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Li-Fraumeni Syndrome
Hierarchy: | ∟ ∟ ∟ ∟ Li-Fraumeni Syndrome 20 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Li-Fraumeni Syndrome 20 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Li-Fraumeni Syndrome 20 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ |
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historyNote*: | 92
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publicMeSHNote*: | 92
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Scope note: | Rare autosomal dominant syndrome characterized by mesenchymal and epithelial neoplasms at multiple sites. MUTATION of the p53 tumor suppressor gene, a component of the DNA DAMAGE response pathway, apparently predisposes family members who inherit it to develop certain cancers. The spectrum of cancers in the syndrome was shown to include, in addition to BREAST CANCER and soft tissue sarcomas (SARCOMA); BRAIN TUMORS; OSTEOSARCOMA; LEUKEMIA; and ADRENOCORTICAL CARCINOMA.
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activeMeSHYear*: | |
dateCreated*: | 1991-06-21X |
dateEstablished*: | 1992-01-01X |
dateRevised*: | 2005-06-30X |
recordAuthorizer*: | sjnX |
recordMaintainer*: | nnsX |
recordOriginator*: | AGSX |
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Labels and equivalent concepts: | Li-Fraumenin syöpäoireyhtymä (fi) XSíndrome de Li-Fraumeni (es) σύνδρομο Li-Fraumeni (el) Li-Fraumeni-Syndrom (de) Li-Fraumeni syndrom (cs) |
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