Myoclonic epilepsy

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
JUVENILE MYOCLONIC EPILEPSY
C0270853307MONDO:0009696
CAPRIN1 Causal — Disgenet —
GABRA1 Causal
23756480
Disgenet, Orphanet
All24 Causal2 Unknown22
Related Diseases Diseases that share the most curated genes with Myoclonic epilepsy.
5 View disease cluster →
Idiopathic generalized epilepsy 4 shared genesGABRD, GABRA1, CACNB4, CLCN2 Related via 4 shared genes including GABRD, GABRA1, CACNB4. Familial adult myoclonic epilepsy 3 shared genesRAPGEF2, TNRC6A, SAMD12 Related via 3 shared genes including RAPGEF2, TNRC6A, SAMD12. Adult myoclonic epilepsy 3 shared genesRAPGEF2, TNRC6A, SAMD12 Related via 3 shared genes including RAPGEF2, TNRC6A, SAMD12. Dravet syndrome 3 shared genesGABRA1, SCN1A, STXBP1 Related via 3 shared genes including GABRA1, SCN1A, STXBP1. Benign infantile epilepsy 2 shared genesCHRNA2, KCNQ3 Related via 2 shared genes including CHRNA2, KCNQ3.