MeSH Browser

MeSH Supplementary: Corneal Dystrophy, Posterior Polymorphous, 1
Unique ID: C562745
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C562745
Entry Term(s): Corneal Dystrophy, Hereditary Polymorphous Posterior; Posterior Polymorphous Corneal Dystrophy; Ppcd1 Posterior polymorphous corneal dystrophy 1
Registry Number: 0
Heading Mapped to: *Corneal Dystrophies, Hereditary
Frequency: 41
Note: Hereditary corneal dystrophy characterized by metaplasia and overgrowth of corneal endothelial cells. Symptoms can vary significantly, even within the same family. It is caused by a mutation in the OVOL2 gene. OMIM: 122000
Date of Entry: 2012/11/05
Revision Date: 2019/06/19

Corneal Dystrophy, Posterior Polymorphous, 1 MeSH Supplementary Concept Data 2024