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Diseases
Genes (807)
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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
LMNA
Premature Ventricular Contraction
Cardiomyopathy, Dilated, 1e
Limb–girdle Muscular Dystrophy
Boxer Cardiomyopathy
Focal Segmental Glomerulosclerosis
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
DES
Cardiomyopathy, Dilated, 1e
Limb–girdle Muscular Dystrophy
Boxer Cardiomyopathy
ABHD5
Cerebral Creatine Deficiency
NBEAL2
Gray Platelet Syndrome
NAA10
Premature Ventricular Contraction
Ogden Syndrome
GAMT
Guanidinoacetate Methyltransferase Deficiency
TRDN
Premature Ventricular Contraction
Ventricular Tachycardia, Catecholaminergic Polymorphic, 4
TREX1
Aicardi–goutières Syndrome
IFT140
Conorenal Syndrome
TRPC6
Focal Segmental Glomerulosclerosis
KANSL1
Alopecia, Androgenetic, 1
17q21.31 Microdeletion 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
TCAP
Cardiomyopathy, Dilated, 1e
Limb–girdle Muscular Dystrophy
TGFBR1
Alopecia, Androgenetic, 1
Loeys–dietz Syndrome