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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

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