Night Blindness, Congenital Stationary, Autosomal Dominant 3 Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C566475
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Genes

1 genes/proteins associated with the disease Night Blindness, Congenital Stationary, Autosomal Dominant 3 from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
GNAT1 guanine nucleotide binding protein (G protein), alpha transducing activity polypeptide 1 2.88009