Disease Information
Disease Name Gene Name Type UMLS Association Type Score Source
Myofibrillar Myopathy BAG3 disease C2678065 Biomarker 0.8 disgenet
Myofibrillar Myopathy BAG3 disease C2678065 CausalMutation 0.8 disgenet
Myofibrillar Myopathy BAG3 disease C2678065 GeneticVariation 0.8 disgenet
Myofibrillar Myopathy DES disease C2678065 CausalMutation 0.7 disgenet
Myofibrillar Myopathy DES disease C2678065 Biomarker 0.7 disgenet
Myofibrillar Myopathy DES disease C2678065 GeneticVariation 0.7 disgenet
Myofibrillar Myopathy DES disease C2678065 AlteredExpression 0.7 disgenet
Myofibrillar Myopathy CRYAB disease C2678065 GeneticVariation 0.48 orphanet , disgenet
Myofibrillar Myopathy CRYAB disease C2678065 CausalMutation 0.48 orphanet , disgenet
Myofibrillar Myopathy CRYAB disease C2678065 Biomarker 0.48 orphanet , disgenet
Myofibrillar Myopathy TTN disease C2678065 GeneticVariation 0.46 disgenet
Myofibrillar Myopathy TTN disease C2678065 Biomarker 0.46 disgenet
Myofibrillar Myopathy LDB3 disease C2678065 Biomarker 0.41 disgenet
Myofibrillar Myopathy LDB3 disease C2678065 GeneticVariation 0.41 disgenet
Myofibrillar Myopathy LDB3 disease C2678065 CausalMutation 0.41 disgenet
Myofibrillar Myopathy PYROXD1 disease C2678065 Biomarker 0.32 disgenet
Myofibrillar Myopathy PYROXD1 disease C2678065 GeneticVariation 0.32 disgenet
Myofibrillar Myopathy KY disease C2678065 Biomarker 0.3 orphanet , disgenet
Myofibrillar Myopathy MATR3 disease C2678065 Biomarker 0.3 disgenet
Myofibrillar Myopathy MYOT disease C2678065 AlteredExpression 0.2 disgenet
Myofibrillar Myopathy MYOT disease C2678065 GeneticVariation 0.2 disgenet
Myofibrillar Myopathy MYOT disease C2678065 CausalMutation 0.2 disgenet
Myofibrillar Myopathy MYOT disease C2678065 Biomarker 0.2 disgenet
Myofibrillar Myopathy FLNC disease C2678065 GeneticVariation 0.2 disgenet
Myofibrillar Myopathy FLNC disease C2678065 Biomarker 0.2 disgenet
Myofibrillar Myopathy FHL1 disease C2678065 GeneticVariation 0.15 disgenet
Myofibrillar Myopathy FHL1 disease C2678065 Biomarker 0.15 disgenet
Myofibrillar Myopathy DNAJB6 disease C2678065 Biomarker 0.13 disgenet
Myofibrillar Myopathy DNAJB6 disease C2678065 GeneticVariation 0.13 disgenet
Myofibrillar Myopathy ACTA1 disease C2678065 Biomarker 0.12 disgenet
Myofibrillar Myopathy ACTA1 disease C2678065 GeneticVariation 0.12 disgenet
Myofibrillar Myopathy CFL2 disease C2678065 Biomarker 0.11 disgenet
Myofibrillar Myopathy CFL2 disease C2678065 GeneticVariation 0.11 disgenet
Myofibrillar Myopathy PTEN disease C2678065 Biomarker 0.1 disgenet
Myofibrillar Myopathy KLHL40 disease C2678065 Biomarker 0.1 disgenet
Myofibrillar Myopathy AKT1 disease C2678065 Biomarker 0.1 disgenet
Myofibrillar Myopathy TTR disease C2678065 CausalMutation 0.1 disgenet
Myofibrillar Myopathy ACTB disease C2678065 Biomarker 0.06 disgenet
Myofibrillar Myopathy ACTB disease C2678065 GeneticVariation 0.06 disgenet
Myofibrillar Myopathy ZASP disease C2678065 Biomarker 0.03 disgenet
Myofibrillar Myopathy ZASP disease C2678065 GeneticVariation 0.03 disgenet
Myofibrillar Myopathy GFAP disease C2678065 GeneticVariation 0.02 disgenet
Myofibrillar Myopathy KHDRBS1 disease C2678065 Biomarker 0.02 disgenet
Myofibrillar Myopathy GFAP disease C2678065 AlteredExpression 0.02 disgenet
Myofibrillar Myopathy TARDBP disease C2678065 Biomarker 0.02 disgenet
Myofibrillar Myopathy SQSTM1 disease C2678065 Biomarker 0.02 disgenet
Myofibrillar Myopathy HSPB8 disease C2678065 Biomarker 0.02 orphanet , disgenet
Myofibrillar Myopathy NUP62 disease C2678065 Biomarker 0.02 disgenet
Myofibrillar Myopathy PDLIM5 disease C2678065 GeneticVariation 0.02 disgenet
Myofibrillar Myopathy GTF2H1 disease C2678065 Biomarker 0.02 disgenet
Myofibrillar Myopathy DCTN4 disease C2678065 Biomarker 0.02 disgenet
Myofibrillar Myopathy CPT1B disease C2678065 Biomarker 0.01 disgenet
Myofibrillar Myopathy USH2A disease C2678065 GeneticVariation 0.01 disgenet
Myofibrillar Myopathy NRAP disease C2678065 GeneticVariation 0.01 disgenet
Myofibrillar Myopathy SLC24A1 disease C2678065 Biomarker 0.01 disgenet
Myofibrillar Myopathy XIRP2 disease C2678065 GeneticVariation 0.01 disgenet
Myofibrillar Myopathy CAPN3 disease C2678065 GeneticVariation 0.01 disgenet
Myofibrillar Myopathy SYNM disease C2678065 Biomarker 0.01 disgenet
Myofibrillar Myopathy CHD7 disease C2678065 GeneticVariation 0.01 disgenet
Myofibrillar Myopathy MYH7 disease C2678065 GeneticVariation 0.01 disgenet
Myofibrillar Myopathy TPM2 disease C2678065 Biomarker 0.01 disgenet
Myofibrillar Myopathy SLC7A10 disease C2678065 Biomarker 0.01 disgenet
Myofibrillar Myopathy FN1 disease C2678065 GeneticVariation 0.01 disgenet
Myofibrillar Myopathy XIRP1 disease C2678065 GeneticVariation 0.01 disgenet
Myofibrillar Myopathy PSME1 disease C2678065 Biomarker 0.01 disgenet
Myofibrillar Myopathy CBS disease C2678065 Biomarker 0.01 disgenet
Myofibrillar Myopathy PLN disease C2678065 Biomarker 0.01 disgenet
Myofibrillar Myopathy CBSL disease C2678065 Biomarker 0.01 disgenet
Myofibrillar Myopathy GSN disease C2678065 Biomarker 0.01 disgenet
Myofibrillar Myopathy PRDX6 disease C2678065 Biomarker 0.01 disgenet
Myofibrillar Myopathy ATP2A1 disease C2678065 Biomarker 0.01 disgenet
Myofibrillar Myopathy LMNA disease C2678065 GeneticVariation 0.01 disgenet
Myofibrillar Myopathy DMD disease C2678065 AlteredExpression 0.01 disgenet
Myofibrillar Myopathy HMBS disease C2678065 Biomarker 0.01 disgenet
Myofibrillar Myopathy COX5A disease C2678065 Biomarker 0.01 disgenet
Myofibrillar Myopathy IL1B disease C2678065 Biomarker 0.01 disgenet
Myofibrillar Myopathy CPOX disease C2678065 Biomarker 0.01 disgenet
Myofibrillar Myopathy COX8A disease C2678065 Biomarker 0.01 disgenet
Myofibrillar Myopathy ANO5 disease C2678065 Biomarker 0.01 disgenet
Myofibrillar Myopathy WASHC5 disease C2678065 Biomarker 0.01 disgenet
Myofibrillar Myopathy UCHL1 disease C2678065 AlteredExpression 0.01 disgenet
Myofibrillar Myopathy ACTC1 disease C2678065 GeneticVariation 0.01 disgenet
Myofibrillar Myopathy CS disease C2678065 Biomarker 0.01 disgenet
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