"Gilbert Disease" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
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.
| Descriptor ID |
D005878
|
| MeSH Number(s) |
C16.320.565.300.528 C18.452.648.300.528
|
| Concept/Terms |
Gilbert Disease- Gilbert Disease
- Disease, Gilbert
- Gilbert's Disease
- Disease, Gilbert's
- Gilberts Disease
- Gilbert's Syndrome
- Gilberts Syndrome
- Syndrome, Gilbert's
- Hyperbilirubinemia 1
- Hyperbilirubinemia 1s
- Unconjugated Benign Bilirubinemia
- Hyperbilirubinemia, Arias Type
- Arias Type Hyperbilirubinemia
- Arias Type Hyperbilirubinemias
- Hyperbilirubinemias, Arias Type
- Constitutional Liver Dysfunction
- Familial Nonhemolytic Jaundice
- Gilbert-Lereboullet Syndrome
- Meulengracht Syndrome
- Gilbert Syndrome
- Syndrome, Gilbert
- Hyperbilirubinemia I
|
Below are MeSH descriptors whose meaning is more general than "Gilbert Disease".
Below are MeSH descriptors whose meaning is more specific than "Gilbert Disease".
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Below are the most recent publications written about "Gilbert Disease" by people in Profiles.
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Phosphofructokinase deficiency (Tarui disease) associated with hepatic glucuronyltransferase deficiency (Gilbert's syndrome): a case and family study. Isr J Med Sci. 1990 Jun; 26(6):328-33.