Phenotype #0000045631

Individual ID 00059042
Associated disease DFNB3
Phenotype details congenital, profound hearing loss
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Zippi Brownstein
Database submission license Creative Commons Attribution-NonCommercial 4.0 InternationalCreative Commons License
Created by Zippi Brownstein
Date created 2016-02-18 18:18:33 +01:00 (CET)
Date last edited 2016-03-08 18:56:46 +01:00 (CET)

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