Global Variome shared LOVD

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Phenotype #0000045611 Individual ID 00059023 Associated disease DFNB3 Phenotype details congenital profound hearing loss 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 2016-02-15 19:38:23 +01:00 (CET) Date last edited 2016-02-18 01:24:41 +01:00 (CET)

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