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.
Also Known As:
Constitutional Liver Dysfunction; Familial Nonhemolytic Jaundice; Gilbert Syndrome; Gilbert's Disease; Gilbert's Syndrome; Gilbert-Lereboullet Syndrome; Hyperbilirubinemia 1; Hyperbilirubinemia I; Hyperbilirubinemia, Arias Type; Meulengracht Syndrome; Unconjugated Benign Bilirubinemia; Arias Type Hyperbilirubinemia; Arias Type Hyperbilirubinemias; Disease, Gilbert; Disease, Gilbert's; Gilberts Disease; Gilberts Syndrome; Hyperbilirubinemia 1s; Hyperbilirubinemias, Arias Type; Syndrome, Gilbert; Syndrome, Gilbert's