20p duplication (Q91022): Difference between revisions
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Revision as of 18:01, 15 August 2026
Trisomy 20p is a chromosomal disorder resulting from duplication of all or part of the short arm of chromosome 20. It is mostly characterised by normal growth, mild to moderate intellectual disability, speech delay, poor coordination and evocative facial features.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1396883815 |
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| English | 20p duplication |
Trisomy 20p is a chromosomal disorder resulting from duplication of all or part of the short arm of chromosome 20. It is mostly characterised by normal growth, mild to moderate intellectual disability, speech delay, poor coordination and evocative facial features. |
Statements
CID11:ID_1396883815
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