Focal epilepsy

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
FOCAL EPILEPSY
MONDO:0005384
DEPDC5 Causal
23542697 23542701 24283814 29481864 29708509 29761115 29861134 29950950
ClinGen, Disgenet
CLASP1 Unknown — GenCC
NPRL2 Unknown
26505888 27173016 28199897 29281825 30093711 31835056 34376795 37259768
ClinGen, GWAS catalog
NPRL3 Unknown
26285051 26505888 26786403 27173016 34868250 35136953
ClinGen, GWAS catalog
All4 Causal1 Unknown3
Related Diseases Diseases that share the most curated genes with Focal epilepsy.
5 View disease cluster →
Familial focal epilepsy with variable foci 3 shared genesDEPDC5, NPRL2, NPRL3 Related via 3 shared genes including DEPDC5, NPRL2, NPRL3. Roifman syndrome 1 shared geneCLASP1 Related via 1 shared gene including CLASP1. Epilepsy with auditory features 1 shared geneDEPDC5 Related via 1 shared gene including DEPDC5. Lateral temporal lobe epilepsy 1 shared geneDEPDC5 Related via 1 shared gene including DEPDC5. Progressive myoclonic epilepsy 3 shared genesDEPDC5, NPRL2, NPRL3 Related via 3 shared genes including DEPDC5, NPRL2, NPRL3.