Catalog

Spinocerebellar ataxia type 7

No MMS code

Link to WHO Definition

Spinocerebellar ataxia type 7 – http://id.who.int/icd/entity/625800545

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.