16q24.3 deletion (Q104436): Difference between revisions

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description / pt-brdescription / pt-br
 
A síndrome de microdeleção 16q24.3 é uma anomalia cromossômica associada a atraso variável no desenvolvimento, dismorfismo facial (testa alta, orelhas grandes, filtro liso, queixo pontudo e boca larga), convulsões e transtorno do espectro autista.
description / endescription / en
 
16q24.3 microdeletion syndrome is a chromosomal anomaly associated with variable developmental delay, facial dysmorphism (high forehead, large ears, smooth philtrum, pointed chin and wide mouth), seizures and autistic spectrum disorder.
Property / Canonical URI
 
Property / Canonical URI: https://id.who.int/icd/entity/875703691 / rank
 
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Property / CURIE
 
CID11:ID_875703691
Property / CURIE: CID11:ID_875703691 / rank
 
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Property / Canary Token
 
dki-india-ID_875703691
Property / Canary Token: dki-india-ID_875703691 / rank
 
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Property / Verification Status
 
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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Property / Collection date
 
16 August 2026
Timestamp+2026-08-16T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0
Property / Collection date: 16 August 2026 / rank
 
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Latest revision as of 10:17, 17 August 2026

16q24.3 microdeletion syndrome is a chromosomal anomaly associated with variable developmental delay, facial dysmorphism (high forehead, large ears, smooth philtrum, pointed chin and wide mouth), seizures and autistic spectrum disorder.
Language Label Description Also known as
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ID_875703691
    English
    16q24.3 deletion
    16q24.3 microdeletion syndrome is a chromosomal anomaly associated with variable developmental delay, facial dysmorphism (high forehead, large ears, smooth philtrum, pointed chin and wide mouth), seizures and autistic spectrum disorder.

      Statements

      CID11:ID_875703691
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      dki-india-ID_875703691
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      Concluído
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      16 August 2026
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