Mannose-p-dolichol utilization defect 1

Preferred Label : Mannose-p-dolichol utilization defect 1;

Symbol : MPDU1;

CISMeF acronym : MPDU1;

Type : Gene;

Alternative titles and symbols : Suppressor of lec15; SL15; LEC35;

Ensembl ID : ENSG00000129255;

Prefixed ID : *604041;

Details

Origin ID

604041;

UMLS CUI

C1417235;

Automatic exact mappings (from CISMeF team)
- Congenital disorder of glycosylation type 1f (disorder) [SNOMED CT concept]
- mannose-P-dolichol utilization defect 1 [ORDO Gene]
- mannose-P-dolichol utilization defect 1 [HGNC gene]
HGNC gene
- mannose-P-dolichol utilization defect 1 [HGNC gene]
NCIt concept(s)
- MPDU1 Gene [NCIt concept]
- MPDU1 wt Allele [NCIt concept]
- Mannose-P-Dolichol Utilization Defect 1 Protein [NCIt concept]
ORDO concept(s)
- mannose-P-dolichol utilization defect 1 [ORDO Gene]
Phenotypes related
- Congenital disorder of glycosylation, type if [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- MPDU1 Gene [NCIt concept]
- mannose-P-dolichol utilization defect 1 [HGNC gene]

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