Global Variome shared LOVD

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Phenotype #0000132429 Individual ID 00167565 Associated disease PDS;TDH2B Phenotype details Cochlear hypoplasia, nodular goiter, hypothyroidism, high thyroglobulin, PDT negative Diagnosis/Initial Pendred syndrome Inheritance Familial, autosomal recessive Diagnosis/Definite - 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 Anne-Françoise Roux Date created 2014-09-05 17:19:10 +02:00 (CEST) Date last edited N/A

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