Phenotype #0000227908

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00289016
Associated disease	-
Phenotype details	RP, night blindness, pericentral field loss
Diagnosis/Initial	retinitis pigmentosa
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	-
Age/Examination	11y (11 years)
Age/Diagnosis	-
Age/Onset	10y
Phenotype/Onset	-
Protein	-
Owner name	Sandro Banfi
Database submission license	No license selected
Created by	Johan den Dunnen
Date created	2020-05-03 16:46:49 +02:00 (CEST)
Date last edited	2020-08-25 10:48:31 +02:00 (CEST)

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