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Boli A-Z 3-Methylglutaconic Aciduria Accessory Mitral Valve Tissue Achalasia Acquired Metabolic Disease Acrocallosal Syndrome Acrofacial Dysostosis Acute Myocardial Infarction Acute Myocarditis Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of Adenocarcinoma Adie Pupil Aging Alcoholic Cardiomyopathy Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Amyloidosis Androgen Insensitivity Syndrome, Mild Aneurysm Angina Pectoris Aniridia 1 Anorexia Nervosa 1 Aromatic Alpha-Keto Acid Reductase Arrhythmogenic Right Ventricular Cardiomyopathy Arteries, Anomalies of Arteriovenous Fistula Arthrochalasia Ehlers-Danlos Syndrome Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Ataxia Neuropathy Spectrum Atrial Fibrillation Atrial Standstill 1 Atrial Tachyarrhythmia with Short Pr Interval Atrioventricular Block Atrioventricular Septal Defect Beckwith-Wiedemann Syndrome 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 Bohring-Opitz Syndrome Bornholm Eye Disease Brugada Syndrome Burns Cardiac Arrest Cardiac Conduction Defect Cardiac Rupture Cardiac Sarcoidosis Cardiac Tamponade Cardioencephalomyopathy Cardiofaciocutaneous Syndrome 1 Cardiogenic Shock Cardiomyopathy, Dilated, 1e Cardiomyopathy, Familial Hypertrophic, 1 Cardiomyopathy, Familial Hypertrophic, 21 Cardiomyopathy, Familial Hypertrophic, 4 Cardiomyopathy, Familial Hypertrophic, 6 Cardiomyopathy, Infantile Hypertrophic Cardioneuromyopathy with Hyaline Masses and Nemaline Rods Cataract Central Core Disease of Muscle Chagas Disease Chromosomal Triplication Chronic Fatigue Syndrome Combined Oxidative Phosphorylation Deficiency 9 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Complete Atrioventricular Canal Congenital Cataract-Hypertrophic Cardiomyopathy-Mitochondrial Myopathy Syndrome Congenital Cytomegalovirus Congenital Disorder of Glycosylation, Type Ia Congestive Heart Failure Constrictive Pericarditis Cornelia De Lange Syndrome Coronary Stenosis Cor Triatriatum Costello Syndrome Cranioectodermal Dysplasia 1 Crouzon Syndrome Crouzon Syndrome with Acanthosis Nigricans Cytomegalovirus Infection Cytoplasmic Body Myopathy Danon Disease Dextrocardia Diabetes Mellitus Diastolic Heart Failure Diffuse Lymphatic Malformation Dilated Cardiomyopathy Disseminated Intravascular Coagulation Donohue Syndrome Down Syndrome Dwarfism Dysostosis Ebstein Anomaly Encephalomyopathy Encephalopathy Endocardial Fibroelastosis Endocarditis Endocrine-Cerebroosteodysplasia Endomyocardial Fibrosis Endotheliitis End Stage Renal Failure Epilepsy Extrinsic Cardiomyopathy Fabry Disease Facial Hemiatrophy Factor Vii Deficiency Factor X Deficiency 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 Familial Isolated Restrictive Cardiomyopathy Fasciitis Fatal Infantile Cytochrome C Oxidase Deficiency Fatal Infantile Encephalocardiomyopathy Fibroblastic Rheumatism Fibromatosis Fibromuscular Dysplasia Gastric Adenocarcinoma Gigantism Gitelman Syndrome Glycogen Storage Disease Glycogen Storage Disease Ii Glycogen Storage Disease, Type Ixd Gonadal Dysgenesis Heart Disease Hemifacial Atrophy, Progressive Hemopericardium Hemophagocytic Lymphohistiocytosis, Familial, 1 Hemophagocytic Lymphohistiocytosis, Familial, 2 Hepatic Adenomas, Familial Hepatitis Hepatitis C Hepatitis C Virus Hereditary Spherocytosis Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hypercholesterolemia, Autosomal Dominant, 3 Hypercholesterolemia, Familial Hyperinsulinemic Hypoglycemia Hyperinsulinemic Hypoglycemia, Familial, 3 Hyperinsulinemic Hypoglycemia, Familial, 4 Hyperinsulinism Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertensive Heart Disease Hyperthyroidism Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypoglycemia Hypotonia Hypoxia Inclusion Body Myositis Infective Endocarditis Inferior Myocardial Infarction Insulin-Like Growth Factor I Interstitial Nephritis Intrinsic Cardiomyopathy Ischemia Ischemic Heart Disease Lactic Acidosis Laryngeal Cleft Laryngitis Left Ventricular Noncompaction Leiomyosarcoma Lentigines Leopard Syndrome Limb-Girdle Muscular Dystrophy Limb Ischemia Lipodystrophy Lissencephaly 1 Liver Cirrhosis Loeffler Endocarditis Long Qt Syndrome Lymphoma Macs Syndrome Marfan Syndrome Mitochondrial Disorders Mitochondrial Encephalomyopathy Mitochondrial Myopathy Miyoshi Muscular Dystrophy 1 Morbid Obesity Motor Neuron Disease Mucolipidosis Ii Alpha/beta Muscle Hypertrophy Muscular Dystrophy Muscular Dystrophy, Limb-Girdle, Type 2a Muscular Dystrophy, Limb-Girdle, Type 2f Mutism Myocardial Infarction Myocardial Stunning Myocarditis Myoclonus Myopathy Myopathy, Spheroid Body Myosin Storage Myopathy Myositis Myotonic Dystrophy Nemaline Myopathy Nephrotic Syndrome Neurofibromatosis-Noonan Syndrome Neuronal Ceroid Lipofuscinosis Neuronitis Neutropenia Noonan Syndrome 1 Noonan Syndrome with Multiple Lentigines Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy Ovarian Cyst Pancreatitis Parametritis Pericardial Effusion Pericarditis Pheochromocytoma Phosphorylase Kinase Deficiency Platelet Glycoprotein Iv Deficiency Posterior Urethral Valves Progressive Familial Heart Block, Type Ib Pulmonary Edema Pulmonary Embolism Pulmonary Hypertension Pulmonary Interstitial Glycogenosis Pulmonary Valve Stenosis Pulmonary Vein Stenosis Pulmonic Stenosis Renal Glucosuria Renal Hypodysplasia/aplasia 1 Restrictive Cardiomyopathy Rheumatic Heart Disease Right Bundle Branch Block Rigid Spine Muscular Dystrophy 1 Sarcoidosis 2 Schnyder Corneal Dystrophy Sengers Syndrome Sensorineural Hearing Loss Septal Myocardial Infarction Short Qt Syndrome Short Stature, Auditory Canal Atresia, Mandibular Hypoplasia, and Skeletal Abnormalities Sick Sinus Syndrome Sideroblastic Anemia Siderosis Situs Inversus Sleep Apnea Spasticity Spinocerebellar Atrophy Spiradenoma Splenic Infarction Spondyloocular Syndrome Subacute Cerebellar Degeneration Subaortic Stenosis, Membranous Subendocardial Myocardial Infarction Subpulmonary Stenosis Subvalvular Aortic Stenosis Syncope Systolic Heart Failure Tetralogy of Fallot Three M Syndrome 1 Thrombocytopenia Thrombosis Tyrosinemia Ventricular Septal Defect Vitamin B12 Deficiency Williams-Beuren Syndrome Wolff-Parkinson-White Syndrome Wolf-Hirschhorn Syndrome