Ablepharon, unilateral (Q98945): Difference between revisions

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description / pt-brdescription / pt-br
 
Trata-se da ausência congênita de pálpebras. É um componente da síndrome ablefaria-macrostomia. O diagnóstico é pela ocorrência em um olho.
description / endescription / en
 
This is the congenital absence of the eyelids. It is a component of the Ablepharon macrostomia syndrome. This diagnosis is occurring in one eye.
Property / Canonical URI
 
Property / Canonical URI: https://id.who.int/icd/entity/914726589 / rank
 
Normal rank
Property / CURIE
 
CID11:ID_914726589
Property / CURIE: CID11:ID_914726589 / rank
 
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Property / Canary Token
 
dki-india-ID_914726589
Property / Canary Token: dki-india-ID_914726589 / 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
 
15 August 2026
Timestamp+2026-08-15T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0
Property / Collection date: 15 August 2026 / rank
 
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Latest revision as of 15:36, 16 August 2026

This is the congenital absence of the eyelids. It is a component of the Ablepharon macrostomia syndrome. This diagnosis is occurring in one eye.
Language Label Description Also known as
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ID_914726589
    English
    Ablepharon, unilateral
    This is the congenital absence of the eyelids. It is a component of the Ablepharon macrostomia syndrome. This diagnosis is occurring in one eye.

      Statements

      CID11:ID_914726589
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      dki-india-ID_914726589
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      Concluído
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      15 August 2026
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