| Dataset | GAD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | A cerebellar disease characterized by ataxia originating in the cerebellum. (Human Disease Ontology, DOID_0050753) |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the disease cerebellar ataxia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| CACNA1A | calcium channel, voltage-dependent, P/Q type, alpha 1A subunit |
