Phenotype #0000058631
Individual ID |
00078872 |
Associated disease |
LGMDR12;LGMD2L |
Phenotype details |
- |
Diagnosis/Initial |
- |
Inheritance |
Familial, autosomal dominant |
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 |
2013-06-28 23:10:26 +02:00 (CEST) |
Date last edited |
2013-06-29 20:56:42 +02:00 (CEST) |
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