Atrial fibrillation, familial, 10
|
(OMIM:614022)
|
Cardiomyopathy, dilated, 1AA with or without left ventricular noncompaction
|
(OMIM:612158)
|
Cardiomyopathy, dilated, 1DD
|
(OMIM:613172)
|
Cardiomyopathy, dilated, 1E
|
(OMIM:601154)
|
Cardiomyopathy, dilated, 1EE
|
(OMIM:613252)
|
Cardiomyopathy, familial hypertrophic, 2
|
(OMIM:115195)
|
Cardiomyopathy, familial restrictive, 3
|
(OMIM:612422)
|
Catecholaminergic polymorphic ventricular tachycardia
|
(Orphanet:3286)
|
Fabry disease
|
(Orphanet:324)
|
Familial atrial tachyarrhythmia-infra-Hisian cardiac conduction disease
|
(Orphanet:436242)
|
Hemochromatosis, type 2A
|
(OMIM:602390)
|
Histiocytoid cardiomyopathy
|
(Orphanet:137675)
|
Hyperammonemia due to N-acetylglutamate synthetase deficiency
|
(Orphanet:927)
|
Incessant infant ventricular tachycardia
|
(Orphanet:45453)
|
MERRF
|
(Orphanet:551)
|
McLeod neuroacanthocytosis syndrome
|
(Orphanet:59306)
|
Multifocal atrial tachycardia
|
(Orphanet:3282)
|
Premature ageing appearance-developmental delay-cardiac arrhythmia syndrome
|
(Orphanet:276432)
|
Pyruvate dehydrogenase E3-binding protein deficiency
|
(Orphanet:255182)
|
Uhl anomaly
|
(Orphanet:3403)
|