Spinocerebellar ataxia type 13 (Q101088): 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/1191033828 / rank | |||
Normal rank | |||
Revision as of 17:53, 16 August 2026
Spinocerebellar ataxia type 13 (SCA13) is a very rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterised by onset in childhood marked by delayed motor and cognitive development followed by mild progression of cerebellar ataxia.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1191033828 |
||
| English | Spinocerebellar ataxia type 13 |
Spinocerebellar ataxia type 13 (SCA13) is a very rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterised by onset in childhood marked by delayed motor and cognitive development followed by mild progression of cerebellar ataxia. |
