Heart Diseases | Page 1

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