Informaţii despre

Nume Atrial Standstill 1
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificari ICD10 Cardiomyopathy due to drugs and other external agents; Cardiomyopathy in other diseases classified elsewhere; Cardiomyopathy, unspecified; Other specified heart block
Clasificare anatomică Malacards Boli cardiovasculare
Boli din aceeaşi familie Atrial Standstill 2

Vezi şi

Boli A-Z Acute Myocardial Infarction Acute Myocarditis Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency of Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of Adams-Oliver Syndrome Aging Alcoholic Cardiomyopathy Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alport Syndrome, X-Linked Al-Raqad Syndrome Amyloidosis Aneurysm Aneurysm of Sinus of Valsalva Angiosarcoma Aniridia 1 Anorexia Nervosa 1 Anterolateral Myocardial Infarction Antiphospholipid Syndrome Aortic Valve Disease 2 Aortitis Aromatic Alpha-Keto Acid Reductase Arrhythmogenic Right Ventricular Cardiomyopathy Arrhythmogenic Right Ventricular Dysplasia, Familial, 1 Arrhythmogenic Right Ventricular Dysplasia, Familial, 8 Arrhythmogenic Right Ventricular Dysplasia, Familial, 9 Arthritis Arthrochalasia Ehlers-Danlos Syndrome Aseptic Meningitis Aspergillosis Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Atrial Fibrillation Atrial Standstill Atrial Standstill 2 Atrioventricular Block Atrioventricular Septal Defect Autoimmune Hepatitis Autosomal Dominant Limb-Girdle Muscular Dystrophy Autosomal Dominant Polycystic Kidney Disease Barth Syndrome Benign Chronic Pemphigus Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Brugada Syndrome Brugada Syndrome 5 Cardiac Arrest Cardiac Conduction Defect Cardiac Sarcoidosis Cardiac Tamponade Cardiomyopathy, Dilated, 1a Cardiomyopathy, Dilated, 1e Cardiomyopathy, Dilated, 1h Cardiomyopathy, Dilated, 3b Cardiomyopathy, Dilated, with Woolly Hair and Keratoderma Cardiomyopathy, Familial Hypertrophic, 1 Cardiomyopathy, Familial Hypertrophic, 4 Cardioneuromyopathy with Hyaline Masses and Nemaline Rods Cardiovascular Syphilis Carnitine Deficiency, Systemic Primary Carnitine Palmitoyltransferase Ii Deficiency, Infantile Central Core Disease of Muscle Chronic Progressive External Ophthalmoplegia Conduct Disorder Congenital Fiber-Type Disproportion Congenitally Corrected Transposition of the Great Arteries Congestive Heart Failure Connective Tissue Disease Coronary Artery Anomaly Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome Cytoplasmic Body Myopathy Danon Disease Dengue Hemorrhagic Fever Dengue Shock Syndrome Dextrocardia Dextrocardia with Situs Inversus Diastolic Heart Failure Digitalis Poisoning Dilated Cardiomyopathy Distal Muscular Dystrophy Double Discordia Dowling-Degos Disease 1 Ebstein Anomaly Ectodermal Dysplasia/skin Fragility Syndrome Ehrlichiosis Emerinopathy Emery-Dreifuss Muscular Dystrophy 2, Autosomal Dominant Endocardial Fibroelastosis Endocarditis Epidermolysis Bullosa, Lethal Acantholytic Extracardiac Rhabdomyoma Fabry Disease Familial Isolated Arrhythmogenic Ventricular Dysplasia, Biventricular Form Familial Isolated Arrhythmogenic Ventricular Dysplasia, Left Dominant Form Familial Isolated Arrhythmogenic Ventricular Dysplasia, Right Dominant Form Familial Isolated Dilated Cardiomyopathy Familial Isolated Restrictive Cardiomyopathy Familial Progressive Cardiac Conduction Defect First-Degree Atrioventricular Block Gas Gangrene Giant Cell Myocarditis Gigantism Glycogen Storage Disease Ii Grover's Disease Heart Block, Congenital Heart Conduction Disease Heart Disease Hemorrhagic Fever Hemosiderosis Hepatitis Herpes Zoster Hydrops Fetalis Hydrops Fetalis, Nonimmune, and/or Atrial Septal Defect Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hyperekplexia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertrophic Cardiomyopathy Hypoaldosteronism Hypoplastic Left Heart Syndrome Hypoxia Infective Endocarditis Inferior Myocardial Infarction Intermediate Coronary Syndrome Intracranial Aneurysm Intrinsic Cardiomyopathy Kearns-Sayre Syndrome Klippel-Feil Syndrome Laryngitis Left Ventricular Noncompaction Leptospirosis Limb-Girdle Muscular Dystrophy Listeriosis Long-Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency Long Qt Syndrome Lupus Erythematosus Lyme Disease Lymphoma Macroglossia Malignant Spiradenoma Meckel Syndrome, Type 1 Mediastinitis Meningitis Meningococcemia Merkel Cell Carcinoma Microcolon Mitochondrial Dna Depletion Syndrome 4a Mitochondrial Myopathy Mixed Connective Tissue Disease Muscular Dystrophy Muscular Dystrophy, Congenital Merosin-Deficient, 1a Muscular Dystrophy, Duchenne Type Muscular Dystrophy, Limb-Girdle, Type 1b Muscular Dystrophy, Limb-Girdle, Type 1e Muscular Dystrophy, Limb-Girdle, Type 2a Myocardial Infarction Myocarditis Myofibrillar Myopathy Myoglobinuria, Recurrent Myopathy Myopathy, Myofibrillar, 1 Myopathy, Myofibrillar, 2 Myopathy, Myofibrillar, 4 Myopathy, Proximal, and Ophthalmoplegia Myopathy, Spheroid Body Myopathy, X-Linked, with Excessive Autophagy Myotonia Myotonia Atrophica Nail-Patella Syndrome Natural Killer Cell Leukemia Naxos Disease Neonatal Lupus Erythematosus Neonatal Systemic Lupus Erythematosus Neuritis Neuromuscular Disease Neuropathy Neuropathy, Hereditary Sensory and Autonomic, Type Iii Neutrophilic Dermatosis, Acute Febrile Oliver Syndrome Optic Neuritis Palmoplantar Keratoderma and Woolly Hair Paragonimiasis Paraneoplastic Pemphigus Pelger-Huet Anomaly Pemphigus Pemphigus Vulgaris Pericardial Effusion Pericarditis Peripartum Cardiomyopathy Phosphatase, Acid, of Tissues Pituitary Hormone Deficiency, Combined, 2 Placenta Accreta Poems Syndrome Polycystic Kidney Disease Polymorphic Reticulosis Polyradiculoneuropathy Posterior Myocardial Infarction Prieto X-Linked Mental Retardation Syndrome Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 3 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 Progressive Familial Heart Block Progressive Familial Heart Block, Type Ia Progressive Familial Heart Block, Type Ib Progressive Familial Heart Block, Type Ii Pulmonary Edema Pulmonary Embolism Pulmonary Hemosiderosis Pulmonary Tuberculosis Purpura Relapsing Polychondritis Restrictive Cardiomyopathy Rheumatic Fever Rheumatic Fever-Related Antigen Rheumatoid Arthritis Right Bundle Branch Block Rigid Spine Muscular Dystrophy 1 Sarcoidosis 2 Scarlet Fever Schimmelpenning-Feuerstein-Mims Syndrome Second-Degree Atrioventricular Block Seizure Disorder Sensorineural Hearing Loss Sickle Cell Disease Sick Sinus Syndrome Silent Myocardial Infarction Sino-Auricular Heart Block Situs Inversus Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity Spinal and Bulbar Muscular Atrophy, X-Linked 1 Spondylitis Spondyloarthropathy Spondyloarthropathy 1 Spondyloocular Syndrome Subacute Bacterial Endocarditis Syncope Syphilis Systemic Lupus Erythematosus Systemic Scleroderma Systolic Heart Failure Thalassemia Third-Degree Atrioventricular Block Thyroiditis Thyrotoxic Periodic Paralysis Transposition of the Great Arteries Tricuspid Atresia Undifferentiated Connective Tissue Disease Undifferentiated Pleomorphic Sarcoma Ventricular Fibrillation, Paroxysmal Familial, 1 Ventricular Septal Defect Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy Werner Syndrome Wild Type Attr Amyloidosis Wolff-Parkinson-White Syndrome