SE-ATLAS

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