Night Blindness, Congenital Stationary, Autosomal Dominant 3 (CSNBAD3)

Night Blindness, Congenital Stationary, Autosomal Dominant 3, also known as congenital stationary night blindness autosomal dominant 3, is related to cone-rod dystrophy 2 and night blindness, congenital stationary, autosomal dominant 2. An important gene associated with Night Blindness, Congenital Stationary, Autosomal Dominant 3 is GNAT1 (G Protein Subunit Alpha Transducin 1), and among its related pathways/superpathways are Organelle biogenesis and maintenance and Bardet-Biedl syndrome. Related phenotypes are congenital stationary night blindness and adipose tissue