Complete trisomy 13 (Q46805): Difference between revisions
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dki-india-LD40.1 | |||||||||||||||
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13 August 2026
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Latest revision as of 15:37, 13 August 2026
Trisomy 13 is a chromosomal anomaly caused by the presence of an extra chromosome 13 and is characterised by brain malformations (holoprosencephaly), facial dysmorphism, ocular anomalies, postaxial polydactyly, visceral malformations (cardiopathy) and severe psychomotor retardation.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | LD40.1 |
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| English | Complete trisomy 13 |
Trisomy 13 is a chromosomal anomaly caused by the presence of an extra chromosome 13 and is characterised by brain malformations (holoprosencephaly), facial dysmorphism, ocular anomalies, postaxial polydactyly, visceral malformations (cardiopathy) and severe psychomotor retardation. |
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CID11:LD40.1
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dki-india-LD40.1
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Concluído
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13 August 2026
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