Global Variome shared LOVD

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Phenotype #0000054935 Individual ID 00075160 Associated disease STGD1 Phenotype details Stargardt disease; bilateral impairment of central vision, appearance of perimacular and peripheral yellow-white flecks, moderate fundus changes; OD 20/250, OS 20/250, affected color vision, numerous yellowish-white fundus lesions throughout posterior pole, Diagnosis/Initial - Inheritance Unknown Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset 9y Phenotype/Onset decreased visual acuity 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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