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Terminology chevron_right Concepts chevron_right 304737009

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The component that hold information about this concept.
Familial hyperkalemic periodic paralysis (disorder)
Gamstorp disease
Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Familial hyperkalemic periodic paralysis (disorder)

SCTID: 304737009, Primitive, Active


304737009|Familial hyperkalemic periodic paralysis (disorder)|
  • en Adynamia episodica hereditaria
  • en Familial hyperkalaemic periodic paralysis
  • en Familial hyperkalemic periodic paralysis
  • en Familial hyperkalemic periodic paralysis (disorder)
  • en Hyperkalaemic periodic paralysis
  • en Hyperkalemic periodic paralysis
  • en Gamstorp disease
  • en Periodic paralysis ii

304737009 |Familial hyperkalemic periodic paralysis (disorder)|

<<< 267607008 |Familial periodic paralysis (disorder)| :
        { 363698007 |Finding site (attribute)| = 127954009 |Skeletal muscle structure (body structure)| }
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