Phenotype #0000305726

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00413761
Associated disease	-
Phenotype details	night blindness, followed by loss of peripheral visual field and later loss of central vision, often leading to complete blindness
Diagnosis/Initial	Autosomal-recessive RP (arRP)
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	LOVD
Database submission license
Created by	Julia Lopez
Date created	2022-07-22 03:34:11 +02:00 (CEST)
Date last edited	N/A

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