Complete trisomy 18 (Q46806): Difference between revisions
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Revision as of 15:37, 13 August 2026
Trisomy 18 is a chromosomal abnormality associated with the presence of an extra chromosome 18 and characterised by growth delay, dolichocephaly, a characteristic facies, limb anomalies and visceral malformations.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | LD40.2 |
||
| English | Complete trisomy 18 |
Trisomy 18 is a chromosomal abnormality associated with the presence of an extra chromosome 18 and characterised by growth delay, dolichocephaly, a characteristic facies, limb anomalies and visceral malformations. |
Statements
CID11:LD40.2
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dki-india-LD40.2
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Concluído
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13 August 2026
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