Disease #07273 (DEE87 (encephalopathy, developmental and epileptic, type 87), OMIM:618916)
| Official abbreviation |
DEE87 |
| Name |
encephalopathy, developmental and epileptic, type 87 |
| OMIM ID |
618916 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
CDK19 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2026-07-20 13:45:18 +02:00 (CEST) |
| Date last edited |
N/A |
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