Informaţii despre

Nume Transposition of the Great Arteries
Pagina Web
Clasificare globală Malacards Boli rare

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Boli A-Z 16p11.2 Duplication 46,xy Partial Gonadal Dysgenesis Accessory Mitral Valve Tissue Acute Myocardial Infarction Aging Alport Syndrome, X-Linked Al-Raqad Syndrome Aneurysm Aniridia 1 Anorexia Nervosa 1 Aortic Aneurysm Aortic Coarctation Aortic Valve Atresia Aortic Valve Insufficiency Aortopulmonary Window Arthrochalasia Ehlers-Danlos Syndrome Atrial Fibrillation Atrial Heart Septal Defect Atrioventricular Block Atrioventricular Septal Defect Azygos Continuation of the Inferior Vena Cava Biliary Atresia Blood Group--Ahonen Blood Group, Dombrock System Blood Group, Junior 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 Brain Injury Cardiac Arrest Cardiofaciocutaneous Syndrome 1 Cerebritis Communicating Hydrocephalus Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Complete Atrioventricular Canal Complete Atrioventricular Canal-Left Heart Obstruction Syndrome Complete Atrioventricular Canal-Tetralogy of Fallot Syndrome Complete Atrioventricular Canal-Ventricle Hypoplasia Syndrome Congenitally Corrected Transposition of the Great Arteries Conotruncal Heart Malformations Coronary Artery Anomaly Coronary Stenosis Cor Triatriatum Cor Triatriatum Sinister Criss-Cross Heart Cyanosis, Transient Neonatal Dextrocardia Dextro-Looped Transposition of the Great Arteries Diaphragmatic Hernia, Congenital Diaphragm Disease Double Discordia Down Syndrome Ebstein Anomaly Endocardial Fibroelastosis Endocarditis Esophageal Atresia/tracheoesophageal Fistula Familial Atrial Fibrillation Fetal Hydantoin Syndrome Galactose Epimerase Deficiency Heart Disease Heart Septal Defect Heterotaxy Heterotaxy, Visceral, 1, X-Linked Hydrocephalus Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypoplastic Left Heart Syndrome Hypoxia Interatrial Communication Intestinal Atresia Isolated Congenitally Uncorrected Transposition of the Great Arteries Jackson-Weiss Syndrome Juxtaposition of the Atrial Appendages Keratomalacia Klippel-Feil Syndrome Mesocardia Mitral Atresia Mitral Valve Stenosis Myocardial Infarction Oeis Complex Omphalocele Pancreatic Agenesis Partial Atrioventricular Canal Patent Ductus Arteriosus 1 Patent Foramen Ovale Pulmonary Artery Hypoplasia Pulmonary Hypertension Pulmonary Interstitial Glycogenosis Pulmonary Sequestration Pulmonary Valve Disease Pulmonary Valve Insufficiency Pulmonary Valve Stenosis Pulmonary Vein Stenosis Pulmonic Stenosis Right Aortic Arch Right Ventricle Hypoplasia Scalp-Ear-Nipple Syndrome Sick Sinus Syndrome Single Ventricular Heart Situs Inversus Sternal Cleft Subclavian Steal Syndrome Subpulmonary Stenosis Tetralogy of Fallot Thrombocytopenia Thrombosis Total Anomalous Pulmonary Venous Return 1 Tracheobronchomalacia Transposition of the Great Arteries, Dextro-Looped 1 Trichohepatoenteric Syndrome 1 Tricuspid Atresia Tricuspid Valve Disease Tricuspid Valve Insufficiency Tuberous Sclerosis Twin-to-Twin Transfusion Syndrome Univentricular Heart Vaginitis Ventricular Septal Defect Visceral Heterotaxy Vitamin E, Familial Isolated Deficiency of Wolff-Parkinson-White Syndrome