congenital disorder of glycosylation type 1F

Preferred Label : congenital disorder of glycosylation type 1F;

MeSH synonym : congenital disorder of glycosylation, type IF;

Origin ID

C535744;

UMLS CUI

C1836669;

Automatic exact mappings (from CISMeF team)
- ALG13-CDG [ORDO Disease]
- Congenital disorder of glycosylation type 1s (disorder) [SNOMED CT concept]
- Congenital disorder of glycosylation, type in [OMIM Phenotype]
- Congenital disorder of glycosylation, type it [OMIM Phenotype]
- Developmental and epileptic encephalopathy 36 [OMIM Phenotype]
- Mannose-P-dolichol utilisation defect 1 [ICD-11 More detail]
- PGM1-CDG [ORDO Disease]
- RFT1-CDG [ORDO Disease]
Currated CISMeF NLP mapping
- Congenital Disorder of Glycosylation Type If [NCIt concept]
- Congenital disorder of glycosylation type 1f (disorder) [SNOMED CT concept]
- Congenital disorder of glycosylation, type if [OMIM Phenotype]
- MPDU1-CDG [ORDO Disease]
MeSH term(s) associated for indexing
- congenital disorders of glycosylation [MeSH Descriptor]
Record concept(s)
- Congenital disorder of glycosylation type 1F [MeSH concept]
See also inter- (CISMeF)
- Congenital disorder of glycosylation type 1n (disorder) [SNOMED CT concept]
- Phosphoglucomutase 1-related congenital disorder of glycosylation (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital Disorder of Glycosylation Type If [NCIt concept]
- Congenital disorder of glycosylation type 1f (disorder) [SNOMED CT concept]
- Congenital disorder of glycosylation, type if [OMIM Phenotype]
- MPDU1-CDG [ORDO Disease]