DiseaseID 28587
骨尤文肉瘤/骨外周原始神经外胚层肿瘤
Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor Of Bone
NCI2016_02D:A spectrum of malignant tumors arising from the bone and characterized morphologically by the presence of small round cells. Ewing sarcoma and peripheral primitive neuroectodermal tumor represent the ends of
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Disease: 1Symptom: 1Target: 12Links: 13
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 28587
- Core Entity Id
- 121155
- Source Entity Count
- 1
- Preferred Name
- Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor Of Bone
- Name Cn
- 骨尤文肉瘤/骨外周原始神经外胚层肿瘤
- Name Pinyin
- Gu You Wen Rou Liu / Gu Wai Zhou Yuan Shi Shen Jing Wai Pei Ceng Zhong Liu
- Name En
- Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor Of Bone
- Name Latin
- Bilingual Status
- complete
- Disease Type
- Umls Disease Type
- Disgenet Type
- Mesh Class
- Do Class
- Hpo Class
- Mesh Class Name
- Hpo Class Name
- Do Class Name
- Disease Definition
- NCI2016_02D:A spectrum of malignant tumors arising from the bone and 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. Pain and the presence of a mass are the most common clinical symptoms.
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor Of Bone
Role
preferred
Cross References
Trusted external identifiers retained for this final record.
Umls
C1333481
Sym Map
SMDE08529
Itcmdb Generated
ITX-DISEASE-7FBE97E966CE
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Disease Definition
NCI2016_02D:A spectrum of malignant tumors arising from the bone and 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. Pain and the presence of a mass are the most common clinical symptoms.