Disease Information
Disease Name Gene Name Type UMLS Association Type Score Source
Muir-Torre Syndrome MSH2 disease C1321489 GermlineCausalMutation 0.8 orphanet , disgenet
Muir-Torre Syndrome MLH1 disease C1321489 GeneticVariation 0.8 orphanet , disgenet
Muir-Torre Syndrome MSH2 disease C1321489 Biomarker 0.8 orphanet , disgenet
Muir-Torre Syndrome MLH1 disease C1321489 Biomarker 0.8 orphanet , disgenet
Muir-Torre Syndrome MSH2 disease C1321489 AlteredExpression 0.8 orphanet , disgenet
Muir-Torre Syndrome MLH1 disease C1321489 AlteredExpression 0.8 orphanet , disgenet
Muir-Torre Syndrome MLH1 disease C1321489 CausalMutation 0.8 orphanet , disgenet
Muir-Torre Syndrome MLH1 disease C1321489 GermlineCausalMutation 0.8 orphanet , disgenet
Muir-Torre Syndrome MSH2 disease C1321489 GeneticVariation 0.8 orphanet , disgenet
Muir-Torre Syndrome MSH2 disease C1321489 CausalMutation 0.8 orphanet , disgenet
Muir-Torre Syndrome MSH6 disease C1321489 GeneticVariation 0.57 orphanet , disgenet
Muir-Torre Syndrome MSH6 disease C1321489 Biomarker 0.57 orphanet , disgenet
Muir-Torre Syndrome MSH6 disease C1321489 GermlineCausalMutation 0.57 orphanet , disgenet
Muir-Torre Syndrome FHIT disease C1321489 Biomarker 0.21 disgenet
Muir-Torre Syndrome MRC1 disease C1321489 GeneticVariation 0.05 disgenet
Muir-Torre Syndrome MUTYH disease C1321489 GeneticVariation 0.02 disgenet
Muir-Torre Syndrome MYH1 disease C1321489 GeneticVariation 0.01 disgenet
Muir-Torre Syndrome PMS2 disease C1321489 AlteredExpression 0.01 disgenet
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