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GTR Home > Conditions/Phenotypes > Mirror movements 3

Summary

Any familial congenital mirror movements in which the cause of the disease is a mutation in the DNAL4 gene. [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: MRMV3, PIG27, DNAL4
    Summary: dynein axonemal light chain 4

Clinical features

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