Nogo-interacting mitochondrial protein deficiency

Synonym(s)
- Optic atrophy type 10
Type

Disease
External link(s)
- IEMbase
Gene
- RTN4IP1 / Reticulon 4 Interacting Protein 1
  6q21
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Reticulon 4 interacting protein 1
Disease group(s)
- 11.4 Miscellaneous disorders associated with mitochondrial dysfunction