Phenotype #0000254267

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curators: Céline Helsmoortel and Elisa Cappuyns

Individual ID	00358969
Associated disease	-
Phenotype details	see paper; ...
Diagnosis/Initial	Leber Congenital Amaurosis
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	LOVD
Database submission license
Created by	Johan den Dunnen
Date created	2021-03-18 12:15:00 +01:00 (CET)
Date last edited	N/A

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