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Results 1 - 10 of 44 for Glycogen storage "disease," type II
  1. ... glucosidase, alpha; acid glucosidase, alpha; acid (Pompe disease, glycogen storage disease type II) LYAG LYAG_HUMAN lysosomal alpha-glucosidase Tests of ...
  2. ... 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 disease, type ...
  3. Newborn Screening Tests (Nemours Foundation)  
    Newborn Screening/Start Here ... Newborn Screening ... Nemours Foundation ... newborn screening tests, metabolic disorders, genetic disorders, pku, phenylketonuria, ...
  4. Newborn Screening Tests for Your Baby (March of Dimes Foundation)  
    Newborn Screening/Specifics ... Newborn Screening ... March of Dimes Foundation ... All babies in the U.S. receive newborn screening tests before leaving the hospital ...
  5. ... Glycogen storage disease type 2B Glycogen storage disease type IIb Lysosomal glycogen storage disease with normal acid maltase Lysosomal glycogen storage disease without acid maltase deficiency X-linked pseudoglycogenosis II X-linked vacuolar cardiomyopathy and myopathy Genetic Testing ...
  6. Carbohydrate Metabolism Disorders (National Library of Medicine)  
    Metabolism is the process your body uses to make energy from the food you eat. Food is made up of proteins, carbohydrates, and fats. Chemicals in your digestive ...
  7. Disease Treatments (American Society of Gene & Cell Therapy)  
    Genes and Gene Therapy/Specifics ... Genes and Gene Therapy ... American Society of Gene & Cell Therapy
  8. ... gene are known to cause a form of glycogen storage disease type IX (GSD IX) called GSD IXa or X- ...
  9. Pompe Disease From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    ... disease (also known as acid-maltase disease and glycogen storage disease II) is a rare genetic disorder that causes progressive weakness to the heart and skeletal muscles. It is caused by mutations in a ... body uses to break down glycogen, a stored form of sugar used for energy.
  10. Galactosemia (American Liver Foundation)  
    Carbohydrate Metabolism Disorders/Specifics ... Carbohydrate Metabolism Disorders ... Liver Diseases/Children ... Liver Diseases ... Galactosemia is an inherited disorder ...
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