Phenotype #0000262586

Individual ID 00367248
Associated disease -
Phenotype details At the age of 13, the BCVA (RE) was 0,15 and the BCVA (LE) was 0,15. At the age of 13 the fundus showed: Macular atrophy. Widespread yellow-white round flecks beyond the vasular arcade.
Diagnosis/Initial Stargardt disease
Inheritance Unknown
Diagnosis/Definite STGD1
Age/Examination -
Age/Diagnosis -
Age/Onset 7y
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

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.