An epilepsy syndrome characterized by adult-onset cortical myoclonus typically first seen as tremulous finger movements and myoclonus of the extremities.
| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Benign adult familial myoclonic epilepsy | MONDO:0019448 | ||
| Epilepsy, familial adult myoclonic, 1 | MONDO:0010985 | SAMD12 | |
| Epilepsy, familial adult myoclonic, 2 | MONDO:0011930 | STARD7 | |
| Epilepsy, familial adult myoclonic, 3 | MONDO:0013322 | MARCHF6 | |
| Epilepsy, familial adult myoclonic, 4 | MONDO:0014055 | ||
| Epilepsy, familial adult myoclonic, 5 | MONDO:0014167 | CNTN2 | |
| Epilepsy, familial adult myoclonic, 6 | MONDO:0054846 | ||
| Epilepsy, familial adult myoclonic, 7 | MONDO:0054847 |
Rare disease
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