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Disease Ontology Browser
cone dystrophy (DOID:0050795)
Alliance: disease page
Synonyms: retinal cone dystrophy
Alt IDs: OMIM:180020, OMIM:610024, OMIM:610356, OMIM:610478, OMIM:613093
Definition: A retinal disease that is characterized by the loss of cone cells, the photoreceptors responsible for both central and color vision.

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
MGI 6.14
The Jackson Laboratory