SE-ATLAS

Benign recurrent intrahepatic cholestasis Congenital bile acid synthesis defect Wilson disease Cerebrotendinous xanthomatosis Autoimmune hepatitis Secondary short bowel syndrome Bile acid synthesis defect with cholestasis and malabsorption Progressive familial intrahepatic cholestasis type 5 Progressive familial intrahepatic cholestasis type 4 Isolated biliary atresia Hirschsprung disease MYO5B-related progressive familial intrahepatic cholestasis Benign recurrent intrahepatic cholestasis type 2 Benign recurrent intrahepatic cholestasis type 1 Congenital bile acid synthesis defect type 4 Choledochal cyst Hereditary North American Indian childhood cirrhosis Familial intrahepatic cholestasis Bile acid CoA ligase deficiency and defective amidation Primitive portal vein thrombosis Progressive familial intrahepatic cholestasis Down syndrome Congenital bile acid synthesis defect type 3 Congenital bile acid synthesis defect type 1 Alpha-1-antitrypsin deficiency Progressive familial intrahepatic cholestasis type 2 Congenital bile acid synthesis defect type 2 Progressive familial intrahepatic cholestasis type 1 Progressive familial intrahepatic cholestasis type 3 Familial hypercholanemia