SE-ATLAS

Familial atrial tachyarrhythmia-infra-Hisian cardiac conduction disease Cardiogenic shock Congenital aortic valve stenosis Jervell and Lange-Nielsen syndrome Aneurysm of sinus of Valsalva Primary pulmonary vein stenosis Congenital left ventricular aneurysm Familial restrictive cardiomyopathy Anomaly of the mitral subvalvular apparatus Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome Congenital contractural arachnodactyly Congenital pulmonary valvar stenosis Congenitally corrected transposition of the great arteries Subpulmonary stenosis Loeys-Dietz syndrome Brugada syndrome Dextrocardia Isolated pulmonary artery sling Noonan syndrome Congenital heart block CHARGE syndrome Idiopathic pulmonary artery dilatation Familial idiopathic dilatation of the right atrium Cardiac diverticulum Idiopathic giant cell myocarditis Romano-Ward syndrome Familial isolated dilated cardiomyopathy Mesocardia His bundle tachycardia Congenital aortic valve atresia Partial atrioventricular septal defect with ventricular hypoplasia Double outlet right ventricle with subaortic or doubly committed ventricular septal defect with pulmonary stenosis Straddling or overriding tricuspid valve Sinoatrial node dysfunction and deafness Tetralogy of Fallot Double outlet right ventricle with non-committed subpulmonary ventricular septal defect Pulmonary artery coming from patent ductus arteriosus Congenital mitral valve insufficiency and/or stenosis Pulmonary valve agenesis-intact ventricular septum-persistent ductus arteriosus syndrome Abnormal origin of right or left pulmonary artery from the aorta Discrete fibromuscular subaortic stenosis Congenital mitral stenosis Hypoplasia of the mitral valve annulus Accessory mitral valve tissue Pseudoxanthoma elasticum Mitral valve agenesis Intermediate atrioventricular septal defect Aortic arch interruption Aorto-left ventricular tunnel Aorto-right ventricular tunnel Familial long QT syndrome Encircling double aortic arch Timothy syndrome Persistent fifth aortic arch Anomalous aortic origin of the right coronary artery Right aortic arch Ectopia cordis EPHB4-related lymphatic-related hydrops fetalis Congenital anomaly of the inferior vena cava Pulmonary artery hypoplasia Double outlet right ventricle with subaortic or doubly committed ventricular septal defect Dysphagia lusoria Anomalous aortic origin of the left coronary artery Right sided atrial isomerism Peripheral pulmonary stenosis Coronary ostial stenosis or atresia Abnormal number of coronary ostia Interventricular septum aneurysm Congenital Gerbode defect Cor triatriatum sinister Glycogen storage disease due to LAMP-2 deficiency Sarcoidosis Atrial septal defect, ostium secundum type Atrial septal defect, coronary sinus type Atrial septal defect, ostium primum type Persistent left superior vena cava connecting to the roof of left-sided atrium Right superior vena cava connecting to left-sided atrium Marfan syndrome type 2 Tropical endomyocardial fibrosis Familial patent arterial duct Right inferior vena cava connecting to left-sided atrium Loeffler endocarditis Coronary sinus atresia Persistent eustachian valve Inferior vena cava interruption without azygos continuation Congenital stenosis of the inferior vena cava Rare lymphatic system anomaly Neonatal Marfan syndrome Congenital complete agenesis of pericardium Truncus arteriosus Congenital partial agenesis of pericardium X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome X-linked severe syndromic thoracic aortic aneurysm and dissection Aorto-ventricular tunnel Uhl anomaly Familial atrial fibrillation Ebstein malformation of the tricuspid valve Isolated ectopia lentis Heart-hand syndrome, Slovenian type Extracranial carotid artery aneurysm Quadricuspid aortic valve Double outlet left ventricle Down syndrome Familial progressive cardiac conduction defect Primary superior vena cava aneurysm Brachydactyly-long thumb syndrome Diabetic embryopathy Familial sick sinus syndrome Familial short QT syndrome Torsade-de-pointes syndrome with short coupling interval Shprintzen-Goldberg syndrome Familial isolated restrictive cardiomyopathy Congenital pulmonary venous return anomaly Inherited isolated arrhythmogenic cardiomyopathy, dominant-right variant Congenitally uncorrected transposition of the great arteries with cardiac malformation Progressive sensorineural hearing loss-hypertrophic cardiomyopathy syndrome Congenital anomaly of the great veins Andersen-Tawil syndrome Congenital aortic valve dysplasia Tricuspid atresia Cutis laxa-Marfanoid syndrome Situs inversus totalis Hypoplastic left heart syndrome Familial dilated cardiomyopathy with conduction defect due to LMNA mutation Multifocal atrial tachycardia Catecholaminergic polymorphic ventricular tachycardia Tricuspid valve agenesis Congenital tricuspid stenosis Partial atrioventricular septal defect without ventricular hypoplasia Congenitally uncorrected transposition of the great arteries with coarctation Double outlet right ventricle with subpulmonary ventricular septal defect Familial mitral valve prolapse Cleft mitral valve Discrete fixed membranous subaortic stenosis Complete atrioventricular septal defect without ventricular hypoplasia Tunnel subaortic stenosis Valvular pulmonary stenosis Congenital supravalvular mitral ring Double-orifice mitral valve Congenital unguarded mitral orifice Shone complex Straddling and/or overriding mitral valve Familial thoracic aortic aneurysm and aortic dissection Complete atrioventricular septal defect with ventricular hypoplasia Premature closure of the arterial duct Congenital patent ductus arteriosus aneurysm Congenital coronary artery aneurysm Kommerell diverticulum Cervical aortic arch Neuhauser anomaly Congenital anomaly of superior vena cava Cor triatriatum dexter Congenital pericardium anomaly Atrial septal defect, sinus venosus type Atrial septal aneurysm Persistent left superior vena cava connecting through coronary sinus to left-sided atrium Marfan syndrome type 1 Subaortic course of innominate vein Absence of innominate vein Agenesis of the superior vena cava Coronary sinus stenosis Anomalous aortic origin of coronary artery Idiopathic ventricular fibrillation, non Brugada type Azygos continuation of the inferior vena cava Complete atrioventricular septal defect Partial atrioventricular septal defect Congenital total pulmonary venous return anomaly Congenital partial pulmonary venous return anomaly Pleuro-pericardial cyst Aneurysm-osteoarthritis syndrome Heart-hand syndrome type 3 Atrial standstill Fabry disease Heart-hand syndrome type 2 Anomalous origin of coronary artery from the pulmonary artery Pulmonary valve agenesis-tetralogy of Fallot-absence of ductus arteriosus syndrome Congenitally uncorrected transposition of the great arteries Patent ductus arteriosus-bicuspid aortic valve-hand anomalies syndrome Congenital tricuspid valve dysplasia Infective endocarditis Holt-Oram syndrome Idiopathic neonatal atrial flutter Incessant infant ventricular tachycardia Primary inferior vena cava aneurysm Congenital mitral malformation Transposition of the great arteries and conotruncal cardiac anomaly Cardiac anomalies-heterotaxy syndrome Pulmonary artery or pulmonary branch anomaly Mid-Aortic-Syndrom Aortenisthmusstenose Criss-Cross-Herz Rechtsventrikuläre Hypoplasie, isolierte Form Triatriales Herz Herz, univentrikuläres Ehlers-Danlos-Syndrom, kardio-valvulärer Typ AL-Amyloidose AA-Amyloidose Interatriale Kommunikation Atriumseptumdefekt mit atrio-ventrikulären Reizleitungsstörungen Kardiomyopathie, histiozytoide Gaucher-Krankheit Typ 1 Fehlen der Pulmonalarterie Fibroelastose, endokardiale Alagille-Syndrom durch JAG1-Gen-Punktmutationen Linksventrikuläre Noncompaction-Kardiomyopathie Aorto-pulmonale Fenster, kongenitales Koronarfistel Kardiomyopathie, hypertrophe, nicht-familiäre Form Alagille-Syndrom durch NOTCH2-Gen-Punktmutationen Hereditäre isolierte arrhythmogene Kardiomyopathie, linksdominante Form Williams-Syndrom Linksisomerie Syndrom der chronischen atrialen und intestinalen Rhythmusstörung Lebervene, kongenitale Anomalie der Fehlstellung eines Koronarostiums Portosystemischer Shunt, kongenitaler Kardiomyopathie, dilatative, familiäre Form Kardiomyopathie, dilatative, nicht-familiäre Form Marfan-Syndrom Subaortenstenose, fixierte Alagille-Syndrom HEC-Syndrom Kardiomyopathie, nicht klassifizierte Desminopathie Hereditäre isolierte arrhythmogene Kardiomyopathie, biventrikuläre Form Seltene kombinierte vaskuläre Fehlbildung Transposition der großen Arterien Postkardiotomie-Syndrom mit rechtsventrikulären Versagen Trikuspidalklappe mit akzessorischem Gewebe Kompletter atrioventrikulärer Septumdefekt mit Fallot-Tetralogie Pulmonalvenenatresie, kongenitale Gliedergürtelmuskeldystrophie, autosomal-rezessive, Typ 2X Intelligenzminderung-Herzrhythmusstörung-Syndrom durch GNB5-Mangel Subaortenstenose-Kleinwuchs-Syndrom Aortenstenose, supravalvuläre Mitralatresie Pulmonalatresie mit intaktem Ventrikelseptum Rechter Doppelausstromventrikel mit atrioventrikulärem Septumdefekt, Pulmonalstenose und Heterotaxie Herztumor, primärer, des Kindes Alagille-Syndrom durch Mikrodeletion 20p12 Pulmonalstenose, supravalvuläre Kardiomyopathie, restriktive, nicht-familiäre Form Isolierte kongenitale unkorrigierte Transposition der großen Arterien Bikuspide Aortenklappe, familiäre Form Pulmonalatresie mit Ventrikelseptumdefekt Scimitar-Syndrom