SE-ATLAS

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