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Congenital Disorders of Glycosylation MeSH Descriptor Data 2022


MeSH Heading
Congenital Disorders of Glycosylation
Tree Number(s)
C16.320.565.202.125
C18.452.648.202.125
Unique ID
D018981
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D018981
Scope Note
A genetically heterogeneous group of heritable disorders resulting from defects in protein N-glycosylation.
Entry Term(s)
Carbohydrate-Deficient Glycoprotein Syndrome
Glycoprotein Syndrome, Carbohydrate-Deficient
Previous Indexing
Carbohydrate Metabolism, Inborn Errors (1991-1995)
Glycoproteins (1977-1995)
Public MeSH Note
2011; CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME (1996-2010)
History Note
2011(1996)
Date Established
1996/01/01
Date of Entry
1995/05/24
Revision Date
2010/06/25
Congenital Disorders of Glycosylation Preferred
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