Meesmann corneal dystrophy 2 Disease Ontology Browser

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Disease Ontology Browser

Meesmann corneal dystrophy 2 (DOID:0080671)
Alliance: disease page
Alt IDs: OMIM:618767
Definition: A Messmann corneal dystrophy that is characterized by fragility of the anterior corneal epithelium and the presence of intraepithelial microcysts and that has_material_basis_in heterozygous mutation in the KRT3 gene on chromosome 12q13.

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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