Phenotype #0000056968

Individual ID	00077193
Associated disease	STGD1
Phenotype details	Stargardt disease, late onset; y52: Visual actuity: OD 20/40, OS 20/30, Small yellowish spots in the macula with zone of increased background FAF and mottled decreased FAF para- and perifoveal.
Diagnosis/Initial	-
Inheritance	Isolated (sporadic)
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	48y
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