Disease association ontology term - MONDO:0012784 - autosomal recessive ataxia due to ubiquinone deficiency
Term summary
- ID
- MONDO:0012784
- Name
- autosomal recessive ataxia due to ubiquinone deficiency
- Ontology or CV name
- Disease association
- Definition
- This syndrome is characterized by childhood-onset progressive ataxia and cerebellar atrophy.
