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 |
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