All diseases

OMIM ID
602668
OMIM term:
MYOTONIC DYSTROPHY 2; DM2
Alternative terms:
DYSTROPHIA MYOTONICA 2
PROXIMAL MYOTONIC MYOPATHY; PROMM
MYOTONIC MYOPATHY, PROXIMAL
RICKER SYNDROME
(∗) Location:
3q21.3  
(†) Associated OMIM genes:
ZNF9  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/p0cr1syz