Informaţii despre

Nume Atrioventricular Block
Pagina Web www.malacards.org
Clasificari ICD10 Other and unspecified atrioventricular block
Clasificare anatomică Malacards Boli cardiovasculare

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Boli A-Z Achalasia Acute Myocardial Infarction Acute Myocarditis Adenocarcinoma Aging Alcohol Abuse Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Al-Raqad Syndrome Amyloidosis Andersen Cardiodysrhythmic Periodic Paralysis Aneurysm Aniridia 1 Anorexia Nervosa 1 Anteroseptal Myocardial Infarction Aortic Aneurysm Aortitis Appendicitis Argininosuccinic Aciduria Arrhythmogenic Right Ventricular Dysplasia, Familial, 5 Arteries, Anomalies of Arthrochalasia Ehlers-Danlos Syndrome Aseptic Meningitis Ataxia with Vitamin E Deficiency Atrial Fibrillation Atrial Heart Septal Defect Atrial Septal Defect 1 Atrial Standstill 1 Atrioventricular Dissociation Atrioventricular Septal Defect B-Cell Lymphomas Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Bronchogenic Cyst Brugada Syndrome Cardiac Arrest Cardiac Arrhythmia Cardiac Conduction Defect Cardiac Conduction Disease with or Without Dilated Cardiomyopathy Cardiac Sarcoidosis Cardiac Tamponade Cardiogenic Shock Cardiomyopathy, Dilated, 1e Catecholaminergic Polymorphic Ventricular Tachycardia Cavernous Hemangioma Cerebral Palsy Cerebritis Cholecystitis Chromosomal Triplication Chronic Progressive External Ophthalmoplegia Congenitally Corrected Transposition of the Great Arteries Connective Tissue Disease Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome Cytomegalovirus Infection Digitalis Poisoning Dilated Cardiomyopathy Double Discordia Dowling-Degos Disease 1 Dysautonomia Ebstein Anomaly Emery-Dreifuss Muscular Dystrophy Encephalomyopathy Endocardial Fibroelastosis Endocarditis Epilepsy Extrapulmonary Tuberculosis Fabry Disease Familial Atrial Fibrillation Familial Long Qt Syndrome Familial Progressive Cardiac Conduction Defect Familial Short Qt Syndrome Familial Sick Sinus Syndrome First-Degree Atrioventricular Block Gastric Dilatation Giant Cell Myocarditis Gingivitis Heart Block, Congenital Heart Conduction Disease Heart Disease Heart Septal Defect Hemangioma Hemophagocytic Lymphohistiocytosis Heterotaxy Heterotaxy, Visceral, 1, X-Linked His Bundle Tachycardia Hyaline Fibromatosis Syndrome Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertonia Hypertrophic Cardiomyopathy Hypokalemia Hypopituitarism Hypoplastic Left Heart Syndrome Infectious Myocarditis Infective Endocarditis Inferior Myocardial Infarction Intrinsic Cardiomyopathy Jervell and Lange-Nielsen Syndrome 1 Kearns-Sayre Syndrome Laryngitis Left Ventricular Noncompaction Leiomyoma Levocardia Lissencephaly 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 Lymphangitis Lymphoma Melanoma Meningitis Mitochondrial Encephalomyopathy Mixed Connective Tissue Disease Mobitz Type Ii Atrioventricular Block Muscular Dystrophy Myocardial Infarction Myocarditis Myopathy Myositis Myxedema Nonsyndromic Paraganglioma Patent Foramen Ovale Pericardial Effusion Peripartum Cardiomyopathy Pheochromocytoma Pneumothorax Polymorphic Reticulosis Polymyositis Posterior Myocardial Infarction Posteroinferior 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 Ib Pseudopseudohypoparathyroidism Pulmonary Embolism Pulmonary Hypertension Pulmonary Valve Disease Pulmonary Valve Stenosis Restrictive Cardiomyopathy Rheumatic Fever Rheumatic Fever-Related Antigen Right Atrial Isomerism Right Bundle Branch Block Sarcoidosis 2 Satb2-Associated Syndrome Second-Degree Atrioventricular Block Septal Myocardial Infarction Short Qt Syndrome Sick Sinus Syndrome Single Ventricular Heart Sinusitis Sudden Infant Death Syndrome Supravalvular Aortic Stenosis Syncope Systolic Heart Failure Takayasu Arteritis Tetralogy of Fallot Third-Degree Atrioventricular Block Thrombocytopenia Timothy Syndrome Tonsillitis Transposition of the Great Arteries Trichinosis Tricuspid Atresia Univentricular Heart 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 Wild Type Attr Amyloidosis Wolff-Parkinson-White Syndrome