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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.

expand / collapse MeSH information
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.


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This graph shows the total number of publications written about "Aspartylglucosaminuria" by people in this website by year, and whether "Aspartylglucosaminuria" was a major or minor topic of these publications.
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