SE-ATLAS

Glycogen storage disease due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form Hereditary ATTR amyloidosis Alagille syndrome due to a NOTCH2 point mutation Primary sclerosing cholangitis Progressive familial intrahepatic cholestasis Primitive portal vein thrombosis Neonatal hemochromatosis Fanconi-Bickel syndrome CADDS Acute fatty liver of pregnancy Mitochondrial DNA depletion syndrome, hepatocerebrorenal form Glycogen storage disease due to glycogen branching enzyme deficiency, childhood neuromuscular form Primary biliary cholangitis Cholestasis-lymphedema syndrome Primary systemic amyloidosis Rare metabolic liver disease Glycogen storage disease due to glycogen branching enzyme deficiency, adult neuromuscular form Growth retardation-mild developmental delay-chronic hepatitis syndrome Rare parenchymal liver disease Rare vascular liver disease Acute infantile liver failure-multisystemic involvement syndrome Congenital bile acid synthesis defect type 1 Rare biliary tract disease Primary localized amyloidosis Steroid dehydrogenase deficiency-dental anomalies syndrome Congenital bile acid synthesis defect type 2 Hereditary fructose intolerance Isolated polycystic liver disease Congenital bile acid synthesis defect type 3 Progressive familial intrahepatic cholestasis type 3 AL amyloidosis Familial hypercholanemia Progressive familial intrahepatic cholestasis type 2 AA amyloidosis Progressive familial intrahepatic cholestasis type 1 Tyrosinemia type 1 Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 ATTRV30M amyloidosis ATTRV122I amyloidosis Amyloidosis Hereditary amyloidosis with primary renal involvement Hepatic veno-occlusive disease Hyperbiliverdinemia Wild type ATTR amyloidosis Rare hereditary hemochromatosis Benign recurrent intrahepatic cholestasis Galactosemia TFR2-related hemochromatosis Cirrhotic cardiomyopathy Peroxisome biogenesis disorder Nodular regenerative hyperplasia of the liver Adult polyglucosan body disease Infantile Refsum disease Cerebrotendinous xanthomatosis Pulmonary fibrosis-hepatic hyperplasia-bone marrow hypoplasia syndrome Autoimmune hepatitis Hepatoportal sclerosis Glycogen storage disease due to glycogen branching enzyme deficiency Bile acid synthesis defect with cholestasis and malabsorption Reynolds syndrome Dubin-Johnson syndrome Transient infantile hypertriglyceridemia and hepatosteatosis Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins Hemochromatosis type 4 Low phospholipid-associated cholelithiasis FTH1-related iron overload Intrahepatic cholestasis of pregnancy Neonatal ichthyosis-sclerosing cholangitis syndrome Rotor syndrome Generalized galactose epimerase deficiency Isolated biliary atresia Dietary iron overload disease Glycogen storage disease due to liver phosphorylase kinase deficiency Caroli disease Benign recurrent intrahepatic cholestasis type 1 Inflammatory pseudotumor of the liver HJV or HAMP-related hemochromatosis Benign recurrent intrahepatic cholestasis type 2 Congenital bile acid synthesis defect type 4 Crigler-Najjar syndrome type 2 Crigler-Najjar syndrome type 1 Galactokinase deficiency Transient familial neonatal hyperbilirubinemia Variant ABeta2M amyloidosis Congenital respiratory-biliary fistula Budd-Chiari syndrome Classic galactosemia AApoAII amyloidosis AApoAI amyloidosis Galactose epimerase deficiency Rare hepatic disease AFib amyloidosis Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency Hereditary North American Indian childhood cirrhosis Alagille syndrome due to 20p12 microdeletion Glycogen storage disease due to glycogen branching enzyme deficiency, fatal perinatal neuromuscular form Fulminant viral hepatitis Glycogen storage disease due to glycogen branching enzyme deficiency, congenital neuromuscular form Glycogen storage disease due to glucose-6-phosphatase deficiency type Ia Familial intrahepatic cholestasis Bile acid CoA ligase deficiency and defective amidation Hepatic veno-occlusive disease-immunodeficiency syndrome Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib Alagille syndrome due to a JAG1 point mutation Neonatal adrenoleukodystrophy Alagille syndrome Biliary atresia with splenic malformation syndrome Glycogen storage disease due to glucose-6-phosphatase deficiency Glycogen storage disease due to liver glycogen phosphorylase deficiency ALys amyloidosis Wilson disease Glycogen storage disease due to glycogen branching enzyme deficiency, progressive hepatic form Zellweger syndrome Glycogen storage disease due to glycogen branching enzyme deficiency, non progressive hepatic form Solitary necrotic nodule of the liver Wild type ABeta2M amyloidosis AGel amyloidosis Crigler-Najjar syndrome Idiopathic copper-associated cirrhosis Erythrocyte galactose epimerase deficiency