Ontology of Drug Adverse Events

Last uploaded: January 12, 2019
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Preferred Name

Neuroblastoma [Disease/Finding]
Synonyms
ID

http://evs.nci.nih.gov/ftp1/NDF-RT/NDF-RT.owl#N0000002167
code

C4512
Display_Name

Neuroblastoma
imported from

http://evs.nci.nih.gov/ftp1/NDF-RT/NDF-RT.owl
label

Neuroblastoma [Disease/Finding]
MeSH_CUI

M0014699
MeSH_Definition

A common neoplasm of early childhood arising from neural crest cells in the sympathetic nervous system, and characterized by diverse clinical behavior, ranging from spontaneous remission to rapid metastatic progression and death. This tumor is the most common intraabdominal malignancy of childhood, but it may also arise from thorax, neck, or rarely occur in the central nervous system. Histologic features include uniform round cells with hyperchromatic nuclei arranged in nests and separated by fibrovascular septa. Neuroblastomas may be associated with the opsoclonus-myoclonus syndrome. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, pp2099-2101; Curr Opin Oncol 1998 Jan;10(1):43-51)
MeSH_DUI

D009447
MeSH_Name

Neuroblastoma
NUI

N0000002167
prefixIRI

NDF-RT:N0000002167
prefLabel

Neuroblastoma [Disease/Finding]
RxNorm_CUI

1026096
SNOMED_CID

87364003
UMLS_CUI

C0027819
subClassOf

http://evs.nci.nih.gov/ftp1/NDF-RT/NDF-RT.owl#N0000003715
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