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Diseases
Genes (631)
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SCN5A
Premature Ventricular Contraction
Cardiomyopathy, Dilated, 1e
Ventricular Fibrillation, Paroxysmal Familial, 1
Ventricular Tachycardia, Catecholaminergic Polymorphic, 3
Boxer Cardiomyopathy
Arrhythmia
RYR2
Premature Ventricular Contraction
Ventricular Fibrillation, Paroxysmal Familial, 1
Ventricular Tachycardia, Catecholaminergic Polymorphic, 3
Boxer Cardiomyopathy
TTN
Premature Ventricular Contraction
Cardiomyopathy, Dilated, 1e
Limb–girdle Muscular Dystrophy
Boxer Cardiomyopathy
DSG2
Premature Ventricular Contraction
Cardiomyopathy, Dilated, 1e
Boxer Cardiomyopathy
Arrhythmogenic Right Ventricular Dysplasia, Familial, 10
LMNA
Premature Ventricular Contraction
Cardiomyopathy, Dilated, 1e
Limb–girdle Muscular Dystrophy
Boxer Cardiomyopathy
Fragile X-Associated Tremor/ataxia Syndrome
DES
Cardiomyopathy, Dilated, 1e
Limb–girdle Muscular Dystrophy
Boxer Cardiomyopathy
PMM2
Pmm2 Deficiency
ASL
Argininosuccinic Aciduria
NAA10
Premature Ventricular Contraction
Ogden Syndrome
TRDN
Premature Ventricular Contraction
Ventricular Tachycardia, Catecholaminergic Polymorphic, 3
FMR1
Ventricular Fibrillation, Paroxysmal Familial, 1
Renpenning's Syndrome
Fg Syndrome
Fragile X-Associated Tremor/ataxia Syndrome
PQBP1
Renpenning's Syndrome
SGCD
Cardiomyopathy, Dilated, 1e
Limb–girdle Muscular Dystrophy
MED12
Fg Syndrome
CALM1
Ventricular Fibrillation, Paroxysmal Familial, 1
Ventricular Tachycardia, Catecholaminergic Polymorphic, 3
CASQ2
Premature Ventricular Contraction
Ventricular Tachycardia, Catecholaminergic Polymorphic, 3
TCAP
Cardiomyopathy, Dilated, 1e
Limb–girdle Muscular Dystrophy
FKTN
Cardiomyopathy, Dilated, 1e
Limb–girdle Muscular Dystrophy
SGCG
Limb–girdle Muscular Dystrophy
MYOT
Limb–girdle Muscular Dystrophy