Disease #06406 (EPM9 (epilepsy, progressive myoclonic, type 9), OMIM:616540)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	EPM9
Name	epilepsy, progressive myoclonic, type 9
OMIM ID	616540
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	LMNB2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-12-10 23:20:41 +01:00 (CET)
Date last edited	2025-04-17 19:22:48 +02:00 (CEST)

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