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Results 1 - 6 of 6 for Glycogen storage disease type 13
  1. Glycogen storage disease type V 
    Glycogen storage disease type V (also known as GSDV or McArdle disease) is an inherited disorder caused by an inability to break down a complex sugar called glycogen ...
    https://medlineplus.gov/.../glycogen-storage-disease-type-v - Genetics
  2. Danon disease 
    ... linked traits to their children with Y chromosomes. Glycogen storage disease type 2B Glycogen storage disease type IIb Lysosomal glycogen storage disease with normal acid ...
    https://medlineplus.gov/genetics/condition/danon-disease - Genetics
  3. GAA gene 
    ... glucosidase, alpha; acid glucosidase, alpha; acid (Pompe disease, glycogen storage disease type II) LYAG LYAG_HUMAN lysosomal alpha-glucosidase Tests ... gene in 40 Italian patients with late onset glycogen storage disease type II. Hum Mutat. 2006 Oct;27(10):999- ...
    https://medlineplus.gov/genetics/gene/gaa - Genetics
  4. PYGM gene 
    ... the PYGM gene have been found to cause glycogen storage disease type V (GSDV). One mutation that is common in North American and European populations is written as Arg50Ter or R50X. This ... of glycogen. Other mutations that cause GSDV may severely reduce ...
    https://medlineplus.gov/genetics/gene/pygm - Genetics
  5. PHKA1 gene 
    ... gene are known to cause a form of glycogen storage disease type IX (GSD IX) called GSD IXd or X- ...
    https://medlineplus.gov/genetics/gene/phka1 - Genetics
  6. LAMP2 gene 
    ... Wright GB, Kanter RJ, Seidman CE, Seidman JG. Glycogen storage diseases ... and autophagy. Mol Biol Cell. 2002 Sep;13(9):3355-68. doi: 10.1091/mbc.e02- ...
    https://medlineplus.gov/genetics/gene/lamp2 - Genetics