cone-rod dystrophy 21 Disease Ontology Browser

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Disease Ontology Browser

cone-rod dystrophy 21 (DOID:0081447)
Alliance: disease page
Alt IDs: OMIM:616502
Definition: A cone-rod dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the DRAM2 gene on chromosome 1p13.

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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