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Diseases
Genes (523)
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SCN5A
Premature Ventricular Contraction
Cardiomyopathy, Dilated, 1e
Ventricular Fibrillation, Paroxysmal Familial, 1
Ventricular Tachycardia, Catecholaminergic Polymorphic, 4
Boxer Cardiomyopathy
Arrhythmia
RYR2
Premature Ventricular Contraction
Ventricular Fibrillation, Paroxysmal Familial, 1
Ventricular Tachycardia, Catecholaminergic Polymorphic, 4
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
CALM1
Ventricular Fibrillation, Paroxysmal Familial, 1
Ventricular Tachycardia, Catecholaminergic Polymorphic, 4
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
FKTN
Cardiomyopathy, Dilated, 1e
Limb–girdle Muscular Dystrophy
DSG2
Premature Ventricular Contraction
Cardiomyopathy, Dilated, 1e
Boxer Cardiomyopathy
SGCG
Limb–girdle Muscular Dystrophy
MYOT
Limb–girdle Muscular Dystrophy
CAV3
Limb–girdle Muscular Dystrophy
MYBPC3
Premature Ventricular Contraction
Cardiomyopathy, Dilated, 1e
Boxer Cardiomyopathy
TECRL
Ventricular Tachycardia, Catecholaminergic Polymorphic, 4
FKRP
Limb–girdle Muscular Dystrophy