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Chromosome 17p13.3 duplication syndrome
rare17p13.3 microduplication syndrome is characterized by variable psychomotor delay and dysmorphic features.
- Identifiers
- MONDO:0013182 OMIM:613215Orphanet:217385
- Part of
- Multiple congenital anomalies/dysmorphic syndrome-intellectual disabilityPartial duplication of the short arm of chromosome 17
- Also known as
- 17p13.3 duplication syndrome · 17p13.3 microduplication syndrome · dup(17)(p13.3) · trisomy 17p13.3
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