Facioscapulohumeral muscular dystrophy (Q41386): Difference between revisions

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Distrofia muscular fácio-escápulo-umeral (FSHD) é uma doença muscular hereditária autossômica dominante caracterizada por fraqueza muscular progressiva com envolvimento focal inicial dos músculos de face, ombro e braço.
description / endescription / en
 
Facioscapulohumeral muscular dystrophy (FSHD) is an autosomal dominantly inherited muscle disease characterised by progressive muscle weakness with initial focal involvement of the facial, shoulder and arm muscles.
Property / Canonical URI
 
Property / Canonical URI: https://id.who.int/icd/entity/621965073 / rank
 
Normal rank
Property / CURIE
 
CID11:8C70.3
Property / CURIE: CID11:8C70.3 / rank
 
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Property / Canary Token
 
dki-india-8C70.3
Property / Canary Token: dki-india-8C70.3 / 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: G71.0 / rank
 
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Latest revision as of 07:32, 13 August 2026

Facioscapulohumeral muscular dystrophy (FSHD) is an autosomal dominantly inherited muscle disease characterised by progressive muscle weakness with initial focal involvement of the facial, shoulder and arm muscles.
Language Label Description Also known as
default for all languages
8C70.3
    English
    Facioscapulohumeral muscular dystrophy
    Facioscapulohumeral muscular dystrophy (FSHD) is an autosomal dominantly inherited muscle disease characterised by progressive muscle weakness with initial focal involvement of the facial, shoulder and arm muscles.

      Statements

      CID11:8C70.3
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      dki-india-8C70.3
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      Concluído
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      13 August 2026
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      0 references