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autosomal dominant keratitis (DOID:0111383)
Alliance: disease page
Synonyms: hereditary keratitis
Alt IDs: OMIM:148190, MESH:C537022, ORDO:2334, UMLS_CUI:C1835698
Definition: A keratitis characterized by corneal opacification and vascularization and foveal hypoplasia that has_material_basis_in heterozygous mutation in the PAX6 gene on chromosome 11p13.

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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Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory