Phenotype #0000288628

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00395429
Associated disease	-
Phenotype details	Vision impairment, nystagmus, best corrected visual acuity hand movement/hand movement
Diagnosis/Initial	-
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	Leber congenital amaurosis
Age/Examination	29y (29 years)
Age/Diagnosis	-
Age/Onset	<1y
Phenotype/Onset	-
Protein	-
Owner name	LOVD
Database submission license
Created by	Anna Tracewska
Date created	2021-12-06 14:47:57 +01:00 (CET)
Date last edited	N/A

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