Global Variome shared LOVD

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Phenotype #0000128900 Individual ID 00163777 Associated disease DFNB86 Phenotype details congenital profound hearing loss Diagnosis/Initial hearing loss Inheritance Familial, autosomal recessive Diagnosis/Definite DFNB86 Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset congenital Protein - Owner name Nada Danial-Farran Database submission license No license selected Created by Nada Danial-Farran Date created 2018-04-11 09:14:32 +02:00 (CEST) Date last edited 2026-09-04 14:12:08 +02:00 (CEST)

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