Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0017638
Disease: Glioma
Glioma
0.310 GeneticVariation disease BEFREE The few known PMS2 mutations show a striking association with the presence of gliomas, which are the hallmark of the Turcot variant of HNPCC. 14518071 2003
CUI: C0017638
Disease: Glioma
Glioma
0.310 CausalMutation disease CGI