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  • MYH6
    • Cardiomyopathy, Dilated, 1y
    • Cardiomyopathy, Familial Hypertrophic, 14
  • NEXN
    • Cardiomyopathy, Familial Hypertrophic, 20
    • Cardiomyopathy, Dilated, 1y
  • ABHD5
    • Cerebral Creatine Deficiency
  • LIPA
    • Lysosomal Acid Lipase Deficiency
  • GAMT
    • Guanidinoacetate Methyltransferase Deficiency
  • PLN
    • Cardiomyopathy, Dilated, 1y
    • Cardiomyopathy, Familial Hypertrophic, 18
  • SCO2
    • Abdominal Aortic Aneurysm
    • Cardioencephalomyopathy, Fatal Infantile, Due To Cytochrome C Oxidase Deficiency 2
  • FLNC
    • Cardiomyopathy, Dilated, 1y
    • Cardiomyopathy, Familial Hypertrophic, 26
  • MYL2
    • Cardiomyopathy, Dilated, 1y
    • Cardiomyopathy, Familial Hypertrophic, 10
  • MMP9
    • Aneurysm
    • Abdominal Aortic Aneurysm
    • Cholesteatoma
  • TTN
    • Cardiomyopathy, Dilated, 1y
  • PLD1
    • Cardiac Valvular Defect, Developmental
  • COA6
    • Cardioencephalomyopathy, Fatal Infantile, Due To Cytochrome C Oxidase Deficiency 2
  • FOXF1
    • Alveolar Capillary Dysplasia With Misalignment Of Pulmonary Veins
  • COL3A1
    • Aneurysm
    • Abdominal Aortic Aneurysm
    • Uterine Rupture
  • MMP14
    • Abdominal Aortic Aneurysm
  • SOD2
    • Abdominal Aortic Aneurysm
  • DAB2IP
    • Abdominal Aortic Aneurysm
  • COX15
    • Cardioencephalomyopathy, Fatal Infantile, Due To Cytochrome C Oxidase Deficiency 2
  • COA5
    • Cardioencephalomyopathy, Fatal Infantile, Due To Cytochrome C Oxidase Deficiency 2

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