Global Variome shared LOVD

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Phenotype #0000046728 Individual ID 00060243 Associated disease DFNB7 Phenotype details Congenital, profound NSHL Diagnosis/Initial - Inheritance Familial, autosomal recessive 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 2016-03-16 11:50:22 +01:00 (CET) Date last edited 2016-03-28 09:59:40 +02:00 (CEST)

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