5C58.01 Gilbert syndrome

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2026-01

Gilbert's syndrome is an inherited liver disorder characterised by jaundice due to unconjugated hyperbilirubinemia, resulting from a partial deficiency in hepatic bilirubin glucuronosyltransferase activity.

synonyms

• Gilbert syndrome
• Gilbert cholaemia
• Gilbert disease
• Gilbert--Lereboullet syndrome
• Hyperbilirubinaemia type 1
• Meulengracht icterus
• Meulengracht syndrome
• benign unconjugated bilirubinaemia syndrome
• cholaemia familiaris simplex
• chronic intermittent juvenile jaundice
• congenital familial cholaemia
• constitutional hepatic dysfunction
• constitutional hyperbilirubinaemia (in part)
• familial cholaemia
• familial nonhaemolytic bilirubinaemia
• familial nonhaemolytic jaundice
• hereditary nonhaemolytic bilirubinaemia
• hereditary nonhaemolytic jaundice
• icterus intermittens juvenilis
• idiopathic hyperbilirubinaemia (in part)
• idiopathic unconjugated hyperbilirubinaemia
• low-grade chronic hyperbilirubinaemia syndrome
• physiologic cholaemia

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