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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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last database update
01/24/2023
MGI 6.22
The Jackson Laboratory