Phenotype #0000260820

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00365482
Associated disease	-
Phenotype details	At the age of 28, the BCVA was : 20/250 OD and 20/200 OS. Ultrawidefield fundus autofluorescence type was: Central atrophy with or without flecks confined to posterior pole—No findings outside 55° field of view
Diagnosis/Initial	Stargardt disease
Inheritance	Unknown
Diagnosis/Definite	STGD1
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	unknown
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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