Gilbert Syndrome

Preferred Label : Gilbert Syndrome;

NCIt synonyms : Gilbert Disease;

NCIt related terms : Gilbert's Syndrome;

NCIt definition : An autosomal recessive inherited disorder characterized by unconjugated hyperbilirubinemia, resulting in harmless intermittent jaundice.;

Details

Origin ID

C84729;

UMLS CUI

C0017551;

Automatic exact mappings (from CISMeF team)
- Gilbert disease [PASCAL descriptor]
- Gilbert syndrome [DO Concept]
- liver diseases [MedlinePlus Topic]
Currated CISMeF NLP mapping
- Gilbert Meulengracht Syndrome [Disease (Nov.)]
- Gilbert syndrome [ICD-10 Sub-category]
- Gilbert syndrome [ICD-11 Sub-sub category]
- Gilbert syndrome [OMIM Phenotype]
- Gilbert syndrome [ORDO Disease]
- Gilbert's syndrome [MedDRA Preferred Term]
- Gilbert's syndrome (disorder) [SNOMED CT concept]
- Gilberts syndrome [ICD-10 Sub-category (who)]
- gilbert disease [MeSH Descriptor]
- gilbert disease [MeSH concept]
- gilbert's syndrome [SNOMED Notion]
DO Cross reference
- Gilbert syndrome [DO Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Gilbert Meulengracht Syndrome [Disease (Nov.)]
- Gilbert syndrome [ORDO Disease]
- Gilbert syndrome [OMIM Phenotype]
- Gilbert syndrome [ICD-10 Sub-category]
- Gilbert syndrome [DO Concept]
- Gilbert syndrome [ICD-11 Sub-sub category]
- Gilbert's syndrome [MedDRA Preferred Term]
- Gilbert's syndrome (disorder) [SNOMED CT concept]
- Gilberts syndrome [ICD-10 Sub-category (who)]
- gilbert disease [MeSH concept]
- gilbert disease [MeSH Descriptor]
- gilbert's syndrome [SNOMED Notion]
concept_is_in_subset
- GDC Terminology [NCIt concept]
- GDC Value Terminology [NCIt concept]
disease_has_finding
- Rare Lesion [NCIt concept]
disease_mapped_to_gene
- UGT1A1 Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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