Benign myoclonic epilepsy

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
BENIGN ADULT FAMILIAL MYOCLONIC EPILEPSY
C4273988MONDO:0019448
ADRA2B Unknown
24114805
Disgenet, GWAS catalog
CNTN2 Unknown
23518707
Disgenet, GWAS catalog
CTNND2 Unknown
29127138
Disgenet, GWAS catalog
MARCHF6 Unknown
31664039
CTD, Disgenet
SAMD12 Unknown
29939203
Disgenet, GWAS catalog —
YEATS2 Unknown
31539032
Disgenet, GWAS catalog —
All6 Causal0 Unknown6
Related Diseases Diseases that share the most curated genes with Benign myoclonic epilepsy.
5 View disease cluster →
Adult myoclonic epilepsy 6 shared genesCTNND2, ADRA2B, CNTN2, MARCHF6, SAMD12, YEATS2 Related via 6 shared genes including CTNND2, ADRA2B, CNTN2. Familial adult myoclonic epilepsy 5 shared genesADRA2B, CNTN2, MARCHF6, SAMD12, YEATS2 Related via 5 shared genes including ADRA2B, CNTN2, MARCHF6. Benign adult familial myoclonic epilepsy 2 shared genesADRA2B, SAMD12 Related via 2 shared genes including ADRA2B, SAMD12. Cri-du-chat syndrome 1 shared geneCTNND2 Related via 1 shared gene including CTNND2. Early onset epilepsy with developmental delay 1 shared geneCNTN2 Related via 1 shared gene including CNTN2.