Phenotype #0000058065

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00078290
Associated disease	STGD1
Phenotype details	Stargardt disease; y43, visual acuity OD: 20/400, OS: 20/200, geographic atrophy at the macular, fleck distribution: choriocapillaris, resorbed/reticular peripapillary sparing.
Diagnosis/Initial	-
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	9y
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

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