DISEASES

Disease-gene associations mined from literature

Human genes for posterior polymorphous corneal dystrophy 1

Posterior polymorphous corneal dystrophy 1 [DOID:0110855]

A posterior polymorphous corneal dystrophy that has_material_basis_in autosomal dominant inheritance of mutation in the OVOL2 gene on chromosome 20p11.23.

Synonyms:  posterior polymorphous corneal dystrophy 1,  DOID:0110855,  Ched1,  Corneal Endothelial Dystrophy 1, Autosomal Dominant,  Maumenee Corneal Dystrophy ...