autosomal dominant non-syndromic intellectual disability 5 (Q50349609)
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An autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of SYNGAP1 on chromosome 6p21.32.
- autosomal dominant mental retardation 5
- MRD5
- MENTAL RETARDATION, AUTOSOMAL DOMINANT 5
- Mental Retardation, Autosomal Dominant type 5
- MENTAL RETARDATION, AUTOSOMAL DOMINANT 5; MRD5
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | autosomal dominant non-syndromic intellectual disability 5 |
An autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of SYNGAP1 on chromosome 6p21.32. |
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Statements
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Identifiers
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Sitelinks
Wikipedia(1 entry)
- dewiki SYNGAP-Syndrom