Human Phenotype Ontology 
Grandparent Node:
expand
Abnormal cornea morphology (HP:0000481)help
Parent Node:
expand
Abnormal corneal endothelium morphology (HP:0011488)help
..Starting node
..expand
Abnormal migration of corneal endothelium (HP:0011489)help
Term ID: 11489
Name: Abnormal migration of corneal endothelium
Synonym:
Definition: Abnormal migration of corneal endothelium.
Comments:
Reference: HP:0011489
Genes and Diseases:
 
       Child Nodes:
........expandPolymorphous posterior corneal dystrophy (HP:0007915) help

 Sister Nodes: 
..expandAbnormal Descemet membrane morphology (HP:0011490) help
..expandCorneal keratic precipitates (HP:0025341) help
..expandReduced number of corneal endothelial cells (HP:0011491) 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:0011489HP:0011489Abnormal migration of corneal endothelium0OVOL2 CL E G H5849515804OMIM:122000Corneal dystrophy, posterior polymorphous, 14
HP:0011489HP:0007915Polymorphous posterior corneal dystrophy1OVOL2 CL E G H5849515804OMIM:122000Corneal dystrophy, posterior polymorphous, 14


Genes (1) :OVOL2

Diseases (1) :OMIM:122000
 

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