Phenotype #0000061383

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00081742
Associated disease	WGVRP
Phenotype details	see paper; ..., ocular phenotypes includes empty vitreous with fibrillary condensations, avascular membrane, perivascular sheathing, progressive chorioretinal dystrophy (similar to Wagner syndrome)
Diagnosis/Initial	-
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Johan den Dunnen
Database submission license
Created by	Johan den Dunnen
Date created	2016-10-21 19:35:35 +02:00 (CEST)
Date last edited	N/A

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