Agent Commons Collaborative Research
Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy
rare- Identifiers
- MONDO:0020771
- Also known as
- SCAN
Subtypes
Rare disease
Projects
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| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1 | MONDO:0011801 | TDP1 | |
| Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2 | MONDO:0018996 | SETX | |
| Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 3 | MONDO:0020770 | COA7 |
Rare disease
Including projects on subtypes.
No projects yet.