Informaţii despre

Nume Conotruncal Heart Malformations
Pagina Web
Clasificare globală Malacards Boli fetale; Boli genetice; Boli rare
Clasificari ICD10 Caf; Common arterial trunk; Double outlet right ventricle
Clasificare anatomică Malacards Boli cardiovasculare; Boli de piele

Vezi şi

Boli A-Z Adie Pupil Aging Al-Raqad Syndrome Aneurysm Aniridia 1 Anorexia Nervosa 1 Aortic Aneurysm Aortic Coarctation Aortopulmonary Window Arrhythmogenic Right Ventricular Dysplasia, Familial, 5 Arteriovenous Malformation Arthrochalasia Ehlers-Danlos Syndrome Atrial Heart Septal Defect Atrioventricular Septal Defect Beemer Ertbruggen Syndrome Blood Group--Ahonen Blood Group, Dombrock System Cardiofaciocutaneous Syndrome 1 Cardiomyopathy, Dilated, 1e Chromosomal Triplication Chromosome 3p Duplication Cleft Larynx, Posterior Collecting Duct Carcinoma 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 Congestive Heart Failure Cornelia De Lange Syndrome Coronary Artery Anomaly Cor Triatriatum Criss-Cross Heart Cyanosis, Transient Neonatal Dextrocardia Dextro-Looped Transposition of the Great Arteries Diaphragmatic Hernia, Congenital Discrete Subaortic Stenosis Double Discordia Double Outlet Left Ventricle Double Outlet Right Ventricle with Subaortic or Doubly Committed Ventricular Septal Defect with Pulmonary Stenosis Down Syndrome Ebstein Anomaly Ectopia Cordis Endocarditis Facial Dysmorphism-Anorexia-Cachexia-Eye and Skin Anomalies Syndrome Familial Atrial Fibrillation Familial Bicuspid Aortic Valve Fanconi Anemia, Complementation Group E Heart Septal Defect Heparin-Induced Thrombocytopenia Hepatic Adenomas, Familial Heterotaxy Heterotaxy, Visceral, 1, X-Linked Holt-Oram Syndrome Hydrocephalus Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertrophic Cardiomyopathy Hypoplastic Left Heart Syndrome Infective Endocarditis Jacobsen Syndrome Levocardia Microcephaly Mitral Atresia Moebius Syndrome Myotonic Dystrophy Neurodegeneration with Brain Iron Accumulation 2a Partial Atrioventricular Canal Patent Ductus Arteriosus 1 Patent Foramen Ovale Pentalogy of Cantrell Phaeochromocytoma Phenylketonuria Pulmonary Arteriovenous Malformation Pulmonary Atresia with Ventricular Septal Defect Pulmonary Embolism Pulmonary Valve Disease Pulmonary Valve Stenosis Pulmonic Stenosis Right Aortic Arch Right Atrial Isomerism Scalp-Ear-Nipple Syndrome Situs Inversus Subvalvular Aortic Stenosis Tetralogy of Fallot Third-Degree Atrioventricular Block Thoracoabdominal Syndrome Thrombocytopenia Total Anomalous Pulmonary Venous Return 1 Tracheal Agenesis Tracheal Stenosis Tracheoesophageal Fistula Transposition of the Great Arteries Trichohepatoenteric Syndrome 1 Tricuspid Atresia Tricuspid Valve Disease Velocardiofacial Syndrome Ventricular Septal Defect Visceral Heterotaxy Vitamin E, Familial Isolated Deficiency of