RFT1 homolog - CISMeF

Preferred Label : RFT1 homolog;

Approved symbol HGNC : RFT1;

Name synonyms HGNC : congenital disorder of glycosylation 1N;

Alias symbols HGNC : CDG1N;

Chromosome HGNC : 3p21.1;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000163933;

Details

Origin ID

HGNC:30220;

UMLS CUI

C1538829;

Automatic exact mappings (from CISMeF team)
- Congenital disorder of glycosylation, type in [OMIM Phenotype]
- RFT1 homolog [ORDO Gene]
- Rft1 homolog [OMIM gene]
- congenital disorder of glycosylation In [DO Concept]
OMIM gene
- Rft1 homolog [OMIM gene]
Orphanet gene
- RFT1 homolog [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- Rft1 homolog [OMIM gene]

Keyword's position in hierarchy(ies) :

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