ATRIAL FIBRILLATION, FAMILIAL, 15; ATFB15
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(OMIM:615770)
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Atrial fibrillation, familial, 10
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(OMIM:614022)
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Atrial tachyarrhythmia with short PR interval
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(Orphanet:844)
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BRUGADA SYNDROME 7
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(OMIM:613120)
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Brugada syndrome
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(Orphanet:130)
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Cardiomyopathy, dilated, 1E
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(OMIM:601154)
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Cardiomyopathy, familial restrictive 2
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(OMIM:609578)
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Chronic atrial and intestinal dysrhythmia syndrome
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(Orphanet:435988)
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Familial atrial fibrillation
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(Orphanet:334)
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Familial atrial tachyarrhythmia-infra-Hisian cardiac conduction disease
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(Orphanet:436242)
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Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
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(Orphanet:300751)
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Familial progressive cardiac conduction defect
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(Orphanet:871)
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Familial sick sinus syndrome
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(Orphanet:166282)
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Idiopathic neonatal atrial flutter
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(Orphanet:45452)
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Lymphedema - atrial septal defects - facial changes
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(Orphanet:86915)
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Senile systemic amyloidosis
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(Orphanet:330001)
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Sinus node disease and myopia
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(OMIM:182190)
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Steinert myotonic dystrophy
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(Orphanet:273)
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X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome
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(Orphanet:324410)
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[DEL] CARDIAC CONDUCTION DISEASE WITH OR WITHOUT DILATED CARDIOMYOPATHY
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(OMIM:616117)
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