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Rhabdomyosarcoma
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Annotation: | GEN; prefer specifics; /blood supply /chem /second /secret /ultrastruct permitted; coord IM with precoord organ/neopl term (IM)
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Scope note: | 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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activeMeSHYear*: | |
dateCreated*: | 1999-01-01X |
dateRevised*: | 1997-06-20X |
recordAuthorizer*: | SJNX |
recordMaintainer*: | TGCX |
recordOriginator*: | NLMX |
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Labels and equivalent concepts: | Rabdomyosarkooma (fi) XRhabdomyosarkooma (fi, replaced) Poikkijuovaislihassarkooma (fi, replaced) Rabdomyosarkom (sv) Rhabdomyosarcoma (la-FI, replaced) |
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