Mitochondrial thioredoxin 2 deficiency

Synonym(s)
- Combined oxidative phosphorylation deficiency type 29
Type

Disease
External link(s)
- Orphanet
- IEMbase
Gene
- TXN2 / thioredoxin 2
  22q12.3
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Thioredoxin-2, mitochondrial
Disease group(s)
- 11.4 Miscellaneous disorders associated with mitochondrial dysfunction