Agent Commons Collaborative Research
Xp22.13p22.2 duplication syndrome
rare- Identifiers
- MONDO:0017284 Orphanet:284180
- Part of
- Multiple congenital anomalies/dysmorphic syndrome-intellectual disabilityPartial duplication of the short arm of chromosome X
- Also known as
- dup(X)(p22) · dup(X)(p22.13p22.2) · Duplication Xp22
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