Heart Diseases | Page 1

176 diseases found in 2 pages

2 Diseases

22q11.2 deletion syndrome

A Diseases

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

B Diseases

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

C Diseases

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 CREST syndrome Cystic medial necrosis of aorta

D Diseases

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

E Diseases

Ebstein's anomaly Ellis-Van Creveld syndrome Ellis Yale Winter syndrome Eosinophilic granulomatosis with polyangiitis

F Diseases

Fabry disease Familial atrial fibrillation Familial dilated cardiomyopathy Familial hypertrophic cardiomyopathy Familial progressive cardiac conduction defect Familial thoracic aortic aneurysm and dissection Fibrocartilaginous embolism Fibromuscular dysplasia Friedreich ataxia Fucosidosis

G Diseases

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

H Diseases

Heart-hand syndrome, Slovenian type Heart-hand syndrome, Spanish type HEC syndrome His bundle tachycardia Holt-Oram syndrome Human HOXA1 Syndromes Hurler–Scheie syndrome Hurler syndrome Hypereosinophilic syndrome Hypoplastic left heart syndrome

I Diseases

Infantile histiocytoid cardiomyopathy Intracranial arteriovenous malformation Isobutyryl-CoA dehydrogenase deficiency Ivemark syndrome

J Diseases

Jervell Lange-Nielsen syndrome

K Diseases

Kallikrein hypertension Kawasaki disease Kearns-Sayre syndrome

L Diseases

LCHAD deficiency Leber hereditary optic neuropathy Left ventricular noncompaction LEOPARD syndrome

The RareGuru disease database is regularly updated using data generously provided by GARD, the United States Genetic and Rare Disease Information Center.

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