Disease #07185 (DEE118 (encephalopathy, developmental and epileptic, type 118), OMIM:621250)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	DEE118
Name	encephalopathy, developmental and epileptic, type 118
OMIM ID	621250
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	TMEM63B
Associated tissues	-
Disease features	-
Remarks	-
Date created	2025-09-30 18:05:06 +02:00 (CEST)
Date last edited	N/A

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