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Disease Ontology Browser
cone-rod dystrophy 16 (DOID:0111022)
Alliance: disease page
Synonyms: CORD16; retinal dystrophy with early macular involvement
Alt IDs: OMIM:614500
Definition: A cone-rod dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the C8ORF37 gene on chromosome 8q22.

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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last database update
12/03/2019
MGI 6.14
The Jackson Laboratory