Spinocerebellar ataxia type 7 (Q101071): 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/625800545 / rank | |||
Normal rank | |||
Revision as of 17:52, 16 August 2026
Spinocerebellar ataxia type 7 (SCA7) is an autosomal dominant disorder that involves progressive ataxia, dysarthria, dysphagia, as well as central vision loss due to cone-rod retinal dystrophy.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_625800545 |
||
| English | Spinocerebellar ataxia type 7 |
Spinocerebellar ataxia type 7 (SCA7) is an autosomal dominant disorder that involves progressive ataxia, dysarthria, dysphagia, as well as central vision loss due to cone-rod retinal dystrophy. |
