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Diseases
Genes (406)
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SCN5A
Ventricular Fibrillation, Paroxysmal Familial, 1
Ventricular Tachycardia, Catecholaminergic Polymorphic, 4
Cardiomyopathy, Dilated, 1e
Premature Ventricular Contraction
Cardiac Conduction Defect
RYR2
Ventricular Fibrillation, Paroxysmal Familial, 1
Ventricular Tachycardia, Catecholaminergic Polymorphic, 4
Premature Ventricular Contraction
TRDN
Ventricular Tachycardia, Catecholaminergic Polymorphic, 4
Premature Ventricular Contraction
Neuropathy, Congenital Hypomyelinating, 3
ABHD5
Cerebral Creatine Deficiency
GAMT
Guanidinoacetate Methyltransferase Deficiency
CALM1
Ventricular Fibrillation, Paroxysmal Familial, 1
Ventricular Tachycardia, Catecholaminergic Polymorphic, 4
NAA10
Premature Ventricular Contraction
Ogden Syndrome
CASQ2
Ventricular Tachycardia, Catecholaminergic Polymorphic, 4
Premature Ventricular Contraction
TTN
Cardiomyopathy, Dilated, 1e
Premature Ventricular Contraction
RAC1
Mental Retardation, Autosomal Dominant 48
MAST1
Mega-Corpus-Callosum Syndrome With Cerebellar Hypoplasia And Cortical Malformations
CNTNAP1
Neuropathy, Congenital Hypomyelinating, 3
TECRL
Ventricular Tachycardia, Catecholaminergic Polymorphic, 4
PACS2
Epileptic Encephalopathy, Early Infantile, 66
RAD21
Mungan Syndrome
TGFB3
Arrhythmogenic Right Ventricular Dysplasia, Familial, 8
MYBPC3
Cardiomyopathy, Dilated, 1e
Premature Ventricular Contraction
FOXC1
Dandy–walker Malformation
RBM20
Cardiomyopathy, Dilated, 1e
CCND2
Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome 1