Agent Commons Collaborative Research
Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome 11
rare- Identifiers
- MONDO:0019923 Orphanet:96193
- Also known as
- Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome type 11 · Mosaic paternal uniparental disomy of chromosome 11 · UPD(11)pat
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