"OMIM mapping confirmed by DO. [SN]."^^ . "DOID:3883"^^ . "GARD:9905"^^ . "hereditary nonpolyposis colorectal cancer"@en . _:vb50952421 . "UMLS_CUI:C0009405"^^ . . _:vb50952421 . "ORDO:144"^^ . "Lynch syndrome"^^ . "NCI:C120083"^^ . . _:vb50952421 . "DOID:0050586"^^ . "disease_ontology"^^ . . "hereditary nonpolyposis colorectal neoplasm"@en . _:vb50952421 . . . "Hereditary Defective Mismatch Repair syndrome"@en . "DOID:3040"^^ . "COCA 1"@en . "A syndrome that is characterized by an increased risk for colon cancer and cancers of the endometrium, ovary, stomach, small intestine, hepatobiliary tract, urinary tract, brain, and skin and has_material_basis_in mutation of mismatch repair genes that increases the risk of many types of cancers."^^ . _:vb50952421 . "MESH:D003123"^^ . "HNPCC - hereditary nonpolyposis colon cancer"@en . . "OMIM:PS120435"^^ . "UMLS_CUI:C1333990"^^ . "SNOMEDCT_US_2021_09_01:315058005"^^ .