Disease Information
Disease Name Gene Name Type UMLS Association Type Score Source
Familial Periodic Paralyses KCNJ2 disease C0030443 Biomarker 0.4 disgenet
Familial Periodic Paralyses KCNJ2 disease C0030443 GeneticVariation 0.4 disgenet
Familial Periodic Paralyses SCN4A disease C0030443 Biomarker 0.2 disgenet
Familial Periodic Paralyses SCN4A disease C0030443 GeneticVariation 0.2 disgenet
Familial Periodic Paralyses KCNJ18 disease C0030443 Biomarker 0.11 orphanet , disgenet
Familial Periodic Paralyses CACNA1S disease C0030443 GeneticVariation 0.11 orphanet , disgenet
Familial Periodic Paralyses CACNA1S disease C0030443 Biomarker 0.11 orphanet , disgenet
Familial Periodic Paralyses FAH disease C0030443 Biomarker 0.1 disgenet
Familial Periodic Paralyses ABCB6 disease C0030443 Biomarker 0.1 disgenet
Familial Periodic Paralyses SLC4A1 disease C0030443 Biomarker 0.1 disgenet
Familial Periodic Paralyses KCNE3 disease C0030443 GeneticVariation 0.04 disgenet
Familial Periodic Paralyses KCNE3 disease C0030443 Biomarker 0.04 disgenet
Familial Periodic Paralyses H19 disease C0030443 GeneticVariation 0.02 disgenet
Familial Periodic Paralyses RYR1 disease C0030443 Biomarker 0.02 disgenet
Familial Periodic Paralyses RYR1 disease C0030443 GeneticVariation 0.02 disgenet
Familial Periodic Paralyses COL4A5 disease C0030443 GeneticVariation 0.01 disgenet
Familial Periodic Paralyses HLA-B disease C0030443 GeneticVariation 0.01 disgenet
Familial Periodic Paralyses MCM3AP disease C0030443 GeneticVariation 0.01 disgenet
Familial Periodic Paralyses KCNH2 disease C0030443 GeneticVariation 0.01 disgenet
Familial Periodic Paralyses PRKAA1 disease C0030443 Biomarker 0.01 disgenet
Familial Periodic Paralyses PRKAB1 disease C0030443 Biomarker 0.01 disgenet
Familial Periodic Paralyses MB disease C0030443 Biomarker 0.01 disgenet
Familial Periodic Paralyses PRKAA2 disease C0030443 Biomarker 0.01 disgenet
Familial Periodic Paralyses MT-ATP8 NA C0030443 NA NA orphanet
Familial Periodic Paralyses MT-ATP6 NA C0030443 NA NA orphanet
Familial Periodic Paralyses GABRA3 NA C0030443 NA NA orphanet
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