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References OMIM Gene GeneReviews HGMD HGNC
last update : 20-03-2009
Symbol OED
Location Xp21.1
Name blindness, night, congenital, stationary 2,
Other name(s)
  • Oregon eye disease
  • Duchenne muscular dystrophy
  • Corresponding gene DMD
    Other symbol(s) CSNBX3
    Main clinical features
  • some incomplete forms, with persistence of slight rod function (dystrophin defect)
  • Genetic determination sex linked
    Function/system disorder
    Type disease
    Gene product
    Name dystrophin (DMD)