cone-rod dystrophy 10 Disease Ontology Browser

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Disease Ontology Browser

cone-rod dystrophy 10 (DOID:0111017)
Alliance: disease page
Synonyms: CORD10
Alt IDs: OMIM:610283, MESH:C564597
Definition: A cone-rod dystrophy that has_material_basis_in compound heterozygous mutation in the SEMA4A gene on chromosome 1q22.

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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