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.