Global Variome shared LOVD

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Phenotype #0000128213 Individual ID 00163076 Associated disease DFNA1 Phenotype details Cardiac hypertrophy and QT interval prolongation Diagnosis/Initial deafness, nonsyndromic (DFNA) Inheritance Familial, autosomal dominant Diagnosis/Definite DFNA-22 Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Anne-Françoise Roux Database submission license Creative Commons Attribution 4.0 International Created by David Baux Date created 2015-01-14 18:28:04 +01:00 (CET) Date last edited 2015-01-16 16:23:04 +01:00 (CET)

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