Disease #03404 (DEE11 (encephalopathy, developmental and epileptic, type 11), OMIM:613721)
| Official abbreviation |
DEE11 |
| Name |
encephalopathy, developmental and epileptic, type 11 |
| OMIM ID |
613721 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
7 |
| Phenotype entries for this disease |
7 |
| Associated with 1 gene |
SCN2A |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2022-04-07 09:19:02 +02:00 (CEST) |
Individuals
|