Phenotype #0000273028

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Global Variome, with Curator vacancy

Individual ID	00377882
Associated disease	-
Phenotype details	-
Diagnosis/Initial	Leber Congenital Amaurosis
Inheritance	Isolated (sporadic)
Diagnosis/Definite	-
Age/Examination	7m
Age/Diagnosis	-
Age/Onset	<1y
Phenotype/Onset	-
Protein	-
Owner name	LOVD
Database submission license
Created by	Julia Lopez
Date created	2021-08-02 20:37:33 +02:00 (CEST)
Date last edited	N/A

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