cone-rod dystrophy 12 Disease Ontology Browser

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Disease Ontology Browser

cone-rod dystrophy 12 (DOID:0111019)
Alliance: disease page
Synonyms: CORD12
Alt IDs: OMIM:612657, MESH:C567206
Definition: A cone-rod dystrophy that has_material_basis_in homozygous or heterozygous mutation in the PROM1 gene on chromosome 4p15.

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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