Disease Information
Disease Name Gene Name Type UMLS Association Type Score Source
3-methylcrotonyl CoA carboxylase 1 deficiency MCCC1 disease C0268600 CausalMutation 0.73 orphanet , disgenet
3-methylcrotonyl CoA carboxylase 1 deficiency MCCC1 disease C0268600 Biomarker 0.73 orphanet , disgenet
3-methylcrotonyl CoA carboxylase 1 deficiency MCCC1 disease C0268600 GeneticVariation 0.73 orphanet , disgenet
3-methylcrotonyl CoA carboxylase 1 deficiency MCCC1 disease C0268600 GermlineCausalMutation 0.73 orphanet , disgenet
3-methylcrotonyl CoA carboxylase 1 deficiency MCCC2 disease C0268600 GeneticVariation 0.52 orphanet , disgenet
3-methylcrotonyl CoA carboxylase 1 deficiency MCCC2 disease C0268600 GermlineCausalMutation 0.52 orphanet , disgenet
3-methylcrotonyl CoA carboxylase 1 deficiency MCCC2 disease C0268600 Biomarker 0.52 orphanet , disgenet
3-methylcrotonyl CoA carboxylase 1 deficiency PER2 disease C0268600 GeneticVariation 0.01 disgenet
3-methylcrotonyl CoA carboxylase 1 deficiency MED17 disease C0268600 GeneticVariation 0.01 disgenet
3-methylcrotonyl CoA carboxylase 1 deficiency MCC disease C0268600 GeneticVariation 0.01 disgenet
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