Global Variome shared LOVD

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Phenotype #0000275780 Individual ID 00381938 Associated disease - Phenotype details BCVA OD-OS:1/35-1/35; nystagmus; cataract Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite Leber congenital amaurosis Age/Examination 27y (27 years) Age/Diagnosis - Age/Onset 6m Phenotype/Onset - Protein - Owner name LOVD Database submission license Creative Commons Attribution 4.0 International Created by Anna Tracewska Date created 2021-09-06 14:12:14 +02:00 (CEST) Date last edited N/A

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