Phenotype #0000334382

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	00445129
Associated disease	CTRCT
Phenotype details	see paper; ..., congenital cataract, microphthalmia, nystagmus
Diagnosis/Initial	cataract
Inheritance	Isolated (sporadic)
Diagnosis/Definite	CTRCT2
Age/Examination	00y00m15d (15 days)
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Johan den Dunnen
Database submission license
Created by	Johan den Dunnen
Date created	2024-01-02 21:30:52 +01:00 (CET)
Date last edited	N/A

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