hereditary sensory and autonomic neuropathy type 7

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
hereditary sensory and autonomic neuropathy type 7
SCN11A Causal — ClinGen
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with hereditary sensory and autonomic neuropathy type 7.
5 View disease cluster →
Dominantly inherited sensory neuropathy 1 shared geneSCN11A Related via 1 shared gene including SCN11A. Episodic pain syndrome 1 shared geneSCN11A Related via 1 shared gene including SCN11A. Erythromelalgia 1 shared geneSCN11A Related via 1 shared gene including SCN11A. Congenital pain insensitivity 1 shared geneSCN11A Related via 1 shared gene including SCN11A. Paroxysmal extreme pain disorder 1 shared geneSCN11A Related via 1 shared gene including SCN11A.