The causes are: Hepatitis B, hepatitis C, long term alcohol consumption, hemochromatosis (This inherited disorder causes your body to absorb and store too much iron. It can build up in your liver and cause cirrhosis), hepatitis A, autoimmune hepatitis, cirrhosis, primary sclerosing cholangitis (Primary sclerosing cholangitis (PSC) is a long-term progressive disease of the liver and gallbladder characterized by inflammation and scarring of the bile ducts which normally allow bile to drain from the gallbladder.), oxalosis, Wilson’s disease, alpha-1 antitrypsin deficiency (This genetic condition can lead to lung or liver disease.), liver cancer, liver adenoma, fatty liver disease, Alagille syndrome (A genetic disorder that results in fewer bile ducts than normal in the liver), Lysosomal acid lipase deficiency (LAL-D, With this genetic condition, the patient cannot produce an enzyme called lysosomal acid lipase (LAL), which helps body break down fats and cholesterol in cells. As a result, fats stay in the liver and cause damage).