Phenotype #0000051969

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00072264
Associated disease	CCTRCT
Phenotype details	no ocular abnormality (-HP:?), clinically insignificant fine opacities in the red reflect (HP:?)
Diagnosis/Initial	-
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	01y
Phenotype/Onset	-
Protein	-
Owner name	Jamie Zeegers
Database submission license	No license selected
Created by	Jamie Zeegers
Date created	2016-06-03 10:10:30 +02:00 (CEST)
Date last edited	2016-06-12 14:16:46 +02:00 (CEST)

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