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Terminology chevron_right Concepts chevron_right 5523002

Production
The component that hold information about this concept.
Idiopathic myoglobinuria (disorder)
Meyer-betz disease
Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Idiopathic myoglobinuria (disorder)

SCTID: 5523002, Defined, Active


5523002|Idiopathic myoglobinuria (disorder)|
  • en Acute paroxysmal myoglobinuria
  • en Idiopathic myoglobinuria
  • en Idiopathic myoglobinuria (disorder)
  • en Non-exertional myoglobinuria
  • en Spontaneous myoglobinuria
  • en Meyer-betz disease

5523002 |Idiopathic myoglobinuria (disorder)|

=== 48165008 |Myoglobinuria (finding)| +
    41969006 |Idiopathic disease (disorder)| +
    2704003 |Acute disease (disorder)| +
    106102002 |Abnormal urinary product (finding)| :
        { 363713009 |Has interpretation (attribute)| = 260373001 |Detected (qualifier value)|,
          363714003 |Interprets (attribute)| = 32375007 |Myoglobin measurement, urine (procedure)| }
        { 263502005 |Clinical course (attribute)| = 424124008 |Sudden onset and/or short duration (qualifier value)| }
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