Coffin-Siris syndrome 2 (Q50349618)

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An autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of ARID1A on chromosome 1p36.11.
  • MRD14
  • autosomal dominant mental retardation 14
  • CSS2
  • Mental Retardation, Autosomal Dominant type 14
  • MENTAL RETARDATION, AUTOSOMAL DOMINANT 14; MRD14
  • MENTAL RETARDATION, AUTOSOMAL DOMINANT 14
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Language Label Description Also known as
English
Coffin-Siris syndrome 2
An autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of ARID1A on chromosome 1p36.11.
  • MRD14
  • autosomal dominant mental retardation 14
  • CSS2
  • Mental Retardation, Autosomal Dominant type 14
  • MENTAL RETARDATION, AUTOSOMAL DOMINANT 14; MRD14
  • MENTAL RETARDATION, AUTOSOMAL DOMINANT 14

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