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Terminology chevron_right Concepts chevron_right 110997000

Production
The component that hold information about this concept.
Fahr's syndrome (disorder)
Fahr disease
Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Fahr's syndrome (disorder)

SCTID: 110997000, Primitive, Active


110997000|Fahr's syndrome (disorder)|
  • en Cerebral symmetric calcification
  • en Cerebrovascular ferrocalcinosis
  • en Idiopathic nonarteriosclerotic cerebrovascular calcification
  • en Fahr disease
  • en Fahr syndrome
  • en Fahr's syndrome (disorder)
  • en Fahr's syndrome

110997000 |Fahr's syndrome (disorder)|

<<< 230311004 |Basal ganglia degeneration with calcification (disorder)| +
    62914000 |Cerebrovascular disease (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 18115005 |Pathologic calcification, calcified structure (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 28661005 |Cerebrovascular system structure (body structure)| }
        { 116676008 |Associated morphology (attribute)| = 18115005 |Pathologic calcification, calcified structure (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 32610002 |Basal ganglion structure (body structure)| }
        { 363713009 |Has interpretation (attribute)| = 263654008 |Abnormal (qualifier value)|,
          363714003 |Interprets (attribute)| = 363847004 |Movement observable (observable entity)| }
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