All diseases

OMIM ID
310500
OMIM term:
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1A; CSNB1A
Alternative terms:
CSNB, COMPLETE, X-LINKED
NIGHT BLINDNESS, CONGENITAL STATIONARY, WITH MYOPIA
HEMERALOPIA-MYOPIA
MYOPIA-NIGHT BLINDNESS; NBM1 NYCTALOPIA, INCLUDED
(∗) Location:
Xp11.4  
(†) Associated OMIM genes:
NYX  
(‡) Associated MGI genes:
Nyx  

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