Phenotype #0000057551

Individual ID 00077776
Associated disease STGD1
Phenotype details Stargardt disease; y45: Visual acuity OD 0 logMAR, OS 0 logMAR, mottled retinal pigment epithelial changes and/or localized parafoveal yellow-white flecks, ERG was not available.
Diagnosis/Initial -
Inheritance Unknown
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset 45y
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

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.