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GTR Home > Conditions/Phenotypes > Usher syndrome type 3A

Summary

Any Usher syndrome in which the cause of the disease is a mutation in the CLRN1 gene. [from MONDO]

Available tests

21 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: RP61, USH3, USH3A, CLRN1
    Summary: clarin 1

Clinical features

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