Disease #03049 (EPM-3 (epilepsy, myoclonic, progressive, type 3 (EPM-3)), OMIM:611726)

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	Curator: Johan T. den Dunnen

Official abbreviation	EPM-3
Name	epilepsy, myoclonic, progressive, type 3 (EPM-3)
OMIM ID	611726
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	KCTD7
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A