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Congenital disorder of glycosylation, type 2C MeSH Supplementary Concept Data 2022


MeSH Supplementary
Congenital disorder of glycosylation, type 2C
Unique ID
C535755
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C535755
Entry Term(s)
CDG2C
Congenital Disorder Of Glycosylation, Type IIC
LAD2
Leukocyte Adhesion Deficiency, Type II
Leukocyte adhesion deficiency, type 2
Rambam Hasharon syndrome
Rambam-Hasharon Syndrome
Registry Number
0
Heading Mapped to
*Congenital Disorders of Glycosylation
Frequency
9
Date of Entry
2010/08/25
Revision Date
2012/12/01
Congenital disorder of glycosylation, type 2C Preferred
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