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31
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Glycogen storage disease
- 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 ...
- 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 ...
- 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 ...
- 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 ...
- 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 ...
- 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 ...
- 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 ...
- 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 ...
- ... 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): ...
- ... deficiency AMD Deficiency of alpha-glucosidase GAA deficiency Glycogen storage disease type II Glycogenosis type II GSD II GSD2 Pompe's disease Genetic Testing Registry: Glycogen storage disease type II, infantile Genetic Testing Registry: Glycogen storage ...
