Phenotype #0000056955

Individual ID	00077180
Associated disease	STGD1
Phenotype details	Stargardt disease, late onset; y61: Visual actuity: OD count fingers, OS count fingers, Foveal changes with parafoveal yellow-white dots and mottled decreased FAF in macula, dark choroid.
Diagnosis/Initial	-
Inheritance	Isolated (sporadic)
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	58y
Phenotype/Onset	The onset of STGD1 was defined as the age at initial symptoms. In asymptomatic cases, we used the age at first diagnosis, defined as the age at which macular abnormalities were diagnosed for the first time by an ophthalmologist
Protein	-
Owner name	Stéphanie Cornelis
Database submission license
Created by	Stéphanie Cornelis
Date created	2016-02-22 12:22:09 +01:00 (CET)
Date last edited	N/A

Global Variome shared LOVD