(Q50349640)
English
autosomal dominant non-syndromic intellectual disability 36
An autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of PPP2R1A on chromosome 19q13.41.
- autosomal dominant mental retardation 36
- MRD36
- Mental Retardation, Autosomal Dominant type 36
- MENTAL RETARDATION, AUTOSOMAL DOMINANT 36
- MENTAL RETARDATION, AUTOSOMAL DOMINANT 36; MRD36
Statements
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Identifiers
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