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Diseases
Genes (1810)
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SCN5A
Premature Ventricular Contraction
Cardiomyopathy, Dilated, 1e
Ventricular Tachycardia, Catecholaminergic Polymorphic, 4
Ventricular Fibrillation, Paroxysmal Familial, 1
TTN
Premature Ventricular Contraction
Cardiomyopathy, Dilated, 1e
Limb–girdle Muscular Dystrophy
RYR2
Premature Ventricular Contraction
Ventricular Tachycardia, Catecholaminergic Polymorphic, 4
Ventricular Fibrillation, Paroxysmal Familial, 1
LMNA
Premature Ventricular Contraction
Cardiomyopathy, Dilated, 1e
Limb–girdle Muscular Dystrophy
ALX4
Enlarged Parietal Foramina
MSX2
Enlarged Parietal Foramina
Matthew-Wood Syndrome
DES
Cardiomyopathy, Dilated, 1e
Limb–girdle Muscular Dystrophy
NAA10
Premature Ventricular Contraction
Ogden Syndrome
TRDN
Premature Ventricular Contraction
Ventricular Tachycardia, Catecholaminergic Polymorphic, 4
COL2A1
Collagen, Type Ii, Alpha-1
MMP2
Multicentric Osteolysis Nodulosis And Arthropathy
Matthew-Wood Syndrome
GALNS
Premature Ventricular Contraction
Ventricular Fibrillation, Paroxysmal Familial, 1
Mucopolysaccharidosis Type Iva
CDAN1
Congenital Dyserythropoietic Anemia Type I
USB1
Poikiloderma With Neutropenia
STRA6
Matthew-Wood Syndrome
CALM1
Ventricular Tachycardia, Catecholaminergic Polymorphic, 4
Ventricular Fibrillation, Paroxysmal Familial, 1
RECQL4
Baller-Gerold Syndrome
Poikiloderma With Neutropenia
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