Behr syndrome

Synonym(s)
- OPA1 deficiency
Type

Disease
External link(s)
- Orphanet
- IEMbase
Gene
- OPA1 / OPA1, Mitochondrial Dynamin Like GTPase
  3q29
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Mitochondrial dynamin-like GTPase
Disease group(s)
- 19.2 Disorders of mitochondrial and peroxisomal dynamics
Child entries
- Optic atrophy type 1