Nizon-isidor syndrome

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Nizon-Isidor syndrome
MONDO_0030030
MED12L Causal
31155615 35920825 36212160 37883018 40957966
ClinGen, Open Targets
KCNA2 Unknown
37883018 31155615
Open Targets
All2 Causal1 Unknown1
Related Diseases Diseases that share the most curated genes with Nizon-isidor syndrome.
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Epileptic encephalopathy, early infantile, 32 1 shared geneKCNA2 Related via 1 shared gene including KCNA2. Platelet-type bleeding disorder 1 shared geneMED12L Related via 1 shared gene including MED12L. Language development disorders 1 shared geneKCNA2 Related via 1 shared gene including KCNA2. Genetic developmental and epileptic encephalopathy 1 shared geneKCNA2 Related via 1 shared gene including KCNA2. Digestive system disease 1 shared geneMED12L Related via 1 shared gene including MED12L.