Phenotype #0000277171

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	00383386
Associated disease	CCTRCT
Phenotype details	Not determined Irregular spot-like cataract in the middle of the lens
Diagnosis/Initial	congenital cataract
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	-
Age/Examination	3m
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	LOVD
Database submission license
Created by	Anna Tracewska
Date created	2021-09-29 09:56:40 +02:00 (CEST)
Date last edited	N/A

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