Human Phenotype Ontology 
Grandparent Node:
Abnormal eye physiology (HP:0012373)help
Grandparent Node:
Internal hemorrhage (HP:0011029)help
Parent Node:
Hemorrhage of the eye (HP:0011885)help
..Starting node
Choroid hemorrhage (HP:0011887)help
Term ID: 11887
Name: Choroid hemorrhage
Synonym: Choroidal hemorrhage
Definition: Hemorrhage from the vessels of the choroid.
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.