All diseases

OMIM ID
608390
OMIM term:
MYOTONIA, POTASSIUM-AGGRAVATED
Alternative terms:
MYOTONIA FLUCTUANS
MYOTONIA PERMANENS
SODIUM CHANNEL MUSCLE DISEASE
MYOTONIA CONGENITA, ACETAZOLAMIDE-RESPONSIVE
MYOTONIA CONGENITA, ATYPICAL LARYNGOSPASM, SEVERE NEONATAL EPISODIC, INCLUDED; SNEL, INCLUDED
(∗) Location:
17q23.3  
(†) Associated OMIM genes:
SCN4A  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/w4cmsaj6