Mitochondrial methionyl-trna formyltransferase

Preferred Label : Mitochondrial methionyl-trna formyltransferase;

Symbol : MTFMT;

CISMeF acronym : MTFMT;

Type : Gene;

Ensembl ID : ENSG00000103707;

Prefixed ID : *611766;

Details

Origin ID

611766;

UMLS CUI

C1826321;

Automatic exact mappings (from CISMeF team)
- mitochondrial methionyl-tRNA formyltransferase [ORDO Gene]
Currated CISMeF NLP mapping
- MTFMT gene [LOINC component]
- mitochondrial methionyl-tRNA formyltransferase [HGNC gene]
HGNC gene
- mitochondrial methionyl-tRNA formyltransferase [HGNC gene]
ORDO concept(s)
- mitochondrial methionyl-tRNA formyltransferase [ORDO Gene]
Phenotypes related
- Combined oxidative phosphorylation deficiency 15 [OMIM Phenotype]
- Mitochondrial complex I deficiency, nuclear type 27 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- MTFMT gene [LOINC component]
- mitochondrial methionyl-tRNA formyltransferase [HGNC gene]

Keyword's position in hierarchy(ies) :

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