Spinocerebellar ataxia, autosomal recessive 22

Definition

Any autosomal recessive cerebellar ataxia in which the cause of the disease is a mutation in the VWA3B gene.

Also known as autosomal recessive cerebellar ataxia caused by mutation in VWA3B, SCAR22, spinocerebellar ataxia, autosomal recessive 22, spinocerebellar ataxia, autosomal recessive 22; SCAR22, spinocerebellar ataxia, autosomal recessive type 22, VWA3B autosomal recessive cerebellar ataxia — per MONDO

Also identified as

• DOID 0111614 per MONDO
• OMIM 616948 per MONDO
• UMLS C4310781 per MONDO