FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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Term familial periodic paralysis ID (Ontology) DOID:1029 (Human Disease)
Definition A metal metabolism disorder that is characterized by episodes of muscle paralysis in which the affected muscles become flaccid and the deep tendon reflexes disappear. Between the episodes the affected muscles usually work normally, and that are caused by mutations in genes involved in the sodium and calcium channels in nerve cells.
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  inherited metabolic disorder
   |__metal metabolism disorder
       |__familial periodic paralysis  2 rec.
           |__hyperkalemic periodic paralysis 1 rec.
           |__hypokalemic periodic paralysis 2 rec.
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GARD:6422
ICD10CM:G72.3
MESH:D010245
NCI:C84709
SNOMEDCT_US_2023_03_01:193241004
UMLS_CUI:C0030443