Disease Information
Disease Name Gene Name Type UMLS Association Type Score Source
Hyperpigmentation, Familial Progressive KITLG disease C1840392 GeneticVariation 0.73 orphanet , disgenet
Hyperpigmentation, Familial Progressive KITLG disease C1840392 Biomarker 0.73 orphanet , disgenet
Hyperpigmentation, Familial Progressive KITLG disease C1840392 GermlineCausalMutation 0.73 orphanet , disgenet
Hyperpigmentation, Familial Progressive KITLG disease C1840392 CausalMutation 0.73 orphanet , disgenet
Hyperpigmentation, Familial Progressive DUH2 disease C1840392 Biomarker 0.01 disgenet
Hyperpigmentation, Familial Progressive ADIPOQ disease C1840392 AlteredExpression 0.01 disgenet
click here to return to the previous page