Global Variome shared LOVD

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Phenotype #0000258639 Individual ID 00363274 Associated disease USH Diagnosis/Initial Usher syndrome, type II Diagnosis/Definite - Phenotype details no retinal dystrophy at time the genetic diagnosis Inheritance Familial, autosomal recessive Age/Examination 1y (1 year) Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name LOVD Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2021-04-26 15:58:48 +02:00 (CEST) Date last edited N/A

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