retinal cone dystrophy 1 Disease Ontology Browser

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Disease Ontology Browser

retinal cone dystrophy 1 (DOID:0081024)
Alliance: disease page
Alt IDs: OMIM:180020, MESH:C566719
Definition: A cone dystrophy that is characterized as autosomal dominant form of diffuse cone degeneration.

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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