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Terminology chevron_right Concepts chevron_right 230191005

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

Rasmussen syndrome (disorder)

SCTID: 230191005, Primitive, Active


230191005|Rasmussen syndrome (disorder)|
  • en Rasmussen syndrome (disorder)
  • en Rasmussen encephalitis
  • en Rasmussen syndrome

230191005 |Rasmussen syndrome (disorder)|

<<< 230189002 |Focal encephalitis (disorder)| +
    298364001 |Finding of head region (finding)| +
    1340125003 |Epilepsy syndrome with progressive neurological deterioration (disorder)| +
    230381009 |Focal epilepsy (disorder)| +
    5294002 |Developmental disorder (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 103625009 |Focal inflammation (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 372073000 |Cerebral hemisphere structure (body structure)| }
        { 363698007 |Finding site (attribute)| = 12738006 |Brain structure (body structure)|,
          370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        { 116676008 |Associated morphology (attribute)| = 103625009 |Focal inflammation (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 280369009 |Brain tissue structure (body structure)| }
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