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Disease Ontology Browser
cone dystrophy (DOID:0050795)
Alliance: disease page
Synonyms: retinal cone dystrophy
Alt IDs: MESH:D000077765
Definition: A retinal disease that is characterized by the loss of cone cells, the photoreceptors responsible for both central and color vision.

Disease References using Mouse Models (1)

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
12/10/2024
MGI 6.24
The Jackson Laboratory