(Q50349610)

English

autosomal dominant non-syndromic intellectual disability 6

An autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of GRIN2B on chromosome 12p13.1.

  • MRD6
  • autosomal dominant mental retardation 6
  • MENTAL RETARDATION, AUTOSOMAL DOMINANT 6
  • MENTAL RETARDATION, AUTOSOMAL DOMINANT 6; MRD6
  • Mental Retardation, Autosomal Dominant type 6
  • GRIN2B-related neurodevelopmental disorder

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