Phenotype #0000130103
| Individual ID |
00164007 |
| Associated disease |
AHC |
| Diagnosis/Initial |
AHC |
| Diagnosis/Definite |
AHC |
| Phenotype details |
Hemiplegia first onset at 7m, 2-3 times/m, dystonia, epileptic seizure, automatic dysfunction, dysphagia, respiritary disturbance, slight developmental delay, language delay |
| Inheritance |
Familial, autosomal dominant |
| Age/Examination |
02y (2 years) |
| Age/Diagnosis |
02y |
| Age/Onset |
00y07m |
| Phenotype/Onset |
Dystonia and hemiplegia |
| Protein |
- |
| Owner name |
Xiaoxu Yang |
| Database submission license |
No license selected |
| Created by |
Xiaoxu Yang |
| Date created |
2018-07-02 01:45:41 +02:00 (CEST) |
| Date last edited |
2018-07-02 14:04:51 +02:00 (CEST) |
|