Disease #05435 (DEE92;IECEE2 (encephalopathy, developmental and epileptic, type92 (IECEE2)), OMIM:617829)
| Official abbreviation |
DEE92;IECEE2 |
| Name |
encephalopathy, developmental and epileptic, type92 (IECEE2) |
| OMIM ID |
617829 |
| 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 |
GABRB2 |
| Associated tissues |
- |
| Disease features |
autosomal dominant |
| Remarks |
- |
| Date created |
2018-06-01 14:38:04 +02:00 (CEST) |
| Date last edited |
2023-10-23 12:25:49 +02:00 (CEST) |
Individuals
|