Disease #04668 (DEE117;CMS18 (encephalopathy, developmental and epileptic, type 117), OMIM:616330)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	DEE117;CMS18
Name	encephalopathy, developmental and epileptic, type 117
OMIM ID	616330
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SNAP25
Associated tissues	-
Disease features	-
Remarks	-
Date created	2015-09-23 10:25:23 +02:00 (CEST)
Date last edited	2025-09-30 18:07:24 +02:00 (CEST)

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