Global Variome shared LOVD

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Phenotype #0000307401 Individual ID 00415621 Associated disease - Phenotype details VA(R/L): 2.0/2.0; photophobia; night vision problems Diagnosis/Initial Retinal dystrophy with early macular involvement Inheritance Familial, autosomal dominant Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset 25y Phenotype/Onset Central visual loss 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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