A usually aggressive malignant bone-forming mesenchymal neoplasm arising from the bone. It may arise de novo or from a pre-existing lesion of the bone. Pain and a palpable mass are the most frequent clinical sign and symptom. It may spread to other anatomic sites, particularly the lungs. [ NCIT:C53707 ]
Synonyms: osteosarcoma, somatic primary osteosarcoma of bone bone osteosarcoma osteosarcoma of bone osteosarcoma, somatic mutation
Term information
- MEDGEN:108437 (MONDO:equivalentTo)
- DOID:3376 (MONDO:equivalentTo)
- SCTID:307576001 (MONDO:equivalentTo)
- ICD9:170.9 (MONDO:relatedTo)
- NCIT:C53707 (MONDO:equivalentTo)
- OMIM:259500 (Orphanet:668/e)
- MedDRA:10031291 (Orphanet:668/e)
- Orphanet:668 (OMIM:259500)
- GARD:7284 (MONDO:GARD)
- UMLS:C0585442 (MONDO:equivalentTo)
gard_rare, matrix_llm__is_cancer_other, ordo_disorder, matrix_txgnn_grouping_cancer_or_benign_tumor, harrisons_view_connective_tissue_disorder, mondo_top_grouping_member, matrix_llm__txgnn_other, nord_rare, matrix_included, mondo_top_grouping_cancer_or_benign_tumor, matrix_txgnn_grouping_member, rare, harrisons_view_musculoskeletal_system_disorder, orphanet_rare, matrix_llm__is_glucose_dysfunction_other, otar, matrix_llm__tag_qualy_lost_other, matrix_llm__medical_specialization_other, mondo_top_grouping_musculoskeletal_system_disorder, matrix_llm__tag_existing_treatment_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, harrisons_view_cancer_or_benign_tumor, harrisons_view_member, mondo_top_grouping_connective_tissue_disorder
http://linkedlifedata.com/resource/umls/id/C0585442
https://omim.org/entry/259500
http://purl.obolibrary.org/obo/DOID_3376
http://www.orpha.net/ORDO/Orphanet_668
http://identifiers.org/snomedct/307576001
http://identifiers.org/medgen/108437
http://purl.obolibrary.org/obo/NCIT_C53707
https://github.com/monarch-initiative/mondo/issues/5537
https://github.com/monarch-initiative/mondo/issues/4521