mannose-P-dolichol utilization defect 1

Preferred Label : mannose-P-dolichol utilization defect 1;

Approved symbol HGNC : MPDU1;

Alias symbols HGNC : PQLC5; SLC66A5; Lec35; CDGIf; SL15;

Chromosome HGNC : 17p13.1;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000129255;

Details

Origin ID

HGNC:7207;

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 [OMIM gene]
- mannose-P-dolichol utilization defect 1 [ORDO Gene]
NCIt concept
- MPDU1 Gene [NCIt concept]
OMIM gene
- Mannose-p-dolichol utilization defect 1 [OMIM gene]
Orphanet gene
- mannose-P-dolichol utilization defect 1 [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- MPDU1 Gene [NCIt concept]
- Mannose-p-dolichol utilization defect 1 [OMIM gene]

Keyword's position in hierarchy(ies) :

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