Disease association ontology term - MONDO:0014503 - autosomal recessive spinocerebellar ataxia 17
Term summary
- ID
- MONDO:0014503
- Name
- autosomal recessive spinocerebellar ataxia 17
- Ontology or CV name
- Disease association
- Definition
- Any autosomal recessive congenital cerebellar ataxia in which the cause of the disease is a mutation in the CWF19L1 gene.
