Human Phenotype Ontology 
Grandparent Node:
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Abnormal eye physiology (HP:0012373)help
Grandparent Node:
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Internal hemorrhage (HP:0011029)help
Parent Node:
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Abnormal vitreous humor morphology (HP:0004327)help
Parent Node:
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Hemorrhage of the eye (HP:0011885)help
..Starting node
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Vitreous hemorrhage (HP:0007902)help
Term ID: 7902
Name: Vitreous hemorrhage
Synonym: Vitreous haemorrhage
Definition: Bleeding within the vitreous compartment of the eye.
Comments:
Reference: HP:0007902
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandChoroid hemorrhage (HP:0011887) help
..expandHyphema (HP:0011886) help
..expandRetinal hemorrhage (HP:0000573) help
..expandSubconjunctival hemorrhage (HP:0011896) 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:0007902HP:0007902Vitreous hemorrhage0BAP1 CL E G H8314950ORPHA:39044Uveal melanomaHP:0040283 - Occasional184
HP:0007902HP:0007902Vitreous hemorrhage0BEST1 CL E G H743912703OMIM:193220VITREORETINOCHOROIDOPATHY.182
HP:0007902HP:0007902Vitreous hemorrhage0CAPN5 CL E G H7261482OMIM:193235Vitreoretinopathy, neovascular inflammatory.6
HP:0007902HP:0007902Vitreous hemorrhage0CTNNB1 CL E G H14992514ORPHA:891Familial exudative vitreoretinopathyHP:0040283 - Occasional88
HP:0007902HP:0007902Vitreous hemorrhage0CYSLTR2 CL E G H5710518274ORPHA:39044Uveal melanomaHP:0040283 - Occasional1
HP:0007902HP:0007902Vitreous hemorrhage0FZD4 CL E G H83224042OMIM:133780Exudative vitreoretinopathy 1.109
HP:0007902HP:0007902Vitreous hemorrhage0FZD4 CL E G H83224042ORPHA:891Familial exudative vitreoretinopathyHP:0040283 - Occasional109
HP:0007902HP:0007902Vitreous hemorrhage0FZD4 CL E G H83224042ORPHA:90050Retinopathy of prematurityHP:0040283 - Occasional109
HP:0007902HP:0007902Vitreous hemorrhage0GNA11 CL E G H27674379ORPHA:39044Uveal melanomaHP:0040283 - Occasional16
HP:0007902HP:0007902Vitreous hemorrhage0GNAQ CL E G H27764390ORPHA:39044Uveal melanomaHP:0040283 - Occasional7
HP:0007902HP:0007902Vitreous hemorrhage0LRP5 CL E G H40416697OMIM:133780Exudative vitreoretinopathy 1.125
HP:0007902HP:0007902Vitreous hemorrhage0LRP5 CL E G H40416697OMIM:601813Exudative vitreoretinopathy 4.125
HP:0007902HP:0007902Vitreous hemorrhage0LRP5 CL E G H40416697ORPHA:891Familial exudative vitreoretinopathyHP:0040283 - Occasional125
HP:0007902HP:0007902Vitreous hemorrhage0LRP5 CL E G H40416697ORPHA:90050Retinopathy of prematurityHP:0040283 - Occasional125
HP:0007902HP:0007902Vitreous hemorrhage0NDP CL E G H46937678ORPHA:891Familial exudative vitreoretinopathyHP:0040283 - Occasional39
HP:0007902HP:0007902Vitreous hemorrhage0NDP CL E G H46937678ORPHA:90050Retinopathy of prematurityHP:0040283 - Occasional39
HP:0007902HP:0007902Vitreous hemorrhage0PROC CL E G H56249451OMIM:612304Thrombophilia due to protein C deficiency, autosomal recessive.65
HP:0007902HP:0007902Vitreous hemorrhage0RB1 CL E G H59259884OMIM:180200RETINOBLASTOMA.365
HP:0007902HP:0007902Vitreous hemorrhage0RS1 CL E G H624710457OMIM:312700Retinoschisis 1, X-linked, juvenile148
HP:0007902HP:0007902Vitreous hemorrhage0SF3B1 CL E G H2345110768ORPHA:39044Uveal melanomaHP:0040283 - Occasional19
HP:0007902HP:0007902Vitreous hemorrhage0TSPAN12 CL E G H2355421641ORPHA:891Familial exudative vitreoretinopathyHP:0040283 - Occasional39
HP:0007902HP:0007902Vitreous hemorrhage0ZNF408 CL E G H7979720041ORPHA:891Familial exudative vitreoretinopathyHP:0040283 - Occasional14


Genes (16) :BAP1 BEST1 CAPN5 CTNNB1 CYSLTR2 FZD4 GNA11 GNAQ LRP5 NDP PROC RB1 RS1 SF3B1 TSPAN12 ZNF408

Diseases (10) :ORPHA:39044 OMIM:193220 OMIM:193235 ORPHA:891 OMIM:133780 ORPHA:90050 OMIM:601813 OMIM:612304 OMIM:180200 OMIM:312700
 

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