| 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 | |
