Preferred Name |
Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor |
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Synonyms |
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ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#Ewing_s_Sarcoma_Peripheral_Primitive_Neuroectodermal_Tumor |
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DEFINITION |
A spectrum of malignant tumors, affecting mostly males under age 20, characterized morphologically by the presence of small round cells. Ewing sarcoma and peripheral primitive neuroectodermal tumor represent the ends of a spectrum, with Ewing sarcoma lacking evidence of neural differentiation and the markers that characterize the peripheral primitive neuroectodermal tumor. Ewing sarcoma and peripheral primitive neuroectodermal tumor may share cytogenetic abnormalities, proto-oncogene expression, cell culture and immunohistochemical abnormalities. These tumors may occur in the soft tissues or the bones. Pain and the presence of a mass are the most common clinical symptoms. |
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FULL_SYN |
Ewing sarcoma family of tumors Ewing Family of Tumors Ewing's Family of Tumors Tumors of Ewing's Family Ewing's Sarcoma/Peripheral Primitive Neuroectodermal Tumor Ewing's Family of Tumours EFTs Tumors of the Ewing's Family |
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label |
Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor |
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prefixIRI |
Thesaurus:Ewing_s_Sarcoma_Peripheral_Primitive_Neuroectodermal_Tumor |
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prefLabel |
Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor |
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subClassOf |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#Embryonal_Neoplasm |
Delete | Mapping To | Ontology | Source |
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http://purl.obolibrary.org/obo/MONDO_0021038 | EFO | LOOM | |
http://purl.obolibrary.org/obo/MONDO_0021038 | MONDO | LOOM | |
http://purl.obolibrary.org/obo/NCIT_C27291 | BERO | LOOM | |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C27291 | NCIT | LOOM | |
http://purl.obolibrary.org/obo/MONDO_0021038 | DOVES | LOOM |