Disease #07101 (DEE116 (encephalopathy, developmental and epileptic, type 116), OMIM:620806)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	DEE116
Name	encephalopathy, developmental and epileptic, type 116
OMIM ID	620806
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	GLUL
Associated tissues	-
Disease features	-
Remarks	-
Date created	2024-09-05 19:39:40 +02:00 (CEST)
Date last edited	N/A

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