Phenotype #0000057842

Individual ID 00078067
Associated disease STGD1
Phenotype details Stargardt disease, moderate/severe; y17, visual acuity OD: 40/200, OS: 40/200. y9: Beaten-bronze maculopathy with fine lipofuscin containing flecks, alternating with atrophic flecks.
Diagnosis/Initial -
Inheritance Isolated (sporadic)
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset 6y
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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