C2orf69 deficiency

Type

Disease
Gene
- C2orf69 / Uncharacterized Protein C2orf69
  2q33.1
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Uncharacterized protein C2orf69
Disease group(s)
- 11.4 Miscellaneous disorders associated with mitochondrial dysfunction