Medical Subject Headings

Last uploaded: January 31, 2024
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Preferred Name

Gilbert Disease
Synonyms

Syndrome, Gilbert's
Definitions

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.
ID

http://purl.bioontology.org/ontology/MESH/D005878
altLabel

Syndrome, Gilbert's

Gilberts Disease

Hyperbilirubinemia I

Hyperbilirubinemia 1

Hyperbilirubinemias, Arias Type

Syndrome, Gilbert

Unconjugated Benign Bilirubinemia

Gilbert Syndrome

Arias Type Hyperbilirubinemias

Gilbert-Lereboullet Syndrome

Gilberts Syndrome

Gilbert's Disease

Disease, Gilbert

Arias Type Hyperbilirubinemia

Hyperbilirubinemia, Arias Type

Gilbert's Syndrome

Meulengracht Syndrome

Hyperbilirubinemia 1s

Disease, Gilbert's

Familial Nonhemolytic Jaundice

Constitutional Liver Dysfunction
AQL

BL CF CI CL CO DG DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RH RT SU TH UR VE VI
cui

C0017551
DC

1
definition

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.
DX

19910101
HN

2000(1975)
Inverse of AQ

http://purl.bioontology.org/ontology/MESH/Q000097

http://purl.bioontology.org/ontology/MESH/Q000178

http://purl.bioontology.org/ontology/MESH/Q000175

http://purl.bioontology.org/ontology/MESH/Q000628

http://purl.bioontology.org/ontology/MESH/Q000276

http://purl.bioontology.org/ontology/MESH/Q000134

http://purl.bioontology.org/ontology/MESH/Q000139

http://purl.bioontology.org/ontology/MESH/Q000266

http://purl.bioontology.org/ontology/MESH/Q000378

http://purl.bioontology.org/ontology/MESH/Q000517

http://purl.bioontology.org/ontology/MESH/Q000662

http://purl.bioontology.org/ontology/MESH/Q000469

http://purl.bioontology.org/ontology/MESH/Q000150

http://purl.bioontology.org/ontology/MESH/Q000821

http://purl.bioontology.org/ontology/MESH/Q000191

http://purl.bioontology.org/ontology/MESH/Q000196

http://purl.bioontology.org/ontology/MESH/Q000473

http://purl.bioontology.org/ontology/MESH/Q000145

http://purl.bioontology.org/ontology/MESH/Q000382

http://purl.bioontology.org/ontology/MESH/Q000451

http://purl.bioontology.org/ontology/MESH/Q000453

http://purl.bioontology.org/ontology/MESH/Q000534

http://purl.bioontology.org/ontology/MESH/Q000532

http://purl.bioontology.org/ontology/MESH/Q000503

http://purl.bioontology.org/ontology/MESH/Q000188

http://purl.bioontology.org/ontology/MESH/Q000235

http://purl.bioontology.org/ontology/MESH/Q000201

http://purl.bioontology.org/ontology/MESH/Q000209

http://purl.bioontology.org/ontology/MESH/Q000208

http://purl.bioontology.org/ontology/MESH/Q000601

http://purl.bioontology.org/ontology/MESH/Q000000981

http://purl.bioontology.org/ontology/MESH/Q000652

http://purl.bioontology.org/ontology/MESH/Q000523

http://purl.bioontology.org/ontology/MESH/Q000401
Machine permutation

2000; see GILBERT'S DISEASE 1991-1999, see HYPERBILIRUBINEMIA, HEREDITARY 1975-90
MDA

19990101
MMR

20130708
MN

C18.452.648.300.528

C16.320.565.300.528
notation

D005878
prefLabel

Gilbert Disease
TERMUI

T770119

T768909

T740550

T841493

T017775

T811558

T768910

T841492

T841491

T017776

T841489

T841490
TH

OMIM (2013)

NLM (1975)

UNK (19XX)

GHR (2014)

NLM (2011)

ORD (2010)
tui

T047
subClassOf

http://purl.bioontology.org/ontology/MESH/D006933
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http://purl.bioontology.org/ontology/MDRGER/10018267 MDRGER CUI
http://purl.bioontology.org/ontology/NDFRT/N0000001333 NDFRT CUI
http://purl.bioontology.org/ontology/SCTSPA/27503000 SCTSPA CUI
http://purl.bioontology.org/ontology/OMIM/143500 OMIM CUI
http://purl.bioontology.org/ontology/SNMI/D6-85100 SNMI CUI
http://purl.bioontology.org/ontology/SNOMEDCT/27503000 SNOMEDCT CUI
http://purl.bioontology.org/ontology/RCD/C3742 RCD CUI
http://purl.bioontology.org/ontology/OMIM/MTHU031877 OMIM CUI
http://purl.bioontology.org/ontology/CSP/1654-1020 CRISP CUI
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0017551 MEDLINEPLUS CUI
http://purl.bioontology.org/ontology/ICPC2P/T99013 ICPC2P CUI
http://purl.bioontology.org/ontology/MEDDRA/10018267 MEDDRA CUI
http://purl.bioontology.org/ontology/MDRFRE/10018267 MDRFRE CUI
http://purl.bioontology.org/ontology/ICD10/E80.4 ICD10 CUI
http://purl.bioontology.org/ontology/ICD10CM/E80.4 ICD10CM CUI
http://purl.bioontology.org/ontology/MSHFRE/D005878 MSHFRE CUI
http://purl.bioontology.org/ontology/OMIM/191740 OMIM CUI
http://id.nlm.nih.gov/mesh/D005878 MDM LOOM
http://purl.obolibrary.org/obo/OMIT_0007073 OMIT LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#5493 OCHV LOOM
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0017551 MEDLINEPLUS LOOM
http://purl.jp/bio/4/id/200906054369582797 IOBC LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C16.320.565.300.528 RH-MESH LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C18.452.648.300.528 RH-MESH LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#D005878 RH-MESH LOOM
http://www.phoc.org.cn/pmo/class/PMO_00036679 PMAPP-PMO LOOM