Phenotype #0000262545

Individual ID 00367207
Associated disease -
Phenotype details at least one of the following features of STGD1: yellow-white pisciform flecks in the retinal pigment epithelium of the posterior pole which were hyperautofluorescent on fundus autofluorescence imaging; and/or progressive atrophy of the macular retinal pigment epithelium
Diagnosis/Initial Stargardt disease
Inheritance Unknown
Diagnosis/Definite STGD1
Age/Examination -
Age/Diagnosis -
Age/Onset 62y
Phenotype/Onset initial symptoms
Protein -
Owner name Stéphanie Cornelis
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Stéphanie Cornelis
Date created 2021-05-03 14:25:36 +02:00 (CEST)
Date last edited N/A

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
  Powered by LOVD v.3.0 Build 30b
LOVD software ©2004-2024 Leiden University Medical Center
Database contents © by their respective submitters and curators
 There are currently no updates.