Disease Information
Disease Name Gene Name Type UMLS Association Type Score Source
Hirschsprung disease ganglioneuroblastoma PHOX2B disease C2751683 SusceptibilityMutation 0.6 orphanet , disgenet
Hirschsprung disease ganglioneuroblastoma PHOX2B disease C2751683 Biomarker 0.6 orphanet , disgenet
Hirschsprung disease ganglioneuroblastoma PHOX2B disease C2751683 CausalMutation 0.6 orphanet , disgenet
click here to return to the previous page