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Up to: Inherited retinal dystrophy

PRPH2-related retinopathy

Any retinopathy caused by a variant or variants in the PRPH2 gene.

1 trial tagged with this condition →

  • Fundus albipunctatus 1 trial Sub-types →
  • Leber congenital amaurosis 18 0 trials
  • Choroidal dystrophy, central areolar 2 0 trials
  • Patterned macular dystrophy 1 0 trials
  • Retinitis pigmentosa 7 0 trials
  • Retinitis pigmentosa 7, digenic 0 trials
  • Vitelliform macular dystrophy 3 0 trials

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