Disease #07065 (DEE99 (encephalopathy, developmental and epileptic, type 99), OMIM:619606)
| Official abbreviation |
DEE99 |
| Name |
encephalopathy, developmental and epileptic, type 99 |
| OMIM ID |
619606 |
| 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 |
ATP1A3 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2024-01-26 15:23:29 +01:00 (CET) |
| Date last edited |
N/A |
Individuals
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