Disease Information
Disease Name Gene Name Type UMLS Association Type Score Source
Peroxisome Biogenesis Disorder, Complementation Group G FRAXA disease C1864172 GeneticVariation 0.01 disgenet
Peroxisome Biogenesis Disorder, Complementation Group G GLS disease C1864172 GeneticVariation 0.01 disgenet
Peroxisome Biogenesis Disorder, Complementation Group G SLC22A5 disease C1864172 GeneticVariation 0.01 disgenet
Peroxisome Biogenesis Disorder, Complementation Group G GGCT disease C1864172 GeneticVariation 0.01 disgenet
Peroxisome Biogenesis Disorder, Complementation Group G TYR disease C1864172 GeneticVariation 0.01 disgenet
Peroxisome Biogenesis Disorder, Complementation Group G FRAXE disease C1864172 GeneticVariation 0.01 disgenet
Peroxisome Biogenesis Disorder, Complementation Group G FMR1 disease C1864172 GeneticVariation 0.01 disgenet
Peroxisome Biogenesis Disorder, Complementation Group G LDLR disease C1864172 GeneticVariation 0.01 disgenet
Peroxisome Biogenesis Disorder, Complementation Group G DOCK11 disease C1864172 GeneticVariation 0.01 disgenet
Peroxisome Biogenesis Disorder, Complementation Group G AGA disease C1864172 GeneticVariation 0.01 disgenet
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