Global Variome shared LOVD

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Phenotype #0000056553 Individual ID 00076778 Associated disease STGD1 Phenotype details Stargardt disease; y32: Visual acuity OD Count fingers OS Count fingers, peripapillary atrophy in both eyes, flecks in the macula, flecks in the extramacular retina in both eyes, atrophy in the macula in both eyes, relative loss of generalized cone function Diagnosis/Initial - Inheritance Unknown Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset 10y 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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