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hypokalemic periodic paralysis, type 2

Disease Summary
Associated Targets (1)
Tclin

1


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:0013234:  hypokalemic periodic paralysis, type 2
MESH:C567635: 
UMLS:C2750061: