Global Variome shared LOVD

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Phenotype #0000054970 Individual ID 00075195 Associated disease STGD1 Phenotype details Stargardt disease; bilateral impairment of central vision, appearance of perimacular and/or peripheral yellow-white flecks; OD <20/400, OS <20/400, affected color vision, extensive atrophic-appearing RPE changes, Diagnosis/Initial - Inheritance Unknown Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset <24y 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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