Disease #05590 (FAME7;FMCTE7 (epilepsy, myoclonic, familial adult, type 7 (FAME7, FMCTE7)), OMIM:618075)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	FAME7;FMCTE7
Name	epilepsy, myoclonic, familial adult, type 7 (FAME7, FMCTE7)
OMIM ID	618075
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	RAPGEF2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2019-04-10 21:14:40 +02:00 (CEST)
Date last edited	2019-12-19 19:19:37 +01:00 (CET)

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