Human Phenotype Ontology 
Grandparent Node:
expand
Abnormal anterior eye segment morphology (HP:0004328)help
Grandparent Node:
expand
Aplasia/Hypoplasia affecting the eye (HP:0008056)help
Parent Node:
expand
Aplasia/Hypoplasia affecting the anterior segment of the eye (HP:0008062)help
..Starting node
..expand
Anterior segment of eye aplasia (HP:0007779)help
Term ID: 7779
Name: Anterior segment of eye aplasia
Synonym:
Definition:
Comments:
Reference: HP:0007779
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAplasia/Hypoplasia of the iris (HP:0008053) help
..expandAplasia/Hypoplasia of the lens (HP:0008063) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0007779HP:0007779Anterior segment of eye aplasia0FOXE3 CL E G H2301610256Congenital primary aphakia610256C1853230OMIM131863808601094
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (1) :FOXE3

Diseases (1) :610256
 

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