Oguchi disease Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Oguchi disease is an autosomal recessive retinal disorder characterized by congenital stationary night blindness (see this term) and the Mizuo-Nakamura phenomenon. (Orphanet Rare Disease Ontology, Orphanet_75382)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C537743
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2 genes/proteins associated with the disease Oguchi disease from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
GRK1 G protein-coupled receptor kinase 1 2.88009
SAG S-antigen; retina and pineal gland (arrestin) 2.88009