Phenotype #0000259316

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00363978
Associated disease	-
Phenotype details	At the age of 49 the fundus of the patient showed extensive chorioretinal atrophy over the entire fundus. At that time the Best corrected visual acuity was FC OD and FC OS.
Diagnosis/Initial	Stargardt disease
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	STGD1
Age/Examination	-
Age/Diagnosis	-
Age/Onset	8y
Phenotype/Onset	visual effects noted for the first time
Protein	-
Owner name	Stéphanie Cornelis
Database submission license
Created by	Stéphanie Cornelis
Date created	2021-05-03 14:25:36 +02:00 (CEST)
Date last edited	N/A

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