Disease #04458 (DEE33 (encephalopathy, developmental and epileptic, type 33), OMIM:616409)
| Official abbreviation |
DEE33 |
| Name |
encephalopathy, developmental and epileptic, type 33 |
| OMIM ID |
616409 |
| 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 |
EEF1A2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2015-09-23 10:25:22 +02:00 (CEST) |
| Date last edited |
2024-02-02 17:33:40 +01:00 (CET) |
Individuals
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