Phenotype #0000285541

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	00392263
Associated disease	-
Phenotype details	congenital cataract, myopia
Diagnosis/Initial	-
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	Cataract 3, multiple types
Age/Examination	12y (12 years)
Age/Diagnosis	21d
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	LOVD
Database submission license
Created by	Anna Tracewska
Date created	2021-11-22 09:44:22 +01:00 (CET)
Date last edited	2021-11-22 12:40:53 +01:00 (CET)

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