Disease Information
Disease Name Gene Name Type UMLS Association Type Score Source
Dystonia 12 ATP1A3 disease C1868681 GeneticVariation 0.8 orphanet , disgenet
Dystonia 12 ATP1A3 disease C1868681 Biomarker 0.8 orphanet , disgenet
Dystonia 12 ATP1A3 disease C1868681 GermlineCausalMutation 0.8 orphanet , disgenet
Dystonia 12 ATP1A3 disease C1868681 CausalMutation 0.8 orphanet , disgenet
Dystonia 12 GCH1 disease C1868681 Biomarker 0.02 disgenet
Dystonia 12 SLC2A1 disease C1868681 GeneticVariation 0.01 disgenet
Dystonia 12 PNKD disease C1868681 Biomarker 0.01 disgenet
Dystonia 12 PRKN disease C1868681 Biomarker 0.01 disgenet
Dystonia 12 HSP90B2P disease C1868681 Biomarker 0.01 disgenet
Dystonia 12 CIT disease C1868681 GeneticVariation 0.01 disgenet
Dystonia 12 TOR1A disease C1868681 GeneticVariation 0.01 disgenet
Dystonia 12 PRKRA disease C1868681 GeneticVariation 0.01 disgenet
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