Phenotype #0000308427

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00416915
Associated disease	EVR2
Phenotype details	all relatives of the proband description: symptoms of retinal traction, peripheral vitreous opacities, and subretinal and intraretinal exudates
Diagnosis/Initial	-
Inheritance	Familial, X-linked recessive
Diagnosis/Definite	familial exudative vitreoretinopathy
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	LOVD
Database submission license
Created by	Anna Tracewska
Date created	2022-09-09 19:20:30 +02:00 (CEST)
Date last edited	N/A

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