Human Phenotype Ontology 
Grandparent Node:
expand
Abnormal eye physiology (HP:0012373)help
Grandparent Node:
expand
Internal hemorrhage (HP:0011029)help
Parent Node:
expand
Hemorrhage of the eye (HP:0011885)help
..Starting node
..expand
Hyphema (HP:0011886)help
Term ID: 11886
Name: Hyphema
Synonym:
Definition: Bleeding in the anterior chamber of the eye.
Comments:
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 entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011886HP:0011886Hyphema0ATOH7 CL E G H22020213907OMIM:221900Persistent hyperplastic primary vitreous, autosomal recessive.4
HP:0011886HP:0011886Hyphema0ZEB2 CL E G H983914881ORPHA:261552Mowat-Wilson syndrome due to a ZEB2 point mutationHP:0040284 - Very rare362


Genes (2) :ATOH7 ZEB2

Diseases (2) :OMIM:221900 ORPHA:261552
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.