Disease Information
Disease Name Gene Name Type UMLS Association Type Score Source
Hypokalemic Periodic Paralysis SCN4A disease C0238358 GeneticVariation 0.9 orphanet , disgenet
Hypokalemic Periodic Paralysis SCN4A disease C0238358 CausalMutation 0.9 orphanet , disgenet
Hypokalemic Periodic Paralysis SCN4A disease C0238358 Biomarker 0.9 orphanet , disgenet
Hypokalemic Periodic Paralysis CACNA1S disease C0238358 GeneticVariation 0.7 orphanet , disgenet
Hypokalemic Periodic Paralysis CACNA1S disease C0238358 CausalMutation 0.7 orphanet , disgenet
Hypokalemic Periodic Paralysis CACNA1S disease C0238358 Biomarker 0.7 orphanet , disgenet
Hypokalemic Periodic Paralysis KCNE3 disease C0238358 GeneticVariation 0.31 orphanet , disgenet
Hypokalemic Periodic Paralysis ATP1A2 disease C0238358 Biomarker 0.31 disgenet
Hypokalemic Periodic Paralysis DPYS disease C0238358 GeneticVariation 0.09 disgenet
Hypokalemic Periodic Paralysis DPYD disease C0238358 GeneticVariation 0.09 disgenet
Hypokalemic Periodic Paralysis KCNJ2 disease C0238358 GeneticVariation 0.02 disgenet
Hypokalemic Periodic Paralysis KCNJ18 disease C0238358 GeneticVariation 0.02 disgenet
Hypokalemic Periodic Paralysis RYR1 disease C0238358 Biomarker 0.02 disgenet
Hypokalemic Periodic Paralysis RYR1 disease C0238358 GeneticVariation 0.02 disgenet
Hypokalemic Periodic Paralysis PRRT2 disease C0238358 GeneticVariation 0.01 disgenet
Hypokalemic Periodic Paralysis TNS3 disease C0238358 Biomarker 0.01 disgenet
Hypokalemic Periodic Paralysis FXYD1 disease C0238358 Biomarker 0.01 disgenet
Hypokalemic Periodic Paralysis BCHE disease C0238358 Biomarker 0.01 disgenet
Hypokalemic Periodic Paralysis CLCN1 disease C0238358 GeneticVariation 0.01 disgenet
Hypokalemic Periodic Paralysis GJB1 disease C0238358 GeneticVariation 0.01 disgenet
Hypokalemic Periodic Paralysis ADRB2 disease C0238358 GeneticVariation 0.01 disgenet
Hypokalemic Periodic Paralysis STAC3 disease C0238358 AlteredExpression 0.01 disgenet
Hypokalemic Periodic Paralysis KCNQ5 disease C0238358 Biomarker 0.01 disgenet
Hypokalemic Periodic Paralysis GABRA3 disease C0238358 GeneticVariation 0.01 disgenet
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