SE-ATLAS

HEC syndrome Supravalvular aortic stenosis Idiopathic pulmonary artery dilatation Anomaly of the tricuspid subvalvular apparatus Congenital complete agenesis of pericardium Non-genetic cardiac rhythm disease Congenital systemic veins anomaly Familial bicuspid aortic valve Double outlet right ventricle with subaortic or doubly committed ventricular septal defect with pulmonary stenosis Accessory mitral valve tissue Congenital unguarded mitral orifice Neuhauser anomaly Congenital Gerbode defect Absence of innominate vein Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome Torsade-de-pointes syndrome with short coupling interval Pulmonary artery or pulmonary branch anomaly Atrioventricular valve anomaly Dilated cardiomyopathy Dilated cardiomyopathy with ataxia Idiopathic ventricular fibrillation, non Brugada type Mitochondrial disease with hypertrophic cardiomyopathy Levocardia Accessory tricuspid valve tissue Loeffler endocarditis Congenital valvular dysplasia Autosomal dominant coarctation of aorta Fixed subaortic stenosis Familial idiopathic dilatation of the right atrium Congenital supravalvular mitral ring Kommerell diverticulum Persistent fifth aortic arch Laubry-Pezzi syndrome Persistent left superior vena cava connecting to the roof of left-sided atrium Aortic malformation Generalized congenital lipodystrophy with myopathy Aortic arch defects Congenitally uncorrected transposition of the great arteries with coarctation Atypical coarctation of aorta Rare hypertrophic cardiomyopathy Congenital aortic valve stenosis Coronary artery congenital malformation Congenital aortic valve atresia Agenesis of the superior vena cava Pleuro-pericardial cyst Conotruncal heart malformations Heterotaxia Idiopathic giant cell myocarditis Double outlet right ventricle with non-committed subpulmonary ventricular septal defect Cleft mitral valve Shone complex Congenital anomaly of the inferior vena cava Aorto-ventricular tunnel Congenitally uncorrected transposition of the great arteries Atrioventricular septal defect Histiocytoid cardiomyopathy Syndrome associated with dilated cardiomyopathy Congenital anomaly of the great veins Familial mitral valve prolapse Aorta coarctation Congenital partial agenesis of pericardium Absence of the pulmonary artery Congenital aortopulmonary window Double outlet right ventricle with subpulmonary ventricular septal defect Double outlet right ventricle with subaortic ventricular septal defect Congenital mitral valve insufficiency and/or stenosis Mitral valve agenesis Inherited arrhythmogenic cardiomyopathy Cervical aortic arch Congenital anomaly of superior vena cava Subaortic course of innominate vein Truncus arteriosus Glycogen storage disease due to muscle and heart glycogen synthase deficiency Congenital tricuspid malformation Hypertrophic cardiomyopathy due to intensive athletic training Familial restrictive cardiomyopathy Non-familial restrictive cardiomyopathy Multifocal atrial tachycardia Rare cardiac rhythm disease Lown-Ganong-Levine syndrome Congenital mitral malformation Dysphagia lusoria Cor triatriatum sinister Microcephaly-cardiomyopathy syndrome Pulmonary valve agenesis-intact ventricular septum-persistent ductus arteriosus syndrome Arterial duct anomaly Aneurysm or dilatation of ascending aorta Heart-hand syndrome, Slovenian type Congenital anomaly of the great arteries His bundle tachycardia Uhl anomaly Familial atrial fibrillation Endocardial fibroelastosis Congenital aortic valve insufficiency Double outlet right ventricle with doubly committed ventricular septal defect Straddling and/or overriding mitral valve Univentricular cardiopathy Right aortic arch Congenital anomaly of the coronary sinus Cor triatriatum dexter Cardiofaciocutaneous syndrome Hypoplastic right heart syndrome Pulmonary valve agenesis Familial dilated cardiomyopathy Brugada syndrome Left ventricular noncompaction Complete atrioventricular septal defect with ventricular hypoplasia Peripheral pulmonary stenosis Ectasia of the right atrial appendage Congenital heart block Mitral atresia Abnormal origin of right or left pulmonary artery from the aorta Glycogen storage disease due to LAMP-2 deficiency Rare congenital non-syndromic heart malformation Andersen-Tawil syndrome Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency Criss-cross heart Interatrial communication Pulmonary artery hypoplasia Juxtaposition of the atrial appendages Coronary sinus stenosis Coronary sinus atresia Heart-hand syndrome type 3 Glycogen storage disease with hypertrophic cardiomyopathy Coronary arterial fistula Dextrocardia Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome Familial dilated cardiomyopathy with conduction defect due to LMNA mutation Pulmonary artery coming from patent ductus arteriosus Complete atrioventricular canal-left heart obstruction syndrome Ascending aorta anomaly Sensorineural deafness with dilated cardiomyopathy Inherited isolated arrhythmogenic cardiomyopathy Abnormal origin of the pulmonary artery Isolated congenitally uncorrected transposition of the great arteries Congenital aortic valve dysplasia Catecholaminergic polymorphic ventricular tachycardia Tetralogy of Fallot Premature closure of the arterial duct Right sided atrial isomerism Isolated right ventricular hypoplasia Atrial septal defect-atrioventricular conduction defects syndrome Discrete fibromuscular subaortic stenosis Familial isolated restrictive cardiomyopathy Progressive sensorineural hearing loss-hypertrophic cardiomyopathy syndrome Brachydactyly-long thumb syndrome Syndrome associated with hypertrophic cardiomyopathy Non-familial dilated cardiomyopathy Aneurysm of sinus of Valsalva Situs ambiguus Pulmonary atresia with ventricular septal defect Triatrial heart Jervell and Lange-Nielsen syndrome Transposition of the great arteries Univentricular heart with single atrio-ventricular valve Complete atrioventricular septal defect-tetralogy of Fallot Aortopulmonary coronary arterial course Atrial septal defect, ostium secundum type Persistent eustachian valve Atrial standstill Pulmonary atresia-intact ventricular septum syndrome Scimitar syndrome Situs inversus totalis Hypoplastic left heart syndrome Discrete fixed membranous subaortic stenosis Aortic arch interruption Rare atrial defect and interatrial communication Cirrhotic cardiomyopathy Univentricular heart Anomaly of the mitral subvalvular apparatus Fatal infantile hypertrophic cardiomyopathy due to mitochondrial complex I deficiency Unclassified cardiomyopathy Cardiac diverticulum Tricuspid atresia Coronary artery intramyocardial course Ectasia of the left atrial appendage Right inferior vena cava connecting to left-sided atrium Cardiomyopathy-cataract-hip spine disease syndrome Sino-auricular heart block Congenital pericardium anomaly X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome Tricuspid valve agenesis Valvular pulmonary stenosis Double-orifice mitral valve Aorto-left ventricular tunnel Congenital coronary artery aneurysm Intramural coronary arterial course Atrial septal defect, sinus venosus type Complete atrioventricular septal defect Congenital stenosis of the inferior vena cava Double outlet right ventricle Congenital pulmonary veins atresia or stenosis Maladie cardiaque rare Déficit combiné de la phosphorylation oxydative type 17 Embryopathie diabétique Syndrome de Holt-Oram Syndrome de tubulopathie rénale-cardiomyopathie dilatée Cardiomyopathie arythmogène héréditaire isolée, variante droite-dominante Trouble génétique du rythme cardiaque Canal atrioventriculaire partiel Ventricule gauche à double issue Sténose subaortique en tunnel Tunnel aorto-ventriculaire droit Anomalie de naissance ou de trajet de l'artère coronaire Sténose ou atrésie ostiale coronaire Anomalie des auricules Communication interauriculaire type sinus coronaire Continuation azygos de la veine cave inférieure Flutter auriculaire idiopathique du nouveau-né Anomalie congénitale des veines pulmonaires Maladie de Naxos Cardiomyopathie dilatée familiale isolée Syndrome du QT long familial Syndrome de Carvajal Amylose ATTRV122I Sténose valvulaire pulmonaire congénitale Anomalie de position d'un ostium coronaire Anévrisme du septum interauriculaire Anomalie congénitale partielle du retour veineux pulmonaire Maladie rare en chirurgie cardiaque Sténose tricuspide congénitale Valve tricuspide en parachute Trouble familial progressif de la conduction cardiaque Tachycardie ventriculaire incessante du nouveau-né Cardiomyopathie hypertrophique non familiale Cardiomyopathie restrictive Sténose sous-pulmonaire Syndrome de Romano-Ward Transposition congénitalement non corrigée des gros vaisseaux avec malformation cardiaque Anévrisme du canal artériel Anomalie de nombre des ostia coronaires Communication interauriculaire type ostium primum Interruption de la veine cave inférieure sans continuation azygos Cardiomyopathie-surdité dues à une mutation de l'ADN mitochondrial Syndrome de Costello Prolapsus valvulaire tricuspide Straddling ou overriding de la valve tricuspide Insertion anormale congénitale des cordages de la tricuspide Maladie rythmique auriculaire familiale Syndrome cardiomélique type 2 Cardiomyopathie hypertrophique avec anomalies rénales dues à une mutation de l'ADN mitochondrial Cardiomyopathie rare Cardiomyopathie Tako-Tsubo Hypoplasie de l'anneau mitral Aorte encerclante Anévrisme du septum interventriculaire Abouchement de la veine cave supérieure gauche dans l'oreillette gauche par le sinus coronaire Abouchement de la veine cave supérieure droite dans l'oreillette gauche Fibrose endomyocardique tropicale Transposition des gros vaisseaux et anomalie conotroncale du coeur Cardiomyopathie arythmogène héréditaire isolée, variante gauche-dominante Maladie mitochondriale avec cardiomyopathie dilatée Transposition congénitalement corrigée des gros vaisseaux Sténose supravalvulaire pulmonaire Syndrome de Timothy Anomalie congénitale du retour veineux pulmonaire Syndrome d'agénésie de la valve pulmonaire-tétralogie de Fallot-absence du canal artériel Syndrome du QT court familial Rétrécissement mitral congénital Persistance du foramen ovale Anomalie congénitale totale du retour veineux pulmonaire Anomalie de position du coeur Syndrome de cardiomyopathie-hypotonie-acidose lactique Syndrome progéroïde cardio-cutané lié à LMNA Mésocardie Dysfonction sinusale et surdité Malformation d'Ebstein de la valve tricuspide Trouble familial rare avec cardiomyopathie hypertrophique Cardiomyopathie ventriculaire arythmogène héréditaire isolée, variante biventriculaire Cardiomyopathie hypertrophique mitochondriale avec acidose lactique par déficit en MTO1