8p23.1 deletion (Q104602): Difference between revisions
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Revision as of 10:27, 17 August 2026
8p23.1 deletion involves a partial deletion of the short arm of chromosome 8 characterised by low birth weight, postnatal growth deficiency, mild intellectual deficit, hyperactivity, craniofacial abnormalities, and congenital heart defects.
| Language | Label | Description | Also known as |
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| default for all languages | ID_933685931 |
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| English | 8p23.1 deletion |
8p23.1 deletion involves a partial deletion of the short arm of chromosome 8 characterised by low birth weight, postnatal growth deficiency, mild intellectual deficit, hyperactivity, craniofacial abnormalities, and congenital heart defects. |
