Global Variome shared LOVD

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Phenotype #0000242569 Individual ID 00322211 Associated disease EDS Inheritance - Diagnosis/Initial - Age/Examination - Diagnosis/Definite - Age/Onset - Phenotype/Onset - Phenotype details Osteogenesis imperfecta/Ehlers-Danlos syndrome overlap, Hearing/Loss - Protein - CK-level - EMG - Muscle/Biopsy - Age/Diagnosis - Owner name Simon Bodek Database submission license No license selected Created by Simon Bodek Date created 2014-10-22 14:26:39 +02:00 (CEST) Date last edited 2014-10-24 09:15:26 +02:00 (CEST)

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