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GTR Home > Conditions/Phenotypes > Retinitis pigmentosa 32

Summary

A retinitis pigmentosa that has material basis in variation in the chromosome region 1p21.3-p13.3. [from MONDO]

Available tests

2 tests are in the database for this condition.

Genes See tests for all associated and related genes

  • Also known as: ERAC1, MCLC, RP32, CLCC1
    Summary: chloride channel CLIC like 1

Clinical features

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