autosomal dominant non-syndromic intellectual disability 19 (Q50349623)
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An autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of CTNNB1 on chromosome 3p22.1.
- MRD19
- autosomal dominant mental retardation 19
- Intellectual disability, autosomal dominant 19
- Mental Retardation, Autosomal Dominant type 19
- CTNNB1-related intellectual disability
- MENTAL RETARDATION, AUTOSOMAL DOMINANT 19
- neurodevelopmental disorder with spastic diplegia and visual defects
- Severe intellectual disability-progressive spastic diplegia syndrome
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | autosomal dominant non-syndromic intellectual disability 19 |
An autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of CTNNB1 on chromosome 3p22.1. |
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C176897
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