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Nutritional and Metabolic Diseases > Metabolic Diseases > Metabolism, Inborn Errors > Hyperbilirubinemia, Hereditary > Gilbert Disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Metabolism, Inborn Errors > Hyperbilirubinemia, Hereditary > Gilbert Disease

Preferred term

Gilbert Disease  

Type

  • Topical Descriptor

Broader concept

Entry terms

  • Arias Type Hyperbilirubinemia
  • Arias Type Hyperbilirubinemias
  • Constitutional Liver Dysfunction
  • Disease, Gilbert's
  • Familial Nonhemolytic Jaundice
  • Gilbert-Lereboullet Syndrome
  • Gilbert's Disease
  • Gilberts Disease
  • Gilbert's Syndrome
  • Gilberts Syndrome
  • Gilbert Syndrome
  • Hyperbilirubinemia 1
  • Hyperbilirubinemia 1s
  • Hyperbilirubinemia, Arias Type
  • Hyperbilirubinemia I
  • Hyperbilirubinemias, Arias Type
  • Meulengracht Syndrome
  • Syndrome, Gilbert
  • Syndrome, Gilbert's
  • Unconjugated Benign Bilirubinemia

Scope note

  • A benign familial disorder, transmitted as an autosomal dominant trait. It is characterized by low-grade chronic hyperbilirubinemia with considerable daily fluctuations of the bilirubin level.

History note

  • 2000(1975)

In other languages

URI

http://www.yso.fi/onto/mesh/D005878

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