"Mucopolysaccharidoses" 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.
Group of lysosomal storage diseases each caused by an inherited deficiency of an enzyme involved in the degradation of glycosaminoglycans (mucopolysaccharides). The diseases are progressive and often display a wide spectrum of clinical severity within one enzyme deficiency.
| Descriptor ID |
D009083
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| MeSH Number(s) |
C16.320.565.202.715 C16.320.565.595.600 C17.300.550.575 C18.452.648.202.715 C18.452.648.595.600
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| Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Mucopolysaccharidoses".
Below are MeSH descriptors whose meaning is more specific than "Mucopolysaccharidoses".
This graph shows the total number of publications written about "Mucopolysaccharidoses" by people in this website by year, and whether "Mucopolysaccharidoses" was a major or minor topic of these publications.
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click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2001 | 0 | 1 | 1 |
| 2008 | 1 | 0 | 1 |
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Below are the most recent publications written about "Mucopolysaccharidoses" by people in Profiles.
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Martin DC, Atmuri V, Hemming RJ, Farley J, Mort JS, Byers S, Hombach-Klonisch S, Csoka AB, Stern R, Triggs-Raine BL. A mouse model of human mucopolysaccharidosis IX exhibits osteoarthritis. Hum Mol Genet. 2008 Jul 01; 17(13):1904-15.
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Csoka AB, Frost GI, Stern R. The six hyaluronidase-like genes in the human and mouse genomes. Matrix Biol. 2001 Dec; 20(8):499-508.