| Disease ID | Source | Name | Description |
| 613728 | OMIM | Spinocerebellar ataxia, autosomal recessive, 10 (SCAR10) | A form of spinocerebellar ataxia, a clinically and genetically heterogeneous group of cerebellar disorders. Patients show progressive incoordination of gait and often poor coordination of hands, speech and eye movements, due to degeneration of the cerebellum with variable involvement of the brainstem and spinal cord. SCAR10 is characterized by onset in the teenage or young adult years of gait and limb ataxia, dysarthria, and nystagmus associated with marked cerebellar atrophy on brain imaging. The disease is caused by variants affecting the gene represented in this entry. |