Global Variome shared LOVD

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Phenotype #0000056549 Individual ID 00076774 Associated disease STGD1 Phenotype details Stargardt disease; y35: Visual acuity OD Hand movements OS Hand movements, peripapillary atrophy in both eyes, flecks in the extramacular retina in both eyes, atrophy in the macula, atrophy in the extramacular retina in both eyes, relative loss of generalized cone function Diagnosis/Initial - Inheritance Unknown Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset 11y Phenotype/Onset visual symptoms or of first ophthalmic consultation where a diagnosis of Stargardt disease 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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