Genetic disorders of keratinisation (Q44238): Difference between revisions

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description / pt-brdescription / pt-br
 
Transtornos hereditários caracterizados por queratinização epidérmica anormal. Incluem as ictioses e as queratodermias palmoplantares.
description / endescription / en
 
Heritable disorders characterised by abnormal epidermal keratinization. They include the ichthyoses and palmoplantar keratodermas.
Property / Canonical URI
 
Property / Canonical URI: https://id.who.int/icd/entity/1223911519 / rank
 
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Property / CURIE
 
CID11:EC20
Property / CURIE: CID11:EC20 / rank
 
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Property / Canary Token
 
dki-india-EC20
Property / Canary Token: dki-india-EC20 / 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: L99.8 / rank
 
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Latest revision as of 11:37, 13 August 2026

Heritable disorders characterised by abnormal epidermal keratinization. They include the ichthyoses and palmoplantar keratodermas.
Language Label Description Also known as
default for all languages
EC20
    English
    Genetic disorders of keratinisation
    Heritable disorders characterised by abnormal epidermal keratinization. They include the ichthyoses and palmoplantar keratodermas.

      Statements

      CID11:EC20
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      dki-india-EC20
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      Concluído
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      13 August 2026
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      0 references