Phenotype #0000325414

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	00435214
Associated disease	LCA6
Phenotype details	-
Diagnosis/Initial	Leber congenital amaurosis
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	LCA6
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Kaoruko Torii
Database submission license
Created by	Kaoruko Torii
Date created	2023-06-12 11:33:28 +02:00 (CEST)
Date last edited	2023-06-12 14:49:05 +02:00 (CEST)

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