obsolete_Muir-Torre syndrome true Orphanet:587 OMIM:158320 cutaneous sebaceous neoplasms and keratoacanthomas, multiple, with gastrointestinal and Other carcinomas Muir-Torre syndrome http://purl.obolibrary.org/obo/MONDO_0008018 multiple keratoacanthoma, Muir-Torre type MRTES DOID:0050465 Replaced with Mondo term. ICD10:L72.8 GARD:0006821 MUIR-Torre syndrome cutaneous sebaceous neoplasms and keratoacanthomas multiple with gastrointestinal and other carcinomas MESH:D055653 SCTID:403824007 NCIT:C84905 MedDRA:10063042 Muir-Torre syndrome (MTS) is a form of hereditary nonpolyposis colon cancer (HNPCC) characterized by cutaneous sebaceous tumors, keratoacanthomas and at least one visceral malignancy, most frequently gastrointestinal carcinoma. UMLS:C1321489 3.41.0