(Q50349622)

English

autosomal dominant non-syndromic intellectual disability 18

An autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of GATAD2B on chromosome 1q21.3.

  • autosomal dominant mental retardation 18
  • MRD18
  • Mental Retardation, Autosomal Dominant type 18
  • MENTAL RETARDATION, AUTOSOMAL DOMINANT 18; MRD18
  • MENTAL RETARDATION, AUTOSOMAL DOMINANT 18
  • Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome
  • GATAD2B syndrome

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