Phenotype #0000054920

Individual ID 00075145
Associated disease STGD1
Phenotype details Stargardt disease; rapid disease progression with central atrophy of the macula and numerous flecks in the midperiphery
Diagnosis/Initial -
Inheritance Unknown
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset 24y
Phenotype/Onset -
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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