Global Variome shared LOVD

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Phenotype #0000262600 Individual ID 00367262 Associated disease - Phenotype details At the age of 68, the BCVA (RE) was 0,6 and the BCVA (LE) was 0,4. At the age of 67 the fundus showed: Macular atrophy. Widespread reticular pattern of pigmentary changes. Diagnosis/Initial Stargardt disease Inheritance Unknown Diagnosis/Definite STGD1 Age/Examination - Age/Diagnosis - Age/Onset 66y Phenotype/Onset unknown Protein - Owner name Stéphanie Cornelis Database submission license Creative Commons Attribution 4.0 International Created by Stéphanie Cornelis Date created 2021-05-03 14:25:36 +02:00 (CEST) Date last edited N/A

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