Phenotype #0000055715

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00075940
Associated disease	STGD1
Phenotype details	Stargardt disease; progressive retinal dystrophy with beaten-metal atrophy of the macula and/or yellow–white pisciform flecks in the posterior pole with onset of bilateral central vision loss in childhood or earlyadulthood, at 13 years of age: OD 20/200, OS 20/63
Diagnosis/Initial	-
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	10y
Phenotype/Onset	unknown
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