Global Variome shared LOVD

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

Phenotype #0000058211 Individual ID 00078436 Associated disease STGD1 Phenotype details Stargardt disease; y53: Visual acuity OD:20/25 OS:20/200 Perifoveal RPE atrophy lesions in OD, macular RPE atrophy in OS, small yellow-white spots in perifoveal region in both eyes. Foveal sparing in the right eye, post foveal sparing in the left eye. Diagnosis/Initial - Inheritance Unknown Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset 39y Phenotype/Onset Paracentral scotoma 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.