SE-ATLAS

HEC-Syndrom Aortenstenose, supravalvuläre Pulmonalarteriendilatation, idiopathische Trikuspider subvalvulärer Apparat, Anomalie des Perikardagenesie, kongenitale, komplette Herzrhythmusstörung, erworbene Venenanomalie, kongenitale sytemische Bikuspide Aortenklappe, familiäre Form Rechter Doppelausstromventrikel mit subaortalem oder double-committed Ventrikelseptumdefekt und Pulmonalstenose Mitralklappe mit akzessorischem Gewebe Mitralöffnung, unbedeckte, kongenitale Neuhauser-Anomalie Gerbode-Defekt, kongenitaler Fehlen der Kopf-Armvene Kongenitale Katarakt-hypertrophe Kardiomyopathie-mitochondriale Myopathie-Syndrom Torsade de pointes mit kurzem Kopplungsintervall Anomalien der Lungenarterie oder des Lungenarterienstammes Atrioventrikulären Klappe, Anomalie der Kardiomyopathie, dilatative Dilatative Kardiomyopathie mit Ataxie Kammerflimmern, idiopathisches (nicht Brugada-Typ) Mitochondriale Krankheit mit hypertropher Kardiomyopathie Laevokardie Trikuspidalklappe mit akzessorischem Gewebe Löffler-Endokarditis Herzklappendysplasie, kongenitale Aortenisthmusstenose, dominante Subaortenstenose, fixierte Familiäre idiopathische rechtsseitige Vorhofdilatation Supravalvulärer Mitralring, kongenitaler Kommerell-Divertikel Aortenbogen, fünfter persistierender Laubry-Pezzi-Syndrom Persistenz der linken Vena cava superior mit Verbindung zum dorsalen Bereich des linken Vorhofes Aortenfehlbildung Generalisierte kongenitale Lipodystrophie mit Muskeldystrophie Aortenbogen-Defekte Kongenitale unkorrigierte Transposition der großen Arterien mit Koarktation Aortenisthmusstenose, atypische Seltene hypertrophe Kardiomyopathie Aortenklappenstenose, kongenitale Fehlbildung der Koronararterien, kongenitale Aortenklappenatresie, kongenitale Vena cava superior, Agenesie der Zyste, pleuroperikardiale Herzfehler, konotrunkaler Heterotaxie Riesenzell-Myokarditis, idiopathische Rechter Doppelausstromventrikel mit non-committed subpulmonalem Ventrikelseptumdefekt Mitralklappenspalt Shone-Komplex Vena cava inferior, kongenitale Anomalie der Aorto-ventrikulärer Tunnel Kongenitale unkorrigierte Transposition der großen Arterien Atrioventrikulärer Septumdefekt Kardiomyopathie, histiozytoide Seltenes Syndrom mit assoziierter dilatativer Kardiomyopathie Großen Venen, kongenitale Anomalie der Mitralklappenprolaps, familiärer Aortenisthmusstenose Perikardagenesie, kongenitale, partielle Fehlen der Pulmonalarterie Aorto-pulmonale Fenster, kongenitales Rechter Doppelausstromventrikel mit subpulmonalem Ventrikelseptumdefekt Rechter Doppelausstromventrikel mit subaortalem Ventrikelseptumdefekt Mitralklappeninsuffizienz oder -stenose, kongenitale Mitralklappenagenesie Hereditäre arrhythmogene Kardiomyopathie Aortenbogen, zervikaler Vena cava superior, kongenitale Anomalie der Vena brachiocephalica, subaortaler Verlauf Truncus arteriosus communis Glykogenose durch muskulären Glykogensythasemangel Trikuspidalklappenfehlbildung, kongenitale Hypertrophe Kardiomyopathie durch intensives athletisches Training Kardiomyopathie, restriktive, familiäre Form Kardiomyopathie, restriktive, nicht-familiäre Form Multifokale atriale Tachykardie Herzrhythmusstörung Lown-Ganong-Levine-Syndrom Mitralklappenfehlbildung, kongenitale 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 Rare cardiac disease Combined oxidative phosphorylation defect type 17 Diabetic embryopathy Holt-Oram syndrome Kidney tubulopathy-dilated cardiomyopathy syndrome Inherited isolated arrhythmogenic cardiomyopathy, dominant-right variant Genetic cardiac rhythm disease Partial atrioventricular septal defect Double outlet left ventricle Tunnel subaortic stenosis Aorto-right ventricular tunnel Abnormal origin or aberrant course of coronary artery Coronary ostial stenosis or atresia Atrial appendage anomaly Atrial septal defect, coronary sinus type Azygos continuation of the inferior vena cava Idiopathic neonatal atrial flutter Congenital pulmonary veins anomaly Naxos disease Familial isolated dilated cardiomyopathy Familial long QT syndrome Carvajal syndrome ATTRV122I amyloidosis Congenital pulmonary valvar stenosis Malposition of a coronary ostium Atrial septal aneurysm Congenital partial pulmonary venous return anomaly Rare surgical cardiac disease Congenital tricuspid stenosis Parachute tricuspid valve Familial progressive cardiac conduction defect Incessant infant ventricular tachycardia Non-familial hypertrophic cardiomyopathy Restrictive cardiomyopathy Subpulmonary stenosis Romano-Ward syndrome Congenitally uncorrected transposition of the great arteries with cardiac malformation Congenital patent ductus arteriosus aneurysm Abnormal number of coronary ostia Atrial septal defect, ostium primum type Inferior vena cava interruption without azygos continuation Mitochondrial DNA-related cardiomyopathy and hearing loss Costello syndrome Tricuspid valve prolapse Straddling or overriding tricuspid valve Congenital anomaly of the tricuspid valve chordae Familial sick sinus syndrome Heart-hand syndrome type 2 Hypertrophic cardiomyopathy with kidney anomalies due to mitochondrial DNA mutation Rare cardiomyopathy Tako-Tsubo cardiomyopathy Hypoplasia of the mitral valve annulus Encircling double aortic arch Interventricular septum aneurysm Persistent left superior vena cava connecting through coronary sinus to left-sided atrium Right superior vena cava connecting to left-sided atrium Tropical endomyocardial fibrosis Transposition of the great arteries and conotruncal cardiac anomaly Inherited isolated arrhythmogenic cardiomyopathy, dominant-left variant Mitochondrial disease with dilated cardiomyopathy Congenitally corrected transposition of the great arteries Supravalvular pulmonary stenosis Timothy syndrome Congenital pulmonary venous return anomaly Pulmonary valve agenesis-tetralogy of Fallot-absence of ductus arteriosus syndrome Familial short QT syndrome Congenital mitral stenosis Patent foramen ovale Congenital total pulmonary venous return anomaly Heart position anomaly Cardiomyopathy-hypotonia-lactic acidosis syndrome LMNA-related cardiocutaneous progeria syndrome Mesocardia Sinoatrial node dysfunction and deafness Ebstein malformation of the tricuspid valve Rare familial disorder with hypertrophic cardiomyopathy Inherited isolated arrhythmogenic ventricular dysplasia, biventricular variant Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency