bone osteosarcoma
http://purl.obolibrary.org/obo/MONDO_0002629
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 ]
Term info
- SCTID:307576001 (MONDO:equivalentTo)
- Orphanet:668 (OMIM:259500)
- MedDRA:10031291 (Orphanet:668/e)
- OMIM:259500 (Orphanet:668/e)
- GARD:0007284 (MONDO:equivalentTo)
- NCIT:C53707 (MONDO:equivalentTo)
- ICD9:170.9 (MONDO:relatedTo)
- DOID:3376 (MONDO:equivalentTo)
ordo_disease
https://github.com/monarch-initiative/mondo/issues/5537, https://github.com/monarch-initiative/mondo/issues/4521
http://identifiers.org/meddra/10031291
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.
https://omim.org/entry/259500, http://purl.obolibrary.org/obo/DOID_3376, http://identifiers.org/snomedct/307576001, http://purl.obolibrary.org/obo/NCIT_C53707, http://purl.obolibrary.org/obo/Orphanet_668
osteosarcoma, somatic, primary osteosarcoma of bone, bone osteosarcoma, osteosarcoma of bone, osteosarcoma, somatic mutation
MONDO:0002629