Informaţii despre

Nume Familial Isolated Dilated Cardiomyopathy
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificari ICD10 Dilated cardiomyopathy
Clasificare anatomică Malacards Boli cardiovasculare

Vezi şi

Boli A-Z Acute Myocarditis Alzheimer Disease 4 Angiolipoma Arrhythmogenic Right Ventricular Cardiomyopathy Atrial Standstill 1 Autosomal Recessive Limb-Girdle Muscular Dystrophy Barth Syndrome Benign Metastasizing Leiomyoma Cardiac Arrest Cardiac Conduction Defect Cardiomyopathy, Dilated, 1b Cardiomyopathy, Dilated, 1d Cardiomyopathy, Dilated, 1dd Cardiomyopathy, Dilated, 1e Cardiomyopathy, Dilated, 3b Cardiomyopathy, Familial Hypertrophic, 1 Cardiomyopathy, Familial Hypertrophic, 4 Cardiomyopathy, Familial Restrictive, 1 Cardioneuromyopathy with Hyaline Masses and Nemaline Rods Centronuclear Myopathy Cervical Polyp Congenital Fibrosarcoma Congestive Heart Failure Creatine Phosphokinase, Elevated Serum Cutaneous Fibrous Histiocytoma Cutaneous Leiomyosarcoma Cystic Nephroma Cytoplasmic Body Myopathy Dextrocardia Diastolic Heart Failure Dilated Cardiomyopathy Distal Muscular Dystrophy Early-Onset, Autosomal Dominant Alzheimer Disease Ebstein Anomaly Endocardial Fibroelastosis Epithelioid Leiomyosarcoma Extracardiac Rhabdomyoma Familial Idiopathic Basal Ganglia Calcification 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 Restrictive Cardiomyopathy Familial Sick Sinus Syndrome Fibroblastic Rheumatism Gas Gangrene Gastrointestinal Stromal Tumor Glomus Tumor Heart Disease Hemophagocytic Lymphohistiocytosis, Familial, 2 Hidradenitis Hidradenitis Suppurativa Hypertrophic Cardiomyopathy Infantile Myofibromatosis Intrinsic Cardiomyopathy Isolated Hyperckemia Left Ventricular Noncompaction Limb-Girdle Muscular Dystrophy Microcolon Muscular Dystrophy, Becker Type Muscular Dystrophy, Congenital, 1b Muscular Dystrophy, Congenital Merosin-Deficient, 1a Muscular Dystrophy, Duchenne Type Muscular Dystrophy-Dystroglycanopathy , Type a, 4 Muscular Dystrophy-Dystroglycanopathy , Type C, 5 Muscular Dystrophy, Limb-Girdle, Type 2a Muscular Dystrophy, Limb-Girdle, Type 2b Muscular Dystrophy, Limb-Girdle, Type 2c Muscular Dystrophy, Limb-Girdle, Type 2f Muscular Dystrophy, Limb-Girdle, Type 2h Muscular Dystrophy, Limb-Girdle, Type 2j Myocardial Stunning Myocarditis Myofibrillar Myopathy Myopathy Myopathy, Congenital Myopathy, Myofibrillar, 1 Myopathy, Myofibrillar, 2 Myopathy, Myofibrillar, 3 Myopathy, Myofibrillar, 4 Myopathy, Spheroid Body Myosin Storage Myopathy Ossifying Fibromyxoid Tumor Ovarian Fibrothecoma Parachordoma Peripartum Cardiomyopathy Perivascular Epithelioid Cell Tumor Pleomorphic Liposarcoma Progressive Familial Heart Block Pulmonary Vein Stenosis Reducing Body Myopathy Restrictive Cardiomyopathy Rigid Spine Muscular Dystrophy 1 Short Qt Syndrome Sick Sinus Syndrome Sinoatrial Node Disease Spindle Cell Lipoma Syringocystadenoma Papilliferum Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy