Phenotype #0000298348

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	00405851
Associated disease	-
Phenotype details	-
Diagnosis/Initial	Leber congenital amaurosis (LCA)
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	-
Age/Examination	2y (2 years)
Age/Diagnosis	-
Age/Onset	2m15d
Phenotype/Onset	Nystagmus
Protein	-
Owner name	LOVD
Database submission license
Created by	Julia Lopez
Date created	2022-03-23 03:47:23 +01:00 (CET)
Date last edited	N/A

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