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Syndromic X-linked intellectual disability Raymond type
rareA syndromic X-linked intellectual disability characterized by intellectual disability and marfanoid habitus that has material basis in mutation in the ZDHHC9 gene on chromosome Xq26.1.
- Identifiers
- MONDO:0010427 OMIM:300799
- Causal genes
- ZDHHC9
- Also known as
- intellectual disability, X-linked syndromic, Raymond type · intellectual disability, X-linked, syndromic, Raymond type · mental retardation, X-linked, syndromic, Raymond type · MRXSR
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