Global Variome shared LOVD

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Phenotype #0000274887 Individual ID 00381036 Associated disease - Phenotype details poor vision, nystagmus Diagnosis/Initial Leber congenital amaurosis (LCA) Inheritance Familial, autosomal dominant Diagnosis/Definite - Age/Examination <1y (before 1 year) Age/Diagnosis - Age/Onset 23y Phenotype/Onset - Protein - Owner name LOVD Database submission license Creative Commons Attribution 4.0 International Created by Julia Lopez Date created 2021-08-25 12:56:54 +02:00 (CEST) Date last edited N/A

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