Phenotype #0000056137

Individual ID 00076362
Associated disease STGD1
Phenotype details Stargardt disease; bilateral central vision loss, macular dystrophy and/or atrophy (beaten bronze appearance or large patch of atrophy); At an age between 20 and 35: appearance in the first or second decade of life, bilateral progressive central vision loss, macular atrophy/dystrophy, noteworthy central vision loss.
Diagnosis/Initial -
Inheritance Unknown
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset <20y
Phenotype/Onset unknown
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

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