Disease

Congenital Stationary Night Blindness

About the Disease
Congenital Stationary Night Blindness, also known as night blindness, congenital stationary, is related to night blindness, congenital stationary, type 1a and x-linked congenital stationary night blindness. An important gene associated with Congenital Stationary Night Blindness is NYX (Nyctalopin), and among its related pathways/superpathways are Olfactory Signaling Pathway and CREB Pathway. The drugs Beta carotene and Carotenoids have been mentioned in the context of this disorder. Affiliated tissues include eye, retina and skeletal muscle, and related phenotypes are myopia and reduced visual acuity

Common Targets
GUCY2D | GNB3 | SAG | GRM6 | TRPM1 | RHO | RIMS2 | PDE6B | ABCA4 | LRIT3 | GPR179 | NYX | CACNA1F | GNAT1 | SLC24A1

疾病靶点研报
Congenital Stationary Night Blindness

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