Phenotype #0000308693

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00417183
Associated disease	EVR1
Phenotype details	full-term, uncomplicated pregnancy; temporal dragging of the macula and optic nerve, widespread peripheral retinal avascularity, and extraretinal neovascularization
Diagnosis/Initial	-
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	familial exudative vitreoretinopathy
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	20d
Protein	-
Owner name	LOVD
Database submission license
Created by	Anna Tracewska
Date created	2022-09-13 15:10:40 +02:00 (CEST)
Date last edited	N/A

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