Disease #06818 (DEE58 (encephalopathy, developmental and epileptic, type 58), OMIM:617830)
| Official abbreviation |
DEE58 |
| Name |
encephalopathy, developmental and epileptic, type 58 |
| OMIM ID |
617830 |
| 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 |
NTRK2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2021-12-10 23:20:41 +01:00 (CET) |
| Date last edited |
2023-10-23 11:52:50 +02:00 (CEST) |
Individuals
|