Phenotype #0000130102
| Individual ID |
00164006 |
| Associated disease |
AHC |
| Diagnosis/Initial |
AHC |
| Diagnosis/Definite |
AHC |
| Phenotype details |
Hemiplegia first onset at 1m, quadriplegia, dystonia, epileptic seizure, dysphagia, dysarthria, ataxia, developmental delay, language delay |
| Inheritance |
Familial, autosomal dominant |
| Age/Examination |
17y (17 years) |
| Age/Diagnosis |
17y |
| Age/Onset |
00y01m |
| Phenotype/Onset |
Hemiplegia |
| Protein |
- |
| Owner name |
Xiaoxu Yang |
| Database submission license |
No license selected |
| Created by |
Xiaoxu Yang |
| Date created |
2018-07-02 01:38:59 +02:00 (CEST) |
| Date last edited |
2018-07-02 14:03:59 +02:00 (CEST) |
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