Human Phenotype Ontology 
Grandparent Node:
Abnormal corneal endothelium morphology (HP:0011488)help
Parent Node:
Abnormal migration of corneal endothelium (HP:0011489)help
Parent Node:
Reduced number of corneal endothelial cells (HP:0011491)help
..Starting node
Polymorphous posterior corneal dystrophy (HP:0007915)help
Term ID: 7915
Name: Polymorphous posterior corneal dystrophy
Definition: This corneal dystrophy affects the posterior limiting membrane of the cornea and is characterized by polymorphous plaques of calcium deposits in the deep stromal layers of the cornea, and occasionally by vesicular lesions of the endothelium and edema of the deep corneal stroma.
Reference: HP:0007915
Genes and Diseases:
       Child Nodes:

 Sister Nodes: 
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
HPO disease - gene - phenotype typical associations:
HP:0007915HP:0007915Polymorphous posterior corneal dystrophy0OVOL2 CL E G H58495122000Posterior polymorphous corneal dystrophy 1122000CN029625OMIM1415804616441
HPO disease - gene - phenotype less frequent non-typical associations:

Genes (1) :OVOL2

Diseases (1) :122000

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