"Arias syndrome" information
| LiverAtlas Disease ID | HuLDi00152 | ||
| Name | Arias syndrome | ||
| Description | Xref: | ||
| Definition | Crigler-Najjar syndrome (CNS) is a rare autosomal recessive disorder of bilirubin metabolism. Type 2 Crigler-Najjar syndrome (also called Arias syndrome), first described in 1962 by Arias, presents with a lower serum bilirubin level and responds to phenobarbital treatment. | Xref: URL | |
| Synonym | Crigler-Najjar syndrome, type2 | EXACT | Xref: Clinical Hepatology, 2004:Page 584 |
| Crigler-Najjar syndrome, type II | EXACT | Xref: UMLS2011AA:C0268311 | |
| Crigler-Najjar syndrome, type ?? | EXACT | Xref: UMLS2011AA:C0268311 | |
| Xref | Clinical Hepatology,2004.Page 584 | ||
| Clinical Hepatology,2004.Page 762 | |||
| Schiff's Diseases of the LIVER,10ed:Page 228 | |||
| Genetics Relation | Gene/Protein/Pathway | ||
| Gene:UGT1A1 | |||
| Protein: | |||
