Phenotype #0000319229

Individual ID 00401634
Associated disease deafness
Phenotype details bilateral profound hearing loss
Diagnosis/Initial hearing loss
Inheritance Familial, autosomal recessive
Diagnosis/Definite DFNB2
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Johan den Dunnen
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2022-12-31 16:36:54 +01:00 (CET)
Date last edited N/A

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