| Metadata | |
|---|---|
| ID | DOID:0050979 |
| Name | spinocerebellar ataxia type 30 |
| Definition | An autosomal dominant cerebellar ataxia that is characterized by slowly progressive gait abnormalities and dysarthria, has_material_basis_in mutation in the ODZ3 gene. https://www.omim.org/entry/613371 |
| Xrefs | |
| Subsets |
DO_rare_slim |
| Parent Relationships |