Phenotype #0000084297
Individual ID |
00106493 |
Associated disease |
MYOP |
Phenotype details |
myopathy, congenital; dilated cardiomyopathy (severe) |
Diagnosis/Initial |
- |
Inheritance |
Unknown |
Diagnosis/Definite |
- |
Age/Examination |
- |
Age/Diagnosis |
- |
Age/Onset |
- |
Phenotype/Onset |
- |
Protein |
- |
Owner name |
Tom Winder |
Database submission license |
No license selected |
Created by |
Tom Winder |
Date created |
2014-09-24 19:56:35 +02:00 (CEST) |
Date last edited |
2014-09-28 10:47:59 +02:00 (CEST) |
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