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 Kardio-fazio-kutanes Syndrom Hypoplastische Rechtsherzsyndrom Pulmonalklappenagenesie Kardiomyopathie, dilatative, familiäre Form Brugada-Syndrom Linksventrikuläre Noncompaction-Kardiomyopathie Kompletter atrioventrikulärer Kanal mit Ventrikelhypoplasie Periphere Pulmonalstenose Ektasie des rechten Vorhofohres Herzblock, kongenitaler Mitralatresie Pulmonalarterie, der Aorta entstammend Glykogenose durch LAMP-2-Mangel Herzfehlbildung, seltene, kongenitale, nicht-syndromale Andersen-Tawil-Syndrom Infantile hypertrophe Kardiomyopathie durch MRPL44-Mangel Criss-Cross-Herz Interatriale Kommunikation Pulmonalarterienhypoplasie Juxtaposition der Vorhofohren Koronarsinusstenose Koronarsinusatresie Herz-Hand-Syndrom Typ 3 Glykogen-Speicherkrankheit mit hypertropher Kardiomyopathie Koronarfistel Dextrokardie Kardiomyopathie, dilatative - hypergonadotroper Hypogonadismus Familiäre dilatative Kardiomyopathie mit Reizleitungs-Defekt durch LMNA-Genmutation Pulmonalarterie, dem offenem Ductus arteriosus entstammend Kompletter atrioventrikulärer Kanal - Linksherzobstruktion Aorta ascendens, Anomalie der Sensorineurale Schwerhörigkeit mit dilatativer Kardiomyopathie Hereditäre isolierte arrhythmogene Kardiomyopathie Pulmonalarterie, abnormaler Ursprung Isolierte kongenitale unkorrigierte Transposition der großen Arterien Aortenklappendysplasie, kongenitale Tachykardie, katecholaminerge polymorphe ventrikuläre Fallot-Tetralogie Ductus arteriosus, vorzeitiger Verschluss des Rechtsatriale Isomerie Rechtsventrikuläre Hypoplasie, isolierte Form Atriumseptumdefekt mit atrio-ventrikulären Reizleitungsstörungen Subaortenstenose, diskrete fibromuskuläre Kardiomyopathie, restriktive, familiäre isolierte Progressiver sensorineuraler Hörverlust - hypertrophe Kardiomyopathie Brachydaktylie mit langem Daumen Seltenes Syndrom mit assoziierter hypertropher Kardiomyopathie Kardiomyopathie, dilatative, nicht-familiäre Form Sinus-Valsalva-Aneurysma, kongenitales Situs ambiguus Pulmonalatresie mit Ventrikelseptumdefekt Triatriales Herz Jervell-Lange-Nielsen-Syndrom Transposition der großen Arterien Univentrikuläres Herz mit singulärer atrio-ventrikulärer Klappe Kompletter atrioventrikulärer Septumdefekt mit Fallot-Tetralogie Koronararterien, aberranter Verlauf, aortopulmonal Atriumseptumdefekt, Sekundum-Typ Eustachische Klappe, persistierende Vorhofstillstand Pulmonalatresie mit intaktem Ventrikelseptum Scimitar-Syndrom Situs inversus totalis Hypoplastisches Linksherzsyndrom Subaortenstenose, diskrete fixierte membranöse Aortenbogenunterbrechung Seltener Vorhofdefekt und interatriale Kommunikation Kardiomyopathie, zirrhotische Herz, univentrikuläres Mitralklappe, Anomalie der subvalvulären Strukturen Hypertrophe Kardiomyopathie, fatale infantile, durch Komplex I-Defekt der mitochondriale Atmungskette Kardiomyopathie, nicht klassifizierte Herzdivertikel Trikuspidalatresie Koronararterien, aberranter Verlauf, intramyokardial Ektasie des linken Vorhofohres IVC, rechte, verbunden mit dem linken Vorhof Kardiomyopathie-Katarakt-Hüftwirbelsäulenerkrankung-Syndrom Herzblock, sinuaurikulärer Perikardfehlbildungen, kongenitale X-chromosomale Intelligenzminderung-Kardiomegalie-kongestive Herzinsuffizienz-Syndrom Trikuspidalklappen-Agenesie Valvuläre Pulmonalstenose Double-orifice-Mitralklappe Aorto-linksventrikulärer Tunnel Koronararterienaneurysma, kongenitales Koronararterien, aberranter Verlauf, intramural Atriumseptumdefekt, Sinus venosus Typ Atrioventrikulärer Septumdefekt, kompletter IVC-Stenose, kongenitale Doppelausstromventrikel, rechter Pulmonalvenenatresie oder -stenose, kongenital Herzkrankheit, seltene Kombinierter Defekt der oxidativen Phosphorylierung Typ 17 Diabetes-Embryopathie Holt-Oram-Syndrom Syndrom der Nierentubulopathie mit dilatierter Kardiomyopathie Hereditäre isolierte arrhythmogene Kardiomyopathie, rechtsdominante Form Herzrythmusstörung, genetisch bedingte Atrioventrikulärer Septumdefekt, partieller Doppelausstromventrikel, linker Subaortenstenose vom Tunneltyp Aorto-rechtsventrikulärer Tunnel Abnormaler Ursprung oder aberrante Verlauf der Koronararterie Koronarostium, Stenose oder Atresie, kongenitale Herzohranomalie Atriumseptumdefekt, Koronarsinus Typ Azygoskontinuität der Vena cava inferior Vorhofflattern, idiopathisches neonatales Pulmonalvenenanomalie, kongenitale 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