Phenotype #0000027067

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00033638
Associated disease	STGD
Phenotype details	Stargardt disease, severe; severe cone-rod dystrophy; y37, visual acuity OD: 20/400, OS: 20/400. y32: Severe chorioretinal atrophy, macula up to periphery most affected
Diagnosis/Initial	-
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	-
Age/Examination	>07y (later than 7 years)
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Miriam Bauwens
Database submission license	No license selected
Created by	Miriam Bauwens
Date created	2014-10-11 14:12:32 +02:00 (CEST)
Date last edited	2016-07-15 09:36:40 +02:00 (CEST)

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