Blau syndrome (Q102968): Difference between revisions

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A síndrome de Blau é uma doença autoinflamatória monogênica dominante associada a mutações em um gene chamado NOD2 (símbolo anterior CARD15)
description / endescription / en
 
Blau syndrome is a monogenic dominant autoinflammatory disease associated with mutations in a gene called NOD2 (previous symbol CARD15)
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Property / Canonical URI: https://id.who.int/icd/entity/382488319 / rank
 
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CID11:ID_382488319
Property / CURIE: CID11:ID_382488319 / rank
 
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dki-india-ID_382488319
Property / Canary Token: dki-india-ID_382488319 / rank
 
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Concluído
Property / Verification Status: Concluído / rank
 
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Property / Knowledge Architect
 
Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank
 
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16 August 2026
Timestamp+2026-08-16T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
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Property / Collection date: 16 August 2026 / rank
 
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Latest revision as of 08:46, 17 August 2026

Blau syndrome is a monogenic dominant autoinflammatory disease associated with mutations in a gene called NOD2 (previous symbol CARD15)
Language Label Description Also known as
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ID_382488319
    English
    Blau syndrome
    Blau syndrome is a monogenic dominant autoinflammatory disease associated with mutations in a gene called NOD2 (previous symbol CARD15)

      Statements

      CID11:ID_382488319
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      dki-india-ID_382488319
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      Concluído
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      16 August 2026
      0 references