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Nume Atrial Fibrillation
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificari ICD10 Atrial fibrillation and flutter
Clasificare anatomică Malacards Boli cardiovasculare
Boli din aceeaşi familie Atrial Fibrillation, Familial, 1; Atrial Fibrillation, Familial, 10; Atrial Fibrillation, Familial, 11; Atrial Fibrillation, Familial, 12; Atrial Fibrillation, Familial, 13; Atrial Fibrillation, Familial, 14; Atrial Fibrillation, Familial, 15; Atrial Fibrillation, Familial, 18; Atrial Fibrillation, Familial, 2; Atrial Fibrillation, Familial, 3; Atrial Fibrillation, Familial, 4; Atrial Fibrillation, Familial, 5; Atrial Fibrillation, Familial, 6; Atrial Fibrillation, Familial, 7; Atrial Fibrillation, Familial, 8; Atrial Fibrillation, Familial, 9; Familial Atrial Fibrillation

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Boli A-Z Abcd Syndrome Ablepharon-Macrostomia Syndrome Acrocallosal Syndrome Acth Deficiency, Isolated Acute Liver Failure Acute Myocardial Infarction Acute Myocarditis Acute Pyelonephritis Adie Pupil Afibrinogenemia, Congenital Aganglionosis, Total Intestinal Aging Al Amyloidosis Alcoholic Cardiomyopathy Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alport Syndrome, X-Linked Al-Raqad Syndrome Alzheimer Disease 3 Amyloidosis Anauxetic Dysplasia 1 Andersen Cardiodysrhythmic Periodic Paralysis Androgen Insensitivity Syndrome, Mild Aneurysm Angina Pectoris Angiodysplasia Aniridia 1 Anomalous Left Coronary Artery from the Pulmonary Artery Anorexia Nervosa 1 Anterolateral Myocardial Infarction Antiphospholipid Syndrome Antithrombin Iii Deficiency Anuria Aortic Atherosclerosis Aortic Coarctation Aortic Valve Disease 2 Apert Syndrome Aphasia Arteries, Anomalies of Arteriosclerosis Arteritic Anterior Ischemic Optic Neuropathy Arthrochalasia Ehlers-Danlos Syndrome Asplenia, Isolated Congenital Ataxia Neuropathy Spectrum Atrial Fibrillation and Stroke Atrial Fibrillation, Familial, 1 Atrial Fibrillation, Familial, 2 Atrial Fibrillation, Familial, 5 Atrial Septal Aneurysm Atrial Standstill Atrial Standstill 1 Atrioventricular Block Atrioventricular Septal Defect Autoimmune Myocarditis Autonomic Dysfunction Autonomic Neuropathy Benign Idiopathic Neonatal Seizures Bestrophinopathy, Autosomal Recessive Beta-Thalassemia Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Blood Platelet Disease Body Mass Index Quantitative Trait Locus 10 Body Mass Index Quantitative Trait Locus 11 Body Mass Index Quantitative Trait Locus 12 Body Mass Index Quantitative Trait Locus 14 Body Mass Index Quantitative Trait Locus 18 Body Mass Index Quantitative Trait Locus 4 Body Mass Index Quantitative Trait Locus 7 Body Mass Index Quantitative Trait Locus 8 Body Mass Index Quantitative Trait Locus 9 Brain Injury Brain Ischemia Breast Cancer Bronchogenic Cyst Brugada Syndrome Brugada Syndrome 5 Calciphylaxis Cannabis Abuse Cannabis Dependence Cardiac Arrest Cardiac Arrhythmia Cardiac Conduction Defect Cardiac Conduction Disease with or Without Dilated Cardiomyopathy Cardiac Sarcoidosis Cardiac Tamponade Carotid Artery Disease Carotid Artery Thrombosis Carotid Stenosis Catecholaminergic Polymorphic Ventricular Tachycardia Central Retinal Artery Occlusion Central Sleep Apnea Cerebral Atherosclerosis Cerebritis Cerebrovascular Disease Chlamydia Chronic Pain Clopidogrel Resistance Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congestive Heart Failure Constrictive Pericarditis Coronary Aneurysm Coronary Artery Anomaly Coronary Artery Dissection, Spontaneous Coronary Stenosis Cor Triatriatum Cor Triatriatum Sinister Coumarin Resistance Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome Crouzon Syndrome with Acanthosis Nigricans Cytochrome P450 2d6 Variant Dementia Dengue Hemorrhagic Fever Dextrocardia Dextrocardia with Situs Inversus Diabetes Mellitus Diabetic Autonomic Neuropathy Diabetic Neuropathy Diastolic Heart Failure Dilated Cardiomyopathy Disseminated Intravascular Coagulation Dowling-Degos Disease 1 Dyspepsia Ehlers-Danlos Syndrome Emery-Dreifuss Muscular Dystrophy Endocarditis Endomyocardial Fibrosis Endotheliitis End Stage Renal Failure Enhanced S-Cone Syndrome Epilepsy Esophageal Atresia Esophageal Cancer Esophageal Duplication Cyst Essential Thrombocythemia Esterase C Fabry Disease Factor Vii Deficiency Factor X Deficiency Fainting Familial Atrial Fibrillation Familial Long Qt Syndrome Familial Progressive Cardiac Conduction Defect Familial Short Qt Syndrome Familial Sick Sinus Syndrome Fanconi Anemia, Complementation Group E Fanconi Renotubular Syndrome 1 Fatty Liver Disease Female Breast Cancer Fibular Hypoplasia and Complex Brachydactyly First-Degree Atrioventricular Block Gastric Lymphoma Gastroesophageal Reflux Gastroparesis Genitopatellar Syndrome Glanzmann Thrombasthenia Glomerulonephritis Gout Graves' Disease Heart Conduction Disease Heart Disease Hemochromatosis, Neonatal Hemopericardium Hemophagocytic Lymphohistiocytosis, Familial, 1 Hemophilia Hemorrhagic Disease Hemorrhagic Fever Heparin-Induced Thrombocytopenia Hepatic Adenomas, Familial Hepatitis Hepatitis C Hepatocellular Carcinoma Hepatoportal Sclerosis Hepatorenal Syndrome Hereditary Hemorrhagic Telangiectasia Hinman Syndrome Holt-Oram Syndrome Horseshoe Kidney Hyaline Fibromatosis Syndrome Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hyperglycemia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertensive Heart Disease Hyperthyroidism Hypertrophic Cardiomyopathy Hyperuricemia Hypokalemia Hypoplastic Left Heart Syndrome Hypoxia Ichthyosis Prematurity Syndrome Idiopathic Edema Inferior Myocardial Infarction Inflammatory Bowel Disease Influenza Insulin-Like Growth Factor I Intermittent Claudication Intracranial Aneurysm Intracranial Embolism Intrinsic Cardiomyopathy Irritable Bowel Syndrome Ischemia Ischemic Optic Neuropathy Isolated Optic Neuritis Jackhammer Esophagus Jervell and Lange-Nielsen Syndrome 1 Kindler Syndrome Kniest Dysplasia Left Ventricular Noncompaction Leukoencephalopathy, Hereditary Diffuse, with Spheroids Light Chain Deposition Disease Liver Cirrhosis Liver Disease Long Qt Syndrome Long Qt Syndrome 1 Long Qt Syndrome 12 Long Qt Syndrome 13 Long Qt Syndrome 2 Long Qt Syndrome 3 Long Qt Syndrome 5 Long Qt Syndrome 6 Long Qt Syndrome 9 Lung Cancer Lung Disease Lupus Erythematosus Lymphoma Macroglobulinemia Malignant Hypertension Malignant Pleural Mesothelioma Malignant Spiradenoma Mantle Cell Lymphoma Meckel Syndrome, Type 1 Mediastinitis Membranoproliferative Glomerulonephritis Meningococcal Infection Microvascular Complications of Diabetes 3 Mild Hemophilia a Mitochondrial Dna Depletion Syndrome 4a Mitral Valve Disease Mitral Valve Insufficiency Mitral Valve Stenosis Morbid Obesity Multifocal Atrial Tachycardia Muscular Dystrophy Myocardial Infarction Myocarditis Myopathy Myotonic Dystrophy Nephrosclerosis Neuronitis Neuropathy Neutrophil Actin Dysfunction Nonarteritic Anterior Ischemic Optic Neuropathy Orbital Tenonitis Osteoporotic Fracture Pancytopenia Panic Disorder Papillomatosis, Confluent and Reticulated Patent Foramen Ovale Pediatric Hypertension Pericardial Effusion Pericarditis Peripheral Artery Disease Peripheral Vascular Disease Peritonitis Pfeiffer Syndrome Pituitary Adenoma 1, Multiple Types Platelet Aggregation, Spontaneous Pleomorphic Xanthoastrocytoma Pneumonia Pneumothorax Polycythemia Polycythemia Vera Polymorphic Reticulosis Porphyria Porphyria Variegata Posterior Urethral Valves Prieto X-Linked Mental Retardation Syndrome Progressive Familial Heart Block Progressive Familial Heart Block, Type Ia Progressive Familial Heart Block, Type Ib Prostatitis Psoriasis Psoriasis 13 Psoriasis 2 Psoriasis 7 Pulmonary Artery Agenesis Pulmonary Edema Pulmonary Embolism Pulmonary Hypertension Pulmonary Vein Stenosis Pyelonephritis Qualitative Platelet Defect Ramer Ladda Syndrome Renal Artery Disease Renal Glucosuria Renal Hypertension Renal Tubular Dysgenesis Renovascular Hypertension Resting Heart Rate, Variation in Restrictive Cardiomyopathy Retinal Artery Occlusion Retinal Ischemia Retinal Vascular Occlusion Retinitis Rheumatic Disease Rheumatic Fever Rheumatic Fever-Related Antigen Rheumatic Heart Disease Richards-Rundle Syndrome Right Bundle Branch Block Robinow Syndrome, Autosomal Recessive Rocky Mountain Spotted Fever Sarcoidosis 2 Sarcosinemia Satb2-Associated Syndrome Short Qt Syndrome Short Qt Syndrome 3 Sick Sinus Syndrome Sinoatrial Node Disease Situs Inversus Sleep Apnea Sleep Disorder Splenic Infarction Spondyloocular Syndrome Spotted Fever Stroke, Ischemic Sudden Arrhythmia Death Syndrome Syncope Syndrome of Inappropriate Antidiuretic Hormone Systemic Lupus Erythematosus Systemic Mastocytosis Systolic Heart Failure Testicular Regression Syndrome Tetralogy of Fallot Thalassemia Third-Degree Atrioventricular Block Thoracoabdominal Syndrome Thrombocytopenia Thrombophilia Due to Activated Protein C Resistance Thrombophilia Due to Thrombin Defect Thrombosis Thyroiditis Thyrotoxic Periodic Paralysis Timothy Syndrome Tracheoesophageal Fistula Transposition of the Great Arteries Uncombable Hair Syndrome 1 Ureterolithiasis Vascular Disease Venous Insufficiency Ventricular Fibrillation, Paroxysmal Familial, 1 Ventricular Septal Defect Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy Vitamin E, Familial Isolated Deficiency of Vitamin K Antagonists Toxicity or Dose Selection Von Willebrand's Disease Wolff-Parkinson-White Syndrome