Global Variome shared LOVD

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Phenotype #0000355133 Individual ID 00469988 Associated disease LCA Phenotype details see paper; ..., Leber congenital amaurosis, no vision in light Diagnosis/Initial Leber congenital amaurosis Inheritance Familial, autosomal recessive Diagnosis/Definite LCA1 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 2025-11-24 13:17:04 +01:00 (CET) Date last edited N/A

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