Disease Information
Disease Name Gene Name Type UMLS Association Type Score Source
VLCAD deficiency ACADVL disease C3887523 Biomarker 1 orphanet , disgenet
VLCAD deficiency ACADVL disease C3887523 AlteredExpression 1 orphanet , disgenet
VLCAD deficiency ACADVL disease C3887523 CausalMutation 1 orphanet , disgenet
VLCAD deficiency ACADVL disease C3887523 GeneticVariation 1 orphanet , disgenet
VLCAD deficiency ACADL disease C3887523 Biomarker 0.2 disgenet
VLCAD deficiency CPT1A disease C3887523 Biomarker 0.03 disgenet
VLCAD deficiency CPT1A disease C3887523 GeneticVariation 0.03 disgenet
VLCAD deficiency CPT1B disease C3887523 GeneticVariation 0.01 disgenet
VLCAD deficiency SOCS3 disease C3887523 Biomarker 0.01 disgenet
VLCAD deficiency CHPT1 disease C3887523 GeneticVariation 0.01 disgenet
VLCAD deficiency TGM5 disease C3887523 GeneticVariation 0.01 disgenet
VLCAD deficiency LPIN1 disease C3887523 AlteredExpression 0.01 disgenet
VLCAD deficiency CHKB-CPT1B disease C3887523 GeneticVariation 0.01 disgenet
VLCAD deficiency MT1B disease C3887523 Biomarker 0.01 disgenet
VLCAD deficiency SLC25A20 disease C3887523 Biomarker 0.01 disgenet
VLCAD deficiency MTTP disease C3887523 Biomarker 0.01 disgenet
VLCAD deficiency CPT2 disease C3887523 GeneticVariation 0.01 disgenet
VLCAD deficiency VWF disease C3887523 GeneticVariation 0.01 disgenet
VLCAD deficiency PPARA disease C3887523 Biomarker 0.01 disgenet
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