cone-rod dystrophy 5 Disease Ontology Browser

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Disease Ontology Browser

cone-rod dystrophy 5 (DOID:0111010)
Alliance: disease page
Synonyms: CORD5
Alt IDs: OMIM:600977, MESH:C563415
Definition: A cone-rod dystrophy that has_material_basis_in mutation in the PITPNM3 gene in chromosome region 17p13.2-p13.1.

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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