Global Variome shared LOVD

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

Phenotype #0000045635 Individual ID 00059046 Associated disease DFNB7 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 2016-02-19 02:01:19 +01:00 (CET) Date last edited 2016-03-08 18:45:44 +01:00 (CET)

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