cone-rod dystrophy 20 Disease Ontology Browser

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Disease Ontology Browser

cone-rod dystrophy 20 (DOID:0111026)
Alliance: disease page
Synonyms: CORD20
Alt IDs: OMIM:615973
Definition: A cone-rod dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the POC1B gene on chromosome 12q21.

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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