Gilbert Disease
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.
Year introduced: 2000(1975)
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Subheadings:
Tree Number(s): C16.320.565.300.528, C18.452.648.300.528
MeSH Unique ID: D005878
Entry Terms:
- Disease, Gilbert
- Gilbert's Syndrome
- Gilberts Syndrome
- Syndrome, Gilbert's
- Hyperbilirubinemia 1
- Hyperbilirubinemia 1s
- Hyperbilirubinemia I
- Hyperbilirubinemia, Arias Type
- Arias Type Hyperbilirubinemia
- Arias Type Hyperbilirubinemias
- Hyperbilirubinemias, Arias Type
- Constitutional Liver Dysfunction
- Familial Nonhemolytic Jaundice
- Gilbert-Lereboullet Syndrome
- Meulengracht Syndrome
- Unconjugated Benign Bilirubinemia
- Gilbert's Disease
- Disease, Gilbert's
- Gilberts Disease
- Gilbert Syndrome
- Syndrome, Gilbert