Spinocerebellar ataxia type 32 (Q101104): Difference between revisions

From determinar.ia.br - Determine suas informações
‎Changed label, description and/or aliases in pt-br, en
‎Changed an Item
Property / Canonical URI
 
Property / Canonical URI: https://id.who.int/icd/entity/1372046516 / rank
 
Normal rank

Revision as of 17:54, 16 August 2026

Spinocerebellar ataxia type 32 is a subtype of autosomal dominant cerebellar ataxia type 1 characterised by ataxia, cognitive impairment and azoospermia in males.
Language Label Description Also known as
default for all languages
ID_1372046516
    English
    Spinocerebellar ataxia type 32
    Spinocerebellar ataxia type 32 is a subtype of autosomal dominant cerebellar ataxia type 1 characterised by ataxia, cognitive impairment and azoospermia in males.

      Statements