Phenotype #0000332002
Individual ID |
00442655 |
Associated disease |
NMD |
Diagnosis/Initial |
Limb girdle muscle weakness with cardiac condunction abnormalities |
Diagnosis/Definite |
- |
Phenotype details |
onset childhood; limb-girdle muscle weakness with facial involvement, cardiac conduction disorders and dilating cardiomyopathy; CK = 838 U/l |
Inheritance |
Familial, autosomal dominant |
Age/Examination |
45y (45 years) |
Age/Diagnosis |
- |
Age/Onset |
- |
Phenotype/Onset |
- |
Owner name |
Johan den Dunnen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |
Date created |
2023-11-23 18:48:51 +01:00 (CET) |
Date last edited |
N/A |
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