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Concept information

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

Preferred term

Gilbert Disease  

Type

  • mesh:Descriptor

Definition

  • 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.

Broader concept

Entry terms

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

Allowable Qualifier(s)

In other languages

  • Maladie de Gilbert

    French

  • Cholémie de Gilbert
  • Cholémie familiale
  • Hyperbilirubinémie de type 1
  • Ictère héréditaire de Gilbert

URI

http://data.loterre.fr/ark:/67375/JVR-LHHB0CTN-S

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