Lafora Disease Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_3534)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D020192
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Genes

2 genes/proteins associated with the disease Lafora Disease from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
EPM2A epilepsy, progressive myoclonus type 2A, Lafora disease (laforin) 2.88009
NHLRC1 NHL repeat containing E3 ubiquitin protein ligase 1 2.88009