Zentrum für angeborene und cholestatische Lebererkrankungen am Universitätsklinikum Düsseldorf Assigned 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