loading...| Preferred Name |
Neuroectodermal Tumors, Primitive, Peripheral [Disease/Finding] |
|
| Synonyms |
(pPNET) Peripheral Primitive Neuroectodermal Tumors Neuroepithelioma, Peripheral |
|
| ID |
http://purl.bioontology.org/ontology/NDFRT/N0000003715 |
|
| altLabel |
(pPNET) Peripheral Primitive Neuroectodermal Tumors Neuroectodermal Tumors, Primitive, Peripheral Neuroectodermal Neoplasm, Peripheral Primitive Peripheral Primitive Neuroectodermal Neoplasm Primitive Neuroectodermal Tumor, Extracranial Neuroectodermal Tumor, Peripheral Peripheral Primitive Neuroectodermal Tumors Neuroectodermal Tumor, Peripheral Primitive Extracranial Primitive Neuroectodermal Tumor Neuroepithelioma, Peripheral |
|
| cui |
C0684337 |
|
| MESH DEFINITION |
A group of highly cellular primitive round cell neoplasms which occur extracranially in soft tissue and bone and are derived from embryonal neural crest cells. These tumors occur primarily in children and adolescents and share a number of characteristics with EWING SARCOMA. |
|
| MESH DUI |
D018241 |
|
| MeSH name |
Neuroectodermal Tumors, Primitive, Peripheral |
|
| MESH UI |
M0027470 |
|
| NDFRT kind |
DISEASE_KIND |
|
| notation |
N0000003715 |
|
| NUI |
N0000003715 |
|
| prefLabel |
Neuroectodermal Tumors, Primitive, Peripheral [Disease/Finding] |
|
| SNOMED CID |
253096008 254764001 |
|
| tui |
T191 |
|
| subClassOf |