National Drug File - Reference Terminology

Last uploaded: July 6, 2018
Id http://purl.bioontology.org/ontology/NDFRT/N0000003715
http://purl.bioontology.org/ontology/NDFRT/N0000003715
Preferred Name

Neuroectodermal Tumors, Primitive, Peripheral [Disease/Finding]
Synonyms
(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
Type http://www.w3.org/2002/07/owl#Class

All Properties

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
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prefLabel
Neuroectodermal Tumors, Primitive, Peripheral [Disease/Finding]
notation
N0000003715
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 UI
M0027470
subClassOf
Semantic type UMLS property
MeSH name
Neuroectodermal Tumors, Primitive, Peripheral
NDFRT kind
DISEASE_KIND
type
SNOMED CID
253096008
254764001
tui
T191
NUI
N0000003715
cui
C0684337
MESH DUI
D018241
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