Global Variome shared LOVD

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Phenotype #0000318060 Individual ID 00426922 Associated disease - Phenotype details - Diagnosis/Initial Leber congenital amaurosis Inheritance Familial, autosomal recessive Diagnosis/Definite Leber congenital amaurosis Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name LOVD Database submission license Creative Commons Attribution 4.0 International Created by Anna Tracewska Date created 2022-12-03 18:53:15 +01:00 (CET) Date last edited N/A

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