Phenotype #0000054877

Individual ID	00075102
Associated disease	STGD1
Phenotype details	Stargardt disease; Bilateral regions of macular atrophy, which were roughly symmetrical in size and severity and associated with pigment deposits that were more prominent in the right eye. Numerous yellow flecks were noted in the posterior pole and midperiphery of both eyes.
Diagnosis/Initial	-
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	12y
Phenotype/Onset	gradual decline in visual acuity
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