sarcoma
http://purl.obolibrary.org/obo/MONDO_0005089
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 ]
Term info
- ICD9:171.5 (EFO:0000691)
- NCIT:C9118 (MONDO:equivalentTo)
- SCTID:424413001 (MONDO:equivalentTo)
- ICD9:171.7 (EFO:0000691)
- MESH:D012509 (MONDO:equivalentTo)
- ICDO:8800/3 (NCIT:C9118)
- DOID:1115 (MONDO:equivalentTo)
- ICD9:171.8 (EFO:0000691)
- ICD9:171.9 (MONDO:relatedTo)
- ICD9:171.2 (EFO:0000691)
- ICD9:171.6 (EFO:0000691)
- GARD:0012018 (MONDO:equivalentTo)
- ICD9:171 (EFO:0000691)
- ICD9:171.0 (EFO:0000691)
- ICD9:171.4 (EFO:0000691)
- ICD9:171.3 (EFO:0000691)
- EFO:0000691 (MONDO:equivalentTo)
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.
http://purl.obolibrary.org/obo/DOID_1115, http://purl.obolibrary.org/obo/NCIT_C9118, http://identifiers.org/mesh/D012509, http://identifiers.org/snomedct/424413001
sarcoma, malignant, sarcoma, sarcoma of the soft tissue and bone, sarcoma of soft tissue and bone, mesenchymal tumor, malignant
tumor of soft tissue and skeleton
MONDO:0005089