| Preferred Name |
Hereditary Hyperbilirubinemia |
| ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C84761 |
| code |
C84761 |
| 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. |
| label |
Hereditary Hyperbilirubinemia |
| Preferred_Name |
Hereditary Hyperbilirubinemia |
| prefixIRI |
C84761 |
| prefLabel |
Hereditary Hyperbilirubinemia |
| Semantic_Type |
Disease or Syndrome |
| UMLS_CUI |
C0020435 |
| subClassOf |
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| There are currently no mappings for this class. | |||