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 |
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There are currently no mappings for this class. |