Disease Information
Disease Name Gene Name Type UMLS Association Type Score Source
Atrophy, Multiple System COQ2 phenotype C0393571 Biomarker 0.3 orphanet , disgenet
Atrophy, Multiple System LINC02210-CRHR1 phenotype C0393571 GeneticVariation 0.1 disgenet
Atrophy, Multiple System ELOVL7 phenotype C0393571 GeneticVariation 0.1 disgenet
Atrophy, Multiple System FBXO47 phenotype C0393571 GeneticVariation 0.1 disgenet
Atrophy, Multiple System SNCA phenotype C0393571 AlteredExpression 0.04 disgenet
Atrophy, Multiple System SNCA phenotype C0393571 Biomarker 0.04 disgenet
Atrophy, Multiple System LRRK2 phenotype C0393571 GeneticVariation 0.03 disgenet
Atrophy, Multiple System LRRK2 phenotype C0393571 Biomarker 0.03 disgenet
Atrophy, Multiple System APTX phenotype C0393571 Biomarker 0.01 disgenet
Atrophy, Multiple System ATXN2 phenotype C0393571 Biomarker 0.01 disgenet
Atrophy, Multiple System NEFL phenotype C0393571 AlteredExpression 0.01 disgenet
Atrophy, Multiple System SQSTM1 phenotype C0393571 Biomarker 0.01 disgenet
Atrophy, Multiple System CRYAB phenotype C0393571 Biomarker 0.01 disgenet
Atrophy, Multiple System UBB phenotype C0393571 GeneticVariation 0.01 disgenet
Atrophy, Multiple System YWHAB phenotype C0393571 AlteredExpression 0.01 disgenet
Atrophy, Multiple System PRKN phenotype C0393571 Biomarker 0.01 disgenet
Atrophy, Multiple System ICAM1 phenotype C0393571 GeneticVariation 0.01 disgenet
Atrophy, Multiple System ATXN8OS phenotype C0393571 Biomarker 0.01 disgenet
Atrophy, Multiple System PPP1R1B phenotype C0393571 Biomarker 0.01 disgenet
Atrophy, Multiple System MAPT phenotype C0393571 AlteredExpression 0.01 disgenet
Atrophy, Multiple System CXCL8 phenotype C0393571 GeneticVariation 0.01 disgenet
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