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79 results
  1. ... of the condition. Other Names for This Condition Acid maltase deficiency Acid maltase deficiency disease Alpha-1,4-glucosidase deficiency AMD Deficiency ...
  2. ... maltase</synonym><synonym >Lysosomal glycogen storage disease without acid maltase deficiency</synonym><synonym >X-linked pseudoglycogenosis II</synonym><synonym > ...
  3. ... name><other_name >Lysosomal glycogen storage disease without acid maltase deficiency</other_name><other_name >X-linked pseudoglycogenosis II</ ...
  4. ... Acid lipase deficiency, see Lysosomal acid lipase deficiency Acid maltase deficiency, see Pompe disease Acid maltase deficiency disease, see Pompe disease ACLS, see Acrocallosal syndrome ...
  5. ... for the treatment of Type 1 Gaucher disease. Glycogen Storage Disease type II (Pompe Disease) Eight studies of alglucosidase alfa as treatment for glycogen storage disease type II (Pompe disease) are summarized in Table 10 . 72 – ...
  6. ... see Danon disease Lysosomal glycogen storage disease without acid maltase deficiency, see Danon disease Lysosomal protective protein deficiency, see ...
  7. ... A-T Children's Project About Face International (Canada) Acid Maltase Deficiency Association Action for XP ADCY5.org Adrenoleukodystrophy Foundation ...
  8. ... normal acid maltase Lysosomal glycogen storage disease without acid maltase deficiency X-linked pseudoglycogenosis II X-linked vacuolar cardiomyopathy ...
  9. ... Fucosidosis C10.228.140.163.100.435.340 Glycogen Storage Disease Type II C10.228.140.163.100.435.590 Mucolipidoses ... 295 Fucosidosis C16.320.565.189.435.340 Glycogen Storage Disease Type II C16.320.565.189.435.590 Mucolipidoses C16. ...
  10. ... Nyhan Syndrome Lysosomal Storage Diseases, Nervous System Fucosidosis Glycogen Storage Disease Type II Mucolipidoses Sialic Acid Storage Disease Sphingolipidoses Fabry Disease ...
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