1 Child Term
| Identifier | Name | Description |
|---|---|---|
| DOID:0050954 | spinocerebellar ataxia type 1 | An autosomal dominant cerebellar ataxia that is characterized by ataxia, dysarthria, dysphagia, dystonia and peripheral neuropathy that begins in early adulthood, has_material_basis_in the expanded (CAG)n trinucleotide repeat of ataxin-1 gene on chromosome 6p22. |
1 Parent Term
| Identifier | Name | Description |
|---|---|---|
| DOID:0050951 | hereditary ataxia | A neurodegenerative disease that is characterized by slowly progressive incoordination of gait and often associated with poor coordination of hands, speech, and eye movements. |
