Phenotype #0000055655

Individual ID	00075880
Associated disease	?
Diagnosis/Initial	-
Diagnosis/Definite	-
Phenotype details	Stargardt disease or fundus flavimaculatus; retinal disorder in a family with more than one affected individual and compatible with autosomal recessive inheritance, onset of symptoms in childhood or early adulthood, bilateral central vision loss with ‘‘beaten metal’’ foveal changes and/or yellow-white ‘‘fish-tail’’ flecks scattered through the posterior pole and peripheral retina (FFM), dark choroid in fluorescein angiography (in some but not all cases).
Inheritance	Unknown
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	unknown
Protein	-
Tumor/MSI	-
Diagnosis/Criteria	-
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