Disease #05604 (FFEVF4 (epilepsy, familial focal, with variable foci, type 4 (FFEVF-4)), OMIM:617935)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	FFEVF4
Name	epilepsy, familial focal, with variable foci, type 4 (FFEVF-4)
OMIM ID	617935
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SCN3A
Associated tissues	-
Disease features	autosomal dominant
Remarks	-
Date created	2019-05-24 19:48:29 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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