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Diseases
Genes (483)
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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
IKBKG
Anhidrotic Ectodermal Dysplasia With Immune Deficiency
Hypohidrotic Ectodermal Dysplasia With Immunodeficiency
LMNA
Premature Ventricular Contraction
Cardiomyopathy, Dilated, 1e
Limb–girdle Muscular Dystrophy
Boxer Cardiomyopathy
DES
Cardiomyopathy, Dilated, 1e
Limb–girdle Muscular Dystrophy
Boxer Cardiomyopathy
IDS
Mucopolysaccharidosis, Type Ii
PMM2
Pmm2 Deficiency
Congenital Disorder Of Glycosylation, Type Id
TRDN
Premature Ventricular Contraction
Ventricular Tachycardia, Catecholaminergic Polymorphic, 4
NAA10
Premature Ventricular Contraction
Ogden Syndrome
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
ADNP
Adnp-Related Intellectual Disability And Autism Spectrum Disorder
ALG3
Congenital Disorder Of Glycosylation, Type Id
TCAP
Cardiomyopathy, Dilated, 1e
Limb–girdle Muscular Dystrophy
FKTN
Cardiomyopathy, Dilated, 1e
Limb–girdle Muscular Dystrophy
SGCG
Limb–girdle Muscular Dystrophy
MYOT
Limb–girdle Muscular Dystrophy