DISEASES

Disease-gene associations mined from literature

Human genes for cone dystrophy

Cone dystrophy [DOID:0050795]

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

Synonyms:  cone dystrophy,  DOID:0050795,  cone dystrophies,  retinal cone dystrophy,  retinal cone dystrophies

Linkouts:  OMIM #1 #2 #3 #4