SE-ATLAS

Kongenitale unkorrigierte Transposition der großen Arterien mit Koarktation Supravalvulärer Mitralring, kongenitaler Aortenbogen, fünfter persistierender Infantile hypertrophe Kardiomyopathie durch MRPL44-Mangel Aortenfehlbildung Lungenvenenfehlmündung, kongenitale Laevokardie Pulmonalstenose, supravalvuläre Familiäre dilatative Kardiomyopathie mit Reizleitungs-Defekt durch LMNA-Genmutation Trikuspidalklappe mit akzessorischem Gewebe SVC, rechte, verbunden mit dem linken Vorhof Löffler-Endokarditis Glykogenose durch muskulären Glykogensythasemangel Hypertrophe Kardiomyopathie durch intensives athletisches Training Kardiomyopathie, restriktive, nicht-familiäre Form Mitralklappenanulus, Hypoplasie des- Aortenbogen, doppelter, mit zirkuläre Einengung von Trachea/Ösophagus Septumaneurysma, interventrikuläres Transposition der großen Gefäße - konotrunkale Herzanomalie Hypertrophe Kardiomyopathie - Muskelhypotonie - Laktatazidose Kardiomyopathie, restriktive, familiäre Form HEC-Syndrom Mesokardie Trikuspidalklappe, gespreizte und/oder reitende Ebstein-Anomalie der Trikuspidalklappe Aortenstenose, supravalvuläre Pulmonalarteriendilatation, idiopathische Endomyokardfibrose, tropische Pulmonalklappenagenesie-Fallot-Tetralogie-fehlender Ductus arteriosus-Syndrom Kongenitale Katarakt-hypertrophe Kardiomyopathie-mitochondriale Myopathie-Syndrom Short-QT-Syndrom, familiäres Hereditäre isolierte arrhythmogene Kardiomyopathie, biventrikuläre Form Venenanomalie, kongenitale sytemische Persistenz der linken Vena cava superior mit Mündung in den linken Vorhof über den Koronarsinus Sick-Sinus-Syndrom, familiäres Tako-Tsubo-Kardiomyopathie Noonan-Syndrom mit multiplen Lentigines Dilatative Kardiomyopathie mit Ataxie Herzklappendysplasie, kongenitale Aortenisthmusstenose, dominante Mitralklappeninsuffizienz oder -stenose, kongenitale Mitralklappe mit akzessorischem Gewebe Neuhauser-Anomalie Vena cava superior, kongenitale Anomalie der Gerbode-Defekt, kongenitaler Fehlen der Kopf-Armvene Perikardagenesie, kongenitale, komplette Atrioventrikulären Klappe, Anomalie der Subaortenstenose, fixierte Familiäre idiopathische rechtsseitige Vorhofdilatation Kongenitale unkorrigierte Transposition der großen Arterien mit Herzfehlbildung Bikuspide Aortenklappe, familiäre Form Rechter Doppelausstromventrikel mit subaortalem oder double-committed Ventrikelseptumdefekt und Pulmonalstenose Rechter Doppelausstromventrikel mit subaortalem Ventrikelseptumdefekt Torsade de pointes mit kurzem Kopplungsintervall Fehlbildung der Koronararterien, kongenitale Aortenbogen-Defekte Aortenisthmusstenose, atypische Heterotaxie Aortenklappenstenose, kongenitale Trikuspider subvalvulärer Apparat, Anomalie des Persistenz der linken Vena cava superior mit Verbindung zum dorsalen Bereich des linken Vorhofes Herzfehler, konotrunkaler Kardiomyopathie, histiozytoide Noonan-ähnliches Syndrom mit losem Anagenhaar Mitralöffnung, unbedeckte, kongenitale Kommerell-Divertikel Laubry-Pezzi-Syndrom Aorto-ventrikulärer Tunnel Anomalien der Lungenarterie oder des Lungenarterienstammes Glykogen-Speicherkrankheit mit hypertropher Kardiomyopathie Mitralklappenprolaps, familiärer Kongenitale unkorrigierte Transposition der großen Arterien Aortenisthmusstenose Aortenklappeninsuffizienz, kongenitale Double outlet right ventricle with non-committed subpulmonary ventricular septal defect Shone complex Agenesis of the superior vena cava Pleuro-pericardial cyst Atrioventricular septal defect Absence of the pulmonary artery Congenital aortopulmonary window Inherited isolated arrhythmogenic cardiomyopathy, dominant-right variant Sensorineural deafness with dilated cardiomyopathy Inherited arrhythmogenic cardiomyopathy Univentricular cardiopathy Congenital anomaly of the coronary sinus Truncus arteriosus X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome Inherited isolated arrhythmogenic cardiomyopathy Multifocal atrial tachycardia Lown-Ganong-Levine syndrome Congenital mitral malformation Microcephaly-cardiomyopathy syndrome Congenital aortic valve atresia Subaortic course of innominate vein Congenital partial agenesis of pericardium Congenital tricuspid malformation Double outlet right ventricle with subpulmonary ventricular septal defect Cleft mitral valve Mitral valve agenesis Arterial duct anomaly Cervical aortic arch Congenital anomaly of the inferior vena cava Right sided atrial isomerism His bundle tachycardia Idiopathic ventricular fibrillation, non Brugada type Familial atrial fibrillation Mitochondrial disease with hypertrophic cardiomyopathy Left ventricular noncompaction Dilated cardiomyopathy Pulmonary valve agenesis-intact ventricular septum-persistent ductus arteriosus syndrome Dysphagia lusoria Cor triatriatum sinister Coronary sinus stenosis Cardiofaciocutaneous syndrome Uhl anomaly Congenital anomaly of the great arteries Pulmonary valve agenesis Endocardial fibroelastosis Isolated congenitally uncorrected transposition of the great arteries Congenital aortic valve dysplasia Generalized congenital lipodystrophy with myopathy Brugada syndrome Andersen-Tawil syndrome Rare hypertrophic cardiomyopathy Double outlet right ventricle with doubly committed ventricular septal defect Straddling and/or overriding mitral valve Right aortic arch Cor triatriatum dexter Non-genetic cardiac rhythm disease Hypoplastic right heart syndrome Mitral atresia Aneurysm or dilatation of ascending aorta Inherited isolated arrhythmogenic cardiomyopathy, dominant-left variant Anomaly of the mitral subvalvular apparatus Ectasia of the left atrial appendage Right inferior vena cava connecting to left-sided atrium Heart-hand syndrome type 3 Criss-cross heart Interatrial communication Coronary arterial fistula Dextrocardia Sinoatrial node dysfunction and deafness Abnormal origin of right or left pulmonary artery from the aorta Complete atrioventricular septal defect with ventricular hypoplasia Coronary artery intramyocardial course Peripheral pulmonary stenosis Glycogen storage disease due to LAMP-2 deficiency Rare atrial defect and interatrial communication Abnormal origin of the pulmonary artery Congenital heart block Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome Catecholaminergic polymorphic ventricular tachycardia Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency Hypertrophic cardiomyopathy with kidney anomalies due to mitochondrial DNA mutation Isolated right ventricular hypoplasia Premature closure of the arterial duct Atrial septal defect-atrioventricular conduction defects syndrome Familial isolated restrictive cardiomyopathy Unclassified cardiomyopathy Pulmonary atresia with ventricular septal defect Pulmonary artery coming from patent ductus arteriosus Complete atrioventricular canal-left heart obstruction syndrome Pulmonary artery hypoplasia Ectasia of the right atrial appendage Juxtaposition of the atrial appendages Coronary sinus atresia Rare congenital non-syndromic heart malformation Ascending aorta anomaly Aneurysm of sinus of Valsalva Situs ambiguus Brachydactyly-long thumb syndrome Triatrial heart Genetic cardiac rhythm disease Coronary ostial stenosis or atresia Atrial septal defect, coronary sinus type Azygos continuation of the inferior vena cava Congenital pulmonary veins anomaly Jervell and Lange-Nielsen syndrome Pulmonary atresia-intact ventricular septum syndrome Hypoplastic left heart syndrome Tunnel subaortic stenosis Aortic arch interruption Aorto-right ventricular tunnel Atrial standstill Heart-hand syndrome, Slovenian type Scimitar syndrome Combined oxidative phosphorylation defect type 17 Univentricular heart Familial dilated cardiomyopathy Cardiac diverticulum Sino-auricular heart block Fatal infantile hypertrophic cardiomyopathy due to mitochondrial complex I deficiency Atrial septal defect, ostium secundum type Persistent eustachian valve Discrete fixed membranous subaortic stenosis Discrete fibromuscular subaortic stenosis Univentricular heart with single atrio-ventricular valve Complete atrioventricular septal defect-tetralogy of Fallot Aortopulmonary coronary arterial course Cardiomyopathy-cataract-hip spine disease syndrome Cirrhotic cardiomyopathy Congenitally corrected transposition of the great arteries Congenital anomaly of the great veins Tricuspid atresia Situs inversus totalis Congenital pericardium anomaly Tricuspid valve agenesis Congenital anomaly of the tricuspid valve chordae Double-orifice mitral valve Congenital patent ductus arteriosus aneurysm Congenital coronary artery aneurysm Abnormal number of coronary ostia Atrial septal defect, ostium primum type Complete atrioventricular septal defect Inferior vena cava interruption without azygos continuation Double outlet right ventricle Idiopathic neonatal atrial flutter Naxos disease Restrictive cardiomyopathy Diabetic embryopathy Holt-Oram syndrome Non-familial hypertrophic cardiomyopathy Congenital pulmonary veins atresia or stenosis Noonan syndrome Idiopathic giant cell myocarditis Partial atrioventricular septal defect Double outlet left ventricle Rare cardiomyopathy Kidney tubulopathy-dilated cardiomyopathy syndrome Rare cardiac disease Sténose valvulaire pulmonaire Tunnel aorto-ventriculaire gauche Coronaire intramurale Anomalies des veines sus-hépatiques Communication interauriculaire type sinus venosus Sténose congénitale de la veine cave inférieure Tachycardie ventriculaire incessante du nouveau-né Syndrome Noonan-like avec leucémie myélomonocytaire juvénile Cardiomyopathie dilatée familiale isolée Sténose valvulaire pulmonaire congénitale Syndrome du QT long familial Persistance du foramen ovale Anomalie de position du coeur Syndrome de Noonan et syndrome associé Transposition des gros vaisseaux Sténose tricuspide congénitale Rétrécissement mitral congénital Trouble familial progressif de la conduction cardiaque Trouble familial rare avec cardiomyopathie hypertrophique Maladie mitochondriale avec cardiomyopathie dilatée Syndrome progéroïde cardio-cutané lié à LMNA Sténose sous-pulmonaire Syndrome de Timothy Anévrisme du septum interauriculaire Anomalie congénitale totale du retour veineux pulmonaire Anomalie congénitale partielle du retour veineux pulmonaire Maladie rare en chirurgie cardiaque Prolapsus valvulaire tricuspide Valve tricuspide en parachute Anomalie de position d'un ostium coronaire Cardiomyopathie-surdité dues à une mutation de l'ADN mitochondrial Syndrome de Costello Cardiomyopathie dilatée non familiale Syndrome de Romano-Ward Syndrome de surdité neurosensorielle progressive-cardiomyopathie hypertrophique Syndrome de Carvajal Anomalie de naissance ou de trajet de l'artère coronaire Anomalie des auricules Amylose ATTRV122I Syndrome cardiomélique type 2 Syndrome associé à une cardiomyopathie hypertrophique Syndrome associé à une cardiomyopathie dilatée Tétralogie de Fallot Trouble rare du rythme cardiaque