All diseases

OMIM ID
300071
OMIM term:
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A; CSNB2A
Alternative terms:
CSNB, INCOMPLETE, X-LINKED
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2; CSNB2
(∗) Location:
Xp11.23  
(†) Associated OMIM genes:
CACNA1F  
(‡) Associated MGI genes:
Cacna1f  

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