Phenotype #0000000134

Malaysian Node of the Human Variome Project Database

LOVD v.3.0 Build 30 [ Current LOVD status ]
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Individual ID	00000387
Associated disease	-
Phenotype details	SMEI: Severe myoclonic epilepsy in infancy / Dravet syndrome
Inheritance	-
Owner name	Nuur Athirah Binti Mohd Daud
Database submission license
Created by	Nuur Athirah Binti Mohd Daud
Date created	2021-01-28 13:20:41 +08:00 (CST)
Date last edited	2021-08-01 14:38:08 +08:00 (CST)