Disease Information
Disease Name Gene Name Type UMLS Association Type Score Source
Peroxisome Biogenesis Disorder, Complementation Group D CYBB disease C1863999 Biomarker 0.4 disgenet
Peroxisome Biogenesis Disorder, Complementation Group D CYBB disease C1863999 GeneticVariation 0.4 disgenet
Peroxisome Biogenesis Disorder, Complementation Group D DECR1 disease C1863999 Biomarker 0.06 disgenet
Peroxisome Biogenesis Disorder, Complementation Group D DECR1 disease C1863999 GeneticVariation 0.06 disgenet
Peroxisome Biogenesis Disorder, Complementation Group D NCF1 disease C1863999 GeneticVariation 0.04 disgenet
Peroxisome Biogenesis Disorder, Complementation Group D NCF1 disease C1863999 Biomarker 0.04 disgenet
Peroxisome Biogenesis Disorder, Complementation Group D CAT disease C1863999 Biomarker 0.02 disgenet
Peroxisome Biogenesis Disorder, Complementation Group D SRY disease C1863999 GeneticVariation 0.02 disgenet
Peroxisome Biogenesis Disorder, Complementation Group D CAT disease C1863999 GeneticVariation 0.02 disgenet
Peroxisome Biogenesis Disorder, Complementation Group D CYBA disease C1863999 GeneticVariation 0.01 disgenet
Peroxisome Biogenesis Disorder, Complementation Group D NCF2 disease C1863999 GeneticVariation 0.01 disgenet
Peroxisome Biogenesis Disorder, Complementation Group D IL1A disease C1863999 AlteredExpression 0.01 disgenet
Peroxisome Biogenesis Disorder, Complementation Group D TBC1D9 disease C1863999 AlteredExpression 0.01 disgenet
Peroxisome Biogenesis Disorder, Complementation Group D TNFSF13B disease C1863999 Biomarker 0.01 disgenet
Peroxisome Biogenesis Disorder, Complementation Group D IL4 disease C1863999 Biomarker 0.01 disgenet
Peroxisome Biogenesis Disorder, Complementation Group D G6PD disease C1863999 GeneticVariation 0.01 disgenet
Peroxisome Biogenesis Disorder, Complementation Group D NCF4 disease C1863999 GeneticVariation 0.01 disgenet
Peroxisome Biogenesis Disorder, Complementation Group D ABCB1 disease C1863999 AlteredExpression 0.01 disgenet
Peroxisome Biogenesis Disorder, Complementation Group D IL1B disease C1863999 AlteredExpression 0.01 disgenet
Peroxisome Biogenesis Disorder, Complementation Group D CYTB disease C1863999 GeneticVariation 0.01 disgenet
Peroxisome Biogenesis Disorder, Complementation Group D COG6 NA C1863999 NA NA orphanet
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