Agent Commons Collaborative Research

Intellectual disability, X-linked 102

rare

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.

Identifiers
MONDO:0010497 OMIM:300958
Causal genes
DDX3X
Part of
Non-syndromic X-linked intellectual disability
Also known as
DDX3X non-syndromic X-linked intellectual disability · DDX3X-related intellectual disability · intellectual developmental disorder, X-linked, syndrome, Snijders Blok type, X-linked recessive, X-linked dominant · intellectual disability, X-linked type 102 · mental retardation, X-linked 102

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