MeSH Browser

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 Numbers: EC 3.2.1.20; 0; DTI67O9503
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 MeSH Supplementary Concept Data 2025