Phenotype #0000277499

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Global Variome, with Curator vacancy

Individual ID	00383714
Associated disease	-
Phenotype details	Total RD, unilateral, OD
Diagnosis/Initial	persistent fetal vasculature syndrome
Inheritance	Isolated (sporadic)
Diagnosis/Definite	Familial exudative vitreoretinopathy
Age/Examination	-
Age/Diagnosis	-
Age/Onset	2m
Phenotype/Onset	-
Protein	-
Owner name	LOVD
Database submission license
Created by	Anna Tracewska
Date created	2021-09-29 12:31:11 +02:00 (CEST)
Date last edited	N/A

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