Global Variome shared LOVD

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Phenotype #0000296695 Individual ID 00404106 Associated disease - Phenotype details see paper; ..., typical cone-rod dystrophy, decrease of vision, nyctalopia Diagnosis/Initial cone-rod dystrophy Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2022-02-27 15:58:59 +01:00 (CET) Date last edited 2022-02-27 16:06:47 +01:00 (CET)

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