About: Familial Periodic Paralysis     Goto   Sponge   NotDistinct   Permalink

An Entity of Type : owl:Class, within Data Space : linked.opendata.cz associated with source document(s)

AttributesValues
rdf:type
rdfs:label
  • Familial Periodic Paralysis
rdfs:subClassOf
Semantic_Type
  • Disease or Syndrome
Preferred_Name
  • Familial Periodic Paralysis
UMLS_CUI
  • C0030443
FULL_SYN
  • Familial Periodic ParalysisPTNCI
DEFINITION
  • A group of genetic neurological disorders caused by mutations in genes involved in the sodium and calcium channels in nerve cells. It 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.NCI
code
  • C84709
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