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GAA protein, human MeSH Supplementary Concept Data 2024


MeSH Supplementary
GAA protein, human
Unique ID
C509951
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C509951
Entry Term(s)
LYAG protein, human
Myozyme
Nexviazyme
acid alpha-glucosidase, human
acid maltase, human
alglucosidase alfa
avlglucosidase alfa
glucosidase, alpha; acid (Pompe disease, glycogen storage disease type II), human
lysosomal alpha-glucosidase, human
recombinant human acid alpha-glucosidase
rhGAA
Registry Number
EC 3.2.1.20
Related Numbers
DTI67O9503
Heading Mapped to
*alpha-Glucosidases
Frequency
336
Note
Defects in the gene for this protein cause glycogen storage disease II, also known as Pompe disease, RefSeq NM_000152
Indexing Information
Glycogen Storage Disease Type II
Date of Entry
2006/05/01
Revision Date
2022/05/12
GAA protein, human Preferred
alglucosidase alfa Narrower
Nexviazyme Narrower
avlglucosidase alfa Narrower
Myozyme Narrower
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