8p23.1 deletion (Q104602)
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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 |
|---|---|---|---|
| default for all languages | ID_933685931 |
||
| 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. |
Statements
CID11:ID_933685931
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dki-india-ID_933685931
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Concluído
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16 August 2026
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