Global Variome shared LOVD

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Phenotype #0000221097 Individual ID 00287173 Associated disease DFNA20;DFNA26 Phenotype details moderate hearing loss downward slope into higher frequencies with a gradual worsening over time affecting all frequencies Diagnosis/Initial NSHL Inheritance Familial, autosomal dominant Diagnosis/Definite NSHL Age/Examination 29y (29 years) Age/Diagnosis 15y Age/Onset 15y Phenotype/Onset - Protein - Owner name Camille Cenni Database submission license No license selected Created by Camille Cenni Date created 2020-02-14 11:24:28 +01:00 (CET) Date last edited N/A

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