Acute hepatocellular | Viral hepatitis | Alcohol-associated fatty liver and/or hepatitis | Non-alcoholic steatohepatitis | Drugs | Chronic hepatocellular | Primary sclerosing cholangitis | Primary biliary cholangitis | Drugs | Hepatitis (viral, alcohol, autoimmune) | Cirrhosis of any cause | Multifactorial | Total parental nutrition | Systemic infection | Postoperative | Sickle cell disease/crisis | Organ transplantation (rejection; graft-versus-host disease; venoocclusive disease) | | Miscellaneous | Hypotension/hypoxemia/HF | Budd-Chiari syndrome | Parasitic infection (Clonorchis sinensis; Fasciola hepatica) | Idiopathic adulthood ductopenia | Other cholangiopathies (IgG4 cholangiopathy; ischemic cholangiopathy; COVID-19) | Inherited/endocrine | Benign recurrent intrahepatic cholestasis (BRIC) | Progressive familial intrahepatic cholestasis (PFIC) | Low phospholipid-associated cholestasis (LPAC) | Thyrotoxicosis | Alagille syndrome | Disorders of carbohydrate, lipid, or bile acid metabolism | Caroli's disease | Pregnancy | Protoporphyria | Infiltrative/granulomatous | Amyloidosis | Lymphoma* | Sarcoidosis | Tuberculosis | |