Dubin-Johnson Syndrome

Preferred Label : Dubin-Johnson Syndrome;

NCIt synonyms : Chronic Idiopathic Jaundice;

NCIt definition : An inherited autosomal recessive disorder characterized by the presence of mild jaundice due to abnormalities in the bilirubin transportation from the liver parenchyma to the biliary system.;

Details

Origin ID

C34741;

UMLS CUI

C0022350;

Automatic exact mappings (from CISMeF team)
- Dubin-Johnson syndrome [DO Concept]
- Other disorders of bilirubin metabolism [ICD-10 Sub-category]
- Other disorders of bilirubin metabolism [ICD-10 Sub-category (who)]
Currated CISMeF NLP mapping
- Dubin-Johnson disease [PASCAL descriptor]
- Dubin-Johnson syndrome [ICD-11 Sub-sub category]
- Dubin-Johnson syndrome [MedDRA Preferred Term]
- Dubin-Johnson syndrome [TUV Concept]
- Dubin-Johnson syndrome [ORDO Disease]
- Dubin-Johnson syndrome (disorder) [SNOMED CT concept]
- Dubin-johnson syndrome [OMIM Phenotype]
- chronic idiopathic jaundice [Disease (Nov.)]
- dubin-johnson syndrome [SNOMED Notion]
- jaundice, chronic idiopathic [MeSH Descriptor]
- jaundice, chronic idiopathic [MeSH concept]
DO Cross reference
- Dubin-Johnson syndrome [DO Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Dubin-Johnson syndrome [ORDO Disease]
- Dubin-Johnson syndrome [TUV Concept]
- Dubin-Johnson syndrome [DO Concept]
- Dubin-Johnson syndrome [MedDRA Preferred Term]
- Dubin-Johnson syndrome (disorder) [SNOMED CT concept]
- Dubin-johnson syndrome [OMIM Phenotype]
- chronic idiopathic jaundice [Disease (Nov.)]
- dubin-johnson syndrome [SNOMED Notion]
- jaundice, chronic idiopathic [MeSH concept]
- jaundice, chronic idiopathic [MeSH Descriptor]
disease_mapped_to_gene
- ABCC2 Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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