Global Variome shared LOVD

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Phenotype #0000299742 Individual ID 00407388 Associated disease EDMD1 Phenotype details 30y-complete atrio ventricular; 33y-cardiac conduction disorder; 40y-augmented plasmatic CPK ; 48y-walking problems Diagnosis/Initial Becker muscular Dystrophy Inheritance Familial, X-linked Diagnosis/Definite EDMD1 Age/Examination 40y-45y Age/Diagnosis 40y Age/Onset 30y Phenotype/Onset 30y Protein not available Owner name Emanuele Micaglio Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Emanuele Micaglio Date created 2022-04-06 15:00:42 +02:00 (CEST) Date last edited 2022-04-07 13:22:45 +02:00 (CEST)

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