Phenotype #0000353599

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	00468447
Associated disease	CTRCT
Phenotype details	nuclear cataract; symmetrical opacities
Diagnosis/Initial	bilateral cataract
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	CTRCT9
Age/Examination	-
Age/Diagnosis	-
Age/Onset	0y
Phenotype/Onset	-
Protein	-
Owner name	Johan den Dunnen
Database submission license
Created by	Johan den Dunnen
Date created	2025-11-09 20:53:28 +01:00 (CET)
Date last edited	N/A

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