All diseases

OMIM ID
160900
OMIM term:
MYOTONIC DYSTROPHY 1; DM1
Alternative terms:
DYSTROPHIA MYOTONICA 1
DYSTROPHIA MYOTONICA; DM
STEINERT DISEASE
(∗) Location:
19q13.32  
(†) Associated OMIM genes:
DMPK  
(‡) Associated MGI genes:
Dmpk   Mbnl1  

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