Informaţii despre

Nume Acute Liver Failure
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli metabolice; Boli rare
Clasificari ICD10 Acute and subacute hepatic failure
Clasificare anatomică Malacards Boli gastrointestinale; Boli hepatice
Boli din aceeaşi familie Infantile Liver Failure Syndrome 1; Infantile Liver Failure Syndrome 2; Liver Failure, Infantile, Transient

Vezi şi

Boli A-Z Abdominal Tuberculosis Acute Kidney Tubular Necrosis Acute Pancreatitis Acute Respiratory Distress Syndrome Adenocarcinoma Adie Pupil Adult T-Cell Leukemia Aging Alagille Syndrome 1 Al Amyloidosis Alcoholic Hepatitis Alcoholic Liver Cirrhosis Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alpha-Fetoprotein Deficiency Alport Syndrome, X-Linked Al-Raqad Syndrome Alstrom Syndrome Amyloidosis Analbuminemia Anaplastic Large Cell Lymphoma Aniridia 1 Anorexia Nervosa 1 Antipyrine Metabolism Antithrombin Iii Deficiency Aplastic Anemia Argininemia Arthritis Arthrochalasia Ehlers-Danlos Syndrome Aspergillosis Ataxia and Polyneuropathy, Adult-Onset Ataxia-Telangiectasia Atrial Fibrillation Autoimmune Hepatitis Autoimmune Lymphoproliferative Syndrome, Type V Autoimmune Polyendocrine Syndrome, Type Ii Babesiosis Biliary Atresia Bilirubin Metabolic Disorder Blastomycosis Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Bornholm Eye Disease Brain Edema Brain Injury Branchiootic Syndrome 1 Breast Cancer Budd-Chiari Syndrome Burkitt Lymphoma Burns Central Retinal Vein Occlusion Cerebral Sinovenous Thrombosis Cerebritis Cholangiocarcinoma Cholangitis Cholecystitis Choledocholithiasis Cholestasis Chops Syndrome Compartment Syndrome Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Hepatic Fibrosis Congestive Heart Failure Connective Tissue Disease Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome Cryptogenic Cirrhosis Dengue Hemorrhagic Fever Dihydrolipoamide Dehydrogenase Deficiency Drug Rash with Eosinophilia and Systemic Symptoms Dysfibrinogenemia Encephalopathy Endotheliitis Epidermolysis Bullosa Pruriginosa Epiphyseal Dysplasia, Multiple, with Early-Onset Diabetes Mellitus Esophageal Varix Factor V Deficiency Factor Viii Deficiency Factor X Deficiency Fanconi Anemia, Complementation Group E Fascioliasis Fibromatosis, Gingival, 1 Fournier Gangrene Gastroenteritis Glycerol Kinase Deficiency Hellp Syndrome Hemochromatosis, Neonatal Hemoglobin E Disease Hemophagocytic Lymphohistiocytosis Hemorrhagic Disease Hemorrhagic Fever Hepatic Adenomas, Familial Hepatic Coma Hepatic Encephalopathy Hepatic Tuberculosis Hepatitis Hepatitis a Hepatitis B Hepatitis C Hepatitis C Virus Hepatitis D Hepatitis E Hepatocellular Carcinoma Hepatoportal Sclerosis Hepatorenal Syndrome Herpes Simplex Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance Homocysteinemia Homocystinuria Human Coronavirus Sensitivity Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hypersplenism Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypophosphatemia Hypoxia Infantile Liver Failure Syndrome 1 Infantile Liver Failure Syndrome 2 Inherited Metabolic Disorder Intracranial Hypertension Intrahepatic Cholestasis Intussusception Ischemia Ischemic Colitis Klatskin's Tumor Kwashiorkor Lactic Acidosis Leishmaniasis Leptospirosis Leukemia Livedoid Vasculopathy Liver Cirrhosis Liver Disease Liver Failure, Infantile, Transient Lymphoblastic Leukemia Lymphoma Lymphoma, Hodgkin, Classic Macrophage Activation Syndrome Malignant Spiradenoma Meckel Syndrome, Type 1 Migraine with or Without Aura 1 Miliary Tuberculosis Mixed Connective Tissue Disease Mood Disorder Multiple Mitochondrial Dysfunctions Syndrome 5 Multiple Sclerosis Mycobacterium Kansasii Myocardial Infarction Myopathy Myotonia Congenita, Autosomal Dominant Neonatal Herpes Non-a-E Hepatitis Nonalcoholic Steatohepatitis Nonarteritic Anterior Ischemic Optic Neuropathy Obstructive Jaundice Ocular Motor Apraxia Ornithine Transcarbamylase Deficiency, Hyperammonemia Due to Pancreatitis Paracetamol Poisoning Paraquat Poisoning Patent Ductus Venosus Pepck 1 Deficiency Peripheral T-Cell Lymphoma Polyarteritis Nodosa Porencephaly Porphyria Porphyria Cutanea Tarda Portal Hypertension Portal Vein Thrombosis Post-Thrombotic Syndrome Post-Traumatic Stress Disorder Primary Biliary Cirrhosis Prolymphocytic Leukemia Protein C Deficiency Protein S Deficiency Prothrombin Deficiency, Congenital Pulmonary Alveolar Proteinosis, Acquired Pulmonary Embolism Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 Pure Red-Cell Aplasia Pyridoxine Deficiency Retinal Artery Occlusion Rubella Sagittal Sinus Thrombosis Scalp-Ear-Nipple Syndrome Scott Syndrome Scrub Typhus Short Stature, Optic Nerve Atrophy, and Pelger-Huet Anomaly Short Stature with Optic Atrophy and Pelger-Huët Anomaly Syndrome Sneddon Syndrome Spinal Cord Infarction Splenic Disease Sudden Sensorineural Hearing Loss Surfactant Metabolism Dysfunction, Pulmonary, 2 Surfactant Metabolism Dysfunction, Pulmonary, 3 Surfactant Metabolism Dysfunction, Pulmonary, 4 Systemic Onset Juvenile Idiopathic Arthritis T-Cell Leukemia T-Cell Prolymphocytic Leukemia Thrombophlebitis Thrombosis Tricuspid Valve Insufficiency Tyrosinemia Urea Cycle Disorder Van Der Woude Syndrome 1 Vein Disease Viral Hepatitis Visceral Leishmaniasis Von Willebrand's Disease Wernicke Encephalopathy Wilson Disease