Disease #03200 (EIG8 (epilepsy, idiopathic, generalized, susceptibility to, type 8 (EIG-8)), OMIM:612899)
| Official abbreviation |
EIG8 |
| Name |
epilepsy, idiopathic, generalized, susceptibility to, type 8 (EIG-8) |
| OMIM ID |
612899 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
6 |
| Phenotype entries for this disease |
6 |
| Associated with 1 gene |
CASR |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|