Syndromes affecting the hepatobiliary system

severe pre-eclampsia characterized by hemolysis, elevated liver enzyme and low platelet count

Human disease

Human disease

bilirubin metabolic disorder that involves a build up of bilirubin as bilirubin is not being broken down as a result of a lack or deficiency of the enzyme uridine diphosphate glycosyltransferase (UGT)

congenital disorder of digestive system

rare, autosomal recessive, benign disorder that causes an isolated increase of conjugated bilirubin in the serum

syndrome that is characterized by congenital hypoplasia of lymph vessels, which causes lymphedema of the legs and recurrent cholestasis in infancy, and slow progress to hepatic cirrhosis and giant cell hepatitis with fibrosis of the portal tracts

bile duct disease that is characterized by abnormal dilatation of the intrahepatic bile ducts

complication of cholelithiasis

bypass of the liver by the body's circulatory system

medical condition

human disease