|  Help  |  About  |  Contact Us

DO Term : posterior polymorphous corneal dystrophy 4 [DOID:0080669] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A posterior polymorphous corneal dystrophy that is characterized by an irregular posterior corneal surface with occasional opacities of variable size and shape and that has_material_basis_in heterozygous mutation in the GRHL2 gene on chromosome 8q22.
  • synonyms:
  • 618031,
  • OMIM:618031
Quick Links:
 
Quick Links:
 

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents