Gilbert Disease

"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.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

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 Hyperbilirubinemia I Hyperbilirubinemia, Arias Type Arias Type Hyperbilirubinemia Arias Type Hyperbilirubinemias Hyperbilirubinemias, Arias Type Gilbert's Syndrome Gilberts Syndrome Syndrome, Gilbert's Gilbert Syndrome Syndrome, Gilbert Hyperbilirubinemia 1 Hyperbilirubinemia 1s

Below are MeSH descriptors whose meaning is more general than "Gilbert Disease".

Diseases [C]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Genetic Diseases, Inborn [C16.320]
Metabolism, Inborn Errors [C16.320.565]
Hyperbilirubinemia, Hereditary [C16.320.565.300]
Gilbert Disease [C16.320.565.300.528]
Nutritional and Metabolic Diseases [C18]
Metabolic Diseases [C18.452]
Metabolism, Inborn Errors [C18.452.648]
Hyperbilirubinemia, Hereditary [C18.452.648.300]
Gilbert Disease [C18.452.648.300.528]

Below are MeSH descriptors whose meaning is related to "Gilbert Disease".

Below are MeSH descriptors whose meaning is more specific than "Gilbert Disease".

publications

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