| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| External Link | http://www.omim.org/entry/611726 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the epilepsy, progressive myoclonic 3, with or without intracellular inclusions phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| KCTD7 | potassium channel tetramerization domain containing 7 |
