Global Variome shared LOVD

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Phenotype #0000292841 Individual ID 00399740 Associated disease - Phenotype details - Diagnosis/Initial autosomal recessive, non-syndromic hearing loss (ARNSHL) Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset <0y Phenotype/Onset severe to profound congenital bilateral hearing loss Protein - Owner name LOVD Database submission license Creative Commons Attribution 4.0 International Created by Julia Lopez Date created 2022-01-23 10:23:00 +01:00 (CET) Date last edited N/A

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