Sideroflexin 4 deficiency

Synonym(s)
- Combined oxidative phosphorylation deficiency type 18
Type

Disease
External link(s)
- Orphanet
- IEMbase
Gene
- SFXN4 / Sideroflexin 4
  10q26.11
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Sideroflexin-4
Disease group(s)
- 11.4 Miscellaneous disorders associated with mitochondrial dysfunction