Cardiogenetic disease

Part of

Sub-types of Cardiogenetic disease

• Familial cardiomyopathy 2 trials · 217 incl. sub-types
  9 sub-types

  • Familial hypertrophic cardiomyopathy 2 trials · 85 incl. sub-types Sub-types →
  • Familial restrictive cardiomyopathy 0 trials · 62 incl. sub-types Sub-types →
  • Familial dilated cardiomyopathy 7 trials · 60 incl. sub-types Sub-types →
  • Familial isolated arrhythmogenic right ventricular dysplasia 0 trials · 10 incl. sub-types Sub-types →
  • PRKAG2-related cardiomyopathy 2 trials · 4 incl. sub-types Sub-types →
  • Left ventricular noncompaction 3 trials · 4 incl. sub-types Sub-types →
  • NKX2.5-related congenital, conduction and myopathic heart disease 0 trials
  • Naxos disease 0 trials
  • Fatal infantile encephalocardiomyopathy 0 trials Sub-types →
• Atrial septal defect 45 trials · 78 incl. sub-types
  15 sub-types

  • Patent foramen ovale 36 trials
  • Atrial septal defect, ostium secundum type 8 trials
  • Atrial septal defect 2 1 trial
  • Lutembacher syndrome 0 trials
  • Atrial septal defect 1 0 trials
  • Atrial septal defect 3 0 trials
  • Atrial septal defect 4 0 trials
  • Atrial septal defect 5 0 trials
  • Atrial septal defect 6 0 trials
  • Atrial septal defect 7 0 trials
  • Atrial septal defect 8 0 trials
  • Atrial septal defect 9 0 trials
  • Atrial septal defect, coronary sinus type 0 trials
  • Atrial septal defect, ostium primum type 0 trials
  • Atrial septal defect, sinus venosus type 0 trials
• Postural orthostatic tachycardia syndrome 71 trials
• Cardiogenetic rhythm disorder 2 trials · 67 incl. sub-types
  9 sub-types

  • SCN5A-related cardiac rhythm disorder 0 trials · 47 incl. sub-types Sub-types →
  • Paroxysmal familial ventricular fibrillation 2 trials · 27 incl. sub-types Sub-types →
  • Progressive familial heart block 0 trials · 19 incl. sub-types Sub-types →
  • Ventricular tachycardia, familial 1 trial · 11 incl. sub-types Sub-types →
  • Brugada syndrome 10 trials Sub-types →
  • Familial atrial fibrillation 0 trials · 1 incl. sub-types Sub-types →
  • Short QT syndrome 1 trial Sub-types →
  • Atrial conduction disease 0 trials
  • Familial sick sinus syndrome 0 trials Sub-types →
• Ventricular arrhythmias due to cardiac ryanodine receptor calcium release deficiency syndrome 53 trials
• Tetralogy of fallot 33 trials
• Patent ductus arteriosus 28 trials
  4 sub-types

  • Char syndrome 0 trials
  • PDA1 0 trials
  • Patent ductus arteriosus 2 0 trials
  • Patent ductus arteriosus 3 0 trials
• Ventricular septal defect 24 trials · 26 incl. sub-types
  5 sub-types

  • Double outlet right ventricle 2 trials · 3 incl. sub-types Sub-types →
  • Anterior deviation infundibular septum 0 trials
  • Ventricular septal defect 1 0 trials
  • Ventricular septal defect 2 0 trials
  • Ventricular septal defect 3 0 trials
• Familial bicuspid aortic valve 6 trials · 21 incl. sub-types
  3 sub-types

  • Aortic valve disease 1 16 trials
  • Aortic valve disease 2 12 trials
  • Aortic valve disease 3 0 trials
• NOTCH1-related AOS spectrum disorder 0 trials · 16 incl. sub-types
  2 sub-types

  • Aortic valve disease 1 16 trials
  • Adams-Oliver syndrome 5 0 trials
• Alagille syndrome 15 trials
  3 sub-types

  • Alagille syndrome due to 20p12 microdeletion 0 trials
  • Alagille syndrome due to a JAG1 point mutation 0 trials
  • Alagille syndrome due to a NOTCH2 point mutation 0 trials
• DiGeorge syndrome 11 trials
• Hypoplastic left heart syndrome 9 trials
  2 sub-types

  • Hypoplastic left heart syndrome 1 0 trials
  • Hypoplastic left heart syndrome 2 0 trials
• CHARGE syndrome 4 trials
  1 sub-type

  • CHD7-related CHARGE syndrome 0 trials
• Velocardiofacial syndrome 4 trials
• Supravalvular aortic stenosis 3 trials
• Dextro-looped transposition of the great arteries 2 trials
  4 sub-types

  • Congenital heart defects, multiple types, 6 0 trials
  • Congenitally uncorrected transposition of the great arteries with cardiac malformation 0 trials
  • Congenitally uncorrected transposition of the great arteries with coarctation 0 trials
  • Isolated congenitally uncorrected transposition of the great arteries 0 trials
• Ellis-van Creveld syndrome 1 trial
  1 sub-type

  • Jeune syndrome situs inversus 0 trials
• Coronary artery disease, autosomal dominant, 1 1 trial
• Dextrocardia 1 trial
• Inherited mitral valve disease 0 trials · 1 incl. sub-types
  2 sub-types

  • Familial mitral valve prolapse 0 trials · 1 incl. sub-types Sub-types →
  • Congenital mitral stenosis 0 trials
• Structural congenital heart disease, multiple types - GATA4 0 trials · 1 incl. sub-types
  3 sub-types

  • Atrial septal defect 2 1 trial
  • Atrioventricular septal defect 4 0 trials
  • Ventricular septal defect 1 0 trials
• 8q24.3 microdeletion syndrome 0 trials
• ACTC1-related distal arthrogryposis with congenital heart disease 0 trials
• ACTN2-related cardiac and skeletal myopathy 0 trials
  3 sub-types

  • Dilated cardiomyopathy 1AA 0 trials
  • Myopathy, congenital, with structured cores and z-line abnormalities 0 trials
  • Myopathy, distal, 6, adult-onset, autosomal dominant 0 trials
• CHIME syndrome 0 trials
• COG1-congenital disorder of glycosylation 0 trials
• Ehlers-Danlos syndrome, cardiac valvular type 0 trials
• Ehlers-Danlos syndrome, musculocontractural type 0 trials
  2 sub-types

  • Ehlers-Danlos syndrome, musculocontractural type 1 0 trials
  • Ehlers-Danlos syndrome, musculocontractural type 2 0 trials
• GATA6-related congenital heart disease with or without pancreatic agenesis or neonatal diabetes 0 trials
  2 sub-types

  • Atrial septal defect 9 0 trials
  • Atrioventricular septal defect 5 0 trials
• HAND1 related congenital heart defect 0 trials
• HAND2 related congenital heart defect 0 trials
• Holt-Oram syndrome 0 trials
  1 sub-type

  • Heart-hand syndrome type 3 0 trials
• Hordnes Engebretsen Knudtson syndrome 0 trials
• LMNA-related cardiocutaneous progeria syndrome 0 trials
• Larsen-like syndrome, B3GAT3 type 0 trials
• MGAT2-congenital disorder of glycosylation 0 trials
• MYH-6 related congenital heart defects 0 trials
• PLD1-related congenital heart disease 0 trials
• Peters plus syndrome 0 trials
• RBFOX2-related congenital heart disorder 0 trials
• Sengers syndrome 0 trials
• TARP syndrome 0 trials
• TFAP2B-related congenital heart disease spectrum disorder 0 trials
  2 sub-types

  • Char syndrome 0 trials
  • Patent ductus arteriosus 2 0 trials
• TNNT2-related cardiomyopathy 0 trials
  3 sub-types

  • Cardiomyopathy, familial restrictive, 3 0 trials
  • Dilated cardiomyopathy 1D 0 trials
  • Hypertrophic cardiomyopathy 2 0 trials
• Alveolar capillary dysplasia with misalignment of pulmonary veins 0 trials
• Autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome 0 trials
• Cardiac anomalies - developmental delay - facial dysmorphism syndrome 0 trials
• Cardiac conduction disease with or without cardiomyoopathy 0 trials
  2 sub-types

  • Cardiac conduction disease with or without cardiomyopathy 2 0 trials
  • Cardiac conduction disease with or without dilated cardiomyopathy 1 0 trials
• Cardiac valvular dysplasia, X-linked 0 trials
• Congenital alveolar dysplasia due to FGF10 0 trials
• Congenital alveolar dysplasia due to TBX4 0 trials
• Congenital heart defects, multiple types, 2 0 trials
• Congenital heart defects, multiple types, 3 0 trials
• Congenital heart defects, multiple types, 5 0 trials
• Congenital heart defects, multiple types, 8, with or without heterotaxy 0 trials
• Congenital heart defects, multiple types, 9 0 trials
• Congenital vertebral-cardiac-renal anomalies syndrome 0 trials
  3 sub-types

  • Vertebral, cardiac, renal, and limb defects syndrome 1 0 trials
  • Vertebral, cardiac, renal, and limb defects syndrome 2 0 trials
  • Vertebral, cardiac, renal, and limb defects syndrome 3 0 trials
• Coronary artery disease, autosomal dominant 2 0 trials
• Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome 0 trials
• Familial atrial myxoma 0 trials
• Familial atrioventricular septal defect 0 trials
  6 sub-types

  • Atrioventricular septal defect 0 trials
  • Atrioventricular septal defect 4 0 trials
  • Atrioventricular septal defect 5 0 trials
  • Complete atrioventricular canal 0 trials Sub-types →
  • Congenital heart defects, multiple types, 4 0 trials
  • Partial atrioventricular canal 0 trials
• Familial retinal arterial macroaneurysm 0 trials
• Fibromuscular dysplasia of the coronary arteries 0 trials
• Heart defects-limb shortening syndrome 0 trials
• Lethal left ventricular non-compaction-seizures-hypotonia-cataract-developmental delay syndrome 0 trials
• Mehta lewis patton syndrome 0 trials
• Patent ductus arteriosus-bicuspid aortic valve-hand anomalies syndrome 0 trials
• Pericardial effusion, chronic 0 trials
• Severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome 0 trials
• Sinoatrial node dysfunction and deafness 0 trials
• Transketolase deficiency 0 trials
• Tricuspid atresia 0 trials