Disease #06324 (EPEO2 (epilepsy, early-onset, type 2, with/without developmental delay), OMIM:618832)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	EPEO2
Name	epilepsy, early-onset, type 2, with/without developmental delay
OMIM ID	618832
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SETD1A
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-12-10 23:20:41 +01:00 (CET)
Date last edited	2025-09-04 14:27:17 +02:00 (CEST)

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