Disease #06995 (DEE6B (encephalopathy, developmental and epileptic, type 6B), OMIM:619317)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	DEE6B
Name	encephalopathy, developmental and epileptic, type 6B
OMIM ID	619317
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SCN1A
Associated tissues	-
Disease features	-
Remarks	-
Date created	2023-01-10 15:57:43 +01:00 (CET)
Date last edited	N/A

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