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GTR Home > Conditions/Phenotypes > Retinitis pigmentosa 37

Summary

Any retinitis pigmentosa in which the cause of the disease is a mutation in the NR2E3 gene. [from MONDO]

Available tests

43 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: ESCS, PNR, RNR, RP37, rd7, NR2E3
    Summary: nuclear receptor subfamily 2 group E member 3

Clinical features

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