Phenotype #0000327913
| Individual ID |
00438009 |
| Associated disease |
? |
| Diagnosis/Initial |
- |
| Diagnosis/Definite |
- |
| Phenotype details |
movement disorder; developmental epileptic encephalopathy; developmental delay; 2h-onset epilepsy; structural changes brain; hypotonia; no speech |
| Inheritance |
Unknown |
| Age/Examination |
- |
| Age/Diagnosis |
- |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Protein |
- |
| Tumor/MSI |
- |
| Diagnosis/Criteria |
- |
| Owner name |
Harald Mikkers |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2023-08-14 14:11:00 +02:00 (CEST) |
| Date last edited |
N/A |
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