Global Variome shared LOVD

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Phenotype #0000273053 Individual ID 00377907 Associated disease - Phenotype details nystagmus, poor vision Diagnosis/Initial Leber Congenital Amaurosis Inheritance Isolated (sporadic) Diagnosis/Definite - Age/Examination 4y5m (4 years, 5 months) Age/Diagnosis - Age/Onset 2m Phenotype/Onset - Protein - Owner name LOVD Database submission license Creative Commons Attribution 4.0 International Created by Julia Lopez Date created 2021-08-02 20:37:33 +02:00 (CEST) Date last edited N/A

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