Phenotype #0000262537

Individual ID 00367199
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 48y
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

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