Intellectual disability, X-linked 102

MONDO:0010497

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.

Also known as: DDX3X non-syndromic X-linked intellectual disability, intellectual developmental disorder, X-linked, syndrome, Snijders Blok type, X-linked recessive, X-linked dominant, intellectual disability, X-linked 102, intellectual disability, X-linked type 102, mental retardation, X-linked type 102, non-syndromic X-linked intellectual disability caused by mutation in DDX3X, DDX3X-related intellectual disability, MRX102

29 clinical trials for this condition and its sub-types.

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