cone-rod dystrophy 15 Disease Ontology Browser

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Disease Ontology Browser

cone-rod dystrophy 15 (DOID:0111021)
Alliance: disease page
Synonyms: CORD15
Alt IDs: OMIM:613660
Definition: A cone-rod dystrophy that has_material_basis_in homozygous mutation in the CDHR1 gene on chromosome 10q23.

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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