GTR Home > Conditions/Phenotypes > Intellectual disability, X-linked 99

Summary

Any non-syndromic X-linked intellectual disability in which the cause of the disease is a mutation in the USP9X gene. [from MONDO]

Available tests

19 tests are in the database for this condition.

Genes See tests for all associated and related genes

  • Also known as: DFFRX, FAF, FAF-X, FAM, MRX99, MRXS99F, XLID99, hFAM, USP9X
    Summary: ubiquitin specific peptidase 9 X-linked

Clinical features

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