Phenotype #0000056551

Individual ID 00076776
Associated disease STGD1
Phenotype details Stargardt disease; y18: Visual acuity OD 20/150 OS 20/150, peripapillary atrophy in both eyes, flecks in the macula, flecks in the extramacular retina in both eyes, atrophy in the macula in both eyes, relative loss of generalized cone function
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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