Phenotypes for disease #02249 (EDMD1 (dystrophy, muscular, Emery-Dreifuss, type 1, X-linked (EDMD-1)), OMIM:310300)

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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

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Owner     

Individual ID     
0000299742 30y-complete atrio ventricular; 33y-cardiac conduction disorder; 40y-augmented plasmatic CPK ; 48y-walking problems Becker muscular Dystrophy EDMD1 Familial, X-linked 40y-45y 40y 30y 30y not available Emanuele Micaglio 00407388
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