autosomal dominant non-syndromic intellectual disability 38 (Q50349642)
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An autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of EEF1A2 on chromosome 20q13.33.
- MRD38
- autosomal dominant mental retardation 38
- PRELDS
- psychomotor retardation, epilepsy, and language disability syndrome
- MENTAL RETARDATION, AUTOSOMAL DOMINANT 38
- Mental Retardation, Autosomal Dominant type 38
- MENTAL RETARDATION, AUTOSOMAL DOMINANT 38; MRD38
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | autosomal dominant non-syndromic intellectual disability 38 |
An autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of EEF1A2 on chromosome 20q13.33. |
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