hereditary sensory and autonomic, type VI108
HP:0011885HP:0000573Retinal hemorrhage1EFEMP1 CL E G H22023218ORPHA:75376Familial drusen54
HP:0011885HP:0000573Retinal hemorrhage1ENPP1 CL E G H51673356ORPHA:51608Generalized arterial calcification of infancyHP:0040284 - Very rare151
HP:0011885HP:0000573Retinal hemorrhage1ENPP1 CL E G H51673356ORPHA:758Pseudoxanthoma elasticumHP:0040281 - Very frequent151
HP:0011885HP:0000573Retinal hemorrhage1ERCC6 CL E G H20743438ORPHA:90324Cockayne syndrome type 3HP:0040284 - Very rare199
HP:0011885HP:0000573Retinal hemorrhage1ERCC8 CL E G H11613439ORPHA:90324Cockayne syndrome type 3HP:0040284 - Very rare55
HP:0011885HP:0007902Vitreous hemorrhage1FZD4 CL E G H83224042OMIM:133780Exudative vitreoretinopathy 1.109
HP:0011885HP:0007902Vitreous hemorrhage1FZD4 CL E G H83224042ORPHA:891Familial exudative vitreoretinopathyHP:0040283 - Occasional109
HP:0011885HP:0007902Vitreous hemorrhage1FZD4 CL E G H83224042ORPHA:90050Retinopathy of prematurityHP:0040283 - Occasional109
HP:0011885HP:0000573Retinal hemorrhage1GCDH CL E G H26394189ORPHA:25Glutaryl-CoA dehydrogenase deficiencyHP:0040283 - Occasional115
HP:0011885HP:0007902Vitreous hemorrhage1GNA11 CL E G H27674379ORPHA:39044Uveal melanomaHP:0040283 - Occasional16
HP:0011885HP:0007902Vitreous hemorrhage1GNAQ CL E G H27764390ORPHA:39044Uveal melanomaHP:0040283 - Occasional7
HP:0011885HP:0000573Retinal hemorrhage1HMCN1 CL E G H8387219194OMIM:603075Macular degeneration, age-related, 1262
HP:0011885HP:0000573Retinal hemorrhage1IFNG CL E G H34585438ORPHA:88Idiopathic aplastic anemiaHP:0040283 - Occasional23
HP:0011885HP:0000573Retinal hemorrhage1IKBKG CL E G H85175961OMIM:308300Incontinentia pigmenti.52
HP:0011885HP:0000573Retinal hemorrhage1IKBKG CL E G H85175961ORPHA:464Incontinentia pigmentiHP:0040283 - Occasional52
HP:0011885HP:0000573Retinal hemorrhage1LAMB2 CL E G H39136487OMIM:609049Pierson syndrome92
HP:0011885HP:0007902Vitreous hemorrhage1LRP5 CL E G H40416697OMIM:133780Exudative vitreoretinopathy 1.125
HP:0011885HP:0007902Vitreous hemorrhage1LRP5 CL E G H40416697OMIM:601813Exudative vitreoretinopathy 4.125
HP:0011885HP:0007902Vitreous hemorrhage1LRP5 CL E G H40416697ORPHA:891Familial exudative vitreoretinopathyHP:0040283 - Occasional125
HP:0011885HP:0007902Vitreous hemorrhage1LRP5 CL E G H40416697ORPHA:90050Retinopathy of prematurityHP:0040283 - Occasional125
HP:0011885HP:0000573Retinal hemorrhage1MYD88 CL E G H46157562ORPHA:33226Waldenström macroglobulinemiaHP:0040283 - Occasional9
HP:0011885HP:0007902Vitreous hemorrhage1NDP CL E G H46937678ORPHA:891Familial exudative vitreoretinopathyHP:0040283 - Occasional39
HP:0011885HP:0007902Vitreous hemorrhage1NDP CL E G H46937678ORPHA:90050Retinopathy of prematurityHP:0040283 - Occasional39
HP:0011885HP:0000573Retinal hemorrhage1PRF1 CL E G H55519360ORPHA:88Idiopathic aplastic anemiaHP:0040283 - Occasional58
HP:0011885HP:0007902Vitreous hemorrhage1PROC CL E G H56249451OMIM:612304Thrombophilia due to protein C deficiency, autosomal recessive.65
HP:0011885HP:0011887Choroid hemorrhage1RANBP2 CL E G H59039848ORPHA:88619Familial acute necrotizing encephalopathyHP:0040282 - Frequent57
HP:0011885HP:0007902Vitreous hemorrhage1RB1 CL E G H59259884OMIM:180200RETINOBLASTOMA.365
HP:0011885HP:0007902Vitreous hemorrhage1RS1 CL E G H624710457OMIM:312700Retinoschisis 1, X-linked, juvenile148
HP:0011885HP:0000573Retinal hemorrhage1SBDS CL E G H5111919440ORPHA:88Idiopathic aplastic anemiaHP:0040283 - Occasional26
HP:0011885HP:0007902Vitreous hemorrhage1SF3B1 CL E G H2345110768ORPHA:39044Uveal melanomaHP:0040283 - Occasional19
HP:0011885HP:0000573Retinal hemorrhage1TERC CL E G H701211727ORPHA:88Idiopathic aplastic anemiaHP:0040283 - Occasional48
HP:0011885HP:0000573Retinal hemorrhage1TERT CL E G H701511730ORPHA:88Idiopathic aplastic anemiaHP:0040283 - Occasional238
HP:0011885HP:0000573Retinal hemorrhage1TREX1 CL E G H1127712269OMIM:192315Vasculopathy, retinal, with cerebral leukodystrophy.56
HP:0011885HP:0007902Vitreous hemorrhage1TSPAN12 CL E G H2355421641ORPHA:891Familial exudative vitreoretinopathyHP:0040283 - Occasional39
HP:0011885HP:0000573Retinal hemorrhage1XYLT1 CL E G H6413115516OMIM:264800PSEUDOXANTHOMA ELASTICUM; PXE14
HP:0011885HP:0000573Retinal hemorrhage1XYLT2 CL E G H6413215517OMIM:264800PSEUDOXANTHOMA ELASTICUM; PXE5
HP:0011885HP:0011886Hyphema1ZEB2 CL E G H983914881ORPHA:261552Mowat-Wilson syndrome due to a ZEB2 point mutationHP:0040284 - Very rare362
HP:0011885HP:0007902Vitreous hemorrhage1ZNF408 CL E G H7979720041ORPHA:891Familial exudative vitreoretinopathyHP:0040283 - Occasional14
HP:0011885HP:0031805Intraretinal hemorrhage2 CL E G H
HP:0011885HP:0031611Sub-inner limiting membrane hemorrhage2 CL E G H
HP:0011885HP:0025243Subretinal hemorrhage2 CL E G H
HP:0011885HP:0025574Macular hemorrhage2APOE CL E G H348613OMIM:603075Macular degeneration, age-related, 1HP:0040283 - Occasional39
HP:0011885HP:0025244Subretinal pigment epithelium hemorrhage2ATP6V0A2 CL E G H2354518481ORPHA:357074Autosomal recessive cutis laxa type 2, classic typeHP:0040282 - Frequent140
HP:0011885HP:0025244Subretinal pigment epithelium hemorrhage2ATP6V1A CL E G H523851ORPHA:357074Autosomal recessive cutis laxa type 2, classic typeHP:0040282 - Frequent3
HP:0011885HP:0025244Subretinal pigment epithelium hemorrhage2ATP6V1E1 CL E G H529857ORPHA:357074Autosomal recessive cutis laxa type 2, classic typeHP:0040282 - Frequent2
HP:0011885HP:0025574Macular hemorrhage2CFH CL E G H30754883ORPHA:75376Familial drusenHP:0040283 - Occasional86
HP:0011885HP:0025574Macular hemorrhage2CFHR1 CL E G H30784888OMIM:603075Macular degeneration, age-related, 1HP:0040283 - Occasional
HP:0011885HP:0025574Macular hemorrhage2CFHR3 CL E G H1087816980OMIM:603075Macular degeneration, age-related, 1HP:0040283 - Occasional
HP:0011885HP:0025574Macular hemorrhage2CFI CL E G H34265394ORPHA:75376Familial drusenHP:0040283 - Occasional57
HP:0011885HP:0025574Macular hemorrhage2EFEMP1 CL E G H22023218ORPHA:75376Familial drusenHP:0040283 - Occasional54
HP:0011885HP:0025574Macular hemorrhage2HMCN1 CL E G H8387219194OMIM:603075Macular degeneration, age-related, 1HP:0040283 - Occasional262
HP:0011885HP:0025582Submacular hemorrhage3 CL E G H
HP:0011885HP:0025581Foveal hemorrhage3 CL E G H
HP:0011885HP:0025242Dot-and-blot retinal hemorrhage3 CL E G H
HP:0011885HP:0025241Flame-shaped retinal hemorrhage3 CL E G H


Genes (49) :ABCC6 APOE ARPC1B ATOH7 ATP6V0A2 ATP6V1A ATP6V1E1 BAP1 BEST1 CAPN5 CFH CFHR1 CFHR3 CFI COL4A1 CTNNB1 CYSLTR2 DNM2 DST EFEMP1 ENPP1 ERCC6 ERCC8 FZD4 GCDH GNA11 GNAQ HMCN1 IFNG IKBKG LAMB2 LRP5 MYD88 NDP PRF1 PROC RANBP2 RB1 RS1 SBDS SF3B1 TERC TERT TREX1 TSPAN12 XYLT1 XYLT2 ZEB2 ZNF408

Diseases (35) :ORPHA:51608 ORPHA:758 OMIM:177850 OMIM:264800 OMIM:603075 OMIM:617718 ORPHA:91495 OMIM:221900 ORPHA:357074 ORPHA:39044 OMIM:193220 OMIM:193235 ORPHA:75376 OMIM:611773 OMIM:175780 OMIM:180000 ORPHA:891 OMIM:615368 OMIM:614653 ORPHA:90324 OMIM:133780 ORPHA:90050 ORPHA:25 ORPHA:88 ORPHA:464 OMIM:308300 OMIM:609049 OMIM:601813 ORPHA:33226 OMIM:612304 ORPHA:88619 OMIM:180200 OMIM:312700 OMIM:192315 ORPHA:261552
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.