Chapter 4 - Endocrine, nutritional and metabolic diseases (E00-E89)»Metabolic disorders (E70-E88)»Crigler-Najjar syndrome (E80.5)
E80.5
Crigler-Najjar syndrome
Related indications (MeSH) (1)
Crigler-Najjar Syndrome6 drugs (1 approved, 5 experimental)
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.