Dynamin-like protein 1 deficiency

Synonym(s)
- Optic atrophy type 5,
- encephalopathy due to defective mitochondrial and peroxisomal fission type 1
Type

Disease
External link(s)
- Orphanet
- IEMbase
Gene
- DNM1L / Dynamin 1 Like
  12p11.21
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Dynamin-1-like protein
Disease group(s)
- 19.2 Disorders of mitochondrial and peroxisomal dynamics