All diseases

OMIM ID
168300
OMIM term:
PARAMYOTONIA CONGENITA OF VON EULENBURG; PMC
Alternative terms:
PARALYSIS PERIODICA PARAMYOTONICA PARALYSIS PERIODICA PARAMYOTONIA, INCLUDED
PARAMYOTONIA CONGENITA WITHOUT COLD PARALYSIS, INCLUDED
(∗) Location:
17q23.3  
(†) Associated OMIM genes:
SCN4A  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/edb775ov