Disease association ontology term - MONDO:0013392 - autosomal recessive spinocerebellar ataxia 10
Term summary
- ID
- MONDO:0013392
- Name
- autosomal recessive spinocerebellar ataxia 10
- Ontology or CV name
- Disease association
- Definition
- Any autosomal recessive cerebellar ataxia in which the cause of the disease is a mutation in the ANO10 gene.
