Phenotype #0000046703

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	00060213
Associated disease	CTRCT
Phenotype details	cataract, congenital
Diagnosis/Initial	-
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Juhua Yang
Database submission license	No license selected
Created by	Juhua Yang
Date created	2015-01-14 03:47:46 +01:00 (CET)
Date last edited	N/A

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