NLM Logo

Congenital Disorder Of Glycosylation, Type IIID MeSH Supplementary Concept Data 2024


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 Number
0
Heading Mapped to
*Congenital Disorders of Glycosylation
Frequency
0
Note
mutation of B4GALT1
Date of Entry
2012/11/05
Congenital Disorder Of Glycosylation, Type IIID Preferred
page delivered in 0.005s