1p21.3 deletion (Q105594): Difference between revisions
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16 August 2026
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Latest revision as of 11:56, 17 August 2026
1p21.3 microdeletion syndrome is an extremely rare chromosomal anomaly characterised by severe speech and language delay, intellectual deficiency, autism spectrum disorder.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1367610860 |
||
| English | 1p21.3 deletion |
1p21.3 microdeletion syndrome is an extremely rare chromosomal anomaly characterised by severe speech and language delay, intellectual deficiency, autism spectrum disorder. |
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CID11:ID_1367610860
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dki-india-ID_1367610860
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Concluído
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16 August 2026
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