Disease #05588 (FAME4 (epilepsy, myoclonic, familial adult, type 4 (FAME4)), OMIM:615127)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	FAME4
Name	epilepsy, myoclonic, familial adult, type 4 (FAME4)
OMIM ID	615127
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	YEATS2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2019-04-10 21:08:48 +02:00 (CEST)
Date last edited	2019-12-20 10:19:31 +01:00 (CET)

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