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- B00e9d012b20c2de03831c448d6389e5c hasDbXref "NCIT:C3879" @default.
- B00e9d012b20c2de03831c448d6389e5c type Axiom @default.
- B00e9d012b20c2de03831c448d6389e5c annotatedProperty IAO_0000115 @default.
- B00e9d012b20c2de03831c448d6389e5c annotatedSource MONDO_0015277 @default.
- B00e9d012b20c2de03831c448d6389e5c annotatedTarget "A neuroendocrine carcinoma arising from the C-cells of the thyroid gland. It is closely associated with multiple endocrine neoplasia syndromes. Approximately 10% to 20% of medullary thyroid carcinomas are familial. Patients usually present with a thyroid nodule that is painless and firm. In the majority of cases nodal involvement is present at diagnosis. Surgery is the preferred treatment for both primary lesions and recurrences. This carcinoma is generally not very sensitive to radiation and almost unresponsive to chemotherapy." @default.