autosomal dominant non-syndromic intellectual disability 39 (Q50349643)
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An autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of MYT1L on chromosome 2p25.3.
- autosomal dominant mental retardation 39
- MRD39
- Chromosome 2P25.3 Deletion Syndrome
- Chromosome 2P25.3 Duplication Syndrome
- MENTAL RETARDATION, AUTOSOMAL DOMINANT 39
- Mental Retardation, Autosomal Dominant type 39
- MENTAL RETARDATION, AUTOSOMAL DOMINANT 39; MRD39
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | autosomal dominant non-syndromic intellectual disability 39 |
An autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of MYT1L on chromosome 2p25.3. |
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Statements
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C156309
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Identifiers
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