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bone osteosarcoma

Go to external page 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 ]

Synonyms: osteosarcoma, somatic primary osteosarcoma of bone bone osteosarcoma osteosarcoma of bone osteosarcoma, somatic mutation

This is just here as a test because I lose it

Term information

database cross reference
  • OMIM:259500 (Orphanet:668/e)
  • DOID:3376 (MONDO:equivalentTo)
  • MedDRA:10031291 (Orphanet:668/e)
  • NCIT:C53707 (MONDO:equivalentTo)
  • GARD:7284 (MONDO:GARD)
  • UMLS:C0585442 (MONDO:equivalentTo)
  • MEDGEN:108437 (MONDO:equivalentTo)
  • SCTID:307576001 (MONDO:equivalentTo)
  • ICD9:170.9 (MONDO:relatedTo)
  • Orphanet:668 (OMIM:259500)
Subsets

gard_rare, ordo_disorder, otar, rare, nord_rare, orphanet_rare

closeMatch

http://identifiers.org/meddra/10031291

exactMatch

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

id

MONDO:0002629

term tracker item

https://github.com/monarch-initiative/mondo/issues/5537

https://github.com/monarch-initiative/mondo/issues/4521

Term relations

Subclass of: