Disease #07046 (DEE112 (encephalopathy, developmental and epileptic, type 112), OMIM:620537)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	DEE112
Name	encephalopathy, developmental and epileptic, type 112
OMIM ID	620537
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	KCNH5
Associated tissues	-
Disease features	-
Remarks	-
Date created	2023-12-01 13:40:52 +01:00 (CET)
Date last edited	N/A

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