Phenotype #0000046719

Individual ID 00060231
Associated disease DFNB2
Phenotype details Congenital, severe HL
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 2016-03-14 13:36:03 +01:00 (CET)
Date last edited 2016-03-27 20:44:16 +02:00 (CEST)

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