Global Variome shared LOVD

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Phenotype #0000045632 Individual ID 00059043 Associated disease DFNB;ARNSHL Phenotype details Congenital, profound, non-syndromic 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 2016-02-18 23:51:46 +01:00 (CET) Date last edited 2016-03-08 18:31:19 +01:00 (CET)

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