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Gilbert Disease
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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.
Other names
Syndrome, Gilbert's; Syndrome, Gilbert; Hyperbilirubinemias, Arias Type; Hyperbilirubinemia 1s; Gilberts Syndrome; Gilberts Disease; Disease, Gilbert's; Disease, Gilbert; Arias Type Hyperbilirubinemias; Arias Type Hyperbilirubinemia; Hyperbilirubinemia, Arias Type; Hyperbilirubinemia 1; Gilbert's Syndrome; Gilbert's Disease; Gilbert Syndrome
