Global Variome shared LOVD

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Phenotype #0000165022 Individual ID 00216570 Associated disease CCD Phenotype details no muscle weakness; no contractures; MRI muscle abnormalities mild to modeate Diagnosis/Initial cardiac conduction defect Inheritance Familial Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2008-05-18 14:07:30 +02:00 (CEST) Date last edited 2012-03-04 15:47:20 +01:00 (CET)

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