autosomal dominant non-syndromic intellectual disability 13 (Q50349617)
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An autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of DYNC1H1 on chromosome 14q32.31.
- autosomal dominant mental retardation 13
- MRD13
- mental retardation, autosomal dominant 13, with neuronal migration defects
- Mental Retardation, Autosomal Dominant, 13, With Neuronal Migration Defects
- MENTAL RETARDATION, AUTOSOMAL DOMINANT 13; MRD13
- MENTAL RETARDATION, AUTOSOMAL DOMINANT 13
- Mental Retardation, Autosomal Dominant type 13
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | autosomal dominant non-syndromic intellectual disability 13 |
An autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of DYNC1H1 on chromosome 14q32.31. |
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Statements
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C141424
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Identifiers
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