Mitochondrial intermediate peptidase deficiency

Synonym(s)
- Combined oxidative phosphorylation deficiency type 31
Type

Disease
External link(s)
- Orphanet
- IEMbase
Gene
- MIPEP / Mitochondrial Intermediate Peptidase
  13q12.12
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Mitochondrial intermediate peptidase
Disease group(s)
- 11.3 Disorders of mitochondrial protein quality control