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An Entity of Type : owl:Class, within Data Space : linked.opendata.cz associated with source document(s)

AttributesValues
rdf:type
rdfs:label
  • Sarcoma
equivalentClass
Has_NICHD_Parent
Concept_In_Subset
Semantic_Type
  • Neoplastic Process
Preferred_Name
  • Sarcoma
UMLS_CUI
  • C1261473
Contributing_Source
  • CDISC
  • NICHD
ALT_DEFINITION
  • A cancer of the bone, cartilage, fat, muscle, blood vessels, or other connective or supportive tissue.NCI-GLOSS
  • A malignant mesenchymal tumor for which a distinct line of differentiation cannot be determined. This term may be used for small biopsy specimens for which adequate tissue is not present for definitive classification.NCI
  • A malignant mesenchymal neoplasm. A general term for which the transformed cell type has not been specified.CDISC
ICD-O-3_Code
  • 8800/3
Neoplastic_Status
  • Malignant
Legacy_Concept_Name
  • Sarcoma_of_the_Soft_Tissue_and_Bone
FULL_SYN
  • Sarcoma of the Soft Tissue and BoneSYNCI
  • SARCOMA OF THE SOFT TISSUE AND BONESYCDISC
  • MESENCHYMAL TUMOR, MALIGNANTSYCDISC
  • sarcomaPTNCI-GLOSSCDR0000045562
  • SarcomaSYNCITCGA
  • SarcomaPTNCI
  • SARCOMA, MALIGNANTPTCDISC
  • SARCOMASYCDISC
  • Sarcoma of Soft Tissue and BoneSYNCI
  • SarcomaPTNICHD
  • SARCOMA OF SOFT TISSUE AND BONESYCDISC
DEFINITION
  • A usually aggressive malignant mesenchymal cell tumor most commonly arising from muscle, fat, fibrous tissue, bone, cartilage, and blood vessels. Sarcomas occur in both children and adults. The prognosis depends largely on the degree of differentiation (grade) of the tumor. Representative subtypes are liposarcoma, leiomyosarcoma, osteosarcoma, and chondrosarcoma.NCI
code
  • C9118
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