Charcot-Marie-Tooth disease type 2K (Q104260): Difference between revisions

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A doença de Charcot-Marie-Tooth autossômica dominante, tipo 2K (CMT2K) é uma polineuropatia periférica sensitivomotora de CMT axonal. CMT2K é uma forma rara de CMT com fenótipo leve, início durante a segunda década de vida e progressão muito lenta.
description / endescription / en
 
Autosomal dominant Charcot-Marie-Tooth disease, type 2K (CMT2K) is an axonal CMT peripheral sensorimotor polyneuropathy. CMT2K is a rare form of CMT with a mild phenotype, onset during the second decade of life and very slow progression.
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Property / Canonical URI: https://id.who.int/icd/entity/1720211658 / rank
 
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Property / CURIE
 
CID11:ID_1720211658
Property / CURIE: CID11:ID_1720211658 / rank
 
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Property / Canary Token
 
dki-india-ID_1720211658
Property / Canary Token: dki-india-ID_1720211658 / rank
 
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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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16 August 2026
Timestamp+2026-08-16T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
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After0
Property / Collection date: 16 August 2026 / rank
 
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Latest revision as of 10:07, 17 August 2026

Autosomal dominant Charcot-Marie-Tooth disease, type 2K (CMT2K) is an axonal CMT peripheral sensorimotor polyneuropathy. CMT2K is a rare form of CMT with a mild phenotype, onset during the second decade of life and very slow progression.
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ID_1720211658
    English
    Charcot-Marie-Tooth disease type 2K
    Autosomal dominant Charcot-Marie-Tooth disease, type 2K (CMT2K) is an axonal CMT peripheral sensorimotor polyneuropathy. CMT2K is a rare form of CMT with a mild phenotype, onset during the second decade of life and very slow progression.

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      CID11:ID_1720211658
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      dki-india-ID_1720211658
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      Concluído
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      16 August 2026
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