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Diseases
Genes (522)
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SCN5A
Premature Ventricular Contraction
Cardiomyopathy, Dilated, 1e
Ventricular Tachycardia, Catecholaminergic Polymorphic, 4
Ventricular Fibrillation, Paroxysmal Familial, 1
Boxer Cardiomyopathy
RYR2
Premature Ventricular Contraction
Ventricular Tachycardia, Catecholaminergic Polymorphic, 4
Ventricular Fibrillation, Paroxysmal Familial, 1
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
FMR1
Renpenning's Syndrome
Ventricular Fibrillation, Paroxysmal Familial, 1
Fragile X-Associated Tremor/ataxia Syndrome
TRDN
Premature Ventricular Contraction
Ventricular Tachycardia, Catecholaminergic Polymorphic, 4
PQBP1
Renpenning's Syndrome
PMM2
Pmm2 Deficiency
CALM1
Ventricular Tachycardia, Catecholaminergic Polymorphic, 4
Ventricular Fibrillation, Paroxysmal Familial, 1
CASQ2
Premature Ventricular Contraction
Ventricular Tachycardia, Catecholaminergic Polymorphic, 4
SGCD
Cardiomyopathy, Dilated, 1e
Limb–girdle Muscular Dystrophy
TCAP
Cardiomyopathy, Dilated, 1e
Limb–girdle Muscular Dystrophy
GALE
Galactose Epimerase Deficiency
MAGEL2
Schaaf-Yang Syndrome
TGFB3
Arrhythmogenic Right Ventricular Dysplasia, Familial, 8
Boxer Cardiomyopathy
FKTN
Cardiomyopathy, Dilated, 1e
Limb–girdle Muscular Dystrophy
SGCG
Limb–girdle Muscular Dystrophy
MYOT
Limb–girdle Muscular Dystrophy