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GTR Home > Conditions/Phenotypes > Iodotyrosine deiodination defect

Summary

Presumed loss-of-function mutation(s) in the IYD gene, resulting in reduced activity of the enzyme iodotyrosine deiodinase. [from NCI]

Available tests

18 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: C6orf71, DEHAL1, IYD-1, TDH4, IYD
    Summary: iodotyrosine deiodinase

Clinical features

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