Global Variome shared LOVD

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

Phenotype #0000046725 Individual ID 00060238 Associated disease DFNB2 Phenotype details Congenital profound HL 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 2016-03-15 13:51:11 +01:00 (CET) Date last edited 2016-03-28 08:42:53 +02:00 (CEST)

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