autosomal dominant disease syndrome Lynch syndrome UMLS_CUI:C0009405 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. DOID:3883 ORDO:144 disease_ontology SNOMEDCT_US_2020_03_01:315058005 DOID:3040 HNPCC - hereditary nonpolyposis colon cancer NCI:C120083 MESH:D003123 UMLS_CUI:C1333990 COCA 1 DOID:0050586 Hereditary Defective Mismatch Repair syndrome OMIM:PS120435 GARD:9905 OMIM mapping confirmed by DO. [SN]. hereditary nonpolyposis colorectal cancer hereditary nonpolyposis colorectal neoplasm