MeSH Browser

MeSH Supplementary: Congenital disorder of glycosylation type 1D
Unique ID: C535742
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C535742
Entry Term(s): CDG1D; Carbohydrate-deficient glycoprotein syndrome, type 4; Congenital Disorder Of Glycosylation, Type ID
Registry Number: 0
Heading Mapped to: *Congenital Disorders of Glycosylation
Frequency: 1
Date of Entry: 2010/08/25
Revision Date: 2013/10/24

Congenital disorder of glycosylation type 1D MeSH Supplementary Concept Data 2024