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