loading...| Preferred Name |
Ewing Sarcoma |
| ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C4817 |
| ALT_DEFINITION |
A malignant neoplasm of the bone, or the soft tissue adjacent to bone, that is comprised of primitive neuroectodermal cells. A type of cancer that forms in bone or soft tissue. |
| code |
C4817 |
| Concept_In_Subset |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C116977 |
| Contributing_Source |
CTRP NICHD MedDRA |
| DEFINITION |
A small round cell tumor that lacks morphologic, immunohistochemical, and electron microscopic evidence of neuroectodermal differentiation. It represents one of the two ends of the spectrum called Ewing sarcoma/peripheral neuroectodermal tumor. It affects mostly males under age 20, and it can occur in soft tissue or bone. Pain and the presence of a mass are the most common clinical symptoms. |
| Display_Name |
Ewing Sarcoma |
| FULL_SYN |
Ewing's Tumor Ewing's Sarcoma ES |
| Has_NICHD_Parent | |
| ICD-O-3_Code |
9260/3 |
| label |
Ewing Sarcoma |
| Legacy_Concept_Name |
Ewing_s_Sarcoma |
| Neoplastic_Status |
Malignant |
| NICHD_Hierarchy_Term |
Ewing Sarcoma |
| Preferred_Name |
Ewing Sarcoma |
| prefixIRI |
C4817 |
| prefLabel |
Ewing Sarcoma |
| Semantic_Type |
Neoplastic Process |
| UMLS_CUI |
C0553580 |
| subClassOf |