Corneal Dystrophy, Posterior Polymorphous, 1
MESHC562745
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
Synonyms
- Ppcd1 Posterior polymorphous corneal dystrophy 1
- Posterior Polymorphous Corneal Dystrophy
- Corneal Dystrophy, Hereditary Polymorphous Posterior
Source last updated 2026-05-24T15:30:09.092Z