You are using an outdated browser. Please upgrade your browser to improve your experience.

hypokalemic periodic paralysis, type 1

Disease Summary
Associated Targets (2)
Tclin

2


Uniprot Description An autosomal dominant disorder manifested by episodic flaccid generalized muscle weakness associated with falls of serum potassium levels.
Mondo Term and Equivalent IDs
MONDO:0042979:  hypokalemic periodic paralysis, type 1
UMLS:C3714580: