Disease #04539 (EPM7 (epilepsy, myoclonic, progressive, type 7 (EPM-7)), OMIM:616187)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	EPM7
Name	epilepsy, myoclonic, progressive, type 7 (EPM-7)
OMIM ID	616187
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	KCNC1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2015-09-23 10:25:22 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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