MeSH Browser

MeSH Supplementary: Congenital Disorder Of Glycosylation, Type Im
Unique ID: C563666
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563666
Entry Term(s): CDG1m; CDGIm; Dolichol Kinase Deficiency
Registry Numbers: 0
Heading Mapped to: Phosphotransferases (Alcohol Group Acceptor) / deficiency; *Congenital Disorders of Glycosylation
Frequency: 5
Note: mutation in dolichol kinase (DOLK)
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Concept UI: M0563966
Registry Numbers: 0
Terms: Congenital Disorder Of Glycosylation, Type Im Preferred Term
Term UI T825874
Date07/10/2012
LexicalTag NON
ThesaurusID OMIM (2013); Dolichol Kinase Deficiency
Term UI T803340
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013); CDG1m
Term UI T825872
Date07/10/2012
LexicalTag NON
ThesaurusID OMIM (2013); CDGIm
Term UI T825873
Date07/10/2012
LexicalTag NON
ThesaurusID OMIM (2013)

Congenital Disorder Of Glycosylation, Type Im MeSH Supplementary Concept Data 2025