Myoclonic encephalopathy

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
EARLY MYOCLONIC ENCEPHALOPATHY
C0270855MONDO:0016022
KCND2 Causal — Disgenet
SLC25A22 Causal
15592994
Disgenet, GWAS catalog
All5 Causal2 Unknown3
Related Diseases Diseases that share the most curated genes with Myoclonic encephalopathy.
5 View disease cluster →
KCND2-related neurodevelopmental disorder with or without seizures 1 shared geneKCND2 Related via 1 shared gene including KCND2. Tubulinopathy 1 shared geneTUBA1A Related via 1 shared gene including TUBA1A. 22q11.2 deletion syndrome 1 shared geneJMJD1C Related via 1 shared gene including JMJD1C. Epilepsy of infancy with migrating focal seizures 1 shared geneSLC25A22 Related via 1 shared gene including SLC25A22. Malignant migrating partial seizures of infancy 1 shared geneSLC25A22 Related via 1 shared gene including SLC25A22.