Phenotype #0000154499
| Individual ID |
00206629 |
| Associated disease |
- |
| Phenotype details |
syncope, normokalemia, Short stature (1.4m), LQT, bidirectional VT |
| Diagnosis/Initial |
- |
| Inheritance |
Familial, autosomal dominant |
| Diagnosis/Definite |
- |
| Age/Examination |
- |
| Age/Diagnosis |
35y |
| Age/Onset |
- |
| Phenotype/Onset |
syncope |
| Protein |
- |
| Owner name |
Ikuko Takeda |
| Database submission license |
No license selected |
| Created by |
Ikuko Takeda |
| Date created |
2013-05-22 12:31:07 +02:00 (CEST) |
| Date last edited |
N/A |
|