autosomal dominant non-syndromic intellectual disability 26 (Q50349630)

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An autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of AUTS2 on chromosome 7q11.22.
  • MRD26
  • autosomal dominant mental retardation 26
  • Mental Retardation, Autosomal Dominant type 26
  • AUTS2 syndrome
  • MENTAL RETARDATION, AUTOSOMAL DOMINANT 26
  • MENTAL RETARDATION, AUTOSOMAL DOMINANT 26; MRD26
  • ASD due to AUTS2 deficiency
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English
autosomal dominant non-syndromic intellectual disability 26
An autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of AUTS2 on chromosome 7q11.22.
  • MRD26
  • autosomal dominant mental retardation 26
  • Mental Retardation, Autosomal Dominant type 26
  • AUTS2 syndrome
  • MENTAL RETARDATION, AUTOSOMAL DOMINANT 26
  • MENTAL RETARDATION, AUTOSOMAL DOMINANT 26; MRD26
  • ASD due to AUTS2 deficiency

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