Phenotype #0000027418

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	00034020
Associated disease	CTRCT
Phenotype details	fetal nuclear lamellar cataract
Diagnosis/Initial	-
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Kathryn Burdon
Database submission license
Created by	Kathryn Burdon
Date created	2012-07-25 08:39:33 +02:00 (CEST)
Date last edited	2012-08-31 14:16:59 +02:00 (CEST)

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