Diagnosis or suspected diagnosis of rare liver diseases

This includes the following diseases and groups of diseases:

• Autoimmune liver diseases (autoimmune hepatitis, primary biliary cholangitis, primary sclerosing cholangitis)
• Genetic diseases (e.g. Alfa1 antitrpsin deficiency, Alagille syndrome, progressive familial intrahepatic cholestasis, benign recurrent intrahepatic cholestasis, Wilson’s disease, hereditary fructose intolerance, cystic fibrosis)
• Biliary atresia, Caroli syndrome
• Structural liver diseases (such as biliary malformations)
• Rare liver tumors (polycystic hepatoblastomas)
• vascular liver diseases such asBudd-Chiari syndrome, porto-sinusoidal vascular liver disease, nodular regenerative hyperplasia, portal vein malformations.