maternal uniparental disomy of chromosome 20 (Q55788992)
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human disease
- Maternal UPD(20)
- Maternal uniparental disomy of chromosome type 20
- UPD(20)mat
- Mulchandani-Bhoj-Conlin syndrome
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | maternal uniparental disomy of chromosome 20 |
human disease |
|
Statements
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Identifiers
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