MSH2, mutS homolog 2, 4436

N. diseases: 490; N. variants: 777
Disease: Cholangiocarcinoma ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0206698
Disease: Cholangiocarcinoma
Cholangiocarcinoma 		0.010 GeneticVariation disease LHGDN A case of Muir-Torre syndrome associated with mucinous hepatic cholangiocarcinoma and a novel germline mutation of the MSH2 gene. 17051350 2007
CUI: C0206698
Disease: Cholangiocarcinoma
Cholangiocarcinoma 		0.010 GeneticVariation disease BEFREE A case of Muir-Torre syndrome associated with mucinous hepatic cholangiocarcinoma and a novel germline mutation of the MSH2 gene. 17051350 2007