Phenotype #0000056557

Individual ID 00076782
Associated disease STGD1
Phenotype details Stargardt disease; y63: Visual acuity OD Count fingers OS Hand movements, peripapillary atrophy in both eyes, flecks in the extramacular retina in the right eye, atrophy in the macula, atrophy in the extramacular retina in both eyes, abnormal rod and cone ERGs
Diagnosis/Initial -
Inheritance Unknown
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset 8y
Phenotype/Onset visual symptoms or of first ophthalmic consultation where a diagnosis of Stargardt disease
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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