Oropharyngeal dysphagia

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
OROPHARYNGEAL DYSPHAGIA
C0267071
ATP2B3 Unknown — Disgenet
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Oropharyngeal dysphagia.
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X-linked non progressive cerebellar ataxia 1 shared geneATP2B3 Related via 1 shared gene including ATP2B3. X-linked progressive cerebellar ataxia 1 shared geneATP2B3 Related via 1 shared gene including ATP2B3. Spinocerebellar ataxia, x-linked 1 shared geneATP2B3 Related via 1 shared gene including ATP2B3. Cushing syndrome 1 shared geneATP2B3 Related via 1 shared gene including ATP2B3. Hyperaldosteronism 1 shared geneATP2B3 Related via 1 shared gene including ATP2B3.