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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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Broader categories

Disease (618) Nervous system disorder (217) Hereditary disease (172) Neurodevelopmental disorder (125) Intellectual disability (115) X-linked disease (16) Human disease (14) Hereditary neurological disease (5) Disease of genetic or genomic mechanism (2) Disease by body system or component (0)
Trials to join now! 12 Not yet recruiting 5 Not yet finished but already full! 3 Completed 9
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