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Disease Ontology Browser
cone-rod dystrophy 14 (DOID:0080314)
Alliance: disease page
Alt IDs: OMIM:602093, MESH:C566579, UMLS_CUI:C1838190, UMLS_CUI:C1865869
Definition: A cone-rod dystrophy that is characterized by deterioration of the cone in childhood or early adult life and progressive deterioration of the rod photoreceptor cells in later life that has_material_basis_in mutation in GUCA1A on chromosome 6p21.1.

Disease References using Mouse Models (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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MGI 6.15
The Jackson Laboratory