Disease association ontology term - MONDO:0020771 - spinocerebellar ataxia, autosomal recessive, with axonal neuropathy

Term summary

ID

MONDO:0020771

Name

spinocerebellar ataxia, autosomal recessive, with axonal neuropathy

Ontology or CV name

Disease association

Parents

• is_a autosomal recessive cerebellar ataxia
• is_a DNA repair disease

Annotation