Disease #04347 (FAME2;FMCTE2 (epilepsy, myoclonic, familial adult, type 2 (FAME2)), OMIM:607876)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	FAME2;FMCTE2
Name	epilepsy, myoclonic, familial adult, type 2 (FAME2)
OMIM ID	607876
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	STARD7
Associated tissues	-
Disease features	-
Remarks	-
Date created	2015-09-23 10:25:22 +02:00 (CEST)
Date last edited	2019-12-19 19:05:59 +01:00 (CET)

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