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Mannosidase Deficiency Diseases MeSH Descriptor Data 2021


MeSH Heading
Mannosidase Deficiency Diseases
Tree Number(s)
C16.320.565.202.607
C16.320.565.595.577
C18.452.648.202.607
C18.452.648.595.577
Unique ID
D044904
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D044904
Scope Note
Diseases caused by the loss of one or more enzymes involved in the hydrolysis of mannoside linkages (MANNOSIDASES). The defects in enzyme activity are primarily associated with genetic mutation of the genes that codes for a particular mannosidase isoenzyme.
Entry Version
MANNOSIDASE DEFIC DIS
Entry Term(s)
Mannosidase Deficiency Syndromes
Mannosidosis
Previous Indexing
Mannosidosis (1984-2003)
See Also
Mannosidases
Public MeSH Note
2004; see MANNOSIDOSIS 1984-2003
History Note
2004; use MANNOSIDOSIS, ALPHA B, LYSOSOMAL 1984-2003
Date Established
2004/01/01
Date of Entry
2003/07/09
Revision Date
2013/07/08
Mannosidase Deficiency Diseases Preferred
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