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
Hyphema (HP:0011886)help
Term ID: 11886
Name: Hyphema
Definition: Bleeding in the anterior chamber of the eye.
Reference: HP:0011886
Genes and Diseases:
       Child Nodes:

 Sister Nodes: 
..expandChoroid hemorrhage (HP:0011887) 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:0011886HP:0011886Hyphema0ATOH7 CL E G H220202221900Persistent hyperplastic primary vitreous, autosomal recessive221900C1857299OMIM197513907609875
HPO disease - gene - phenotype less frequent non-typical associations:

Genes (1) :ATOH7

Diseases (1) :221900

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