Gilbert Disease

**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.

**Tree numbers:** - C16.320.565.300.528 - C18.452.648.300.528

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