Phenotype #0000259537

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00364199
Associated disease	-
Phenotype details	At the age of 35 visual acuity was 0.05, central fundus changes were moderate. Colour vision was chaotic. Distribution of flecks: flecks and choroidal atrophy confined to the posterior pole, i.e., within the vascular arcades.
Diagnosis/Initial	Stargardt disease
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	STGD1
Age/Examination	-
Age/Diagnosis	-
Age/Onset	15y
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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