Arrhythmogenic right ventricular dysplasia, familial, 10
|
(OMIM:610193)
|
Arrhythmogenic right ventricular dysplasia, familial, 11
|
(OMIM:610476)
|
Arrhythmogenic right ventricular dysplasia, familial, 13
|
(OMIM:615616)
|
Atrial fibrillation, familial, 7
|
(OMIM:612240)
|
Autosomal recessive limb-girdle muscular dystrophy type 2G
|
(Orphanet:34514)
|
Autosomal recessive limb-girdle muscular dystrophy type 2N
|
(Orphanet:206559)
|
BRUGADA SYNDROME 2
|
(OMIM:611777)
|
BUNDLE BRANCH BLOCK, FAMILIAL ISOLATED COMPLETE RIGHT
|
(OMIM:113950)
|
Brugada syndrome
|
(Orphanet:130)
|
Cardiodysrhythmic potassium-sensitive periodic paralysis
|
(Orphanet:37553)
|
Cardiomyopathy, dilated, 1DD
|
(OMIM:613172)
|
Cardiomyopathy, dilated, 1E
|
(OMIM:601154)
|
Cardiomyopathy, dilated, 1EE
|
(OMIM:613252)
|
Cardiomyopathy, dilated, 1HH
|
(OMIM:613881)
|
Cardiomyopathy, dilated, 1KK
|
(OMIM:615248)
|
Cardiomyopathy, dilated, with woolly hair, keratoderma, and toothagenesis
|
(OMIM:615821)
|
Cardiomyopathy, familial hypertrophic, 1
|
(OMIM:192600)
|
Cardiomyopathy, familial hypertrophic, 3
|
(OMIM:115196)
|
Cardiomyopathy, familial restrictive, 3
|
(OMIM:612422)
|
Desminopathy
|
(Orphanet:98909)
|
Ebstein malformation
|
(Orphanet:1880)
|
Familial atrial tachyarrhythmia-infra-Hisian cardiac conduction disease
|
(Orphanet:436242)
|
Familial progressive cardiac conduction defect
|
(Orphanet:871)
|
Familial short QT syndrome
|
(Orphanet:51083)
|
Glycogen storage disease due to glycogenin deficiency
|
(Orphanet:263297)
|
Idiopathic giant cell myocarditis
|
(Orphanet:329874)
|
Incessant infant ventricular tachycardia
|
(Orphanet:45453)
|
Left vetricular noncompaction 7
|
(OMIM:615092)
|
MERRF
|
(Orphanet:551)
|
Naxos disease
|
(Orphanet:34217)
|
Nestor-Guillermo progeria syndrome
|
(Orphanet:280576)
|
PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IA
|
(OMIM:113900)
|
Senile systemic amyloidosis
|
(Orphanet:330001)
|
[DEL] Arrhythmogenic right ventricular dysplasia, familial, 1
|
(OMIM:107970)
|