Phenotype #0000263957

Individual ID 00368619
Associated disease -
Phenotype details At the age of 35, the BCVA (OD/OS) was: 0.12/0.1, the fundus showed: Macular atrophy, a beaten-bronze appearance and the OCT showed: Hyper-reflective deposition, Thinning of the retina in the macular area.
Diagnosis/Initial Stargardt disease
Inheritance Familial, autosomal recessive
Diagnosis/Definite STGD1
Age/Examination -
Age/Diagnosis -
Age/Onset 20y
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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