- Concept UI
- M0328337
- Scope Note
- An autosomal dominant familial disorder characterized by recurrent episodes of skeletal muscle weakness associated with falls in serum potassium levels. The condition usually presents in the first or second decade of life with attacks of trunk and leg paresis during sleep or shortly after awakening. Symptoms may persist for hours to days and generally are precipitated by exercise or a meal high in carbohydrates. (Adams et al., Principles of Neurology, 6th ed, p1483)
- Terms
-
Hypokalemic Periodic Paralysis
Preferred Term
Term UI
T358337
Date10/12/1999
LexicalTag
NON
ThesaurusID
-
HOKPP
Term UI
T843487
Date05/02/2013
LexicalTag
NON
ThesaurusID
-
Hypokalemic Periodic Paralysis, Familial
Term UI
T372525
Date10/12/1999
LexicalTag
NON
ThesaurusID
NLM (2000)
-
HYPOKPP
Term UI
T843488
Date05/02/2013
LexicalTag
NON
ThesaurusID
-
HYPOPP
Term UI
T843489
Date05/02/2013
LexicalTag
NON
ThesaurusID
-
Familial Hypokalemic Periodic Paralysis
Term UI
T372523
Date10/12/1999
LexicalTag
NON
ThesaurusID
-
Periodic Paralysis- Hypokalemic
Term UI
T764279
Date01/15/2010
LexicalTag
NON
ThesaurusID
-
Primary Hypokalemic Periodic Paralysis
Term UI
T372524
Date10/12/1999
LexicalTag
NON
ThesaurusID
-
Westphall Disease
Term UI
T841723
Date04/18/2013
LexicalTag
NON
ThesaurusID
GHR (2014)
-
Paralysis, Hypokalemic Periodic
Term UI
T451072
Date06/15/2001
LexicalTag
NON
ThesaurusID
NLM (2002)