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Posterior polymorphous corneal dystrophy 1
rareA posterior polymorphous corneal dystrophy that has material basis in autosomal dominant inheritance of mutation in the OVOL2 gene on chromosome 20p11.23.
- Identifiers
- MONDO:0007378 OMIM:122000
- 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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