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Terminology chevron_right Concepts chevron_right 37991008

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

Parinaud's syndrome (disorder)

SCTID: 37991008, Primitive, Active


37991008|Parinaud's syndrome (disorder)|
  • en Dorsal midbrain syndrome
  • en Paralysis of vertical movement
  • en Parinaud's syndrome (disorder)
  • en Parinaud's ophthalmoplegia
  • en Parinaud's syndrome
  • en Parinaud syndrome
  • en Vertical gaze palsy - parinaud

37991008 |Parinaud's syndrome (disorder)|

<<< 95641009 |Disorder of midbrain (disorder)| +
    246773002 |Vertical gaze palsy (disorder)| +
    1370930009 |Cranial nerve palsy (disorder)| :
        { 363698007 |Finding site (attribute)| = 25238003 |Cranial nerve structure (body structure)| }
        { 363698007 |Finding site (attribute)| = 371398005 |Eye region structure (body structure)| }
        { 363698007 |Finding site (attribute)| = 61962009 |Midbrain structure (body structure)| }
        { 363698007 |Finding site (attribute)| = 1264400000 |Structure of motor nervous system (body structure)| }
        { 363713009 |Has interpretation (attribute)| = 2667000 |Absent (qualifier value)|,
          363714003 |Interprets (attribute)| = 363847004 |Movement observable (observable entity)| }
Active
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