Phenotype #0000056939

Individual ID 00077164
Associated disease STGD1
Phenotype details Stargardt disease; y34: Severe (according to the criteria of Scholl HPN, Kremers J, Vonthein R, White K, Weber BH. L- and M-cone driven electroretinograms in Stargardt’s macular dystrophy-fundus flavimaculatus. Invest Ophthalmol Vis Sci 2001;42:1380–1389.), visual acuity OD: FC, OS: FC, color vision:
Diagnosis/Initial -
Inheritance Unknown
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset 6y
Phenotype/Onset Decrease of 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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