posterior polymorphous corneal dystrophy 1 (Q32143867)
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A posterior polymorphous corneal dystrophy that has material basis in autosomal dominant inheritance of mutation in the OVOL2 gene on chromosome 20p11.23.
- Corneal Endothelial Dystrophy 1, Autosomal Dominant
- Ppcd1
- Maumenee Corneal Dystrophy
- Ched1
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | 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. |
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Statements
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Identifiers
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1 reference