Preferred Name |
Crigler-Najjar Syndrome |
ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C84656 |
code |
C84656 |
DEFINITION |
A rare autosomal recessive inherited syndrome characterized by abnormalities in the metabolism of bilirubin. It results in the development of jaundice. It may cause brain damage in infancy. |
label |
Crigler-Najjar Syndrome |
Preferred_Name |
Crigler-Najjar Syndrome |
prefixIRI |
C84656 |
prefLabel |
Crigler-Najjar Syndrome |
Semantic_Type |
Disease or Syndrome |
UMLS_CUI |
C0010324 |
subClassOf |