Phenotype #0000319573

Individual ID 00428668
Associated disease DFNB89
Phenotype details -
Diagnosis/Initial Non-syndromic hearing impairment
Inheritance Familial, autosomal recessive
Diagnosis/Definite DFNB89
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 InternationalCreative Commons License
Created by Yacouba Dia
Date created 2023-01-05 22:41:32 +01:00 (CET)
Date last edited 2023-01-06 10:08:32 +01:00 (CET)

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