autosomal dominant disease Lynch syndrome Muir-Torre syndrome https://www.malacards.org/card/muir_torre_syndrome MONDO:0008018 Orphanet:587 icd11.foundation:229304403 MEDGEN:231157 multiple keratoacanthoma, Muir-Torre type Muir-Torre syndrome OMIM:158320 MRTES GARD:0006821 DOID:0050465 cutaneous sebaceous neoplasms and keratoacanthomas multiple with gastrointestinal and other carcinomas MedDRA:10063042 NCIT:C84905 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 SCTID:403824007 MESH:D055653 obsolete inherited skin tumor hereditary nonpolyposis colon cancer obsolete rare skin tumor or hamartoma benign tumor of palpebral epidermis obsolete palpebral sebaceous gland tumor