Global Variome shared LOVD

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Phenotype #0000307359 Individual ID 00415579 Associated disease - Phenotype details VA: 6/9OD - 6/12OS; astigmatism/ hyperopia Diagnosis/Initial congenital stationary night blindness (CSNB) Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination 40y (40 years) Age/Diagnosis - Age/Onset - Phenotype/Onset night blindness Protein - Owner name LOVD Database submission license Creative Commons Attribution 4.0 International Created by Julia Lopez Date created 2022-08-15 15:41:08 +02:00 (CEST) Date last edited N/A

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