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 Fistel, broncho-biliäre kongenitale Budd-Chiari-Syndrom Sklerosierende Cholangitis Choledochuszyste MEDNIK-Syndrom Duktopenie, idiopathische Biliäre Atresie-Milzfehlbildung-Syndrom Caroli-Syndrom Lebervenen-Verschlusskrankheit - Immunschwäche Menkes-Syndrom Portosystemischer Shunt, kongenitaler Gallenblasenagenesie, isolierte Lebervene, kongenitale Anomalie der Pfortaderthrombose, primäre Alpha-Dystroglykan, qualitative oder quantitative Defekte Pneumopathie, eosinophile idiopathische, chronische Peliosis hepatis, idiopathische Vaskuläre Leberkrankheit, seltene Alpha-1-Antitrypsin-Mangel Zystische Fibrose