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 )

Relationships
is a type of: autosomal dominant disease posterior polymorphous corneal dystrophy