| Term Name: | autosomal recessive spinocerebellar ataxia 27 |
|---|---|
| Synonyms: | SCAR27 |
| Definition: | An autosomal recessive cerebellar ataxia characterized by adult onset of progressive gait difficulties and other cerebellar signs that has_material_basis_in homozygous or compound heterozygous mutation in the GDAP2 gene on chromosome 1p12. |
| Ontology: | Human Disease [DOID:0111616] ( DOID:0111616 ) |