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Crigler-Najjar Syndrome

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.

Drugs by status

Organizations

Organization Involved with Phase 4 Indications (1)

Organization Involved with Phase 2 Indications (3)

Organization Involved with Other Experimental Indications (3)

ICD-10 crosswalk