Arrhythmogenic right ventricular dysplasia, familial, 11
|
(OMIM:610476)
|
Arrhythmogenic right ventricular dysplasia, familial, 8
|
(OMIM:607450)
|
Atrial fibrillation, familial, 3
|
(OMIM:607554)
|
BRUGADA SYNDROME 2
|
(OMIM:611777)
|
BRUGADA SYNDROME 5
|
(OMIM:612838)
|
BRUGADA SYNDROME 6
|
(OMIM:613119)
|
Brugada syndrome
|
(Orphanet:130)
|
Cardiomyopathy, dilated, 1DD
|
(OMIM:613172)
|
Cardiomyopathy, dilated, 1EE
|
(OMIM:613252)
|
Cardiomyopathy, dilated, 1P
|
(OMIM:609909)
|
Cardiomyopathy, familial hypertrophic, 13
|
(OMIM:613243)
|
Catecholaminergic polymorphic ventricular tachycardia
|
(Orphanet:3286)
|
DK1-CDG
|
(Orphanet:91131)
|
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
|
(Orphanet:300751)
|
Familial long QT syndrome
|
(Orphanet:768)
|
Familial short QT syndrome
|
(Orphanet:51083)
|
Hemochromatosis, type 2A
|
(OMIM:602390)
|
Histiocytoid cardiomyopathy
|
(Orphanet:137675)
|
Idiopathic giant cell myocarditis
|
(Orphanet:329874)
|
Idiopathic ventricular fibrillation, not Brugada type
|
(Orphanet:228140)
|
Jervell and Lange-Nielsen syndrome
|
(Orphanet:90647)
|
Long QT syndrome 1
|
(OMIM:192500)
|
Long QT syndrome 2
|
(OMIM:613688)
|
Long QT syndrome 3
|
(OMIM:603830)
|
Long QT syndrome 5
|
(OMIM:613695)
|
Long QT syndrome 6
|
(OMIM:613693)
|
McLeod neuroacanthocytosis syndrome
|
(Orphanet:59306)
|
Multiple acyl-CoA dehydrogenase deficiency
|
(Orphanet:26791)
|
Romano-Ward syndrome
|
(Orphanet:101016)
|
Tako-Tsubo cardiomyopathy
|
(Orphanet:66529)
|
Torsade-de-pointes syndrome with short coupling interval
|
(Orphanet:51084)
|
Uhl anomaly
|
(Orphanet:3403)
|
Ventricular fibrillation, paroxysmal familial, 1
|
(OMIM:603829)
|
Ventricular fibrillation, paroxysmal familial, 2
|
(OMIM:612956)
|
[DEL] Arrhythmogenic right ventricular dysplasia, familial, 1
|
(OMIM:107970)
|