osteosarcoma
http://purl.obolibrary.org/obo/MONDO_0009807
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 ]
Term info
- ICDO:9180/3 (NCIT:C9145)
- NCIT:C9145 (MONDO:equivalentTo)
- MESH:D012516 (https://orcid.org/0000-0003-1967-3726)
- ONCOTREE:OS (MONDO:equivalentTo)
- EFO:0000637 (MONDO:equivalentTo)
- DOID:3347 (MONDO:equivalentTo)
- HP:0002669 (MONDO:otherHierarchy)
https://github.com/monarch-initiative/mondo/issues/5537
osteosarcoma (disease)
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.
http://purl.obolibrary.org/obo/DOID_3347, http://identifiers.org/mesh/D012516, http://purl.obolibrary.org/obo/NCIT_C9145
bone tissue neoplasm
osteoid sarcoma, osteosarcoma, malignant, osteosarcoma (disease), sarcoma of osteoid, osteosarcoma, osteogenic sarcoma
MONDO:0009807