Phenotype #0000054561

Individual ID 00074786
Associated disease STGD1
Phenotype details Stargardt disease; onset before 30 years of age, bilateral central vision loss with “beaten-metal” foveal changes and/or yellow pigment epithelium deposits(“flecks”) in the posterior pole of the eye, typical“dark choroid” in fluorescein angiography
Diagnosis/Initial -
Inheritance Unknown
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset <30y
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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