Global Variome shared LOVD

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Phenotype #0000287557 Individual ID 00394353 Associated disease - Phenotype details USH2A, congenital hearing impairment RP diagnosis about 40 y, ERG Consistent with RP Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite Usher syndrome Age/Examination - Age/Diagnosis 40y Age/Onset - Phenotype/Onset - Protein - Owner name LOVD Database submission license Creative Commons Attribution 4.0 International Created by Anna Tracewska Date created 2021-12-01 10:17:04 +01:00 (CET) Date last edited N/A

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