Posterior polymorphous corneal dystrophy 1

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

Also known as: Maumenee corneal dystrophy, PPCD1, Ppcd1, corneal dystrophy, posterior polymorphous, type 1, posterior polymorphous corneal dystrophy type 1, corneal dystrophy, POSTERIOR polymorphous, 1, corneal dystrophy, hereditary polymorphous posterior, corneal endothelial dystrophy 1, autosomal dominant, formerly

16 clinical trials for this condition and its sub-types.