All diseases

OMIM ID
160800
OMIM term:
MYOTONIA CONGENITA, AUTOSOMAL DOMINANT
Alternative terms:

(∗) Location:
7q34  
(†) Associated OMIM genes:
CLCN1  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/e4mnkxr9