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 entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0007902HP:0007902Vitreous hemorrhage0BEST1 CL E G H7439193220Vitreoretinochoroidopathy193220C1860406OMIM131949212703607854
HP:0007902HP:0007902Vitreous hemorrhage0CAPN5 CL E G H726193235Vitreoretinopathy, neovascular inflammatory193235C0242852OMIM1122331482602537
HP:0007902HP:0007902Vitreous hemorrhage0FZD4 CL E G H8322133780Exudative vitreoretinopathy 1133780C1851402OMIM1912644042604579
HP:0007902HP:0007902Vitreous hemorrhage0LRP5 CL E G H4041133780Exudative vitreoretinopathy 1133780C1851402OMIM12218456697603506
HP:0007902HP:0007902Vitreous hemorrhage0LRP5 CL E G H4041601813Exudative vitreoretinopathy 4601813C1866176OMIM12218456697603506
HP:0007902HP:0007902Vitreous hemorrhage0PROC CL E G H5624612304Thrombophilia, hereditary, due to protein C deficiency, autosomal recessive612304C2676759OMIM13912239451612283
HP:0007902HP:0007902Vitreous hemorrhage0RB1 CL E G H5925180200Retinoblastoma180200C0035335OMIM1111316369884614041
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0007902HP:0007902Vitreous hemorrhage0BAP1 CL E G H831439044ORPHA01191483950603089
HP:0007902HP:0007902Vitreous hemorrhage0CYSLTR2 CL E G H5710539044ORPHA026318274605666
HP:0007902HP:0007902Vitreous hemorrhage0FZD4 CL E G H832290050ORPHA0912644042604579
HP:0007902HP:0007902Vitreous hemorrhage0GNA11 CL E G H276739044ORPHA0111284379139313
HP:0007902HP:0007902Vitreous hemorrhage0GNAQ CL E G H277639044ORPHA06724390600998
HP:0007902HP:0007902Vitreous hemorrhage0LRP5 CL E G H404190050ORPHA02218456697603506
HP:0007902HP:0007902Vitreous hemorrhage0NDP CL E G H469390050ORPHA01672437678300658
HP:0007902HP:0007902Vitreous hemorrhage0RS1 CL E G H6247312700Juvenile retinoschisis312700C0271091OMIM027954810457300839
HP:0007902HP:0007902Vitreous hemorrhage0SF3B1 CL E G H2345139044ORPHA046710768605590


Genes (13) :BAP1 BEST1 CAPN5 CYSLTR2 FZD4 GNA11 GNAQ LRP5 NDP PROC RB1 RS1 SF3B1

Diseases (9) :39044 193220 193235 90050 133780 601813 612304 180200 312700
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is June 2019 release.