A usually aggressive malignant neoplasm of the soft tissue or bone. It arises from muscle, fat, fibrous tissue, bone, cartilage, and blood vessels. Sarcomas occur in both children and adults. The prognosis depends largely on the degree of differentiation (grade) of the neoplasm. Representative subtypes are liposarcoma, leiomyosarcoma, osteosarcoma, and chondrosarcoma. [ NCIT:C9118 ]
Synonyms: sarcoma, malignant sarcoma sarcoma of soft tissue and bone sarcoma of the soft tissue and bone mesenchymal tumor, malignant
Term information
- ICD9:171.6 (EFO:0000691)
- ICD9:171.7 (EFO:0000691)
- ICD9:171.8 (EFO:0000691)
- ICD9:171.4 (EFO:0000691)
- MESH:D012509 (MONDO:equivalentTo)
- ICDO:8800/3 (NCIT:C9118)
- UMLS:C1261473 (MONDO:equivalentTo)
- SCTID:424413001 (MONDO:equivalentTo)
- ICD9:171.3 (EFO:0000691)
- ICD9:171.5 (EFO:0000691)
- DOID:1115 (MONDO:equivalentTo)
- ICD9:171.2 (EFO:0000691)
- ICD9:171.0 (EFO:0000691)
- ICD9:171.9 (MONDO:relatedTo)
- NCIT:C9118 (MONDO:equivalentTo)
- MEDGEN:224714 (MONDO:equivalentTo)
- EFO:0000691 (MONDO:equivalentTo)
- ICD9:171 (EFO:0000691)
matrix_llm__is_cancer_other, matrix_txgnn_grouping_cancer_or_benign_tumor, matrix_llm__is_glucose_dysfunction_other, matrix_excluded, otar, matrix_llm__tag_qualy_lost_other, matrix_llm__medical_specialization_other, mondo_top_grouping_member, matrix_llm__txgnn_other, matrix_llm__tag_existing_treatment_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, mondo_top_grouping_cancer_or_benign_tumor, matrix_txgnn_grouping_member, harrisons_view_cancer_or_benign_tumor, harrisons_view_member
http://purl.obolibrary.org/obo/DOID_1115
http://purl.obolibrary.org/obo/NCIT_C9118
http://identifiers.org/medgen/224714
http://identifiers.org/mesh/D012509
http://linkedlifedata.com/resource/umls/id/C1261473
http://identifiers.org/snomedct/424413001
http://www.ebi.ac.uk/efo/EFO_0000691