Phenotype #0000054289

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00074466
Associated disease	EIG
Phenotype details	Four affected family members over two generations with idiopathic generalizedepilepsy.
Diagnosis/Initial	-
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Bernt Popp
Database submission license	No license selected
Created by	Bernt Popp
Date created	2016-07-03 13:48:35 +02:00 (CEST)
Date last edited	N/A

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