Phenotype #0000056113

Individual ID 00076338
Associated disease STGD1
Phenotype details Stargardt disease; At 46 years of age: OD 20/400, OS 20/400, Anterior segment examination was unremarkable and applanation tonometry measured 12 mmHg OD and 13 mmHg OS. Posterior segment examination and autofluorescence imaging were significant for multifocal small atrophic lesions confined to the fovea OU
Diagnosis/Initial -
Inheritance Unknown
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset 17y
Phenotype/Onset visual acuity loss
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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