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Diseases
Genes (667)
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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
LMNA
Premature Ventricular Contraction
Cardiomyopathy, Dilated, 1e
Limb–girdle Muscular Dystrophy
Boxer Cardiomyopathy
DES
Cardiomyopathy, Dilated, 1e
Limb–girdle Muscular Dystrophy
Boxer Cardiomyopathy
ABHD5
Cerebral Creatine Deficiency
GAMT
Guanidinoacetate Methyltransferase Deficiency
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
MAGEL2
Schaaf-Yang Syndrome
TGFB3
Arrhythmogenic Right Ventricular Dysplasia, Familial, 8
Boxer Cardiomyopathy
FKTN
Cardiomyopathy, Dilated, 1e
Limb–girdle Muscular Dystrophy
DSG2
Premature Ventricular Contraction
Cardiomyopathy, Dilated, 1e
Boxer Cardiomyopathy
TBXT
Limb–girdle Muscular Dystrophy
Chordoma, Susceptibility To
SGCG
Limb–girdle Muscular Dystrophy