A usually aggressive malignant bone-forming mesenchymal neoplasm, predominantly affecting adolescents and young adults. It usually involves bones and less frequently extraosseous sites. It often involves the long bones (particularly distal femur, proximal tibia, and proximal humerus). Pain with or without a palpable mass is the most frequent clinical symptom. It may spread to other anatomic sites, particularly the lungs. [ NCIT:C9145 ]
Synonyms: osteoid sarcoma osteosarcoma, malignant osteosarcoma (disease) sarcoma of osteoid osteosarcoma osteogenic sarcoma
Term information
- ICDO:9180/3 (NCIT:C9145)
- NANDO:2200048 (https://orcid.org/0000-0003-0011-764X)
- MEDGEN:10501 (MONDO:equivalentTo)
- EFO:0000637 (MONDO:equivalentTo)
- MESH:D012516 (https://orcid.org/0000-0003-1967-3726)
- ONCOTREE:OS (MONDO:equivalentTo)
- DOID:3347 (MONDO:equivalentTo)
- HP:0002669 (MONDO:otherHierarchy)
- UMLS:C0029463 (MONDO:equivalentTo)
- NCIT:C9145 (MONDO:equivalentTo)
otar
http://purl.obolibrary.org/obo/DOID_3347
http://linkedlifedata.com/resource/umls/id/C0029463
http://identifiers.org/medgen/10501
http://identifiers.org/mesh/D012516
http://purl.obolibrary.org/obo/NCIT_C9145