Disease Information
Disease Name Gene Name Type UMLS Association Type Score Source
Pallidopyramidal syndrome FBXO7 disease C1850100 CausalMutation 0.77 orphanet , disgenet
Pallidopyramidal syndrome FBXO7 disease C1850100 GermlineCausalMutation 0.77 orphanet , disgenet
Pallidopyramidal syndrome FBXO7 disease C1850100 AlteredExpression 0.77 orphanet , disgenet
Pallidopyramidal syndrome FBXO7 disease C1850100 GeneticVariation 0.77 orphanet , disgenet
Pallidopyramidal syndrome FBXO7 disease C1850100 Biomarker 0.77 orphanet , disgenet
Pallidopyramidal syndrome SNCA disease C1850100 GermlineCausalMutation 0.31 orphanet , disgenet
Pallidopyramidal syndrome SNCA disease C1850100 GeneticVariation 0.31 orphanet , disgenet
Pallidopyramidal syndrome SLC6A3 disease C1850100 GeneticVariation 0.01 disgenet
Pallidopyramidal syndrome SLC18A2 disease C1850100 GeneticVariation 0.01 disgenet
Pallidopyramidal syndrome C19orf12 disease C1850100 GeneticVariation 0.01 disgenet
Pallidopyramidal syndrome SLC2A1 disease C1850100 GeneticVariation 0.01 disgenet
Pallidopyramidal syndrome TOR1A disease C1850100 GeneticVariation 0.01 disgenet
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