Herzkind e.V. Assigned 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