1 Child Term
| Identifier | Name | Description |
|---|---|---|
| DOID:0111612 | autosomal recessive spinocerebellar ataxia 3 | An autosomal recessive cerebellar ataxia characterized by spinocerebellar ataxia with optic and cochlear degeneration that has_material_basis_in homozygous or compound heterozygous mutation in a region on chromosome 6p23-p21. |
1 Parent Term
| Identifier | Name | Description |
|---|---|---|
| DOID:1289 | neurodegenerative disease | A central nervous system disease that results in the progressive deterioration of function or structure of neurons. |
