Global Variome shared LOVD

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Phenotype #0000272397 Individual ID 00377239 Associated disease - Phenotype details see paper Diagnosis/Initial retinal disease Inheritance Familial, autosomal dominant Diagnosis/Definite dystrophy, cone-rod, type 6 (CORD-6) Age/Examination 23y (23 years) Age/Diagnosis 22y Age/Onset 7y Phenotype/Onset - Protein - Owner name LOVD Database submission license Creative Commons Attribution 4.0 International Created by Anna Tracewska Date created 2021-07-16 14:18:12 +02:00 (CEST) Date last edited N/A

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