congenital disorder of glycosylation, type io

Preferred Label : congenital disorder of glycosylation, type io;

MeSH synonym : CDG1o; CDGIo; CDG io;

Origin ID

C567857;

UMLS CUI

C2752007;

Currated CISMeF NLP mapping
- Carbohydrate deficient glycoprotein syndrome type 1o (disorder) [SNOMED CT concept]
- DPM3 congenital disorder of glycosylation [ICD-11 More detail]
- DPM3-CDG [ORDO Disease]
- Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 15 [OMIM Phenotype]
MeSH term(s) associated for indexing
- congenital disorders of glycosylation [MeSH Descriptor]
Record concept(s)
- congenital disorder of glycosylation, type io [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Carbohydrate deficient glycoprotein syndrome type 1o (disorder) [SNOMED CT concept]
- DPM3-CDG [ORDO Disease]
- Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 15 [OMIM Phenotype]