SE-ATLAS

Mapping of Health Care Providers
for People with Rare Diseases


In the following you will find the diseases that are treated in this facility:
Acute fatty liver of pregnancy Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome Acute infantile liver failure-multisystemic involvement syndrome Acute liver failure Alagille syndrome Alpha-1-antitrypsin deficiency Autoimmune hepatitis Benign recurrent intrahepatic cholestasis Benign recurrent intrahepatic cholestasis type 1 Benign recurrent intrahepatic cholestasis type 2 Biliary atresia with splenic malformation syndrome Budd-Chiari syndrome CADDS Caroli disease Cholestasis-lymphedema syndrome Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome Cirrhotic cardiomyopathy 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 Fever-associated acute infantile liver failure syndrome Follicular cholangitis and pancreatitis Fulminant viral hepatitis 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 Growth retardation-mild developmental delay-chronic hepatitis syndrome Hepatic fibrosis-renal cysts-intellectual disability syndrome Hepatic veno-occlusive disease Hepatic veno-occlusive disease-immunodeficiency syndrome Hepatitis delta Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 Hepatoportal sclerosis Hereditary North American Indian childhood cirrhosis Hereditary fructose intolerance Hereditary hemorrhagic telangiectasia Hyperbiliverdinemia Idiopathic copper-associated cirrhosis Inflammatory pseudotumor of the liver Intrahepatic cholestasis of pregnancy Isolated agenesis of gallbladder Isolated biliary atresia Isolated polycystic liver disease Low phospholipid-associated cholelithiasis MYO5B-related progressive familial intrahepatic cholestasis Mitochondrial DNA depletion syndrome, hepatocerebrorenal form Neonatal hemochromatosis Neonatal ichthyosis-sclerosing cholangitis syndrome Nodular regenerative hyperplasia of the liver Peroxisome biogenesis disorder Primary biliary cholangitis Primitive portal vein thrombosis Progressive familial intrahepatic cholestasis Progressive familial intrahepatic cholestasis type 1 Progressive familial intrahepatic cholestasis type 2 Progressive familial intrahepatic cholestasis type 3 Progressive familial intrahepatic cholestasis type 4 Progressive familial intrahepatic cholestasis type 5 Pulmonary fibrosis-hepatic hyperplasia-bone marrow hypoplasia syndrome Rare biliary tract disease Rare hepatic and biliary tract tumor Rare hepatic disease Rare hereditary hemochromatosis Rare metabolic liver disease Rare parenchymal liver disease Rare tumor of gallbladder and extrahepatic biliary tract Rare tumor of liver and intrahepatic biliary tract Rare vascular liver disease Reynolds syndrome Rotor syndrome Sclerosing cholangitis Severe early-onset pulmonary alveolar proteinosis due to MARS deficiency Steroid dehydrogenase deficiency-dental anomalies syndrome Syndromic diarrhea Transient familial neonatal hyperbilirubinemia Transient infantile hypertriglyceridemia and hepatosteatosis Tyrosinemia type 1 Wilson disease