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Gilbert Syndrome - Medical Condition Information

Gilbert Syndrome

Gilbert SyndromeGilbert's DiseaseGilbert-Lereboullet Syndrome
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📋Overview

Gilbert syndrome is a common, benign inherited condition characterized by mild, intermittent unconjugated hyperbilirubinemia due to reduced activity of the enzyme UDP-glucuronosyltransferase 1A1 (UGT1A1). It is a genetic disorder affecting bilirubin metabolism, leading to occasional mild jaundice without liver damage. The term 'Gilbert syndrome' is the preferred modern name.

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This content is provided for general health education and awareness and is based on publicly available medical information. It is not intended to replace professional medical advice, diagnosis, or treatment, and should not be used to make healthcare decisions. Always seek the guidance of a qualified healthcare professional regarding any medical condition, medication, supplement, or procedure.

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Medical codes (for reference)

UMLS CUI: C0017551
ICD-10-CM
E80.4
MeSH
D005878
SNOMED CT (US)
27503000

Codes are provided for reference and interoperability. They are not a diagnosis.

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