Browse

Explore conditions, clinical trials, and the organisations running them.

Up to: Hereditary disease · Heart disorder

Cardiogenetic disease

A heterogeneous group of genetic conditions, with Mendelian (autosomal dominant, recessive, or X-linked) or chromosomal etiology that are characterized by abnormalities in the cardiovascular system.

3 trials tagged with this condition →

Familial cardiomyopathy 2 trials · 217 incl. sub-types Sub-types →
Atrial septal defect 45 trials · 78 incl. sub-types Sub-types →
Postural orthostatic tachycardia syndrome 71 trials
Cardiogenetic rhythm disorder 2 trials · 67 incl. sub-types 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 Sub-types →
Ventricular septal defect 24 trials · 26 incl. sub-types Sub-types →
Familial bicuspid aortic valve 6 trials · 21 incl. sub-types Sub-types →
NOTCH1-related AOS spectrum disorder 0 trials · 16 incl. sub-types Sub-types →
Alagille syndrome 15 trials Sub-types →
DiGeorge syndrome 11 trials
Hypoplastic left heart syndrome 9 trials Sub-types →
CHARGE syndrome 4 trials Sub-types →
Velocardiofacial syndrome 4 trials
Supravalvular aortic stenosis 3 trials
Dextro-looped transposition of the great arteries 2 trials Sub-types →
Ellis-van Creveld syndrome 1 trial Sub-types →
Coronary artery disease, autosomal dominant, 1 1 trial
Dextrocardia 1 trial
Inherited mitral valve disease 0 trials · 1 incl. sub-types Sub-types →
Structural congenital heart disease, multiple types - GATA4 0 trials · 1 incl. sub-types Sub-types →
8q24.3 microdeletion syndrome 0 trials
ACTC1-related distal arthrogryposis with congenital heart disease 0 trials
ACTN2-related cardiac and skeletal myopathy 0 trials Sub-types →
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 Sub-types →
GATA6-related congenital heart disease with or without pancreatic agenesis or neonatal diabetes 0 trials Sub-types →
HAND1 related congenital heart defect 0 trials
HAND2 related congenital heart defect 0 trials
Holt-Oram syndrome 0 trials Sub-types →
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 Sub-types →
TNNT2-related cardiomyopathy 0 trials Sub-types →
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 Sub-types →
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 Sub-types →
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 Sub-types →
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