Disease #05903 (EPM11 (epilepsy, progressive myoclonic, type 11 (EPM11)), OMIM:608873)
| Official abbreviation |
EPM11 |
| Name |
epilepsy, progressive myoclonic, type 11 (EPM11) |
| OMIM ID |
608873 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
SEMA6B |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2021-03-03 09:35:15 +01:00 (CET) |
| Date last edited |
N/A |
Individuals
|