Disease #04665 (MAE (epilepsy, myoclonic-atonic (MAE)), OMIM:616421)
| Official abbreviation |
MAE |
| Name |
epilepsy, myoclonic-atonic (MAE) |
| OMIM ID |
616421 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
4 |
| Phenotype entries for this disease |
5 |
| Associated with 1 gene |
SLC6A1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2015-09-23 10:25:23 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|