Phenotype #0000262569

Individual ID 00367231
Associated disease -
Phenotype details At the age of 48, the BCVA (RE) was 0,2 and the BCVA (LE) was 0,2. At the age of 45 the fundus showed: Foveal atrophy. Small area. Limited number of flecks.
Diagnosis/Initial Stargardt disease
Inheritance Unknown
Diagnosis/Definite STGD1
Age/Examination -
Age/Diagnosis -
Age/Onset 25y
Phenotype/Onset unknown
Protein -
Owner name Stéphanie Cornelis
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Stéphanie Cornelis
Date created 2021-05-03 14:25:36 +02:00 (CEST)
Date last edited N/A

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