Chronic cholestatic liver disease
Extrahepatic biliary atresia
Arteriohepatic dysplasia (Alagille syndrome)
Neonatal hepatitis
Primary sclerosing cholangitis
Caroli's disease
Lanerhan's cell histiocytosis (histiocytosis X)
Inborn errors of metabolism
Alpha-1-antitrypsin deficiency
Tyrosinemia
Wilson's disease
Miscellaneous metabolic or genetic liver disease
Glycogen storage disease, type 1
Glycogen storage disease, type 4
Type 1 hyperoxaluria
Crigler-Najjar syndrome
Ornithine transcarbamylase deficiency
Familial hypercholesterolemia
Protein C deficiency
Niemann-Pick and other lipidosis
Gaucher's disease
Erythropoietic protoporphyria
Hemophilia A
Hemophilia B
Urea cycle enzyme deficiency
Hepatocellular injury
Viral hepatitis
Autoimmune hepatitis
Drug-induced liver failure
Amanita mushroom poisoning
Mass occupying lesions
Hepatoblastoma
Hepatocellular carcinoma (hepatoma)
Polycystic liver disease
Hepatic adenomatosis
Hemangioendothelioma
Miscellaneous
Cystic fibrosis
Congenital hepatic fibrosis
