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National Drug File - Reference Terminology
Last uploaded:
July 6, 2018
| Id | http://purl.bioontology.org/ontology/NDFRT/N0000002628
http://purl.bioontology.org/ontology/NDFRT/N0000002628
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|---|---|
| Preferred Name | Rhabdomyosarcoma [Disease/Finding] |
| Synonyms |
Rhabdomyosarcoma
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| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| altLabel | Rhabdomyosarcoma
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|---|---|
| prefLabel | Rhabdomyosarcoma [Disease/Finding]
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| notation | N0000002628
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| May be treated by |
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| 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)
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| MESH UI | M0019001
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| subClassOf | |
| Semantic type UMLS property | |
| MeSH name | Rhabdomyosarcoma
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| NDFRT kind | DISEASE_KIND
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| type | |
| SNOMED CID | 302847003
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| tui | T191
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| NUI | N0000002628
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| cui | C0035412
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| MESH DUI | D012208
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| Delete | Subject | Author | Type | Created |
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