Phenotype #0000039165

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	00052588
Associated disease	LCA
Phenotype details	Leber congenital amaurosis; poor vision and nystagmus
Diagnosis/Initial	-
Inheritance	Isolated (sporadic)
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	9y
Phenotype/Onset	-
Protein	-
Owner name	Muhammad Ajmal
Database submission license	No license selected
Created by	Muhammad Ajmal
Date created	2015-10-26 17:05:36 +01:00 (CET)
Date last edited	N/A

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