"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".
This graph shows the total number of publications written about "Gilbert Disease" by people in this website by year, and whether "Gilbert Disease" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2000 | 1 | 0 | 1 |
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Below are the most recent publications written about "Gilbert Disease" by people in Profiles.
-
Donor liver uridine diphosphate (UDP)-glucuronosyltransferase-1A1 deficiency causing Gilbert's syndrome in liver transplant recipients. Transplantation. 2000 May 15; 69(9):1882-6.