Phenotype #0000057423

Individual ID 00077648
Associated disease STGD1
Phenotype details Stargardt disease; Bilateral central vision loss; fundus presenting with a beaten-bronze appearance, the presence of orange-yellow flecks in the retina from the posterior pole to the mid periphery, or both; fluorescein angiography showing typical dark choroid; and normal to subnormal electroretinography (ERG) results.
Diagnosis/Initial -
Inheritance Unknown
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset 12y
Phenotype/Onset any symptom of visual impairment
Protein -
Owner name Stéphanie Cornelis
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Stéphanie Cornelis
Date created 2016-02-22 12:22:09 +01:00 (CET)
Date last edited N/A

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