cone-rod dystrophy 24 Disease Ontology Browser

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Disease Ontology Browser

cone-rod dystrophy 24 (DOID:0081449)
Alliance: disease page
Alt IDs: OMIM:620342
Definition: A cone-rod dystrophy that is characterized by night blindness, defective color vision, and reduced visual acuity and that has_material_basis_in heterozygous mutation in the UNC119 gene on chromosome 17q11.

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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