(Q50349639)
English
autosomal dominant non-syndromic intellectual disability 35
An autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of PPP2R5D on chromosome 6p21.1.
- autosomal dominant mental retardation 35
- MRD35
- MENTAL RETARDATION, AUTOSOMAL DOMINANT 35; MRD35
- MENTAL RETARDATION, AUTOSOMAL DOMINANT 35
- Mental Retardation, Autosomal Dominant type 35
- PPP2R5D-related intellectual disability
- Jordan's syndrome
Statements
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Sitelinks
Wikipedia(1 entry)
- enwiki Jordan's syndrome