Lafora disease

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
MYOCLONIC EPILEPSY OF LAFORA 1
254780C5848203MONDO:0958199
EPM2A Causal — ClinVar, Disgenet, HPO, ClinGen
NHLRC1 Causal — Disgenet
MYOCLONIC EPILEPSY OF LAFORA 2
620681MONDO:0800306
NHLRC1 Causal — ClinVar, HPO, ClinGen
All2 Causal2 Unknown0
Related Diseases Diseases that share the most curated genes with Lafora disease.
5 View disease cluster →
Progressive myoclonic epilepsy 1 shared geneNHLRC1 Related via 1 shared gene including NHLRC1. Rolandic epilepsy 1 shared geneEPM2A Related via 1 shared gene including EPM2A. Congenital neurologic anomalies 1 shared geneEPM2A Related via 1 shared gene including EPM2A. Ovarian epithelial cancer 1 shared geneEPM2A Related via 1 shared gene including EPM2A. Biliary tract cancer 1 shared geneNHLRC1 Related via 1 shared gene including NHLRC1.