Phenotype #0000045613

Individual ID 00059024
Associated disease HDR
Phenotype details congenital, moderate-severe hearing loss, kidney disease
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
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 2016-02-15 22:02:18 +01:00 (CET)
Date last edited 2016-02-18 03:53:18 +01:00 (CET)

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