Disease #05964 (DEE59 (encephalopathy, developmental and epileptic, type 59), OMIM:617904)
| Official abbreviation |
DEE59 |
| Name |
encephalopathy, developmental and epileptic, type 59 |
| OMIM ID |
617904 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
GABBR2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2021-08-11 11:46:07 +02:00 (CEST) |
| Date last edited |
2023-10-23 16:03:07 +02:00 (CEST) |
Individuals
|