All diseases

OMIM ID
610445
OMIM term:
NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 1; CSNBAD1
Alternative terms:

(∗) Location:
3q22.1  
(†) Associated OMIM genes:
RHO  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/y33oousz