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Diseases
Genes (403)
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SCN5A
Ventricular Tachycardia, Catecholaminergic Polymorphic, 4
Premature Ventricular Contraction
Cardiomyopathy, Dilated, 1e
Ventricular Fibrillation, Paroxysmal Familial, 1
Boxer Cardiomyopathy
Arrhythmia
RYR2
Ventricular Tachycardia, Catecholaminergic Polymorphic, 4
Premature Ventricular Contraction
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
ABCC9
Cardiomyopathy, Dilated, 1e
Cantú Syndrome
DES
Cardiomyopathy, Dilated, 1e
Limb–girdle Muscular Dystrophy
Boxer Cardiomyopathy
TRDN
Ventricular Tachycardia, Catecholaminergic Polymorphic, 4
Premature Ventricular Contraction
ASL
Argininosuccinic Aciduria
PMM2
Pmm2 Deficiency
OPA3
Costeff Syndrome
NAA10
Premature Ventricular Contraction
Ogden Syndrome
CALM1
Ventricular Tachycardia, Catecholaminergic Polymorphic, 4
Ventricular Fibrillation, Paroxysmal Familial, 1
CASQ2
Ventricular Tachycardia, Catecholaminergic Polymorphic, 4
Premature Ventricular Contraction
SGCD
Cardiomyopathy, Dilated, 1e
Limb–girdle Muscular Dystrophy
TCAP
Cardiomyopathy, Dilated, 1e
Limb–girdle Muscular Dystrophy
B3GLCT
Peters Plus Syndrome
FKTN
Cardiomyopathy, Dilated, 1e
Limb–girdle Muscular Dystrophy
KCNJ8
Ventricular Fibrillation, Paroxysmal Familial, 1
Cantú Syndrome
TECRL
Ventricular Tachycardia, Catecholaminergic Polymorphic, 4