Phenotype #0000259526

Individual ID 00364188
Associated disease -
Phenotype details At the age of 32 visual acuity was 0.05, central fundus changes were severe. Colour vision was chaotic. Distribution of flecks: peripheral flecks and choroidal atrophy extending beyond the vascular arcades.
Diagnosis/Initial Stargardt disease
Inheritance Isolated (sporadic)
Diagnosis/Definite STGD1
Age/Examination -
Age/Diagnosis -
Age/Onset 9y
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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