Phenotype #0000224196

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00296797
Associated disease	EE
Phenotype details	see paper; ..., continuous spike and wave during slow-wave sleep syndrome, verbal dyspraxia
Diagnosis/Initial	epileptic encephalopathy
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	FESD
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Johan den Dunnen
Database submission license
Created by	Johan den Dunnen
Date created	2020-04-13 17:15:23 +02:00 (CEST)
Date last edited	N/A

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