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 InternationalCreative Commons License
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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