eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | autosomal dominant cerebellar ataxia |
| Comorbidity | C0014544|epilepsy |
| Sentences | 1 |
| PubMedID- 24278426 | Spinocerebellar ataxia type 10 (sca10; omim#603516) is an autosomal dominant cerebellar ataxia variably associated with epilepsy and other nervous system disorders [1], [2]. |
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