All diseases

OMIM ID
163500
OMIM term:
NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 2; CSNBAD2
Alternative terms:

(∗) Location:
4p16.3  
(†) Associated OMIM genes:
PDE6B  
(‡) Associated MGI genes:
Pde6b  

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* quick link - http://q.sanger.ac.uk/m76df8dp