1 Child Term
| Identifier | Name | Description |
|---|---|---|
| DOID:0080059 | autosomal recessive spinocerebellar ataxia 7 | An autosomal recessive cerebellar ataxia that is characterized by onset of progressive gait difficulties, eye movement abnormalities, and dysarthria in the first or second decade of life and that has_material_basis_in compound heterozygous mutation in the TPP1 gene on chromosome 11p15. |
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. |
