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GTR Home > Conditions/Phenotypes > Retinitis pigmentosa 1

Summary

Any retinitis pigmentosa in which the cause of the disease is a mutation in the RP1 gene. [from MONDO]

Genes See tests for all associated and related genes

  • Also known as: DCDC4A, ORP1, RP1
    Summary: RP1 axonemal microtubule associated

Clinical features

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