Global Variome shared LOVD

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Phenotype #0000046744 Individual ID 00060255 Associated disease DFNA1 Phenotype details DFNA-6/14/38; congenital NSHL, low-tone, U-shaped audiogram 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 2016-03-22 11:23:56 +01:00 (CET) Date last edited 2016-03-28 10:24:46 +02:00 (CEST)

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