Phenotype #0000347434

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	00459004
Associated disease	LCA
Phenotype details	see paper; ..., Leber congenital amaurosis
Diagnosis/Initial	Leber congenital amaurosis
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	LCA8
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Johan den Dunnen
Database submission license
Created by	Johan den Dunnen
Date created	2024-12-23 15:38:28 +01:00 (CET)
Date last edited	N/A

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