Global Variome shared LOVD

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Phenotype #0000199713 Individual ID 00261208 Associated disease HL Phenotype details see paper; … Diagnosis/Initial autosomal dominant non-syndromic hearing loss Inheritance Familial, autosomal dominant Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2019-08-12 19:37:03 +02:00 (CEST) Date last edited N/A

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