Global Variome shared LOVD

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

Phenotype #0000090303 Individual ID 00114821 Associated disease DFNX2 Phenotype details DFNX2; Hearing_loss Diagnosis/Initial - Inheritance Isolated (sporadic) Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Thomas Parzefall Database submission license No license selected Created by Thomas Parzefall Date created 2013-03-27 19:09:43 +01:00 (CET) Date last edited 2013-03-29 11:56:21 +01:00 (CET)

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