Ontology of Drug Adverse Events

Last uploaded: January 12, 2019
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Preferred Name

Rhabdomyosarcoma [Disease/Finding]
Synonyms
ID

http://evs.nci.nih.gov/ftp1/NDF-RT/NDF-RT.owl#N0000002628
code

C5434
Display_Name

Rhabdomyosarcoma
imported from

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

Rhabdomyosarcoma [Disease/Finding]
MeSH_CUI

M0019001
MeSH_Definition

A malignant solid tumor arising from mesenchymal tissues which normally differentiate to form striated muscle. It can occur in a wide variety of sites. It is divided into four distinct types: pleomorphic, predominantly in male adults; alveolar (RHABDOMYOSARCOMA, ALVEOLAR), mainly in adolescents and young adults; embryonal (RHABDOMYOSARCOMA, EMBRYONAL), predominantly in infants and children; and botryoidal, also in young children. It is one of the most frequently occurring soft tissue sarcomas and the most common in children under 15. (From Dorland, 27th ed; Holland et al., Cancer Medicine, 3d ed, p2186; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, pp1647-9)
MeSH_DUI

D012208
MeSH_Name

Rhabdomyosarcoma
NUI

N0000002628
prefixIRI

NDF-RT:N0000002628
prefLabel

Rhabdomyosarcoma [Disease/Finding]
RxNorm_CUI

1021776
SNOMED_CID

302847003
UMLS_CUI

C0035412
subClassOf

http://evs.nci.nih.gov/ftp1/NDF-RT/NDF-RT.owl#N0000002093
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