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Terminology chevron_right Concepts chevron_right 27503000

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

Gilbert's syndrome (disorder)

SCTID: 27503000, Primitive, Active


27503000|Gilbert's syndrome (disorder)|
  • vi Hội chứng gilbert
  • en Benign unconjugated bilirubinaemia syndrome
  • en Benign unconjugated bilirubinemia syndrome
  • en Cholaemia familiaris simplex
  • en Cholemia familiaris simplex
  • en Chronic intermittent juvenile jaundice
  • en Congenital familial cholaemia
  • en Congenital familial cholemia
  • en Constitutional hepatic dysfunction
  • en Familial nonhaemolytic bilirubinaemia
  • en Familial nonhaemolytic jaundice
  • en Familial nonhemolytic bilirubinemia
  • en Familial nonhemolytic jaundice
  • en Hereditary nonhaemolytic jaundice
  • en Hereditary nonhemolytic jaundice
  • en Low-grade chronic hyperbilirubinaemia syndrome
  • en Low-grade chronic hyperbilirubinemia syndrome
  • en Gilberts syndrome
  • en Gilbert's syndrome (disorder)
  • en Gilbert-lereboullet syndrome
  • en Gilbert's disease
  • en Gilbert's syndrome
  • en Gilbert syndrome
  • en Meulengracht syndrome

27503000 |Gilbert's syndrome (disorder)|

<<< 5655007 |Inherited disorder of bilirubin metabolism (disorder)| :
        { 246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
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