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Results 1 - 10 of 31 for Glycogen storage disease
  1. Glycogen storage disease type IX (also known as GSD IX) is a condition caused by the inability to break down a complex sugar called glycogen. The different forms ...
  2. Glycogen storage disease type IV (GSD IV) is an inherited disorder caused by the buildup of a complex sugar called glycogen in the body's cells. The accumulated ...
  3. 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 ...
  4. Glycogen storage disease type I (also known as GSDI or von Gierke disease) is an inherited disorder caused by the buildup of a complex sugar called glycogen in ...
  5. Glycogen storage disease type 0 (also known as GSD 0) is a condition caused by the body's inability to form a complex sugar called glycogen, which is a major source ...
  6. Glycogen storage disease type VI (also known as GSDVI or Hers disease) is an inherited disorder caused by an inability to break down a complex sugar called glycogen ...
  7. Glycogen storage disease type III (also known as GSDIII or Cori disease) is an inherited disorder caused by the ... GSD III GSD3 Limit dextrinosis Genetic Testing Registry: Glycogen storage disease type III Glycogen storage disease due to glycogen ...
  8. Glycogen storage disease type VII (GSDVII) is an inherited disorder caused by an inability to break down a complex ... deficiency Phosphofructokinase deficiency Tarui disease Genetic Testing Registry: Glycogen storage disease, type VII Glycogen storage disease due to muscle ...
  9. ... linked traits to their children with Y chromosomes. Glycogen storage disease type 2B Glycogen storage disease type IIb Lysosomal glycogen storage disease with normal ...
  10. ... glucosidase, alpha; acid glucosidase, alpha; acid (Pompe disease, glycogen storage disease type II) LYAG LYAG_HUMAN lysosomal alpha-glucosidase ... gene in 40 Italian patients with late onset glycogen storage disease type II. Hum Mutat. 2006 Oct;27(10): ...
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