Epileptic encephalopathy with optic atrophy

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
epileptic encephalopathy with optic atrophy
MONDO_0015000
AP3B2 Unknown
27889060
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Epileptic encephalopathy with optic atrophy.
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Epileptic encephalopathy, early infantile, 48 1 shared geneAP3B2 Related via 1 shared gene including AP3B2. Genetic developmental and epileptic encephalopathy 1 shared geneAP3B2 Related via 1 shared gene including AP3B2. Developmental and epileptic encephalopathy 1 shared geneAP3B2 Related via 1 shared gene including AP3B2. Global developmental delay 1 shared geneAP3B2 Related via 1 shared gene including AP3B2. Autism 1 shared geneAP3B2 Related via 1 shared gene including AP3B2.