Smith-Magenis syndrome (Q86806): Difference between revisions
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| Property / Canonical URI: https://id.who.int/icd/entity/989025532 / rank | |||||||||||||||
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CID11:ID_989025532 | |||||||||||||||
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dki-india-ID_989025532 | |||||||||||||||
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| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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13 August 2026
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Latest revision as of 12:21, 15 August 2026
Smith-Magenis syndrome is a complex genetic disorder characterised by variable intellectual deficit, sleep disturbance, craniofacial and skeletal anomalies, psychiatric disorders, and speech and motor delay.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_989025532 |
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| English | Smith-Magenis syndrome |
Smith-Magenis syndrome is a complex genetic disorder characterised by variable intellectual deficit, sleep disturbance, craniofacial and skeletal anomalies, psychiatric disorders, and speech and motor delay. |
Statements
CID11:ID_989025532
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dki-india-ID_989025532
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Concluído
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13 August 2026
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