MeSH Browser

MeSH Heading: Gilbert Disease
Tree Number(s): C16.320.565.300.528; C18.452.648.300.528
Unique ID: D005878
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D005878
Scope Note: 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.
Entry Version: GILBERT DIS
Entry Term(s): 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
Public MeSH Note: 2000; see GILBERT'S DISEASE 1991-1999, see HYPERBILIRUBINEMIA, HEREDITARY 1975-90
History Note: 2000(1975)
Date Established: 1991/01/01
Date of Entry: 1999/01/01
Revision Date: 2013/07/08

Allowable Qualifiers: blood (BL)

cerebrospinal fluid (CF)

chemically induced (CI)

classification (CL)

complications (CO)

diagnosis (DI)

diagnostic imaging (DG)

diet therapy (DH)

drug therapy (DT)

economics (EC)

embryology (EM)

enzymology (EN)

epidemiology (EP)

ethnology (EH)

etiology (ET)

genetics (GE)

history (HI)

immunology (IM)

metabolism (ME)

microbiology (MI)

mortality (MO)

nursing (NU)

parasitology (PS)

pathology (PA)

physiopathology (PP)

prevention & control (PC)

psychology (PX)

radiotherapy (RT)

rehabilitation (RH)

surgery (SU)

therapy (TH)

urine (UR)

veterinary (VE)

virology (VI)

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]

Nutritional and Metabolic Diseases [C18]
- Metabolic Diseases [C18.452]
  - Metabolism, Inborn Errors [C18.452.648]
    - Hyperbilirubinemia, Hereditary [C18.452.648.300]

Gilbert Disease Preferred

Concept UI: M0009229
Scope Note: 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.
Terms: Gilbert Disease Preferred Term
Term UI T017775
Date03/16/1981
LexicalTag EPO
ThesaurusID; Gilbert's Syndrome
Term UI T770119
Date04/22/2010
LexicalTag EPO
ThesaurusID; Hyperbilirubinemia 1
Term UI T740550
Date02/24/2009
LexicalTag NON
ThesaurusID; Hyperbilirubinemia I
Term UI T811558
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013); Hyperbilirubinemia, Arias Type
Term UI T768910
Date04/07/2010
LexicalTag NON
ThesaurusID; Constitutional Liver Dysfunction
Term UI T841489
Date04/18/2013
LexicalTag NON
ThesaurusID GHR (2014); Familial Nonhemolytic Jaundice
Term UI T841490
Date04/18/2013
LexicalTag NON
ThesaurusID GHR (2014); Gilbert-Lereboullet Syndrome
Term UI T841491
Date04/18/2013
LexicalTag NON
ThesaurusID GHR (2014); Meulengracht Syndrome
Term UI T841492
Date04/18/2013
LexicalTag NON
ThesaurusID GHR (2014); Unconjugated Benign Bilirubinemia
Term UI T841493
Date04/18/2013
LexicalTag NON
ThesaurusID GHR (2014); Gilbert's Disease
Term UI T017776
Date01/01/1999
LexicalTag EPO
ThesaurusID; Gilbert Syndrome
Term UI T768909
Date04/07/2010
LexicalTag EPO
ThesaurusID

Gilbert Disease MeSH Descriptor Data 2024