Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Hereditary Nonpolyposis Colorectal Neoplasms
0.410 CausalMutation group CLINVAR Genomic analysis of an infant with intractable diarrhea and dilated cardiomyopathy. 28701297 2017
Hereditary Nonpolyposis Colorectal Neoplasms
0.410 Biomarker group CTD_human Microsatellite instability: an update. 25701956 2015
Hereditary Nonpolyposis Colorectal Neoplasms
0.410 CausalMutation group CLINVAR Genetic characterization of congenital tufting enteropathy: epcam associated phenotype and involvement of SPINT2 in the syndromic form. 24142340 2014
Hereditary Nonpolyposis Colorectal Neoplasms
0.410 CausalMutation group CLINVAR Absence of cell-surface EpCAM in congenital tufting enteropathy. 23462293 2013
Hereditary Nonpolyposis Colorectal Neoplasms
0.410 GeneticVariation group LHGDN Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3' exons of TACSTD1. 19098912 2009
Hereditary Nonpolyposis Colorectal Neoplasms
0.410 GeneticVariation group CLINVAR