congenital stationary night blindness type 1 autosomal dominant; rhodopsin-related congenital stationary night blindness (CSNBAD1)

Genetics

• associated with defects in rhodopsin gene

More general terms

• congenital stationary night blindness type 1 (CSNB1)

Additional terms

• nyctalopin (NYX, CLRP)

Database

• OMIM: https://mirror.omim.org/entry/610445