Disease Information
Disease Name Gene Name Type UMLS Association Type Score Source
Myopathy, X-Linked, with Excessive Autophagy VMA21 disease C1839615 Biomarker 0.77 disgenet
Myopathy, X-Linked, with Excessive Autophagy VMA21 disease C1839615 GermlineCausalMutation 0.77 disgenet
Myopathy, X-Linked, with Excessive Autophagy VMA21 disease C1839615 CausalMutation 0.77 disgenet
Myopathy, X-Linked, with Excessive Autophagy VMA21 disease C1839615 GeneticVariation 0.77 disgenet
Myopathy, X-Linked, with Excessive Autophagy LAMP2 disease C1839615 GeneticVariation 0.04 disgenet
Myopathy, X-Linked, with Excessive Autophagy LAMP2 disease C1839615 Biomarker 0.04 disgenet
Myopathy, X-Linked, with Excessive Autophagy VCP disease C1839615 GeneticVariation 0.02 disgenet
Myopathy, X-Linked, with Excessive Autophagy GNE disease C1839615 Biomarker 0.02 disgenet
Myopathy, X-Linked, with Excessive Autophagy GNE disease C1839615 GeneticVariation 0.02 disgenet
Myopathy, X-Linked, with Excessive Autophagy HSPB8 disease C1839615 GeneticVariation 0.01 disgenet
Myopathy, X-Linked, with Excessive Autophagy CLN3 disease C1839615 Biomarker 0.01 disgenet
Myopathy, X-Linked, with Excessive Autophagy PYGM disease C1839615 Biomarker 0.01 disgenet
Myopathy, X-Linked, with Excessive Autophagy SQSTM1 disease C1839615 GeneticVariation 0.01 disgenet
Myopathy, X-Linked, with Excessive Autophagy DNAJB6 disease C1839615 GeneticVariation 0.01 disgenet
Myopathy, X-Linked, with Excessive Autophagy CASQ1 disease C1839615 GeneticVariation 0.01 disgenet
Myopathy, X-Linked, with Excessive Autophagy ACTA1 disease C1839615 GeneticVariation 0.01 disgenet
Myopathy, X-Linked, with Excessive Autophagy TRIM32 disease C1839615 GeneticVariation 0.01 disgenet
Myopathy, X-Linked, with Excessive Autophagy EMD disease C1839615 GeneticVariation 0.01 disgenet
Myopathy, X-Linked, with Excessive Autophagy B2M disease C1839615 Biomarker 0.01 disgenet
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