Cone-Rod Dystrophy 5 Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A retinal degeneration that is an inherited progressive disease that causes deterioration of the cone and rod photoreceptor cells and often results in blindness. (Human Disease Ontology, DOID_0050572)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C563415
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Genes

2 genes/proteins associated with the disease Cone-Rod Dystrophy 5 from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
GUCY2D guanylate cyclase 2D, membrane (retina-specific) 2.88009
PITPNM3 PITPNM family member 3 2.88009