Phenotype #0000027133

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00033704
Associated disease	STGD
Phenotype details	Stargardt disease; bilateral impairment of central vision together with irregular hyperfluorescent lesions at the macula and a darkchoroid
Diagnosis/Initial	-
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	09y
Phenotype/Onset	visual deterioration, observed by patient
Protein	-
Owner name	Monika Oldak
Database submission license	No license selected
Created by	Monika Oldak
Date created	2015-02-23 17:49:37 +01:00 (CET)
Date last edited	2016-06-26 21:03:22 +02:00 (CEST)

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