Phenotype #0000054721

Individual ID 00074946
Associated disease STGD1
Phenotype details Stargardt disease; an ophtalmoscopically characteristic retinal disorder, bilateral central visual loss with both "beaten metal" elliptical foveal dystrophy and temporal pallor of the optic discs, documented by retinal color photography, characteristic fluorescein angiographic feature of a dark choroid
Diagnosis/Initial -
Inheritance Unknown
Diagnosis/Definite -
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 2016-02-22 12:22:09 +01:00 (CET)
Date last edited N/A

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