autosomal dominant non-syndromic intellectual disability 42 (Q50349646)
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An autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of GNB1 on chromosome 1p36.33.
- MRD42
- autosomal dominant mental retardation 42
- Mental Retardation, Autosomal Dominant 42
- Mental Retardation, Autosomal Dominant type 42
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | autosomal dominant non-syndromic intellectual disability 42 |
An autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of GNB1 on chromosome 1p36.33. |
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