| Metadata | |
|---|---|
| ID | DOID:0050969 |
| PURL | http://purl.obolibrary.org/obo/DOID_0050969 Copy |
| Name | spinocerebellar ataxia 18 |
| Definition | An autosomal dominant cerebellar ataxia that is characterized by cerebellar ataxia and sensory neuropathy, has_material_basis_in mutation on chromosome 7q22-q23. https://rarediseases.info.nih.gov/diseases/9976/spinocerebellar-ataxia-18 |
| Xrefs | |
| Subsets |
DO_rare_slim |
| Parent Relationships |