Disease Information
Disease Name Gene Name Type UMLS Association Type Score Source
Pain Insensitivity, Congenital SCN9A disease C0002768 GeneticVariation 0.6 orphanet , disgenet
Pain Insensitivity, Congenital SCN9A disease C0002768 GermlineCausalMutation 0.6 orphanet , disgenet
Pain Insensitivity, Congenital SCN9A disease C0002768 Biomarker 0.6 orphanet , disgenet
Pain Insensitivity, Congenital SCN11A disease C0002768 GeneticVariation 0.53 orphanet , disgenet
Pain Insensitivity, Congenital SCN11A disease C0002768 Biomarker 0.53 orphanet , disgenet
Pain Insensitivity, Congenital NTRK1 disease C0002768 GeneticVariation 0.35 disgenet
Pain Insensitivity, Congenital NGF disease C0002768 Biomarker 0.32 disgenet
Pain Insensitivity, Congenital NGF disease C0002768 GermlineCausalMutation 0.32 disgenet
Pain Insensitivity, Congenital NGF disease C0002768 GeneticVariation 0.32 disgenet
Pain Insensitivity, Congenital PRDM12 disease C0002768 Biomarker 0.31 disgenet
Pain Insensitivity, Congenital SCN10A disease C0002768 GeneticVariation 0.31 orphanet , disgenet
Pain Insensitivity, Congenital CLTCL1 disease C0002768 Biomarker 0.3 orphanet , disgenet
Pain Insensitivity, Congenital LIFR disease C0002768 GeneticVariation 0.01 disgenet
Pain Insensitivity, Congenital WNK1 disease C0002768 Biomarker 0.01 disgenet
Pain Insensitivity, Congenital POMC disease C0002768 AlteredExpression 0.01 disgenet
Pain Insensitivity, Congenital ARL6IP1 disease C0002768 GeneticVariation 0.01 disgenet
Pain Insensitivity, Congenital TAC1 disease C0002768 AlteredExpression 0.01 disgenet
Pain Insensitivity, Congenital TRPA1 disease C0002768 GeneticVariation 0.01 disgenet
Pain Insensitivity, Congenital NAA50 disease C0002768 Biomarker 0.01 disgenet
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