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Trisomy 20p
rareTrisomy 20p is a chromosomal disorder resulting from duplication of all or part of the short arm of chromosome 20. It is mostly characterized by normal growth, mild to moderate intellectual disability, speech delay, poor coordination and evocative facial features.
- Identifiers
- MONDO:0016844 Orphanet:261318
- Part of
- Partial trisomy of chromosome 20
- Also known as
- 20p duplication · 20p trisomy · chromosome 20p duplication · dup(20p) · Duplication 20p
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