GAA protein, human

Preferred Label : GAA protein, human;

MeSH note : Defects in the gene for this protein cause glycogen storage disease II, also known as Pompe disease, RefSeq NM_000152;

CISMeF synonym : genzyme brand of recombinant human alglucosidase alfa;

MeSH synonym : LYAG protein, human; acid maltase, human; glucosidase, alpha; acid (Pompe disease, glycogen storage disease type II), human; lysosomal alpha-glucosidase, human; acid alpha-glucosidase, human;

MeSH hyponym : rhGAA; recombinant human acid alpha-glucosidase;

MeSH Related Number : myozyme; alglucosidase alfa; EC 3.2.1.20; DTI67O9503;

Registry Number MeSH : EC 3.2.1.20;

Related CAS MeSH : EC 3.2.1.20 (alglucosidase alfa); EC 3.2.1.20 (Myozyme);

related registry number list (CISMeF) : EC 3.2.1.20;

Is substance : O;

UNII : EC 3.2.1.20;

Details

Origin ID

C509951;

UMLS CUI

C1721422;

ATC code(s)
- alglucosidase alfa [ATC Code]
ATC code(s)
- alglucosidase alfa [ATC Code]
Automatic exact mappings (from CISMeF team)
- Alglucosidase Alfa [NCIt concept]
- alglucosidase alfa [ATC Code]
MeSH indexing information
- glycogen storage disease type ii [MeSH Descriptor]
MeSH term(s) associated for indexing
- alpha-Glucosidases [MeSH Descriptor]
Record concept(s)
- GAA protein, human [MeSH concept]
- Nexviazyme [MeSH concept]
- alglucosidase alfa [MeSH concept]
- avlglucosidase alfa [MeSH concept]
- myozyme [MeSH concept]
Semantic type(s)
- Amino Acid, Peptide, or Protein [UMLS semantic type]
- Enzyme [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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