Disease #07184 (DEE119 (encephalopathy, developmental and epileptic, type 119), OMIM:621304)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	DEE119
Name	encephalopathy, developmental and epileptic, type 119
OMIM ID	621304
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	RNU2-2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2025-09-30 18:03:08 +02:00 (CEST)
Date last edited	N/A

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