"A Lynch syndrome that has_material_basis_in heterozygous deletion of the 3' part of the EPCAM gene and intergenic regions adjacent to the MSH2 gene on chromosome 2p21. This results in transcriptional read-through and silencing of MSH2 in tissues expressing EPCAM."^^ . _:vb50940049 _:vb50940048 . "hereditary nonpolyposis colorectal cancer type 8"^^ . "OMIM:613244"^^ . _:vb50940047 . _:vb50940047 . _:vb50940046 . _:vb50940050 _:vb50940049 . _:vb50940049 . _:vb50940046 _:vb50940050 . . _:vb50940049 . "disease_ontology"^^ . _:vb50940048 . . _:vb50940048 . . _:vb50940050 _:vb50940047 . . _:vb50940046 . _:vb50940050 . _:vb50940048 . _:vb50940047 . "HNPCC8"@en . _:vb50940046 . "DOID:0070270"^^ . _:vb50940047 . _:vb50940048 .