Phenotype #0000093256

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00117868
Associated disease	CDG1P
Phenotype details	unremarkable prenatal and neonatal period, developmental delay, mental retardation, epilepsy, strabismus convergens
Diagnosis/Initial	-
Inheritance	Unknown
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Christian Thiel
Database submission license	No license selected
Created by	Christian Thiel
Date created	2011-11-09 12:29:59 +01:00 (CET)
Date last edited	N/A

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