Disease #00009 (ABCB1 (Epilepsy syndrome), OMIM:171050)

Malaysian Node of the Human Variome Project Database

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Official abbreviation	ABCB1
Name	Epilepsy syndrome
OMIM ID	171050
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	ABCB1
Associated tissues	hippocampus
Disease features	-
Remarks	-
Date created	2017-11-21 07:58:01 +08:00 (CST)
Date last edited	N/A