Phenotype #0000142610
| Individual ID |
00180156 |
| Associated disease |
? |
| Diagnosis/Initial |
epilepsy or seizures associated with neurodevelopmental disorders and/or congenital malformations |
| Diagnosis/Definite |
EIEE-6, Dravet syndrome |
| Phenotype details |
(Pharmacoresistant) epilepsy (HP:0001250), generalized tonic- clonic seizures (HP:0002069), global developmental delay (HP:0001263), developmental regression (HP:0002376). |
| Inheritance |
Familial, autosomal dominant |
| Age/Examination |
- |
| Age/Diagnosis |
- |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Protein |
- |
| Tumor/MSI |
- |
| Diagnosis/Criteria |
- |
| Owner name |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2018-08-24 19:40:22 +02:00 (CEST) |
| Date last edited |
N/A |
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|