All diseases

OMIM ID
170500
OMIM term:
HYPERKALEMIC PERIODIC PARALYSIS; HYPP
Alternative terms:
ADYNAMIA EPISODICA HEREDITARIA WITH OR WITHOUT MYOTONIA
GAMSTORP DISEASE NORMOKALEMIC PERIODIC PARALYSIS, POTASSIUM-SENSITIVE, INCLUDED
(∗) Location:
17q23.3  
(†) Associated OMIM genes:
SCN4A  
(‡) Associated MGI genes:
Scn4a  

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