A malignant cartilaginous matrix-producing mesenchymal neoplasm arising from the bone and soft tissue. It usually affects middle-aged to elderly adults. The pelvic bones, ribs, shoulder girdle, and long bones are the most common sites of involvement. Most chondrosarcomas arise de novo, but some may develop in a preexisting benign cartilaginous lesion. [ NCIT:C2946 ]
Synonyms: chondrosarcoma, malignant chondrosarcoma chondrosarcoma (disease) chondrosarcoma, somatic mutation
Term information
- MESH:D002813 (Orphanet:55880/e)
- DOID:3371 (MONDO:equivalentTo)
- OMIM:215300 (Orphanet:55880/e)
- ICD9:170.9 (MONDO:relatedTo)
- NANDO:2200050 (https://orcid.org/0000-0003-0011-764X)
- MedDRA:10008734 (Orphanet:55880/e)
- UMLS:C0008479 (MONDO:equivalentTo)
- HP:0006765 (MONDO:otherHierarchy)
- EFO:0000333 (MONDO:equivalentTo)
- ICDO:9220/3 (NCIT:C2946)
- ONCOTREE:CHS (MONDO:equivalentTo)
- NCIT:C2946 (MONDO:equivalentTo)
- Orphanet:55880 (OMIM:215300)
- GARD:6055 (MONDO:GARD)
- SCTID:443520009 (MONDO:equivalentTo)
- MEDGEN:3054 (MONDO:equivalentTo)
ordo_disorder, gard_rare, matrix_llm__is_cancer_other, matrix_txgnn_grouping_cancer_or_benign_tumor, harrisons_view_connective_tissue_disorder, matrix_llm__txgnn_other, mondo_top_grouping_member, matrix_included, nord_rare, mondo_top_grouping_cancer_or_benign_tumor, matrix_txgnn_grouping_member, rare, orphanet_rare, matrix_llm__is_glucose_dysfunction_other, otar, matrix_llm__tag_qualy_lost_other, matrix_llm__medical_specialization_other, mondo_top_grouping_hereditary_disease, 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, harrisons_view_hereditary_disease, mondo_top_grouping_connective_tissue_disorder
http://purl.obolibrary.org/obo/NCIT_C2946
http://www.ebi.ac.uk/efo/EFO_0000333
http://identifiers.org/medgen/3054
http://linkedlifedata.com/resource/umls/id/C0008479
http://identifiers.org/snomedct/443520009
http://www.orpha.net/ORDO/Orphanet_55880
http://identifiers.org/mesh/D002813
https://omim.org/entry/215300
http://purl.obolibrary.org/obo/DOID_3371