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GENATLAS PHENOTYPE
last update : 17-02-2012
Symbol CSNB6
Location 3q22.1
Name blindness night congenital, stationary 6
Corresponding gene RHO
Other symbol(s) CSNBAD1
Main clinical features lack of night vision, with normal day vision
Genetic determination autosomal dominant
Function/system disorder eye
Type disease
Gene product
Name rhodopsin (RHO)
Remark(s)