Phenotype #0000057557

Individual ID 00077782
Associated disease STGD1
Phenotype details Stargardt disease; y54: Visual acuity OD 0 logMAR, OS 0 logMAR, patchy parafoveal atrophy surrounded by numerous yellow-white flecks, normal ERGs with or without PERG P50 abnormality.
Diagnosis/Initial -
Inheritance Unknown
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset 54y
Phenotype/Onset visual loss or the latest examination for asymptomatic patients.
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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