BabelNet

bn:00499326n

Noun Concept

Categories: Drugboxes which contain changes to verified fields, Articles without InChI source, Chemicals that do not have a ChemSpider ID assigned, Medical treatments, Drugboxes which contain changes to watched fields

Alglucosidase alfa Acid-alpha glucosidase Acid maltase Aglucosidase alfa Aglucosidase alpha

Alglucosidase alfa, sold under the brand name Myozyme among others, is an enzyme replacement therapy orphan drug for treatment of Pompe disease, a rare lysosomal storage disorder. Wikipedia

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Alglucosidase alfa, sold under the brand name Myozyme among others, is an enzyme replacement therapy orphan drug for treatment of Pompe disease, a rare lysosomal storage disorder. Wikipedia

Enzyme medication Wikidata

IS A

MEDICAL CONDITION TREATED

glycogen storage disease II

glycogen storage disease

Wikipedia

Alglucosidase alfa

Wikidata

Alglucosidase alfa

Wikipedia Redirections

Alglucosidase Alfa, ATC code A16AB07, ATCvet code QA16AB07, C4758H7262N1274O1369S35, Lumizyme, Myozyme

Wikidata Alias

Acid-alpha glucosidase, Acid maltase, Aglucosidase alfa, Aglucosidase alpha, Lumizyme, Lysosomal Alpha-Glucosidase