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extraskeletal myxoid chondrosarcoma
Disease Summary
Associated Targets (5)
Tbio
4
Tchem
1
Mondo Description A rare malignant soft tissue neoplasm of uncertain differentiation, characterized by the presence of chondroblast-like cells in a myxoid stroma and a multinodular growth pattern. The most common sites of involvement are the deep soft tissues of the extremities, particularly the thigh. It usually presents as an enlarging soft tissue mass. Patients may have long survivals, but local recurrences and metastases occur in approximately half of the cases. The most common site of metastasis is the lungs.
Disease Ontology Description An extraosseous chondrosarcoma that has_material_basis_in cells derived from transformed cells that produce cartilage and is characterized by a marked abundance of extracellular mucoid (myxoid) matrix.
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Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Mondo Disease Ontology.
Description from Disease Ontology
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
DOID:6496
MESH:C563195
NCIT:C27502
OMIM:612237
ONCOTREE:EMCHS
Orphanet:209916
SCTID:404079008
UMLS:C1275278
MONDO:0012825
High level summary of knowledge for a disease, including descriptions and datasource references.