SE-ATLAS

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