Global Variome shared LOVD

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Phenotype #0000057159 Individual ID 00077384 Associated disease STGD1 Phenotype details Stargardt disease; Bilateral central vision loss (central and peripheral visual field computerized testing), a retinal “beaten-bronze” foveal appearance and/or yellow-whitish flecks from the posterior pole to the midperiphery, normal caliber of the retinal vessels a typical dark choroid in fluorescein angiography. Diagnosis/Initial - Inheritance Unknown Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset <21y 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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