Global Variome shared LOVD

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Phenotype #0000255379 Individual ID 00359974 Associated disease - Phenotype details Retinal phenotype: Atrophic confluence of yellow‐white lesions, surrounded by STGD1‐like lesions in macula. Peripheral retina showed no abnormalities. Diagnosis/Initial multifocal pattern dystrophy Inheritance Familial, autosomal dominant Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset 44y Phenotype/Onset - Protein - Owner name Manon Peeters Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2021-04-06 16:50:09 +02:00 (CEST) Date last edited N/A

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