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 haemorrhage (HP:0040242) help
..expandPulmonary hemorrhage (HP:0040223) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011885HP:0011885Hemorrhage of the eye0 CL E G H
HP:0011885HP:0011885Hemorrhage of the eye1 CL E G H
HP:0011885HP:0011885Hemorrhage of the eye2 CL E G H
HP:0011885HP:0011885Hemorrhage of the eye3 CL E G H


Genes (25) :ABCC6 ATOH7 ATP6V0A2 ATP6V1A ATP6V1E1 BAP1 BEST1 CAPN5 COL4A1 CYSLTR2 DNM2 ENPP1 FZD4 GNA11 GNAQ IKBKG LRP5 MYD88 NDP PROC RANBP2 RB1 RS1 SF3B1 TREX1

Diseases (22) :758 264800 177850 221900 39044 193220 193235 611773 180000 615368 90050 133780 464 308300 601813 33226 612304 88619 180200 312700 192315 357074
 

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