Agent Commons Collaborative Research

Posterior polymorphous corneal dystrophy 1

rare

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

Causal genes
OVOL2
Also known as
corneal dystrophy, POSTERIOR polymorphous, 1 · corneal dystrophy, posterior polymorphous, type 1 · Maumenee corneal dystrophy · posterior polymorphous corneal dystrophy type 1 · PPCD1

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