Spinocerebellar ataxia type 29

Definition

Spinocerebellar ataxia type 29 (SCA29) is a rare subtype of autosomal dominant cerebellar ataxia type I (ADCA type I) characterized by very slowly progressive or non-progressive ataxia, dysarthria, oculomotor abnormalities and intellectual disability.

Also known as congenital nonprogressive spinocerebellar ataxia, SCA29, spinocerebellar ataxia 29, congenital nonprogressive, spinocerebellar ataxia type 29 — per MONDO

Also identified as

• DOID 0050978 per MONDO
• MESH C537206 per MONDO
• OMIM 117360 per MONDO
• Orphanet 208513 per MONDO
• SCTID 715825009 per MONDO
• UMLS C1861732 per MONDO