- Concept UI
- M0005322
- Scope Note
- A familial form of congenital hyperbilirubinemia transmitted as an autosomal recessive trait. It is characterized by icterus and brain damage caused by a glucuronyl transferase deficiency in the liver and faulty bilirubin conjugation.
- Terms
-
Crigler-Najjar Syndrome
Preferred Term
Term UI
T009939
Date01/01/1999
LexicalTag
EPO
ThesaurusID
-
Crigler Najjar Syndrome
Term UI
T841215
Date04/18/2013
LexicalTag
NON
ThesaurusID
-
Crigler-Najar Syndrome
Term UI
T009940
Date01/03/1979
LexicalTag
EPO
ThesaurusID
UNK (19XX)
-
Familial Nonhemolytic Unconjugated Hyperbilirubinemia
Term UI
T841216
Date04/18/2013
LexicalTag
NON
ThesaurusID
-
Hereditary Unconjugated Hyperbilirubinemia
Term UI
T841217
Date04/18/2013
LexicalTag
NON
ThesaurusID