Search Ontology:
Human Disease

posterior polymorphous corneal dystrophy 4

Term ID
DOID:0080669
Synonyms
Definition
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. https://pubmed.ncbi.nlm.nih.gov/29499165/
References
Ontology
Human Disease   ( DOID:0080669 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models