Intellectual disability, X-linked 1

MONDO:0010656

An X-linked dominant condition caused by mutation(s) in the IQSEC2 gene, encoding IQ motif and SEC7 domain-containing protein 2. It is characterized by substantially impaired intellectual functioning and behavioral abnormalities.

Also known as: IQSEC2-related disorder, IQSEC2-related syndromic intellectual disability, MRX, MRX1, MRX78, intellectual developmental disorder, X-linked 1, X-linked dominant, intellectual disability, X-linked 1, mental retardation, X-linked 1

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

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