MeSH Browser

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: 15
Date of Entry: 2010/08/25
Revision Date: 2012/12/01

Congenital disorder of glycosylation, type 2C MeSH Supplementary Concept Data 2024