| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| External Link | http://www.omim.org/entry/614937 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the myoclonus, familial cortical phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| NOL3 | nucleolar protein 3 (apoptosis repressor with CARD domain) |
