Global Variome shared LOVD

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Phenotype #0000045616 Individual ID 00059027 Associated disease DFNA12 Phenotype details Childhood onset, 2-4y, moderate-severe hearing loss Diagnosis/Initial - Inheritance Familial, autosomal dominant Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Zippi Brownstein Database submission license Creative Commons Attribution-NonCommercial 4.0 International Created by Zippi Brownstein Date created 2016-02-15 23:44:31 +01:00 (CET) Date last edited 2016-02-18 04:21:30 +01:00 (CET)

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