Term Name: familial periodic paralysis
Synonyms:
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.
Ontology: Human Disease [DOID:1029]   ( DOID:1029 )

Relationships
is a type of: metal metabolism disorder
has subtype: hyperkalemic periodic paralysis hypokalemic periodic paralysis