Global Variome shared LOVD

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Phenotype #0000054925 Individual ID 00075150 Associated disease STGD1 Phenotype details Stargardt disease; an ophtalmoscopically characteristic retinal disorder, bilateral central visual loss with both "beaten metal" elliptical foveal dystrophy and temporal pallor of the optic discs, documented by retinal color photography, characteristic fluorescein angiographic feature of a dark choroid Diagnosis/Initial - Inheritance Unknown Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset 6y Phenotype/Onset unknown Protein - Owner name Stéphanie Cornelis Database submission license Creative Commons Attribution 4.0 International Created by Stéphanie Cornelis Date created 2016-02-22 12:22:09 +01:00 (CET) Date last edited N/A

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