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Gilbert syndrome

metabolic disorder in which the liver processes bilirubin slowly
Class type of: bilirubin metabolic disorder Q752216
Gilbert syndrome
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Facts

10 properties
Instance of
class of disease
Subclass of
bilirubin metabolic disorder
Different from
Guillain–Barré syndrome[7]
Discoverer or inventor
Augustin Nicolas Gilbert[3]
Genetic association
UGT1A1[10]
Has phenotype
unconjugated hyperbilirubinemia[12]
Health specialty
hepatology, family medicine[8][9]
NCI Thesaurus ID
C84729[6]
Named after
Augustin Nicolas Gilbert, Einar Meulengracht[4][5]
On focus list of Wikimedia project
WikiProject Medicine[11]
🏷️ Also known as
en Hyperbilirubinemia, Gilbert Type en Gilbert syndrome en Constitutional hyperbilirubinemia en Gilbert Disease en Gilbert's syndrome en Gilbert's disease en GILBERT SYNDROME en Hyperbilirubinemia, Arias Type en hereditary nonhemolytic jaundice en Hyperbilirubinemia 1 en Gilbert-Meulengracht syndrome ar متلازمة غلبرت cs Gilbert-Meulengrachtův syndrom cs Meulengrachtův syndrom cs Gilbertův syndrom cs Icterus intermittens juvenilis cs GS de Morbus Meulengracht de Meulengracht-Krankheit de Morbus Gilbert
🔖 Identifiers · 33
OpenAlex ID
C2776365762
Disease Ontology ID
DOID:2739
DiseasesDB
5218
EMedicine ID
178841
Encyclopædia Britannica Online ID
topic/Gilbert-disease
Exact match
purl.obolibrary.org, identifiers.org, www.orpha.net
Experimental Factor Ontology ID
0005556
Freebase ID
/m/01xg9b
GARD rare disease ID
6507
ICD-10 ID
E80.4
ICD-10-CM
E80.4
ICD-11 ID (Foundation)
1947520963
Show all 33 identifiers +21
ICD-11 ID (MMS)
5C58.01
ICD-9 ID
277.4
KEGG ID
H02055
MeSH descriptor ID
D005878
MeSH tree code
C16.320.565.300.528, C18.452.648.300.528
Medical Dictionary for Regulatory Activities ID
10018267
MedlinePlus ID
000301
Mondo ID
MONDO_0007745
NHS Health A to Z ID
gilberts-syndrome
National Library of Spain SpMaBN ID
XX535328
OMIM ID
143500
Orphanet ID
357
Patientplus ID
gilberts-syndrome-pro
PatientsLikeMe condition ID
gilbert-s-syndrome
Raras disease ID
D00357
SNOMED CT ID
27503000
UK Parliament thesaurus ID
554333
UMLS CUI
C0017551
UniProt disease ID
DI-01659
WikiProjectMed ID
Gilbert's syndrome
WikiSkripta article ID
13449

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🔗 Connections
Health specialty 2
hepatology, family medicine
Created notable works 1
Augustin Nicolas Gilbert
Different from 1
Guillain–Barré syndrome
Discoverer or inventor 1
Augustin Nicolas Gilbert
Genetic association 1
UGT1A1
Named after 1
Augustin Nicolas Gilbert
On focus list of Wikimedia project 1
WikiProject Medicine
Subclass of 1
disease
← Genetic association 1
UGT1A1
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Summary

Gilbert syndrome is a class of disease[1]. It is a type of bilirubin metabolic disorder[2].

Related Entities

disease

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [3] ↑ . wikidata.org.
  2. [4] ↑ . wikidata.org.
  3. [5] ↑ . wikidata.org.
  4. [2] ↑ . Disease Ontology. Retrieved . wikidata.org.
  5. [6] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  6. [7] ↑ . wikidata.org.
  7. [8] ↑ . wikidata.org.
  8. [9] ↑ . wikidata.org.
  9. [10] ↑ . UniProt. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  10. [11] ↑ . wikidata.org.
  11. [12] ↑ . Retrieved . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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APA 4ort.xyz Knowledge Graph. (2026). Gilbert syndrome. Retrieved November 11, 2026, from https://4ort.xyz/entity/gilbert-syndrome
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BibTeX @misc{4ortxyz_gilbert-syndrome_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Gilbert syndrome}}, year = {2026}, url = {https://4ort.xyz/entity/gilbert-syndrome}, note = {Accessed: 2026-11-11}}
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Edit History

Rolling log of changes to this entity's Wikidata record. Values shown reflect the current state of each edited property — follow the history link to see the precise diff for any edit.

  1. 20d ago · ACorrêa (WMB) · 2026-10-24 view diff on Wikidata ↗
    Has phenotype → unconjugated hyperbilirubinemia
    Raras disease ID → D00357
    "Changed the item: QuickStatements 3.0 batch #61469: Raras.org data import"
  2. 19w ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Subclass of → bilirubin metabolic disorder
    Health specialty → hepatology, family medicine
    Genetic association → UGT1A1
    Different from → Guillain–Barré syndrome
    + 4 other properties edited (see Wikidata diff for full list)
    "Changed the item: QuickStatements 3.0 batch #39732: rm redundant subclass"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.