Hereditary Hyperbilirubinemia

Preferred Label : Hereditary Hyperbilirubinemia;

NCIt definition : An inherited disorder affecting the metabolism of bilirubin. It results in increased levels of bilirubin in the blood. Representative examples of this condition include Gilbert syndrome and Crigler-Najjar syndrome.;

Details

Origin ID

C84761;

UMLS CUI

C0020435;

Automatic exact mappings (from CISMeF team)
- bilirubin metabolic disorder [DO Concept]
Currated CISMeF NLP mapping
- hyperbilirubinemia, hereditary [MeSH Descriptor]
- hyperbilirubinemia, hereditary [MeSH concept]
DO Cross reference
- bilirubin metabolic disorder [DO Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- hyperbilirubinemia, hereditary [MeSH Descriptor]
- hyperbilirubinemia, hereditary [MeSH concept]
disease_has_finding
- Rare Lesion [NCIt concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients