Here is the list of all Heart Diseases
- 22q11.2 deletion syndrome
- Abdominal aortic aneurysm
- Aberrant subclavian artery
- Adult polyglucosan body disease
- Alpha-mannosidosis
- Alström syndrome
- Andersen-Tawil syndrome
- Aneurysm of sinus of Valsalva
- Arrhythmogenic right ventricular cardiomyopathy
- Arterial tortuosity syndrome
- Arthrochalasia Ehlers-Danlos syndrome
- Atrial myxoma, familial
- Atrial septal defect ostium primum
- Atrial septal defect sinus venosus
- Baroreflex failure
- Barth syndrome
- Becker muscular dystrophy
- Bidirectional tachycardia
- Blue rubber bleb nevus syndrome
- Brachydactyly long thumb type
- Broken heart syndrome
- Brugada syndrome
- Brugada syndrome 3
- Brugada syndrome 4
- Budd-Chiari syndrome
- Buerger disease
- Cardiac hydatid cysts with intracavitary expansion
- Cardiac rupture
- Cardiac-Valvular Ehlers-Danlos syndrome
- Cardioencephalomyopathy
- Cardiofaciocutaneous syndrome
- Cardiomyopathy cataract hip spine disease
- Cardiomyopathy dilated with woolly hair and keratoderma
- Carney complex
- Carnitine-acylcarnitine translocase deficiency
- Catecholaminergic polymorphic ventricular tachycardia
- Chaotic atrial tachycardia
- CHARGE syndrome
- Chromosome 1p36 deletion syndrome
- COG1-CDG (CDG-IIg)
- COG7-CDG (CDG-IIe)
- Combined oxidative phosphorylation deficiency 16
- Congenital generalized lipodystrophy type 4
- Congenital heart block
- Congenitally corrected transposition of the great arteries
- Cor triatriatum dexter
- Cor triatriatum sinister
- Costello syndrome
- Cystic medial necrosis of aorta
- Danon disease
- DCMA syndrome
- Diffuse cutaneous systemic sclerosis
- Dilated cardiomyopathy
- Dilated cardiomyopathy with hypergonadotropic hypogonadism
- DOLK-CDG (CDG-Im)
- DPM3-CDG (CDG-Io)
- Duchenne muscular dystrophy
- Ebstein’s anomaly
- Ellis Yale Winter syndrome
- Ellis-Van Creveld syndrome
- Eosinophilic granulomatosis with polyangiitis
- Fabry disease
- Familial atrial fibrillation
- Familial dilated cardiomyopathy
- Familial hypertrophic cardiomyopathy
- Familial progressive cardiac conduction defect
- Familial thoracic aortic aneurysm and aortic dissection
- Fibrocartilaginous embolism
- Fibromuscular dysplasia – Not a rare disease
- 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
- Human HOXA1 Syndromes
- Hurler syndrome
- Hurler–Scheie syndrome
- Hypereosinophilic syndrome
- Hypoplastic left heart syndrome
- Infantile histiocytoid cardiomyopathy
- Intracranial arteriovenous malformation
- Isobutyryl-CoA dehydrogenase deficiency
- Ivemark syndrome
- Jervell Lange-Nielsen syndrome
- Kallikrein hypertension
- Kawasaki disease
- Kearns-Sayre syndrome
- LCHAD deficiency
- Leber hereditary optic neuropathy
- Left ventricular noncompaction
- LEOPARD syndrome
- Limb-girdle muscular dystrophy type 1B
- Limb-girdle muscular dystrophy type 2E
- Limb-girdle muscular dystrophy type 2F
- Limb-girdle muscular dystrophy type 2M – See Limb-girdle muscular dystrophy
- Limb-girdle muscular dystrophy, type 2C
- Limb-girdle muscular dystrophy, type 2D
- Limited cutaneous systemic sclerosis
- Limited systemic sclerosis
- Loeys-Dietz syndrome type 2
- Loeys-Dietz syndrome type 4
- Long QT syndrome 1
- Lymphedema and cerebral arteriovenous anomaly
- Lymphocytic vasculitis
- Mannosidosis, beta A, lysosomal
- McLeod neuroacanthocytosis syndrome
- Medulloblastoma
- MGAT2-CDG (CDG-IIa)
- Microcephaly-cardiomyopathy
- Mitochondrial encephalomyopathy lactic acidosis and stroke-like episodes
- Mitochondrial trifunctional protein deficiency
- Mitral atresia
- Mitral valve prolapse, familial, autosomal dominant
- Musculocontractural Ehlers-Danlos syndrome
- Myoclonic epilepsy with ragged red fibers
- Myotonic dystrophy type 1
- Nathalie syndrome
- Naxos disease
- Neonatal stroke
- Neurofibromatosis-Noonan syndrome
- Noonan syndrome
- Noonan syndrome 1 – See Noonan syndrome
- Noonan syndrome 2 – See Noonan syndrome
- Noonan syndrome 3 – See Noonan syndrome
- Noonan syndrome 4 – See Noonan syndrome
- Noonan syndrome 5 – See Noonan syndrome
- Noonan syndrome 6 – See Noonan syndrome
- Noonan-like syndrome with loose anagen hair
- Ostium secundum atrial septal defect
- Paroxysmal ventricular fibrillation
- Patent ductus arteriosus
- Patent ductus venosus
- Peripartum cardiomyopathy
- Peters plus syndrome
- PGM1-CDG
- PHACE syndrome
- Postural orthostatic tachycardia syndrome – Not a rare disease
- Primary carnitine deficiency
- Progressive familial heart block type 1A
- Progressive familial heart block type 1B
- Progressive familial heart block type 2
- Pseudohypoaldosteronism type 2
- Pseudoxanthoma elasticum
- Pulmonary arterial hypertension
- Pulmonary atresia with intact ventricular septum
- Pulmonary atresia with ventricular septal defect
- Pulmonary valve stenosis
- Pulmonary vein stenosis
- Pulmonic stenosis
- Renoprival hypertension
- Retinal arterial macroaneurysm with supravalvular pulmonic stenosis
- Right ventricle hypoplasia
- Sarcoidosis – Not a rare disease
- Sengers syndrome
- Situs inversus
- Sudden Arrhythmia Death Syndrome
- Supravalvular aortic stenosis
- Swyer syndrome
- TANGO2-Related Metabolic Encephalopathy and Arrhythmias
- TARP syndrome
- Tetralogy of Fallot
- Timothy syndrome
- Tricuspid atresia
- Vici syndrome
- VLCAD deficiency
- White forelock with malformations
- Williams syndrome
Source Link -: https://rarediseases.info.nih.gov/diseases/diseases-by-category/4/heart-diseases