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Disease Ontology Browser
cone-rod dystrophy 6 (DOID:0111011)
Alliance: disease page
Synonyms: CORD6; RCD2; retinal cone dystrophy 2
Alt IDs: OMIM:601777
Definition: A cone-rod dystrophy that has_material_basis_in heterozygous mutation in the GUCY2D gene on chromosome 17p13.1.

Disease References using Mouse Models (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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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory