Chondrosarcoma is a malignant bone tumor arising from cartilaginous tissue, most frequently occuring at the ends of the femur and tibia, the proximal end of the humerus and the pelvis; and presenting with a palpable mass and progressive pain. Chondrosarcoma is usually slow growing at low histological grades and can be well managed by intralesional curettage or en-block wide resection.
This is just here as a test because I lose it
Term information
database cross reference
- UMLS:C0008479 (E (Exact mapping: the two concepts are equivalent))
- ICD-10:C49.9 (NTBT (ORPHA code's Narrower Term maps to a Broader Term))
- MeSH:D002813 (E (Exact mapping: the two concepts are equivalent))
- MedDRA:10008734 (E (Exact mapping: the two concepts are equivalent))
- OMIM:215300 (E (Exact mapping: the two concepts are equivalent))
Term relations
Subclass of:
- disease
- has_inheritance some unknown inheritance
- present_in some Europe and has_point_prevalence_range some 1-9 / 100 000
- part_of some Bone sarcoma
- has_inheritance some not genetically inherited
- present_in some Europe and has_lifetime_prevalence_range some 1-9 / 100 000 and has_lifetime_prevalence_average_value value 3.55
- has_age_of_onset some adult
- has_annual_incidence_range some 1-9 / 1 000 000 and present_in some Europe and has_annual_incidence_average_value value 0.24
Related from: