URI(s)
- http://id.loc.gov/authorities/subjects/sh85088232
- http://id.loc.gov/authorities/sh85088232#concept
Variants
- Mucopolysaccharidosis
Broader Terms
Exact Matching Concepts from Other Schemes
Closely Matching Concepts from Other Schemes
Earlier Established Forms
- Mucopolysaccharidosis
Sources
- found: MeSH, June 11, 2018(Mucopolysaccharidoses: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. Mapped to: Lysosomal storage diseases and connective tissue diseases.)
Instance Of
Scheme Membership(s)
Collection Membership(s)
Change Notes
- 1986-02-11: new
- 2018-07-13: revised
Alternate Formats
