Familial acute necrotizing encephalopathy

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
familial acute necrotizing encephalopathy
MONDO_0011953
RANBP2 Causal
17069463 19118815 25128471 26923722 33600493 33777149 34400285 35348941 37090838 40538544 42407393
ClinGen, Open Targets
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Familial acute necrotizing encephalopathy.
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Encephalopathy, acute, infection-induced, 3 1 shared geneRANBP2 Related via 1 shared gene including RANBP2. Paramyotonia congenita 1 shared geneRANBP2 Related via 1 shared gene including RANBP2. Retroperitoneal inflammatory myofibroblastic tumor 1 shared geneRANBP2 Related via 1 shared gene including RANBP2. Hyperkalemic periodic paralysis 1 shared geneRANBP2 Related via 1 shared gene including RANBP2. Christ-siemens-touraine syndrome 1 shared geneRANBP2 Related via 1 shared gene including RANBP2.