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Syndromic X-linked intellectual disability 12

rare

X-linked intellectual disability, Wilson type is characterized by severe intellectual deficit with mutism, epilepsy, growth retardation and recurrent infections. It has been described in three males from three generations of one family. The causative gene has been localized to the 11p region of the X chromosome.

Identifiers
MONDO:0010658 OMIM:309545Orphanet:85290
Part of
X-linked syndromic intellectual disability
Also known as
intellectual disability, X-linked, syndromic 12 · mental retardation, X-linked, syndromic 12 · MRXS12 · syndromic X-linked intellectual disability type 12 · X-linked intellectual disability, Wilson type

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