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Nume Syncope
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Boli A-Z Achalasia Acrocallosal Syndrome Acute Myocarditis Adie Pupil Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Amaurosis Fugax Amyloidosis Andersen Cardiodysrhythmic Periodic Paralysis Androgen Insensitivity Syndrome, Mild Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency Aneurysm Angiosarcoma Aniridia 1 Anorexia Nervosa 1 Anterolateral Myocardial Infarction Arrhythmogenic Right Ventricular Cardiomyopathy Arteries, Anomalies of Arteriovenous Malformation Arthrochalasia Ehlers-Danlos Syndrome Asthma Ataxia Neuropathy Spectrum Atrial Fibrillation Atrial Standstill Atrioventricular Block Autonomic Dysfunction Autonomic Neuropathy Benign Childhood Occipital Epilepsy, Panayiotopoulos Type Bladder Diverticulum Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Body Mass Index Quantitative Trait Locus 10 Body Mass Index Quantitative Trait Locus 11 Body Mass Index Quantitative Trait Locus 12 Body Mass Index Quantitative Trait Locus 14 Body Mass Index Quantitative Trait Locus 18 Body Mass Index Quantitative Trait Locus 4 Body Mass Index Quantitative Trait Locus 7 Body Mass Index Quantitative Trait Locus 8 Body Mass Index Quantitative Trait Locus 9 Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Brain Small Vessel Disease with or Without Ocular Anomalies Breath-Holding Spells Bronchogenic Cyst Brugada Syndrome Burns Calcinosis Cardiac Arrest Cardiac Arrhythmia Cardiac Conduction Defect Cardiac Conduction Disease with or Without Dilated Cardiomyopathy Cardiac Sarcoidosis Carotid Artery Dissection Carotid Artery Occlusion Catecholaminergic Polymorphic Ventricular Tachycardia Central Nervous System Origin Vertigo Central Sleep Apnea Cerebral Hypoxia Cerebral Palsy, Ataxic, Autosomal Recessive Cerebritis Cervicitis Chiari Malformation Choriocarcinoma Chronic Orthostatic Intolerance Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Complex Regional Pain Syndrome Constrictive Pericarditis Coronary Aneurysm Coronary Artery Anomaly Coronary Artery Dissection, Spontaneous Cor Triatriatum Cor Triatriatum Sinister Cystadenoma Deafness, Autosomal Dominant 2a Dementia Dermoid Cyst Dextrocardia Diabetic Neuropathy Dysautonomia Echinococcosis Encephalitis Encephalomyopathy Endocarditis Endomyocardial Fibrosis Endotheliitis Eosinophilic Gastroenteritis Epilepsy Esophageal Disease Exercise-Induced Anaphylaxis Fainting Familial Atrial Fibrillation Familial Long Qt Syndrome Familial Short Qt Syndrome First-Degree Atrioventricular Block Gastroenteritis Glomus Vagale Tumor Glossopharyngeal Neuralgia Glycogen Storage Disease Glycogen Storage Disease 0, Muscle Goiter Griscelli Syndrome Headache Heart Conduction Disease Heart Disease Heart Tumor Hemangioma Hemangiopericytoma, Malignant Hemifacial Spasm Hepatic Adenomas, Familial Hepatitis Hepatitis C Hereditary Sensory Neuropathy Heroin Dependence Histiocytosis Holt-Oram Syndrome Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertensive Heart Disease Hypertrophic Cardiomyopathy Hypoaldosteronism Hypokalemia Hypoparathyroidism Hypoplastic Left Heart Syndrome Hypoxia Idiopathic Edema Infective Endocarditis Inflammatory Myofibroblastic Tumor Intravenous Leiomyomatosis Intrinsic Cardiomyopathy Ischemia Jervell and Lange-Nielsen Syndrome 1 Kearns-Sayre Syndrome Kommerell Diverticulum Langerhans Cell Histiocytosis Laryngitis Left Ventricular Noncompaction Leiomyomatosis Leopard Syndrome Leukemia Liposarcoma Lissencephaly 1 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 Lung Cancer Lupus Erythematosus Lymphoblastic Lymphoma Lymphoma Mediastinitis Melanoma Meningocele Methemoglobinemia Migraine with Aura Mitral Valve Insufficiency Mitral Valve Stenosis Mobitz Type Ii Atrioventricular Block Moebius Syndrome Motion Sickness Mucolipidosis Ii Alpha/beta Myeloid Leukemia Myocardial Infarction Myocarditis Myotonia Myotonia Atrophica Myxedema Nasopharyngeal Carcinoma Nasopharyngitis Neurogenic Hypertension Neuropathy Neurosarcoidosis Nonsyndromic Paraganglioma Ocular Melanoma Orthostatic Intolerance Paine Syndrome Paroxysmal Ventricular Fibrillation Pectus Excavatum Pericarditis Peripartum Cardiomyopathy Pharyngitis Polymorphic Reticulosis Polyneuropathy Posteroinferior Myocardial Infarction Postural Hypotension Postural Orthostatic Tachycardia Syndrome Prieto X-Linked Mental Retardation Syndrome Prinzmetal's Variant Angina Prostatitis Pseudohypoparathyroidism Pulmonary Embolism Pulmonary Hypertension Pure Autonomic Failure Quadriplegia Refractory Anemia Relapsing Polychondritis Retinitis Rheumatic Fever Rheumatic Fever-Related Antigen Right Bundle Branch Block Sarcoidosis 2 Sarcoma Second-Degree Atrioventricular Block Seizure Disorder Short Qt Syndrome Sick Sinus Syndrome Sinoatrial Node Disease Sleep Apnea Sleep Disorder Spindle Cell Sarcoma Squamous Cell Carcinoma Subclavian Steal Syndrome Substance Abuse Substernal Goiter Sudden Infant Death Syndrome Syncope, Familial Vasovagal Syndrome of Inappropriate Antidiuretic Hormone Syringomyelia Systemic Lupus Erythematosus Systemic Mastocytosis Temporal Lobe Epilepsy Third-Degree Atrioventricular Block Thrombocytosis Thrombosis Thyroiditis Timothy Syndrome Trichinosis Tricuspid Atresia Urticaria Urticaria Pigmentosa Ventricular Fibrillation, Paroxysmal Familial, 1 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy Vitamin E, Familial Isolated Deficiency of Wolff-Parkinson-White Syndrome