Phenotype #0000263646

Individual ID 00368308
Associated disease -
Phenotype details At the age of 16 there was: Macular atrophy Central area of hypo-AF with surrounding ring of hyper-AF . SD-OCT showed: IS/OS loss . ERG showed: Normal. BCVA was: 20/80 in both eyes.
Diagnosis/Initial Stargardt disease
Inheritance Unknown
Diagnosis/Definite STGD1
Age/Examination -
Age/Diagnosis -
Age/Onset 14y
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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