Phenotype #0000261625

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00366287
Associated disease	-
Phenotype details	At the age of 17, there was pigment migration and outer retinal atrophy. The BCVA was CF OD and 20/400 OS (Snellen).
Diagnosis/Initial	Stargardt disease
Inheritance	Unknown
Diagnosis/Definite	STGD1
Age/Examination	-
Age/Diagnosis	-
Age/Onset	5y
Phenotype/Onset	symptoms
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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