| Term Name: | posterior polymorphous corneal dystrophy 1 |
|---|---|
| Synonyms: | CHED1, Corneal Endothelial Dystrophy 1, Autosomal Dominant, Maumenee Corneal Dystrophy, PPCD1 |
| Definition: | A posterior polymorphous corneal dystrophy that has_material_basis_in autosomal dominant inheritance of mutation in the OVOL2 gene on chromosome 20p11.23. |
| Ontology: | Human Disease [DOID:0110855] ( DOID:0110855 ) |