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Congenital Disorder Of Glycosylation, Type IIID MeSH Supplementary Concept Data 2025


MeSH Supplementary
Congenital Disorder Of Glycosylation, Type IIID
Unique ID
C564625
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C564625
Entry Term(s)
CDG IID
CDG2D
CDGIID
Registry Numbers
0
Heading Mapped to
*Congenital Disorders of Glycosylation
Frequency
0
Note
mutation of B4GALT1
Date of Entry
2012/11/05
Revision Date
2012/11/05
Congenital Disorder Of Glycosylation, Type IIID Preferred
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