(Q50349631)

English

autosomal dominant non-syndromic intellectual disability 27

An autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of SOX11 on chromosome 2p25.2.

  • MRD27
  • autosomal dominant mental retardation 27
  • MENTAL RETARDATION, AUTOSOMAL DOMINANT 27; MRD27
  • MENTAL RETARDATION, AUTOSOMAL DOMINANT 27
  • Mental Retardation, Autosomal Dominant type 27
  • Coffin-Siris syndrome 9

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