"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
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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 |
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2013 | 1 | 0 | 1 |
2022 | 1 | 0 | 1 |
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Below are the most recent publications written about "Gilbert Disease" by people in Profiles.
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A Novel SPTA1 Mutation in a Patient with Hereditary Spherocytosis without a Family History and Coexisting Gilbert's Syndrome. Intern Med. 2023 Jan 01; 62(1):107-111.
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Genetics of drug-induced hepatotoxicity toxicity in Gilbert's syndrome. Am J Gastroenterol. 2013 Dec; 108(12):1936-7.
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Normal fasting-state levels of serum cholyl-conjugated bile acids in Gilbert's syndrome: an aid to the diagnosis. Hepatology. 1982 May-Jun; 2(3):340-3.
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Effect of splenectomy of hepatic bilirubin clearance in patients with hereditary spherocytosis. Implications for the diagnosis of Gilbert's syndrome. J Lab Clin Med. 1981 Jul; 98(1):37-45.
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Abnormal hepatic transport of indocyanine green in Gilbert's syndrome. Gastroenterology. 1976 Mar; 70(3):385-91.