Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ] Register as submitter | Log in

Phenotype #0000057574 Individual ID 00077799 Associated disease STGD1 Phenotype details Stargardt disease; y57: Visual acuity OD 0.48 logMAR, OS 0.48 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 55y Phenotype/Onset visual loss or the latest examination for asymptomatic patients. Protein - Owner name Stéphanie Cornelis Database submission license Creative Commons Attribution 4.0 International 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.