Phenotype #0000129686

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00164649
Associated disease	STGD
Phenotype details	extensive areas retinal pigment epithelium atrophy throughout posterior pole, extending beyond vascular arcades
Diagnosis/Initial	Stargardt disease, typical
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	STGD-1
Age/Examination	40y (40 years)
Age/Diagnosis	16y
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Johan den Dunnen
Database submission license
Created by	Johan den Dunnen
Date created	2018-06-03 11:01:10 +02:00 (CEST)
Date last edited	2018-06-04 08:29:53 +02:00 (CEST)

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