AL amyloidosis
|
(Orphanet:85443)
|
AORTIC ANEURYSM, FAMILIAL THORACIC 9
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(OMIM:616166)
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ATRIAL FIBRILLATION, FAMILIAL, 1
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(OMIM:608583)
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ATRIAL FIBRILLATION, FAMILIAL, 15; ATFB15
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(OMIM:615770)
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ATRIAL FIBRILLATION, FAMILIAL, 4
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(OMIM:611493)
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ATRIAL FIBRILLATION, FAMILIAL, 6
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(OMIM:612201)
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ATRIAL SEPTAL DEFECT 6
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(OMIM:613087)
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ATTRV122I amyloidosis
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(Orphanet:85451)
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Aneurysm - osteoarthritis syndrome
|
(Orphanet:284984)
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Arrhythmogenic right ventricular dysplasia, familial, 3
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(OMIM:602086)
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Atrial fibrillation, familial, 11
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(OMIM:614049)
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Atrial fibrillation, familial, 3
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(OMIM:607554)
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Atrial septal defect - atrioventricular conduction defects syndrome
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(Orphanet:1479)
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Autosomal recessive Emery-Dreifuss muscular dystrophy
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(Orphanet:98855)
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BRUGADA SYNDROME 3
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(OMIM:611875)
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BRUGADA SYNDROME 4
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(OMIM:611876)
|
Brugada syndrome
|
(Orphanet:130)
|
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 26
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(OMIM:617047)
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CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 3
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(OMIM:614954)
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Cardiac arrhythmia, ankyrin-B-related
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(OMIM:600919)
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Cardiomyopathy, dilated, 1AA with or without left ventricular noncompaction
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(OMIM:612158)
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Cardiomyopathy, dilated, 1BB
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(OMIM:612877)
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Cardiomyopathy, dilated, 1D
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(OMIM:601494)
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Cardiomyopathy, dilated, 1DD
|
(OMIM:613172)
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Cardiomyopathy, dilated, 1E
|
(OMIM:601154)
|
Cardiomyopathy, dilated, 1HH
|
(OMIM:613881)
|
Cardiomyopathy, dilated, 1KK
|
(OMIM:615248)
|
Cardiomyopathy, dilated, 1R
|
(OMIM:613424)
|
Cardiomyopathy, dilated, 1S
|
(OMIM:613426)
|
Cardiomyopathy, dilated, 2B
|
(OMIM:614672)
|
Cardiomyopathy, familial hypertrophic, 16
|
(OMIM:613838)
|
Cardiomyopathy, familial hypertrophic, 18
|
(OMIM:613874)
|
Cardiomyopathy, familial hypertrophic, 20
|
(OMIM:613876)
|
Cardiomyopathy, familial hypertrophic, 3
|
(OMIM:115196)
|
Cardiomyopathy, familial hypertrophic, 6
|
(OMIM:600858)
|
Cardiomyopathy, familial hypertrophic, 7
|
(OMIM:613690)
|
Cardiomyopathy, familial restrictive 2
|
(OMIM:609578)
|
Cardiomyopathy, familial restrictive, 3
|
(OMIM:612422)
|
Catecholaminergic polymorphic ventricular tachycardia
|
(Orphanet:3286)
|
Chronic atrial and intestinal dysrhythmia syndrome
|
(Orphanet:435988)
|
Costello syndrome
|
(Orphanet:3071)
|
Desminopathy
|
(Orphanet:98909)
|
EMERY-DREIFUSS MUSCULAR DYSTROPHY 7, AUTOSOMAL DOMINANT
|
(OMIM:614302)
|
Ebstein malformation
|
(Orphanet:1880)
|
Fabry disease
|
(Orphanet:324)
|
Familial atrial fibrillation
|
(Orphanet:334)
|
Familial atrial tachyarrhythmia-infra-Hisian cardiac conduction disease
|
(Orphanet:436242)
|
Familial cutaneous collagenoma
|
(Orphanet:53296)
|
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
|
(Orphanet:300751)
|
Familial isolated hypertrophic cardiomyopathy
|
(Orphanet:155)
|
Familial isolated restrictive cardiomyopathy
|
(Orphanet:75249)
|
Friedreich ataxia 1
|
(OMIM:229300)
|
Generalized congenital lipodystrophy with myopathy
|
(Orphanet:228429)
|
Hemochromatosis, type 2A
|
(OMIM:602390)
|
Hypertaurinuric cardiomyopathy
|
(OMIM:145350)
|
Idiopathic giant cell myocarditis
|
(Orphanet:329874)
|
Left ventricular noncompaction
|
(Orphanet:54260)
|
Left ventricular noncompaction 1
|
(OMIM:604169)
|
Loeffler endocarditis
|
(Orphanet:75566)
|
Long QT syndrome 13
|
(OMIM:613485)
|
McLeod neuroacanthocytosis syndrome
|
(Orphanet:59306)
|
SHORT QT SYNDROME 2
|
(OMIM:609621)
|
Senile systemic amyloidosis
|
(Orphanet:330001)
|
Sick sinus syndrome 2, autosomal dominant
|
(OMIM:163800)
|
Sinus node disease and myopia
|
(OMIM:182190)
|
Steinert myotonic dystrophy
|
(Orphanet:273)
|
Tropical endomyocardial fibrosis
|
(Orphanet:75565)
|
VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH ORWITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY
|
(OMIM:604772)
|
X-linked Emery-Dreifuss muscular dystrophy
|
(Orphanet:98863)
|
X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome
|
(Orphanet:324410)
|
[DEL] CARDIAC CONDUCTION DISEASE WITH OR WITHOUT DILATED CARDIOMYOPATHY
|
(OMIM:616117)
|