Disease #01954 (EPM4 (epilepsy, progressive myoclonic, type 4, with or without renal failure), OMIM:254900)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	EPM4
Name	epilepsy, progressive myoclonic, type 4, with or without renal failure
OMIM ID	254900
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SCARB2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2021-12-10 22:08:49 +01:00 (CET)

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