Spinocerebellar ataxia type 14 (Q101072): Difference between revisions

From determinar.ia.br - Determine suas informações
‎Created a new Item
 
‎Changed an Item
 
(6 intermediate revisions by the same user not shown)
description / pt-brdescription / pt-br
 
Ataxia espinocerebelar tipo 14 (SCA14) é um subtipo raro e leve de ataxia cerebelar autossômica dominante tipo 1 (ACAD tipo I). É caracterizada por ataxia lentamente progressiva, disartria e nistagmo.
description / endescription / en
 
Spinocerebellar ataxia type 14 (SCA14) is a rare mild subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterised by slowly progressive ataxia, dysarthria and nystagmus.
Property / Canonical URI
 
Property / Canonical URI: https://id.who.int/icd/entity/736357100 / rank
 
Normal rank
Property / CURIE
 
CID11:ID_736357100
Property / CURIE: CID11:ID_736357100 / rank
 
Normal rank
Property / Canary Token
 
dki-india-ID_736357100
Property / Canary Token: dki-india-ID_736357100 / rank
 
Normal rank
Property / Verification Status
 
Concluído
Property / Verification Status: Concluído / rank
 
Normal rank
Property / Knowledge Architect
 
Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank
 
Normal rank
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
 
Normal rank

Latest revision as of 17:52, 16 August 2026

Spinocerebellar ataxia type 14 (SCA14) is a rare mild subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterised by slowly progressive ataxia, dysarthria and nystagmus.
Language Label Description Also known as
default for all languages
ID_736357100
    English
    Spinocerebellar ataxia type 14
    Spinocerebellar ataxia type 14 (SCA14) is a rare mild subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterised by slowly progressive ataxia, dysarthria and nystagmus.

      Statements

      CID11:ID_736357100
      0 references
      dki-india-ID_736357100
      0 references
      Concluído
      0 references
      15 August 2026
      0 references