Phenotype #0000084252
Individual ID |
00106448 |
Associated disease |
MYOP |
Phenotype details |
myopathy, congenital |
Diagnosis/Initial |
- |
Inheritance |
Isolated (sporadic) |
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 |
2011-10-04 17:29:56 +02:00 (CEST) |
Date last edited |
2012-03-09 19:12:55 +01:00 (CET) |
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