congenital disorder of glycosylation type 1D

Preferred Label : congenital disorder of glycosylation type 1D;

MeSH synonym : carbohydrate-deficient glycoprotein syndrome, type 4; CDG1D; congenital disorder of glycosylation, type ID;

Details

Origin ID

C535742;

UMLS CUI

C1832736;

CISMeF manual mappings
- Asparagine-linked glycosylation 3 congenital disorder of glycosylation (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- ALG3-CDG [ORDO Disease]
- Congenital Disorder of Glycosylation Type Id [NCIt concept]
- Congenital disorder of glycosylation, type id [OMIM Phenotype]
MeSH term(s) associated for indexing
- congenital disorders of glycosylation [MeSH Descriptor]
Record concept(s)
- Congenital disorder of glycosylation type 1D [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- ALG3-CDG [ORDO Disease]
- Asparagine-linked glycosylation 3 congenital disorder of glycosylation (disorder) [SNOMED CT concept]
- Congenital Disorder of Glycosylation Type Id [NCIt concept]
- Congenital disorder of glycosylation, type id [OMIM Phenotype]

Keyword's position in hierarchy(ies) :

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