Disease #06907 (EIG18 (epilepsy, idiopathic generalized, susceptibility to, type 18), OMIM:619521)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	EIG18
Name	epilepsy, idiopathic generalized, susceptibility to, type 18
OMIM ID	619521
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	HCN4
Associated tissues	-
Disease features	-
Remarks	-
Date created	2022-04-07 13:29:24 +02:00 (CEST)
Date last edited	N/A

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