Global Variome shared LOVD

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Phenotype #0000045610 Individual ID 00059022 Associated disease DFNB12 Phenotype details congenital severe hearing loss Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Mary-Claire King Database submission license No license selected Created by Mary-Claire King Date created 2016-02-15 19:00:04 +01:00 (CET) Date last edited 2016-03-28 11:10:25 +02:00 (CEST)

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