SE-ATLAS

Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins Alagille syndrome Alpha-1-antitrypsin deficiency Arthrogryposis-renal dysfunction-cholestasis syndrome Autoimmune hepatitis Biliary atresia with splenic malformation syndrome CADDS Caroli disease Caroli syndrome Choledochal cyst Cholesteryl ester storage disease Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome Citrullinemia type II Classic galactosemia Congenital disorder of glycosylation with hepatic involvement Congenital respiratory-biliary fistula Crigler-Najjar syndrome Cystic fibrosis Dietary iron overload disease Dubin-Johnson syndrome FTH1-related iron overload Familial hypercholanemia Familial intrahepatic cholestasis Fanconi-Bickel syndrome Ferro-cerebro-cutaneous syndrome Follicular cholangitis and pancreatitis GRACILE syndrome Galactose epimerase deficiency Glycogen storage disease due to glucose-6-phosphatase deficiency Glycogen storage disease due to glycogen branching enzyme deficiency Glycogen storage disease due to glycogen debranching enzyme deficiency Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency Glycogen storage disease due to liver glycogen phosphorylase deficiency Glycogen storage disease due to liver phosphorylase kinase deficiency Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 Hereditary fructose intolerance Idiopathic ductopenia Intrahepatic cholestasis of pregnancy Isolated agenesis of gallbladder Isolated biliary atresia Isolated polycystic liver disease Low phospholipid-associated cholelithiasis Mitochondrial DNA depletion syndrome, hepatocerebral form Mitochondrial DNA depletion syndrome, hepatocerebrorenal form Neonatal hemochromatosis Peroxisome biogenesis disorder Primary biliary cholangitis Primary intrahepatic lithiasis Rare biliary tract disease Rare hereditary hemochromatosis Rare metabolic liver disease Renal tubulopathy-encephalopathy-liver failure syndrome Reynolds syndrome Rotor syndrome Sclerosing cholangitis Steroid dehydrogenase deficiency-dental anomalies syndrome Tyrosinemia type 1 Wilson disease Wolman disease