Global Variome shared LOVD

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Phenotype #0000262877 Individual ID 00367539 Associated disease - Phenotype details At the age of 37, the BCVA (RE) was: 20/25 and (LE) was: 20/32. Furthermore, there was: Macular dystrophy surrounded by rare yellow?white flecks at the level of the rinal pigment epithelium Normal ffERG responses Diagnosis/Initial Stargardt disease Inheritance Unknown Diagnosis/Definite STGD1 Age/Examination - Age/Diagnosis - Age/Onset 28y Phenotype/Onset unknown Protein - Owner name Stéphanie Cornelis Database submission license Creative Commons Attribution 4.0 International Created by Stéphanie Cornelis Date created 2021-05-03 14:25:36 +02:00 (CEST) Date last edited N/A

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