Structured Summary
Abstract
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.
MeSH Record
Classification
Broader headings
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MeSH Record
Synonyms
21 entry terms
- Constitutional Liver Dysfunction
- Familial Nonhemolytic Jaundice
- Gilbert Syndrome
- Gilbert's Disease
- Gilbert's Syndrome
- Gilbert-Lereboullet Syndrome
- Hyperbilirubinemia 1
- Hyperbilirubinemia I
- Hyperbilirubinemia, Arias Type
- Meulengracht Syndrome
- Unconjugated Benign Bilirubinemia
- Arias Type Hyperbilirubinemia
- Arias Type Hyperbilirubinemias
- Disease, Gilbert
- Disease, Gilbert's
- Gilberts Disease
- Gilberts Syndrome
- Hyperbilirubinemia 1s
- Hyperbilirubinemias, Arias Type
- Syndrome, Gilbert
- Syndrome, Gilbert's
MeSH Record
Aspects Covered
34 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
MeSH Record
History Note
2000(1975)
MeSH Hierarchy
Tree Numbers
AMA Style
References
- National Library of Medicine. Gilbert Disease. Medical Subject Headings (MeSH). 2026. Unique ID D005878. http://id.nlm.nih.gov/mesh/2026/D005878
- Gilbert Disease. In: Wikipedia. https://en.wikipedia.org/wiki/Gilbert%27s_syndrome
- Gilbert Disease. In: Wikidata. https://www.wikidata.org/wiki/Q752216