Congenital disorder of glycosylation type 1I

Preferred Label : Congenital disorder of glycosylation type 1I;

Origin ID

C000623088;

UMLS CUI

C1842836;

Currated CISMeF NLP mapping
- ALG2-CDG [ORDO Disease]
- Congenital disorder of glycosylation type 1i (disorder) [SNOMED CT concept]
- Congenital disorder of glycosylation, type II [OMIM Phenotype]
- Mannosyltransferase 2 deficiency [ICD-11 More detail]
- congenital disorder of glycosylation Ii [DO Concept]
MeSH term(s) associated for indexing
- congenital disorders of glycosylation [MeSH Descriptor]
Record concept(s)
- Congenital disorder of glycosylation type 1I [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital disorder of glycosylation type 1i (disorder) [SNOMED CT concept]
- Congenital disorder of glycosylation, type II [OMIM Phenotype]