Phenotype #0000246706

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Gert Matthijs

Individual ID	00328480
Associated disease	-
Phenotype details	congenital stationary night blindness (HP:0007642)
Diagnosis/Initial	congenital stationary night blindness
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	-
Age/Examination	7y (7 years)
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	LOVD
Database submission license
Created by	Johan den Dunnen
Date created	2021-01-28 09:35:56 +01:00 (CET)
Date last edited	N/A

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