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Diseases
Genes (691)
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SCN5A
Premature Ventricular Contraction
Cardiomyopathy, Dilated, 1e
Ventricular Tachycardia, Catecholaminergic Polymorphic, 4
Ventricular Fibrillation, Paroxysmal Familial, 1
Boxer Cardiomyopathy
Arrhythmia
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
DES
Cardiomyopathy, Dilated, 1e
Pompe Disease
Limb–girdle Muscular Dystrophy
Boxer Cardiomyopathy
GAA
Pompe Disease
MYO15A
Deafness, Autosomal Recessive 3
NAA10
Premature Ventricular Contraction
Ogden Syndrome
TRDN
Premature Ventricular Contraction
Ventricular Tachycardia, Catecholaminergic Polymorphic, 4
CALM1
Ventricular Tachycardia, Catecholaminergic Polymorphic, 4
Ventricular Fibrillation, Paroxysmal Familial, 1
TNNT2
Cardiomyopathy, Dilated, 1e
Pompe Disease
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
KDR
Pompe Disease
Angiosarcoma
KRAS
Angiosarcoma
SGCG
Limb–girdle Muscular Dystrophy
MYOT
Limb–girdle Muscular Dystrophy