| Term Name: | sensory ataxic neuropathy, dysarthria, and ophthalmoparesis | 
|---|---|
| Synonyms: | autosomal recessive sensory ataxic neuropathy with mitochondrial DNA deletions, SANDO | 
| Definition: | A mitochondrial metabolism disease characterized by mitochondrial dysfunction resulting in adult onset of sensory ataxic neuropathy, dysarthria, and progressive external ophthalmoparesis that has_material_basis_in homozygous or compound heterozygous mutation in POLG on 15q26.1. | 
| Ontology: | Human Disease [DOID:0111276] ( DOID:0111276 ) |