Autosomal recessive spinocerebellar ataxia 10

Definition

Any autosomal recessive cerebellar ataxia in which the cause of the disease is a mutation in the ANO10 gene.

Also known as ANO10 autosomal recessive cerebellar ataxia, autosomal recessive cerebellar ataxia caused by mutation in ANO10, autosomal recessive spinocerebellar ataxia type 10, SCAR10, spinocerebellar ataxia, autosomal recessive type 10 — per MONDO

Also identified as

• DOID 0050999 per MONDO
• OMIM 613728 per MONDO
• Orphanet 284289 per MONDO
• UMLS C3150998 per MONDO