Global Variome shared LOVD

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Phenotype #0000045613 Individual ID 00059024 Associated disease HDR Phenotype details congenital, moderate-severe hearing loss, kidney disease Diagnosis/Initial - Inheritance Familial, autosomal dominant 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 2016-02-15 22:02:18 +01:00 (CET) Date last edited 2016-02-18 03:53:18 +01:00 (CET)

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