Phenotype #0000053520

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00017031
Associated disease	CORD
Inheritance	Familial, autosomal recessive
Diagnosis/Initial	-
Age/Examination	34y (34 years)
Diagnosis/Definite	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Phenotype details	BCVA 20/20 both eyes; annular scotoma in the midperiphery; preservation of the peripheral isopter; Typical RCD fundus changes with macular preservation.
Protein	-
Owner name	Marianne Vos (LOVD-team)
Database submission license	No license selected
Created by	Johan den Dunnen
Date created	2016-06-19 11:11:35 +02:00 (CEST)
Date last edited	N/A

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