posterior polymorphous corneal dystrophy 1 Disease Ontology Browser

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Disease Ontology Browser

posterior polymorphous corneal dystrophy 1 (DOID:0110855)
Alliance: disease page
Synonyms: CHED1; Corneal Endothelial Dystrophy 1, Autosomal Dominant; Maumenee Corneal Dystrophy; PPCD1
Alt IDs: OMIM:122000, ICD10CM:H18.50
Definition: A posterior polymorphous corneal dystrophy that has_material_basis_in autosomal dominant inheritance of mutation in the OVOL2 gene on chromosome 20p11.23.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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