Phenotype #0000056258

Individual ID 00076483
Associated disease STGD1
Phenotype details Stargardt disease; Photoreceptor loss, thinner ONL and RPE atrophy Absolute scotoma in the central 2 degrees in both eyes, eccentric PRL (superior retina), speckled macular appearance, visual acuity: OD 20/100, OS 20/100; y25, visual acuity OD 20/150, OS 20/150, bull's eye maculopathy.
Diagnosis/Initial -
Inheritance Unknown
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset 17y
Phenotype/Onset decreased visual acuity
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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