Dystonia due to Hartnup disease (Q98810): Difference between revisions
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Distonia (contrações musculares involuntárias) que ocorre no contexto da doença de Hartnup, um transtorno autossômico recessivo do metabolismo de aminoácidos que leva à erupção cutânea escamosa intermitente avermelhada semelhante à pelagra, ataxia cerebelar, labilidade emocional e disfunção neurológica progressiva. | |||||||||||||||
| description / en | description / en | ||||||||||||||
Dystonia (involuntary muscle contractions) occurring in the setting of Hartnup disease, an autosomal recessive disorder of amino acid metabolism that leads to intermittent pellagra-like red scaly rash, cerebellar ataxia, emotional lability, and progressive neurological dysfunction. | |||||||||||||||
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| Property / Canonical URI: https://id.who.int/icd/entity/1327105709 / rank | |||||||||||||||
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CID11:ID_1327105709 | |||||||||||||||
| Property / CURIE: CID11:ID_1327105709 / rank | |||||||||||||||
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dki-india-ID_1327105709 | |||||||||||||||
| Property / Canary Token: dki-india-ID_1327105709 / rank | |||||||||||||||
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Concluído | |||||||||||||||
| Property / Verification Status: Concluído / rank | |||||||||||||||
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| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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15 August 2026
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| Property / Collection date: 15 August 2026 / rank | |||||||||||||||
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Latest revision as of 15:25, 16 August 2026
Dystonia (involuntary muscle contractions) occurring in the setting of Hartnup disease, an autosomal recessive disorder of amino acid metabolism that leads to intermittent pellagra-like red scaly rash, cerebellar ataxia, emotional lability, and progressive neurological dysfunction.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1327105709 |
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| English | Dystonia due to Hartnup disease |
Dystonia (involuntary muscle contractions) occurring in the setting of Hartnup disease, an autosomal recessive disorder of amino acid metabolism that leads to intermittent pellagra-like red scaly rash, cerebellar ataxia, emotional lability, and progressive neurological dysfunction. |
Statements
CID11:ID_1327105709
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dki-india-ID_1327105709
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Concluído
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15 August 2026
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