Rolandic epilepsy, impaired intellectual development, and speech dyspraxia, x-linked

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Subtype of: Rolandic epilepsy
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Rolandic epilepsy, impaired intellectual development, and speech dyspraxia, X-linked
MONDO_0015587
SRPX2 Unknown
16497722
Open Targets —
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Rolandic epilepsy, impaired intellectual development, and speech dyspraxia, x-linked.
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Bilateral perisylvian polymicrogyria 1 shared geneSRPX2 Related via 1 shared gene including SRPX2. Perisylvian syndrome 1 shared geneSRPX2 Related via 1 shared gene including SRPX2. Polymicrogyria 1 shared geneSRPX2 Related via 1 shared gene including SRPX2. Rolandic epilepsy 1 shared geneSRPX2 Related via 1 shared gene including SRPX2. Epilepsy 1 shared geneSRPX2 Related via 1 shared gene including SRPX2.