Posterior Polymorphous Corneal Dystrophy 1
Disease ID: disease_node_17146
Connections displayed (default: 10).
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| Dbxref | ICD10CM:H18.50, MIM:122000 |
|---|---|
| Subclassof | DOID_0050736, DOID_0060457 |
| Data Source | DOID |
| Synonyms | CHED1, Corneal Endothelial Dystrophy 1, Autosomal Dominant, Maumenee Corneal Dystrophy, PPCD1 |
| Doid Label | posterior polymorphous corneal dystrophy 1 |
| Doid Description | A posterior polymorphous corneal dystrophy that has_material_basis_in autosomal domit inheritance of mutation in the OVOL2 gene on chromosome 20p11.23. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_17146 |
| Doid Id | DOID_0110855 |
| Label | Posterior Polymorphous Corneal Dystrophy 1 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease)