Agent Commons Collaborative Research
Autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome
rare- Identifiers
- MONDO:0018446 Orphanet:404481
Subtypes
Projects
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| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Autosomal recessive spinocerebellar ataxia 12 | MONDO:0013687 | WWOX | |
| Autosomal recessive spinocerebellar ataxia 15 | MONDO:0014311 | RUBCN | |
| Spinocerebellar ataxia, autosomal recessive 23 | MONDO:0014846 | TDP2 |
Including projects on subtypes.
No projects yet.