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Summary Literature (1)
DOID:0050795 - cone dystrophy

Disease Ontology Definition:A retinal disease that is characterized by the loss of cone cells, the photoreceptors responsible for both central and color vision.

Synonyms: retinal cone dystrophy,

Xenbase Genes : pde6c, kcnv2, cacna2d4, guca1al, pde6h, cngb3, gnat2, guca1a

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0000455 - cone dystrophy


Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): retinal disease (is_a)