cone dystrophy Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A retinal disease that is characterized by the loss of cone cells, the photoreceptors responsible for both central and color vision. (Human Disease Ontology, DOID_0050795)
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1 genes associated with the disease cone dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
RDH5 retinol dehydrogenase 5 (11-cis/9-cis)