(Q50349609)

English

autosomal dominant non-syndromic intellectual disability 5

An autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of SYNGAP1 on chromosome 6p21.32.

  • autosomal dominant mental retardation 5
  • MRD5
  • MENTAL RETARDATION, AUTOSOMAL DOMINANT 5
  • Mental Retardation, Autosomal Dominant type 5
  • MENTAL RETARDATION, AUTOSOMAL DOMINANT 5; MRD5

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