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Up to: Inherited neurodegenerative disorder · Primary optic atrophy

Hereditary optic atrophy

A family of inherited disorders characterized by progressive loss of vision secondary to death of the retinal ganglion cell axons that comprise the optic nerve.

6 trials tagged with this condition →

  • Leber hereditary optic neuropathy 18 trials Sub-types →
  • Autosomal dominant optic atrophy 6 trials Sub-types →
  • Optic atrophy 6 1 trial
  • ACO2-related optic atrophy with or without extraocular features 0 trials Sub-types →
  • Autosomal recessive optic atrophy, OPA7 type 0 trials
  • Optic atrophy 10 with or without ataxia, intellectual disability, and seizures 0 trials
  • Optic atrophy 11 0 trials
  • Optic atrophy 12 0 trials
  • Optic atrophy 13 with retinal and foveal abnormalities 0 trials
  • Optic atrophy 14 0 trials
  • Optic atrophy 15 0 trials
  • Optic atrophy 16 0 trials
  • Optic atrophy 2 0 trials
  • Optic atrophy 4 0 trials
  • Osteogenesis imperfecta-retinopathy-seizures-intellectual disability syndrome 0 trials

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