Disease Information
Disease Name Gene Name Type UMLS Association Type Score Source
Molybdenum Cofactor Deficiency, Complementation Group C GPHN disease C1854990 GeneticVariation 0.7 disgenet
Molybdenum Cofactor Deficiency, Complementation Group C GPHN disease C1854990 GermlineCausalMutation 0.7 disgenet
Molybdenum Cofactor Deficiency, Complementation Group C GPHN disease C1854990 Biomarker 0.7 disgenet
Molybdenum Cofactor Deficiency, Complementation Group C GPHN disease C1854990 CausalMutation 0.7 disgenet
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