Aspartylglucosaminuria
"Aspartylglucosaminuria" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A recessively inherited, progressive lysosomal storage disease caused by a deficiency of GLYCOSYLASPARAGINASE activity. The lack of this enzyme activity results in the accumulation of N-acetylglucosaminylasparagine (the linkage unit of asparagine-linked glycoproteins) in LYSOSOMES.
| Descriptor ID |
D054880
|
| MeSH Number(s) |
C16.320.565.595.100 C18.452.648.595.100
|
| Concept/Terms |
Aspartylglucosaminuria- Aspartylglucosaminuria
- Aspartylglucosaminurias
- Glycoasparaginase
- Aspartylglycosaminuria
- Aspartylglycosaminurias
|
Below are MeSH descriptors whose meaning is more general than "Aspartylglucosaminuria".
Below are MeSH descriptors whose meaning is more specific than "Aspartylglucosaminuria".
This graph shows the total number of publications written about "Aspartylglucosaminuria" by people in UAMS Profiles by year, and whether "Aspartylglucosaminuria" was a major or minor topic of these publications.
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Below are the most recent publications written about "Aspartylglucosaminuria" by people in Profiles over the past ten years.