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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
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
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)