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Terminology chevron_right Concepts chevron_right 67305007

Production
The component that hold information about this concept.
Familial essential myoclonus (disorder)
Essential myoclonus
Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Familial essential myoclonus (disorder)

SCTID: 67305007, Primitive, Active


67305007|Familial essential myoclonus (disorder)|
  • en Essential myoclonus
  • en Familial essential myoclonus
  • en Familial essential myoclonus (disorder)

67305007 |Familial essential myoclonus (disorder)|

<<< 127324008 |Myoclonic disorder (disorder)| +
    76349003 |Extrapyramidal disease (disorder)| :
        { 363698007 |Finding site (attribute)| = 76375004 |Extrapyramidal system structure (body structure)| }
        { 363714003 |Interprets (attribute)| = 363847004 |Movement observable (observable entity)| }
Active
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