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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Hemorrhage of the eye (HP:0011885)help
..Starting node
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Choroid hemorrhage (HP:0011887)help
Term ID: 11887
Name: Choroid hemorrhage
Synonym: Choroidal hemorrhage
Definition: Hemorrhage from the vessels of the choroid.
Comments:
Reference: HP:0011887
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandHyphema (HP:0011886) help
..expandRetinal hemorrhage (HP:0000573) help
..expandSubconjunctival hemorrhage (HP:0011896) help
..expandVitreous hemorrhage (HP:0007902) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0011887HP:0011887Choroid hemorrhage0RANBP2 CL E G H590388619ORPHA186849848601181
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (1) :RANBP2

Diseases (1) :88619
 

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