Global Variome shared LOVD

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Phenotype #0000319233 Individual ID 00428324 Associated disease DFNB49 Phenotype details see paper; ..., bilateral hearing loss (moderate to profound) Diagnosis/Initial non-syndromic hearing impairment Inheritance Familial, autosomal recessive Diagnosis/Definite DFNB49 Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset HP:0011474 Protein - Owner name Yacouba Dia Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Yacouba Dia Date created 2022-12-31 20:34:26 +01:00 (CET) Date last edited 2023-01-05 11:02:52 +01:00 (CET)

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