Atrial fibrillation, familial, 7
|
(OMIM:612240)
|
Cardiac arrhythmia, ankyrin-B-related
|
(OMIM:600919)
|
Cardiomyopathy, dilated, 1DD
|
(OMIM:613172)
|
Cardiomyopathy, familial hypertrophic, 6
|
(OMIM:600858)
|
Cardiomyopathy, familial restrictive, 3
|
(OMIM:612422)
|
Catecholaminergic polymorphic ventricular tachycardia
|
(Orphanet:3286)
|
Chronic atrial and intestinal dysrhythmia syndrome
|
(Orphanet:435988)
|
DISTICHIASIS WITH CONGENITAL ANOMALIES OF THE HEART AND PERIPHERALVASCULATURE
|
(OMIM:126320)
|
Fabry disease
|
(Orphanet:324)
|
Familial long QT syndrome
|
(Orphanet:768)
|
Familial progressive cardiac conduction defect
|
(Orphanet:871)
|
Familial sick sinus syndrome
|
(Orphanet:166282)
|
Holt-Oram syndrome
|
(Orphanet:392)
|
Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency
|
(Orphanet:314637)
|
PROGRESSIVE FAMILIAL HEART BLOCK, TYPE II
|
(OMIM:140400)
|
Sick sinus syndrome 1, autosomal recessive
|
(OMIM:608567)
|
Sick sinus syndrome 2, autosomal dominant
|
(OMIM:163800)
|
X-linked Emery-Dreifuss muscular dystrophy
|
(Orphanet:98863)
|