| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| External Link | http://www.omim.org/entry/141500 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the migraine, familial hemiplegic, 1, with progressive cerebellar ataxia phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| CACNA1A | calcium channel, voltage-dependent, P/Q type, alpha 1A subunit |
