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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
:
pde6c,
kcnv2,
cacna2d4,
guca1al,
pde6h,
cngb3,
gnat2,
guca1a
| MONDO:0000455 - attention behavior |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
retinal disease (is_a)