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Diseases

Genetic and Rare Diseases Information Center (GARD)

Search for Rare or Genetic Diseases


Heart Diseases

* This symbol indicates that a condition is not rare but is one for which a question has been answered by the GARD Information Center.

Is Rare Condition? Disease Name
* 22q11.2 deletion syndrome
* Abdominal aortic aneurysm
* Aberrant subclavian artery
* Alpha-mannosidosis type 1
* Alström syndrome
* Andersen-Tawil syndrome
* Aneurysm of sinus of Valsalva
* Arrhythmogenic right ventricular dysplasia
* Arterial tortuosity syndrome
* Athabaskan brainstem dysgenesis
* Atrial fibrillation familial
* Atrial myxoma, familial
* Atrial septal defect ostium primum
* Barth syndrome
* Becker muscular dystrophy
* Bidirectional tachycardia
* Blue rubber bleb nevus syndrome
* Brachydactyly long thumb type
* Brugada syndrome
* Brugada syndrome 3
* Brugada syndrome 4
* Budd-Chiari syndrome
* Buerger disease
* Cardiac hydatid cysts with intracavitary expansion
* Cardiac rupture
* Cardiofaciocutaneous syndrome
* Cardiomyopathy dilated with woolly hair and keratoderma
* Carnitine-acylcarnitine translocase deficiency
* Cataract and cardiomyopathy
* Catecholaminergic polymorphic ventricular tachycardia
* Chaotic atrial tachycardia
* CHARGE syndrome
* Chromosome 1p36 deletion syndrome
* Congenital generalized lipodystrophy type 4
* Congenital heart block
* Costello syndrome
* Cutaneous necrotizing vasculitis
* Cystic medial necrosis of aorta
* Danon disease
* Dilated cardiomyopathy
* Dilated cardiomyopathy with hypergonadotropic hypogonadism
* Ebstein's anomaly
* Ehlers-Danlos syndrome arthrochalasia type
* Ellis Yale Winter syndrome
* Ellis-Van Creveld syndrome
* Emery-Dreifuss muscular dystrophy, X-linked
* Fabry disease
* Familial dilated cardiomyopathy
* Familial hypertrophic cardiomyopathy
* Familial thoracic aortic aneurysm and dissection
* Fibrocartilaginous embolism
*   Fibromuscular dysplasia
* Friedreich ataxia
* Fucosidosis
* Gaucher disease
* Gaucher disease type 1
* Glutaric acidemia type II
* Glycogen storage disease type 2
* Glycogen storage disease type 3
* Glycogen storage disease type 4
* Heart-hand syndrome, Slovenian type
* Heart-hand syndrome,Spanish type
* HEC syndrome
* His bundle tachycardia
* Holt-Oram syndrome
* Hypereosinophilic syndrome
* Hypoplastic left heart syndrome
* Infantile histiocytoid cardiomyopathy
* Intracranial arteriovenous malformation
* Isobutyryl-CoA dehydrogenase deficiency
* Ivemark syndrome
* Jervell and Lange-Nielsen syndrome 2
* Kallikrein hypertension
* Kawasaki syndrome
* Kearns Sayre syndrome
* LCHAD deficiency
* Leber hereditary optic neuropathy
* LEOPARD syndrome
* Limb-girdle muscular dystrophy type 2E
* Limb-girdle muscular dystrophy type 2F
* Limb-girdle muscular dystrophy, type 1B
* Limb-girdle muscular dystrophy, type 2C
* Limb-girdle muscular dystrophy, type 2D
* Limited scleroderma
* Loeys-Dietz syndrome type 1B
* Loeys-Dietz syndrome type 2A
* Loeys-Dietz syndrome type 2B
* Long QT syndrome 1
* Long QT syndrome 8
* Lymphedema and cerebral arteriovenous anomaly
* Lymphocytic vasculitis
* Mannosidosis, beta A, lysosomal
* McLeod neuroacanthocytosis syndrome
* Medulloblastoma
* Mitochondrial encephalomyopathy lactic acidosis and stroke-like episodes
* Mitochondrial trifunctional protein deficiency
* Mitral atresia
* Mitral valve prolapse, familial, autosomal dominant
* Myoclonus with epilepsy with ragged red fibers
* Myotonic dystrophy type 1
* Myxoma-spotty pigmentation-endocrine overactivity
* Naxos disease
* Neonatal stroke
* Noonan syndrome
* Noonan syndrome 1
* Noonan-like syndrome with loose anagen hair
* Paroxysmal ventricular fibrillation
* Patent ductus arteriosus
* Patent ductus venosus
* Peters plus syndrome
* PHACE syndrome
* Polyglucosan body disease, adult
* Primary carnitine deficiency
* Progressive familial heart block type 1A
* Progressive familial heart block type 1B
* Progressive familial heart block type 2
* Pseudoxanthoma elasticum
* Pulmonary arterial hypertension
* Pulmonary atresia with ventricular septal defect
* Pulmonary valve stenosis
* Pulmonary vein stenosis
* Pulmonic stenosis
* Renoprival hypertension
* Right ventricle hypoplasia
*   Sarcoidosis
* Situs inversus
* Stress cardiomyopathy
* Sudden Arrhythmia Death Syndrome
* Supravalvular aortic stenosis
* Swyer syndrome
* Tetralogy of Fallot
* Tricuspid atresia
* Uhl anomaly
* VLCAD deficiency
* Watson syndrome
* Williams syndrome