Kocher-Debre-Semelaigne syndrome (Q106070): Difference between revisions
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| Property / Canonical URI: https://id.who.int/icd/entity/109007822 / rank | |||||||||||||||
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CID11:ID_109007822 | |||||||||||||||
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dki-india-ID_109007822 | |||||||||||||||
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| Property / Verification Status: Concluído / rank | |||||||||||||||
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| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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16 August 2026
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| Property / Collection date: 16 August 2026 / rank | |||||||||||||||
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Latest revision as of 12:51, 17 August 2026
This is a (myopathy) of hypothyroidism in infancy or childhood characterised by lower extremity or generalised muscular hypertrophy, myxoedema, short stature and cretinism.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_109007822 |
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| English | Kocher-Debre-Semelaigne syndrome |
This is a (myopathy) of hypothyroidism in infancy or childhood characterised by lower extremity or generalised muscular hypertrophy, myxoedema, short stature and cretinism. |
Statements
CID11:ID_109007822
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dki-india-ID_109007822
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Concluído
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16 August 2026
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