SE-ATLAS

Primary biliary cholangitis Familial benign copper deficiency Alagille syndrome Rare biliary tract disease Primary qualitative or quantitative defects of alpha-dystroglycan Isolated polycystic liver disease Occipital horn syndrome Hepatic veno-occlusive disease Qualitative or quantitative defects of protein involved in O-glycosylation of alpha-dystroglycan Allergic bronchopulmonary aspergillosis Follicular cholangitis and pancreatitis Wilson disease Nodular regenerative hyperplasia of the liver Disorder of copper metabolism Autoimmune hepatitis Hereditary hemorrhagic telangiectasia Hepatoportal sclerosis Reynolds syndrome Hypersensitivity pneumonitis Transient infantile hypertriglyceridemia and hepatosteatosis Low phospholipid-associated cholelithiasis Arthrogryposis-renal dysfunction-cholestasis syndrome Isolated biliary atresia Caroli disease Rare allergic respiratory disease Primary intrahepatic lithiasis Congenital respiratory-biliary fistula Budd-Chiari syndrome Sclerosing cholangitis Choledochal cyst MEDNIK syndrome Idiopathic ductopenia Biliary atresia with splenic malformation syndrome Caroli syndrome Hepatic veno-occlusive disease-immunodeficiency syndrome Menkes disease Congenital portosystemic shunt Isolated agenesis of gallbladder Congenital anomaly of hepatic vein Primitive portal vein thrombosis Qualitative or quantitative defects of alpha-dystroglycan Idiopathic chronic eosinophilic pneumonia Idiopathic peliosis hepatis Rare vascular liver disease Alpha-1-antitrypsin deficiency Cystic fibrosis