Informaţii despre

Nume Arrhythmogenic Right Ventricular Cardiomyopathy
Pagina Web www.malacards.org
Clasificare globală Malacards Boli rare
Clasificare anatomică Malacards Boli cardiovasculare

Vezi şi

Boli A-Z Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Al-Raqad Syndrome Aneurysm Aniridia 1 Anorexia Nervosa 1 Arrhythmogenic Right Ventricular Dysplasia, Familial, 1 Arrhythmogenic Right Ventricular Dysplasia, Familial, 2 Arrhythmogenic Right Ventricular Dysplasia, Familial, 4 Arrhythmogenic Right Ventricular Dysplasia, Familial, 5 Arrhythmogenic Right Ventricular Dysplasia, Familial, 6 Arrhythmogenic Right Ventricular Dysplasia, Familial, 8 Arrhythmogenic Right Ventricular Dysplasia, Familial, 9 Arthrochalasia Ehlers-Danlos Syndrome Ataxia Neuropathy Spectrum Atrial Standstill 1 Autonomic Dysfunction Blood Group--Ahonen Blood Group, Dombrock System Brugada Syndrome Cardiac Arrest Cardiac Conduction Defect Cardiac Sarcoidosis Cardiomyopathy, Dilated, 1a Cardiomyopathy, Dilated, 1e Cardiomyopathy, Dilated, 1h Cardiomyopathy, Dilated, 3b Cardiomyopathy, Dilated, with Woolly Hair and Keratoderma Cardioneuromyopathy with Hyaline Masses and Nemaline Rods Catecholaminergic Polymorphic Ventricular Tachycardia Central Core Disease of Muscle Central Core Myopathy Centronuclear Myopathy Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Fiber-Type Disproportion Cytoplasmic Body Myopathy Delayed Sleep Phase Disorder Dilated Cardiomyopathy Ectodermal Dysplasia Ectodermal Dysplasia/skin Fragility Syndrome Emerinopathy Emery-Dreifuss Muscular Dystrophy Emery-Dreifuss Muscular Dystrophy 2, Autosomal Dominant Enterobiasis Epidermolysis Bullosa, Lethal Acantholytic Extracardiac Rhabdomyoma Fainting 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 Grover's Disease Hypertrophic Cardiomyopathy Intrinsic Cardiomyopathy Kocher-Debre-Semelaigne Syndrome Left Ventricular Noncompaction Limb-Girdle Muscular Dystrophy Malignant Hyperthermia Malignant Hyperthermia of Anesthesia Mcleod Syndrome Microcolon Mixed Ductal-Endocrine Carcinoma Mucolipidosis Ii Alpha/beta Muscle 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 2a Muscular Dystrophy, Limb-Girdle, Type 2b Muscular Dystrophy, Limb-Girdle, Type 2f Muscular Dystrophy, Limb-Girdle, Type 2j Myocarditis Myofibrillar Myopathy Myopathy Myopathy, Myofibrillar, 1 Myopathy, Myofibrillar, 3 Myopathy, Myofibrillar, 4 Myopathy, Proximal, and Ophthalmoplegia Myopathy, Spheroid Body Native American Myopathy Naxos Disease Neuromuscular Disease Palmoplantar Keratoderma and Woolly Hair Paraneoplastic Pemphigus Pelger-Huet Anomaly Pemphigus Pemphigus Vulgaris Progressive Familial Heart Block, Type Ib Protein-Losing Enteropathy Pulmonary Embolism Reducing Body Myopathy Right Bundle Branch Block Sarcoidosis 2 Skin Pilomatrix Carcinoma Spondyloocular Syndrome Syncope Tetralogy of Fallot Thrombosis Unna-Thost Palmoplantar Keratoderma Ventricular Fibrillation, Paroxysmal Familial, 1 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy