Phenotype #0000057040

Individual ID 00077265
Associated disease STGD1
Phenotype details Stargardt disease; Bilateral progressive central visual loss, macular dystrophy or atrophy, and the presence of yellowish-white flecks, visual acuity: OD 20/40, OS 20/32.
Diagnosis/Initial -
Inheritance Unknown
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset 60y
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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