Informaţii despre

Nume Left Ventricular Noncompaction
Pagina Web www.malacards.org
Clasificare globală Malacards Boli fetale; Boli genetice; Boli rare
Clasificari ICD10 Other cardiomyopathies
Clasificare anatomică Malacards Boli cardiovasculare
Boli din aceeaşi familie Left Ventricular Noncompaction 1; Left Ventricular Noncompaction 10; Left Ventricular Noncompaction 2; Left Ventricular Noncompaction 7; Left Ventricular Noncompaction 8

Vezi şi

Boli A-Z Adie Pupil Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Al-Raqad Syndrome Andersen Cardiodysrhythmic Periodic Paralysis Aneurysm Aniridia 1 Anorexia Nervosa 1 Aortic Coarctation Arrhythmogenic Right Ventricular Cardiomyopathy Arteries, Anomalies of Arthrochalasia Ehlers-Danlos Syndrome Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Atrial Fibrillation Atrial Standstill 1 Atrial Tachyarrhythmia with Short Pr Interval Atrioventricular Block Barth Syndrome Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Brugada Syndrome Cardiac Arrest Cardiac Arrhythmia Cardiac Conduction Defect Cardiac Conduction Disease with or Without Dilated Cardiomyopathy Cardiomyopathy, Dilated, 1dd Cardiomyopathy, Dilated, 1e Cardiomyopathy, Familial Hypertrophic, 1 Cardiomyopathy, Familial Hypertrophic, 4 Catecholaminergic Polymorphic Ventricular Tachycardia Chromosomal Triplication Chromosome 1p36 Deletion Syndrome Coffin-Lowry Syndrome Congenital Fiber-Type Disproportion Congestive Heart Failure Coronary Arterial Fistulas Cranioectodermal Dysplasia 1 Craniosynostosis with Fibular Aplasia Cutaneous Sclerosis Dextrocardia Dilated Cardiomyopathy Double-Orifice Mitral Valve Ebstein Anomaly Endocardial Fibroelastosis Endomyocardial Fibrosis Epidermolysis Bullosa 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 Sick Sinus Syndrome Graves' Disease Heart Conduction Disease Heart Disease Hepatic Adenomas, Familial Hydrops Fetalis Hydrops Fetalis, Nonimmune, and/or Atrial Septal Defect Hypercholesterolemia, Autosomal Dominant, 3 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertrophic Cardiomyopathy Intrinsic Cardiomyopathy Left Ventricular Noncompaction 1 Left Ventricular Noncompaction 2 Limb-Girdle Muscular Dystrophy Long Qt Syndrome Long Qt Syndrome 1 Long Qt Syndrome 12 Long Qt Syndrome 13 Long Qt Syndrome 2 Long Qt Syndrome 5 Long Qt Syndrome 6 Long Qt Syndrome 9 Malignant Hyperthermia Marfan Syndrome Mucolipidosis Ii Alpha/beta Multiminicore Disease Muscle Disorders Muscular Dystrophy Muscular Dystrophy, Limb-Girdle, Type 2j Myocardial Infarction Myopathy Myopathy, Myofibrillar, 3 Myopathy, Myofibrillar, 4 Myopathy, Spheroid Body Myosin Storage Myopathy Myxoid Leiomyosarcoma Neuronal Ceroid Lipofuscinosis Neuronitis Pancytopenia Partial Atrioventricular Canal Peripartum Cardiomyopathy Periventricular Nodular Heterotopia Pheochromocytoma Polycystic Kidney Disease Polymicrogyria Polyneuropathy Pulmonary Atresia with Intact Ventricular Septum Pulmonary Hypertension Recessive Dystrophic Epidermolysis Bullosa Restrictive Cardiomyopathy Second-Degree Atrioventricular Block Sensorineural Hearing Loss Sick Sinus Syndrome Sinoatrial Node Disease Sotos Syndrome 1 Sudden Infant Death Syndrome Syncope Tetanus Neonatorum Tetralogy of Fallot Thalassemia Trichohepatoenteric Syndrome 1 Tricuspid Atresia Ventricular Fibrillation, Paroxysmal Familial, 1 Ventricular Septal Defect Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy