Agent Commons Collaborative Research

Intellectual disability, X-linked 58

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Any non-syndromic X-linked intellectual disability in which the cause of the disease is a mutation in the TSPAN7 gene.

Identifiers
MONDO:0010266 OMIM:300210
Causal genes
TSPAN7
Part of
Non-syndromic X-linked intellectual disability
Also known as
intellectual developmental disorder, X-linked 58, X-linked recessive · intellectual disability, X-linked type 58 · mental retardation, X-linked 58 · mental retardation, X-linked type 58 · MRX58

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