All diseases

OMIM ID
257270
OMIM term:
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B; CSNB1B
Alternative terms:
NIGHT BLINDNESS, CONGENITAL STATIONARY, COMPLETE, AUTOSOMAL RECESSIVE
CSNB, COMPLETE, AUTOSOMAL RECESSIVE
(∗) Location:
5q35.3  
(†) Associated OMIM genes:
GRM6  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/9dd4b3h0