Genetic disorders of skin pigmentation (Q46663): Difference between revisions

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description / pt-brdescription / pt-br
 
Transtornos genéticos da pele caracterizados por alteração da pigmentação, incluindo albinismo e formas hereditárias de lentiginose.
description / endescription / en
 
Genetic disorders of the skin characterised by disordered pigmentation, including albinism and inherited forms of lentiginosis.
Property / Canonical URI
 
Property / Canonical URI: https://id.who.int/icd/entity/1596419171 / rank
 
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Property / CURIE
 
CID11:EC23
Property / CURIE: CID11:EC23 / rank
 
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Property / Canary Token
 
dki-india-EC23
Property / Canary Token: dki-india-EC23 / 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
 
13 August 2026
Timestamp+2026-08-13T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0
Property / Collection date: 13 August 2026 / rank
 
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Property / Linked ICD 10
 
Property / Linked ICD 10: TESSA VIRGINIA DE OLIVEIRA PASSARELLA MADEIRA / rank
 
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Latest revision as of 15:24, 13 August 2026

Genetic disorders of the skin characterised by disordered pigmentation, including albinism and inherited forms of lentiginosis.
Language Label Description Also known as
default for all languages
EC23
    English
    Genetic disorders of skin pigmentation
    Genetic disorders of the skin characterised by disordered pigmentation, including albinism and inherited forms of lentiginosis.

      Statements

      CID11:EC23
      0 references
      dki-india-EC23
      0 references
      Concluído
      0 references
      13 August 2026
      0 references