Phenotype #0000143159

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	00180896
Associated disease	epilepsy
Phenotype details	HP:0001249
Diagnosis/Initial	-
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	03y
Phenotype/Onset	-
Protein	-
Owner name	Anaïs Begemann
Database submission license	No license selected
Created by	Anaïs Begemann
Date created	2018-09-10 11:48:35 +02:00 (CEST)
Date last edited	2018-09-14 12:54:05 +02:00 (CEST)

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