Informaţii despre

Nume Infantile Liver Failure Syndrome 1
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 Acute Liver Failure; Infantile Liver Failure Syndrome 2; Liver Failure, Infantile, Transient

Vezi şi

Boli A-Z Acid Sphingomyelinase Deficiency Acute Liver Failure Acute Pancreatitis Acute Respiratory Distress Syndrome Adenocarcinoma Adult T-Cell Leukemia Aging Alagille Syndrome 1 Al Amyloidosis Alcoholic Hepatitis Alcoholic Liver Cirrhosis Alpha-1-Antitrypsin Deficiency 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 Alveolar Echinococcosis Amyloidosis Anaplastic Large Cell Lymphoma Angiodysplasia Angiosarcoma Aniridia 1 Anorexia Nervosa 1 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 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 Bullous Pemphigoid Burkitt Lymphoma Cardiogenic Shock Cerebritis Cholangiocarcinoma Cholangitis Choledocholithiasis Cholestasis Chops Syndrome Chronic Active Epstein-Barr Virus Infection Chronic Graft Versus Host Disease Citrullinemia, Classic Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Hepatic Fibrosis Congestive Heart Failure Connective Tissue Disease Coq-Responsive Oxphos Deficiency Cortical Blindness Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome Cytophagic Histiocytic Panniculitis Dengue Hemorrhagic Fever Dengue Shock Syndrome Deoxyguanosine Kinase Deficiency Diabetes Insipidus Diabetes Mellitus Dihydrolipoamide Dehydrogenase Deficiency Drug Rash with Eosinophilia and Systemic Symptoms Dyskeratosis Congenita Echinococcosis Eclampsia Encephalopathy Endotheliitis Epidermolysis Bullosa Pruriginosa Epiphyseal Dysplasia, Multiple, with Early-Onset Diabetes Mellitus Facial Paralysis Factor X Deficiency Fanconi Anemia, Complementation Group E Fanconi-Bickel Syndrome Galactosemia Gastroenteritis Glucose Intolerance Glycerol Kinase Deficiency Graft-Versus-Host Disease Hemangioma Hematopoietic Stem Cell Transplantation Hemochromatosis, Neonatal Hemolytic Anemia Hemophagocytic Lymphohistiocytosis Hemorrhagic Disease Hemorrhagic Fever Heparin Cofactor Ii Deficiency Hepatic Adenomas, Familial Hepatic Coma Hepatic Encephalopathy Hepatic Infarction Hepatic Tuberculosis Hepatitis Hepatitis a Hepatitis B Hepatitis C Hepatitis C Virus Hepatitis E Hepatoblastoma Hepatocellular Carcinoma Hepatoportal Sclerosis Hepatorenal Syndrome Hereditary Hemorrhagic Telangiectasia Herpes Simplex Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance Homocystinuria Human Coronavirus Sensitivity Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hyperthyroidism Hypoglycemia Hypophosphatemia Hypoxia Infantile Liver Failure Syndrome 2 Inherited Metabolic Disorder Intracranial Hypertension Intrahepatic Cholangiocarcinoma Intrahepatic Cholestasis Intussusception Invasive Aspergillosis Ischemia Juvenile Xanthogranuloma Klatskin's Tumor Lactic Acidosis Laron Syndrome Leigh Syndrome Leishmaniasis Leptospirosis Leukemia Light Chain Deposition Disease Liver Cirrhosis Liver Disease Liver Failure, Infantile, Transient Long-Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency Lymphoblastic Leukemia Lymphoma Macrophage Activation Syndrome Malignant Spiradenoma Migraine with or Without Aura 1 Miliary Tuberculosis Mitochondrial Complex Iii Deficiency Mixed Connective Tissue Disease Mood Disorder Multiple Mitochondrial Dysfunctions Syndrome 5 Multiple Sclerosis Mycobacterium Kansasii Myocardial Infarction Myopathy Myotonia Congenita, Autosomal Dominant Neonatal Herpes Neuroleptic Malignant Syndrome Neuropathy Niemann-Pick Disease Niemann-Pick Disease, Type B Non-a-E Hepatitis Obstructive Jaundice Ocular Motor Apraxia Ornithine Transcarbamylase Deficiency, Hyperammonemia Due to Pancreatitis Panniculitis Patent Ductus Venosus Pepck 1 Deficiency Peripheral T-Cell Lymphoma Peritonitis Pick Disease of Brain Polyarteritis Nodosa Polycystic Liver Disease Polyneuropathy Porphyria Porphyria Cutanea Tarda Portal Hypertension Post-Traumatic Stress Disorder Pre-Eclampsia Primary Biliary Cirrhosis Prolymphocytic Leukemia Protein S Deficiency Pulmonary Alveolar Proteinosis, Acquired Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 Pure Red-Cell Aplasia Purpura Rapidly Involuting Congenital Hemangioma Retinitis Reye Syndrome Rubella Scalp-Ear-Nipple Syndrome Scrub Typhus Short Bowel Syndrome Short Stature, Optic Nerve Atrophy, and Pelger-Huet Anomaly Short Stature with Optic Atrophy and Pelger-Huët Anomaly Syndrome Shwachman-Diamond Syndrome Siderosis 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 Thrombosis Thrombotic Thrombocytopenic Purpura Thyroiditis Transaldolase Deficiency Tricuspid Valve Insufficiency Tuberculous Uveitis Tyrosinemia Urea Cycle Disorder Uveitis Van Der Woude Syndrome 1 Viral Hepatitis Visceral Leishmaniasis Wernicke Encephalopathy Wilson Disease X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome