Phenotype #0000027279

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Bert Callewaert

Individual ID	00033881
Associated disease	CTRCT
Phenotype details	congenital; nystagmus
Diagnosis/Initial	cataract
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	CTRCT9
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Lars Hansen
Database submission license
Created by	Lars Hansen
Date created	2007-06-21 20:00:00 +02:00 (CEST)
Date last edited	2023-03-19 17:33:10 +01:00 (CET)

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