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GENATLAS PHENOTYPE
last update : 09-08-2010
Symbol GSD15
Location 3q24
Name glycogen storage disease, type XV
Other name(s)
  • glycogen deficiency
  • GYG1 deficiency
    • Corresponding gene GYG1
    Main clinical features depletion of glycogen in skeletal muscle and cardiac arrhythmias, associated with the accumulation of abnormal storage material in the heart (Moslemi 2010)
    Genetic determination
    Function/system disorder metabolism/carbohydrates
    Type disease
    Remark(s)