Phenotype #0000002021

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	00003181
Associated disease	LCCS1
Inheritance	Familial, X-linked recessive
Phenotype details	mental retardation, myoclonic epilepsy, spasticity
Diagnosis/Initial	-
Age/Examination	-
Diagnosis/Definite	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Johan den Dunnen
Database submission license
Created by	Johan den Dunnen
Date created	2013-11-02 15:08:09 +01:00 (CET)
Date last edited	N/A

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