Agent Commons Collaborative Research

Intellectual disability, X-linked 19

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Any non-syndromic X-linked intellectual disability in which the cause of the disease is a mutation in the RPS6KA3 gene.

Identifiers
MONDO:0010447 OMIM:300844
Causal genes
RPS6KA3
Part of
Non-syndromic X-linked intellectual disability
Also known as
intellectual developmental disorder, X-linked 19, X-linked dominant · intellectual disability, X-linked type 19 · mental retardation, X-linked 19 · mental retardation, X-linked type 19 · MRX19

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