cone-rod dystrophy 13 Disease Ontology Browser

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Disease Ontology Browser

cone-rod dystrophy 13 (DOID:0111016)
Alliance: disease page
Synonyms: CORD13
Alt IDs: OMIM:608194, MESH:C567698
Definition: A cone-rod dystrophy that has_material_basis_in mutation in the RPGRIP1 gene on chromosome 14q11.2.

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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