SE-ATLAS

Cholangiocarcinoma Rare metabolic liver disease Rare parenchymal liver disease Porphyria Rare biliary tract disease Neuroendocrine neoplasm Alpha-1-antitrypsin deficiency Genetic polyendocrinopathy Disorder of porphyrin and heme metabolism Chylous ascites Rare genetic gastroenterological disease Rare hereditary hemochromatosis Genetic gastro-esophageal disease TFR2-related hemochromatosis Rare neoplastic disease Genetic pancreatic disease Inherited cancer-predisposing syndrome Mucopolysaccharidosis type 2, severe form Porphyria variegata Mucopolysaccharidosis type 2, attenuated form Hemochromatosis type 4 HJV or HAMP-related hemochromatosis Rare abdominal surgical disease Klatskin tumor Peutz-Jeghers syndrome Genetic digestive tract tumor Genetic neuroendocrine tumor Genetic biliary tract disease Genetic parenchymatous liver disease Congenital erythropoietic porphyria Primary sclerosing cholangitis Mucopolysaccharidosis type 2 VIPoma Hypoinsulinemic hypoglycemia and body hemihypertrophy Rare genetic diabetes mellitus Rare genetic hypothalamic or pituitary disease Primary biliary cholangitis Familial adenomatous polyposis Rare genetic thyroid disease Wilson disease Rare pancreatic disease Lysosomal disease Budd-Chiari syndrome Rare inborn errors of metabolism Genetic intestinal disease Hepatic veno-occlusive disease-immunodeficiency syndrome Hereditary chronic pancreatitis Hyperbiliverdinemia Rare vascular liver disease Rare genetic parathyroid disease and phosphocalcic metabolism disorder Rare genetic adrenal disease