Phenotype #0000053382

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00073646
Associated disease	CCTRCT
Phenotype details	bilateral white central nuclear opacities (HP:?), no other ocular or systemic abnormalities (HP:?)
Diagnosis/Initial	-
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Jamie Zeegers
Database submission license	No license selected
Created by	Jamie Zeegers
Date created	2016-06-13 12:36:52 +02:00 (CEST)
Date last edited	2017-07-18 21:54:20 +02:00 (CEST)

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