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
|