Ferredoxin reductase deficiency

Type

Disease
External link(s)
- Orphanet
- IEMbase
Gene
- FDXR / Ferredoxin Reductase
  17q25.1
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Ferredoxin reductase
Disease group(s)
- 8.2 Disorders of lipoic acid and iron-sulfur metabolism
Child entries
- Auditory neuropathy and optic atrophy