autosomal dominant non-syndromic intellectual disability 41 (Q50349645)
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An autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of TBL1XR1 on chromosome 3q26.32.
- autosomal dominant mental retardation 41
- MRD41
- Mental Retardation, Autosomal Dominant 41
- Mental Retardation, Autosomal Dominant type 41
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | autosomal dominant non-syndromic intellectual disability 41 |
An autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of TBL1XR1 on chromosome 3q26.32. |
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Statements
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Identifiers
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