An inherited condition caused by mutation(s) in the DDX3X gene, encoding ATP-dependent RNA helicase DDX3X. It is characterized by severe intellectual disability and variable neurologic features.
Comprehensive, easy-to-understand information about this condition
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intellectual disability, X-linked 23
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intellectual disability, X-linked 20
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intellectual disability, X-linked 14
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intellectual disability, X-linked 21
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intellectual disability, X-linked 58
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