NLM Logo

Mucopolysaccharidoses MeSH Descriptor Data 2022


MeSH Heading
Mucopolysaccharidoses
Tree 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
Unique ID
D009083
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D009083
Annotation
lysosomal storage dis; types I through VII except V are available as main headings: V = MUCOPOLYSACCHARIDOSIS V see MUCOPOLYSACCHARIDOSIS I; do not use /‌congen & do not coord with INFANT, NEWBORN, DISEASES
Scope Note
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.
Entry Term(s)
Mucopolysaccharidosis
NLM Classification #
QU 265.5.C3
Public MeSH Note
92; was MUCOPOLYSACCHARIDOSIS 1974-91
Online Note
use MUCOPOLYSACCHARIDOSES to search MUCOPOLYSACCHARIDOSIS 1974-91
History Note
92; was MUCOPOLYSACCHARIDOSIS 1974-91
Date Established
1974/01/01
Date of Entry
1999/01/01
Revision Date
2006/07/05
Mucopolysaccharidoses Preferred
page delivered in 0.146s