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Congenital Disorder Of Glycosylation, Type IIH MeSH Supplementary Concept Data 2022


MeSH Supplementary
Congenital Disorder Of Glycosylation, Type IIH
Unique ID
C566987
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C566987
Entry Term(s)
CDG IIIH
CDG2H
CDGIIH
Registry Number
0
Heading Mapped to
*Congenital Disorders of Glycosylation
Frequency
0
Note
mutation in COG8
Date of Entry
2012/11/05
Congenital Disorder Of Glycosylation, Type IIH Preferred
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