Global Variome shared LOVD

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Phenotype #0000128934 Individual ID 00163814 Associated disease DFNB4 Phenotype details congenital profound hearing loss Diagnosis/Initial hearing loss Inheritance Familial, autosomal recessive Diagnosis/Definite DFNB4 Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Nada Danial-Farran Database submission license No license selected Created by Nada Danial-Farran Date created 2018-04-13 11:01:18 +02:00 (CEST) Date last edited 2026-09-04 14:14:54 +02:00 (CEST)

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