Phenotype #0000297738

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00405189
Associated disease	-
Phenotype details	-
Diagnosis/Initial	X-linked congenital stationary night blindness (CSNB1A)
Inheritance	Familial, X-linked
Diagnosis/Definite	-
Age/Examination	16y (16 years)
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	non-progressive stable severe night blindness since early childhood and moderate to high myopia
Protein	-
Owner name	LOVD
Database submission license
Created by	Julia Lopez
Date created	2022-03-16 13:42:42 +01:00 (CET)
Date last edited	N/A

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