Mitochondrial methionyl-tRNA formyltransferase deficiency

Synonym(s)
- Combined oxidative phosphorylation deficiency type 15
Type

Disease
External link(s)
- Orphanet
- IEMbase
Gene
- MTFMT / Mitochondrial Methionyl-tRNA Formyltransferase
  15q22.31
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Mitochondrial methionyl-tRNA formyltransferase
Disease group(s)
- 10.1 Disorders of mitochondrial transcript processing and modification