NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link http://ctdbase.org/detail.go?type=disease&acc=OMIM:257270
Similar Terms
Downloads & Tools

Genes

1 genes/proteins associated with the disease NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
GRM6 glutamate receptor, metabotropic 6 2.88009