mental retardation, autosomal dominant 20 (Q50349624)
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An autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of MEF2C on chromosome 5q14.3.
- Chromosome 5Q14.3 Deletion Syndrome, Proximal
- MENTAL RETARDATION, AUTOSOMAL DOMINANT 20; MRD20
- Mental Retardation, Stereotypic Movements, Epilepsy, And/Or Cerebral Malformations
- autosomal dominant mental retardation 20
- Mental Retardation, Autosomal Dominant type 20
- MRD20
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | mental retardation, autosomal dominant 20 |
An autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of MEF2C on chromosome 5q14.3. |
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