Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ] Register as submitter | Log in

Phenotype #0000127239 Individual ID 00154503 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 Nada Danial-Farran Database submission license No license selected Created by Nada Danial-Farran Date created 2018-03-02 11:33:38 +01:00 (CET) Date last edited 2018-03-02 16:01:21 +01:00 (CET)

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