(Q50349611)
English
autosomal dominant non-syndromic intellectual disability 7
An autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of DYRK1A on chromosome 21q22.13.
- autosomal dominant mental retardation 7
- MRD7
- intellectual disability, autosomal dominant type 7
- MENTAL RETARDATION, AUTOSOMAL DOMINANT 7; MRD7
- Mental Retardation, Autosomal Dominant type 7
- MENTAL RETARDATION, AUTOSOMAL DOMINANT 7
Statements
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Identifiers
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