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GTR Home > Conditions/Phenotypes > Retinitis pigmentosa 13

Summary

Any retinitis pigmentosa in which the cause of the disease is a mutation in the PRPF8 gene. [from MONDO]

Available tests

30 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Genes See tests for all associated and related genes

  • Also known as: HPRP8, PRP8, PRPC8, RP13, SNRNP220, PRPF8
    Summary: pre-mRNA processing factor 8

Clinical features

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