SE-ATLAS

Mapping of Health Care Providers
for People with Rare Diseases


In the following you will find the diseases that this support group organisation focuses on:
ATTRV122I amyloidosis Abnormal number of coronary ostia Abnormal origin of right or left pulmonary artery from the aorta Abnormal origin of the pulmonary artery Abnormal origin or aberrant course of coronary artery Absence of innominate vein Absence of the pulmonary artery Accessory mitral valve tissue Accessory tricuspid valve tissue Agenesis of the superior vena cava Andersen-Tawil syndrome Aneurysm of sinus of Valsalva Aneurysm or dilatation of ascending aorta Anomaly of the mitral subvalvular apparatus Anomaly of the tricuspid subvalvular apparatus Aorta coarctation Aortic arch defects Aortic arch interruption Aortic malformation Aorto-left ventricular tunnel Aorto-right ventricular tunnel Aorto-ventricular tunnel Aortopulmonary coronary arterial course Arterial duct anomaly Ascending aorta anomaly Atrial appendage anomaly Atrial septal aneurysm Atrial septal defect, coronary sinus type Atrial septal defect, ostium primum type Atrial septal defect, ostium secundum type Atrial septal defect, sinus venosus type Atrial septal defect-atrioventricular conduction defects syndrome Atrial standstill Atrioventricular septal defect Atrioventricular valve anomaly Atypical coarctation of aorta Autosomal dominant coarctation of aorta Azygos continuation of the inferior vena cava Brachydactyly-long thumb syndrome Brugada syndrome Cardiac diverticulum Cardiofaciocutaneous syndrome Cardiomyopathy-cataract-hip spine disease syndrome Cardiomyopathy-hypotonia-lactic acidosis syndrome Carvajal syndrome Catecholaminergic polymorphic ventricular tachycardia Cervical aortic arch Cirrhotic cardiomyopathy Cleft mitral valve Combined oxidative phosphorylation defect type 17 Complete atrioventricular canal-left heart obstruction syndrome Complete atrioventricular septal defect Complete atrioventricular septal defect with ventricular hypoplasia Complete atrioventricular septal defect-tetralogy of Fallot Congenital Gerbode defect Congenital anomaly of hepatic vein Congenital anomaly of superior vena cava Congenital anomaly of the coronary sinus Congenital anomaly of the great arteries Congenital anomaly of the great veins Congenital anomaly of the inferior vena cava Congenital anomaly of the tricuspid valve chordae Congenital aortic valve atresia Congenital aortic valve dysplasia Congenital aortic valve insufficiency Congenital aortic valve stenosis Congenital aortopulmonary window Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome Congenital complete agenesis of pericardium Congenital coronary artery aneurysm Congenital heart block Congenital mitral malformation Congenital mitral stenosis Congenital mitral valve insufficiency and/or stenosis Congenital partial agenesis of pericardium Congenital partial pulmonary venous return anomaly Congenital patent ductus arteriosus aneurysm Congenital pericardium anomaly Congenital pulmonary valvar stenosis Congenital pulmonary veins anomaly Congenital pulmonary veins atresia or stenosis Congenital pulmonary venous return anomaly Congenital stenosis of the inferior vena cava Congenital supravalvular mitral ring Congenital systemic veins anomaly Congenital total pulmonary venous return anomaly Congenital tricuspid malformation Congenital tricuspid stenosis Congenital unguarded mitral orifice Congenital valvular dysplasia Congenitally corrected transposition of the great arteries Congenitally uncorrected transposition of the great arteries Congenitally uncorrected transposition of the great arteries with cardiac malformation Congenitally uncorrected transposition of the great arteries with coarctation Conotruncal heart malformations Cor triatriatum dexter Cor triatriatum sinister Coronary arterial fistula Coronary artery congenital malformation Coronary artery intramyocardial course Coronary ostial stenosis or atresia Coronary sinus atresia Coronary sinus stenosis Costello syndrome Criss-cross heart Dextrocardia Diabetic embryopathy Dilated cardiomyopathy Dilated cardiomyopathy with ataxia Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome Discrete fibromuscular subaortic stenosis Discrete fixed membranous subaortic stenosis Double outlet left ventricle Double outlet right ventricle Double outlet right ventricle with doubly committed ventricular septal defect Double outlet right ventricle with non-committed subpulmonary ventricular septal defect Double outlet right ventricle with subaortic or doubly committed ventricular septal defect with pulmonary stenosis Double outlet right ventricle with subaortic ventricular septal defect Double outlet right ventricle with subpulmonary ventricular septal defect Double-orifice mitral valve Dysphagia lusoria Ebstein malformation of the tricuspid valve Ectasia of the left atrial appendage Ectasia of the right atrial appendage Encircling double aortic arch Endocardial fibroelastosis Familial atrial fibrillation Familial bicuspid aortic valve Familial dilated cardiomyopathy Familial dilated cardiomyopathy with conduction defect due to LMNA mutation Familial idiopathic dilatation of the right atrium Familial isolated dilated cardiomyopathy Familial isolated restrictive cardiomyopathy Familial long QT syndrome Familial mitral valve prolapse Familial progressive cardiac conduction defect Familial restrictive cardiomyopathy Familial short QT syndrome Familial sick sinus syndrome Fatal infantile hypertrophic cardiomyopathy due to mitochondrial complex I deficiency Fixed subaortic stenosis Generalized congenital lipodystrophy with myopathy Genetic cardiac rhythm disease Glycogen storage disease due to LAMP-2 deficiency Glycogen storage disease due to muscle and heart glycogen synthase deficiency Glycogen storage disease with hypertrophic cardiomyopathy HEC syndrome Heart position anomaly Heart-hand syndrome type 2 Heart-hand syndrome type 3 Heart-hand syndrome, Slovenian type Heterotaxia His bundle tachycardia Histiocytoid cardiomyopathy Holt-Oram syndrome Hypertrophic cardiomyopathy due to intensive athletic training Hypertrophic cardiomyopathy with kidney anomalies due to mitochondrial DNA mutation Hypoplasia of the mitral valve annulus Hypoplastic left heart syndrome Hypoplastic right heart syndrome Idiopathic giant cell myocarditis Idiopathic neonatal atrial flutter Idiopathic pulmonary artery dilatation Idiopathic ventricular fibrillation, non Brugada type Incessant infant ventricular tachycardia Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency Inferior vena cava interruption without azygos continuation Inherited arrhythmogenic cardiomyopathy Inherited isolated arrhythmogenic cardiomyopathy Inherited isolated arrhythmogenic cardiomyopathy, dominant-left variant Inherited isolated arrhythmogenic cardiomyopathy, dominant-right variant Inherited isolated arrhythmogenic ventricular dysplasia, biventricular variant Interatrial communication Interventricular septum aneurysm Intramural coronary arterial course Isolated congenitally uncorrected transposition of the great arteries Isolated right ventricular hypoplasia Jervell and Lange-Nielsen syndrome Juxtaposition of the atrial appendages Kidney tubulopathy-dilated cardiomyopathy syndrome Kommerell diverticulum LMNA-related cardiocutaneous progeria syndrome Laubry-Pezzi syndrome Left ventricular noncompaction Levocardia Loeffler endocarditis Lown-Ganong-Levine syndrome Malposition of a coronary ostium Mesocardia Microcephaly-cardiomyopathy syndrome Mitochondrial DNA-related cardiomyopathy and hearing loss Mitochondrial disease with dilated cardiomyopathy Mitochondrial disease with hypertrophic cardiomyopathy Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency Mitral atresia Mitral valve agenesis Multifocal atrial tachycardia Naxos disease Neuhauser anomaly Non-familial dilated cardiomyopathy Non-familial hypertrophic cardiomyopathy Non-familial restrictive cardiomyopathy Non-genetic cardiac rhythm disease Noonan syndrome Noonan syndrome and Noonan-related syndrome Noonan syndrome with multiple lentigines Noonan syndrome-like disorder with juvenile myelomonocytic leukemia Noonan syndrome-like disorder with loose anagen hair Parachute tricuspid valve Partial atrioventricular septal defect Patent foramen ovale Peripheral pulmonary stenosis Persistent eustachian valve Persistent fifth aortic arch Persistent left superior vena cava connecting through coronary sinus to left-sided atrium Persistent left superior vena cava connecting to the roof of left-sided atrium Pleuro-pericardial cyst Premature closure of the arterial duct Progressive sensorineural hearing loss-hypertrophic cardiomyopathy syndrome Pulmonary artery coming from patent ductus arteriosus Pulmonary artery hypoplasia Pulmonary artery or pulmonary branch anomaly Pulmonary atresia with ventricular septal defect Pulmonary atresia-intact ventricular septum syndrome Pulmonary valve agenesis Pulmonary valve agenesis-intact ventricular septum-persistent ductus arteriosus syndrome Pulmonary valve agenesis-tetralogy of Fallot-absence of ductus arteriosus syndrome Rare atrial defect and interatrial communication Rare cardiac disease Rare cardiac rhythm disease Rare cardiomyopathy Rare congenital non-syndromic heart malformation Rare familial disorder with hypertrophic cardiomyopathy Rare hypertrophic cardiomyopathy Rare surgical cardiac disease Restrictive cardiomyopathy Right aortic arch Right inferior vena cava connecting to left-sided atrium Right sided atrial isomerism Right superior vena cava connecting to left-sided atrium Romano-Ward syndrome Scimitar syndrome Sensorineural deafness with dilated cardiomyopathy Shone complex Sino-auricular heart block Sinoatrial node dysfunction and deafness Situs ambiguus Situs inversus totalis Straddling and/or overriding mitral valve Straddling or overriding tricuspid valve Subaortic course of innominate vein Subpulmonary stenosis Supravalvular aortic stenosis Supravalvular pulmonary stenosis Syndrome associated with dilated cardiomyopathy Syndrome associated with hypertrophic cardiomyopathy Tako-Tsubo cardiomyopathy Tetralogy of Fallot Timothy syndrome Torsade-de-pointes syndrome with short coupling interval Transposition of the great arteries Transposition of the great arteries and conotruncal cardiac anomaly Triatrial heart Tricuspid atresia Tricuspid valve agenesis Tricuspid valve prolapse Tropical endomyocardial fibrosis Truncus arteriosus Tunnel subaortic stenosis Uhl anomaly Unclassified cardiomyopathy Univentricular cardiopathy Univentricular heart Univentricular heart with single atrio-ventricular valve Valvular pulmonary stenosis X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome