OnlineIMD

Mitofusin 2 deficiency

  • Type
    Disease
  • External link(s)
    • Orphanet
    • IEMbase
  • Gene
    • MFN2 / Mitofusin 2
      • 1p36.22
      • OMIM
      • GnomAD
      • Ensembl
      • HGNC
      • VMH
      • LOVD
  • Gene product
    • Mitofusin-2
  • Disease group(s)
    • 19.2    Disorders of mitochondrial and peroxisomal dynamics
  • Child entries
    • Axonal Charcot-Marie-Tooth type 2A2
    • Hereditary motor and sensory neuropathy type 5
    • Multiple symmetric lipomatosis