Phenotype #0000334390

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00445137
Associated disease	CTRCT
Phenotype details	see paper; ..., bilateral, progressive congenital cataract, developed during embryonic and fetal phases, aggravated with age; mother congenital bilateral cortical opacity
Diagnosis/Initial	cataract
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	CTRCT3
Age/Examination	02y (2 years)
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Johan den Dunnen
Database submission license
Created by	Johan den Dunnen
Date created	2024-01-03 11:51:46 +01:00 (CET)
Date last edited	N/A

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