Disease #03236 (EIG10 (epilepsy, idiopathic, generalized, susceptibility to, type 10 (EIG-10)), OMIM:613060)
| Official abbreviation |
EIG10 |
| Name |
epilepsy, idiopathic, generalized, susceptibility to, type 10 (EIG-10) |
| OMIM ID |
613060 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
GABRD |
| 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) |
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